Riboflavin Missence Mutation Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedClassFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
PRODHchr221890589818905899rs3970559+GA/Gsinglemissense101000GENOMES,BCM_SSAHASNP,CLINSEQ_SNP,EXOME_CHIP,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,SC_SNP,SSMP,TSC-CSHL,20.011183
PRODHchr221890596318905964rs2904552+CC/Tsinglemissense131000GENOMES,ABI,CLINSEQ_SNP,ENSEMBL,EXOME_CHIP,HUMANGENOME_JCVI,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PJP,SSAHASNP,TISHKOFF,TSC-CSHL,20.929709
PRODHchr221890597618905977rs2238731+CC/Tsinglemissense91000GENOMES,CLINSEQ_SNP,EXOME_CHIP,NHLBI-ESP,SC_SNP,SI_EXO,SSMP,TISHKOFF,YUSUKE,20.955779
PRODHchr221891035418910355rs5747933+GG/Tsinglemissense81000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SC_SNP,SEATTLESEQ,SSMP,20.950928
PRODHchr221891267618912677rs11913840+CC/Tsinglemissense61000GENOMES,CLINSEQ_SNP,CSHL-HAPMAP,EXOME_CHIP,NHLBI-ESP,SSMP,20.945209
PRODHchr221892362818923629rs146648839+CC/Tsingleintron,missense31000GENOMES,EXOME_CHIP,NHLBI-ESP,20.960514
PRODHchr221892371218923713rs3815655+GA/Gsingleintron,missense61000GENOMES,COMPLETE_GENOMICS,EXOME_CHIP,HGSV,SSMP,YUSUKE,20.125229
PRODHchr221892374418923745rs2008720-GA/Csingleintron,missense161000GENOMES,ABI,BCM-HGSC-SUB,BGI,CSHL-HAPMAP,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,PJP,SEQUENOM,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,YUSUKE,20.543462
TXNRD2chr221986821719868218rs1139793+AA/Gsinglemissense311000GENOMES,AFFY,AFFY_GWHS,APPLERA_GI,BCMHGSC_JDW,BGI,BL,BUSHMAN,CGAP-GAI,CGM_KYOTO,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,LEE,NHLBI-ESP,PERLEGEN,PJP,SC_SNP,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,YUSUKE,50.247231
TXNRD2chr221987089719870898rs61736941+GA/Gsinglemissense2CORNELL,NHLBI-ESP,20.013513
TXNRD2chr221988298319882984rs5992495+TG/Tsinglemissense201000GENOMES,ABI,AFFY,BUSHMAN,CLINSEQ_SNP,CORNELL,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PJP,SC_SNP,SEATTLESEQ,SSMP,TISHKOFF,20.232925
TXNRD2chr221990328919903290rs61736929+CC/Gsinglemissense91000GENOMES,CLINSEQ_SNP,CORNELL,EXOME_CHIP,GOLDSTEINLAB,ILLUMINA,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.963597
TXNRD2chr221990709819907099rs5748469+CA/Csinglemissense201000GENOMES,BCM-HGSC-SUB,BGI,BL,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,EXOME_CHIP,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SC_SNP,SEATTLESEQ,SSMP,TISHKOFF,20.463202
ACAD9chr3128622921128622922rs115532916+GA/C/GsinglencRNA,missense61000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,20.013100
ACAD9chr3128627886128627887rs4494951+GA/GsinglencRNA,missense111000GENOMES,ABI,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,DEVINE_LAB,EXOME_CHIP,ILLUMINA,NHLBI-ESP,PERLEGEN,SC_JCM,20.011064
ACAD9chr3128634036128634037rs113633667+CC/Tsinglemissense41000GENOMES,CLINSEQ_SNP,COMPLETE_GENOMICS,ILLUMINA,20.989467
ETFDHchr4159601675159601676rs11559290+CC/Tsinglemissense261000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,MGC_GENOME_DIFF,NHLBI-ESP,PERLEGEN,PJP,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,20.323065
MTRRchr578668207866821rs16879259+TC/Tsingleintron,missense131000GENOMES,AFFY,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.065686
MTRRchr578680297868030rs2966952+TC/Tsingleintron,near-gene-5,missense271000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.834742
MTRRchr578709727870973rs1801394+AA/Gsinglenear-gene-5,missense291000GENOMES,ABI,AFFY,APPLERA_GI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGBASE,HUMANGENOME_JCVI,ILLUMINA,KYUGEN,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PHARMGKB_PPII,PJP,SEATTLESEQ,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.572342
MTRRchr578781787878179rs1532268-CA/Gsinglemissense271000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CORNELL,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SNP500CANCER,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,YUSUKE,20.295599
MTRRchr578784237878424rs2303080+TA/Tsinglemissense131000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,HGSV,ILLUMINA,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SSMP,YUSUKE,20.030610
MTRRchr578859067885907rs10064631+CC/Gsinglemissense121000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,SEATTLESEQ,TISHKOFF,WI_SSAHASNP,20.947887
MTRRchr578859587885959rs162036+AA/Gsinglemissense231000GENOMES,ABI,AFFY,BCM_SSAHASNP,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SC_JCM,SEATTLESEQ,SSMP,TISHKOFF,20.774035
MTRRchr578893037889304rs2287780+CC/Tsinglemissense161000GENOMES,APPLERA_GI,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,SEATTLESEQ,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.950050
MTRRchr578915057891506rs16879334+CC/Gsinglemissense111000GENOMES,AFFY,CLINSEQ_SNP,EXOME_CHIP,GMI,ILLUMINA,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.956700
MTRRchr578971907897191rs10380+CC/Tsinglemissense251000GENOMES,AFFY,APPLERA_GI,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,EXOME_CHIP,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,LEE,NHLBI-ESP,PERLEGEN,PHARMGKB_PPII,PJP,SEATTLESEQ,SEQUENOM,SI_EXO,SNP500CANCER,SSMP,TISHKOFF,YUSUKE,20.811339
SDHAchr5223629223630rs1061518+TG/Tsinglemissense1LEE,20.100000
SDHAchr5223645223646rs34635677+AA/Tsinglemissense71000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,LARRIBA,NHLBI-ESP,SI_EXO,20.967633
SDHAchr5233692233693rs1062468+GA/Gsinglemissense2LEE,SEQUENOM,20.120000
SDHAchr5236618236619rs201741295+TC/Tsinglemissense1CLINSEQ_SNP,20.015500
SDHAchr5236627236628rs201139275+CC/Tsinglemissense2CLINSEQ_SNP,EXOME_CHIP,20.962500
SDHAchr5236648236649rs76896145+CC/Tsinglemissense41000GENOMES,CLINSEQ_SNP,EXOME_CHIP,GMI,20.888782
SDHAchr5236675236676rs138277996+GA/Gsinglemissense31000GENOMES,CLINSEQ_SNP,EXOME_CHIP,20.071620
SDHAchr5236677236678rs111387770+GA/Gsinglemissense51000GENOMES,BCM-HGSC-SUB,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,20.122482
SDHAchr5254511254512rs1126568+GA/Gsinglemissense31000GENOMES,LEE,SEQUENOM,20.014233
SDHAchr5254598254599rs6960+AA/Tsinglemissense9BCMHGSC_JDW,BCM_SSAHASNP,CGAP-GAI,CLINSEQ_SNP,EXOME_CHIP,LEE,NHLBI-ESP,SSMP,WI_SSAHASNP,20.864915
SDHAchr5256508256509rs6962+GA/Gsinglemissense191000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,HGSV,ILLUMINA,LARRIBA,LEE,NHLBI-ESP,PJP,SEATTLESEQ,SSMP,TISHKOFF,WI_SSAHASNP,20.177438
ENPP1chr6132129362132129363rs200362492+CA/Csinglemissense11000GENOMES,20.046832
ENPP1chr6132172367132172368rs1044498+AA/Csinglemissense321000GENOMES,ABI,AFFY,APPLERA_GI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,CGAP-GAI,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGBASE,IBARROSO,ILLUMINA,ILLUMINA-UK,IMCJ-GDT,LEE,NHLBI-ESP,OMICIA,OMIM-CURATED-RECORDS,PERLEGEN,PJP,SC_SNP,SEATTLESEQ,SHGC,SSAHASNP,SSMP,TISHKOFF,20.654913
ENPP1chr6132198238132198239rs79079368+CC/Gsinglemissense71000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,20.986298
ENPP1chr6132201075132201076rs115371819+GA/Gsinglemissense61000GENOMES,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.013580
ENPP1chr6132206078132206079rs28933977+CC/Tsinglemissense91000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,PERLEGEN,SSMP,20.975029
ENPP3chr6132030136132030137rs200752094+TA/Tsingleintron,missense1CLINSEQ_SNP,20.011500
ENPP3chr6132030559132030560rs200750273+GA/Gsingleintron,missense3CLINSEQ_SNP,EXOME_CHIP,GMI,20.065065
ENPP3chr6132030965132030966rs202051647+GC/Gsingleintron,missense4CLINSEQ_SNP,EXOME_CHIP,GMI,SSMP,20.095500
ENPP3chr6132031140132031141rs202093315+AA/Csingleintron,missense1CLINSEQ_SNP,20.986500
ENPP3chr6132045179132045180rs58038770+AA/Gsinglemissense81000GENOMES,CLINSEQ_SNP,EXOME_CHIP,HGSV,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SEATTLESEQ,20.987960
ENPP3chr6132047244132047245rs9321309+GA/Gsinglemissense131000GENOMES,AFFY,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,WI_SSAHASNP,20.022033
ENPP3chr6132058567132058568rs77610153+CC/Gsinglemissense41000GENOMES,EXOME_CHIP,ILLUMINA,NHLBI-ESP,20.984903
ENPP3chr6132061419132061420rs17601580+GA/Gsinglemissense101000GENOMES,AFFY,BCM-HGSC-SUB,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SSMP,20.103232
IYDchr6150710631150710632rs111758467+AA/Gsinglemissense61000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,NHLBI-ESP,TISHKOFF,20.987964
IYDchr6150713557150713558rs35217099-CC/Gsinglemissense1APPLERA_GI,20.014706
IYDchr6150716532150716533rs4407723+TA/Tsingleintron,missense191000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,DEVINE_LAB,ENSEMBL,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,20.195807
IYDchr6150716611150716612rs73617694+CC/Tsingleintron,missense51000GENOMES,COMPLETE_GENOMICS,ILLUMINA,NHLBI-ESP,TISHKOFF,20.986697
IYDchr6150716695150716696rs612421-TA/Gsingleintron,missense261000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KWOK,NHLBI-ESP,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.133209
IYDchr6150716696150716697rs4479949+GA/Gsingleintron,missense121000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,CLINSEQ_SNP,ENSEMBL,EXOME_CHIP,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SC_JCM,SSMP,20.153534
IYDchr6150719239150719240rs73619510+GA/Gsinglecoding-synon,missense,untranslated-371000GENOMES,COMPLETE_GENOMICS,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.016934
IYDchr6150719313150719314rs36063028-GC/Tsinglemissense,untranslated-3131000GENOMES,APPLERA_GI,BUSHMAN,CLINSEQ_SNP,EXOME_CHIP,HGSV,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,PERLEGEN,SEATTLESEQ,SSMP,TISHKOFF,20.931895
DLDchr7107531728107531729rs75077312+GA/Gsinglemissense61000GENOMES,BUSHMAN,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,20.010253
DLDchr7107545413107545414rs62001027+CC/Tsinglemissense1CORNELL,20.986111
DLDchr7107569961107569962rs35915664+AA/Gsinglemissense71000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,NHLBI-ESP,SEATTLESEQ,20.984689
PORchr77561438575614386rs56010266+TA/Csinglemissense1XBZ4050KLSIC,20.050505
PORchr77561500575615006rs1057868+CC/Tsinglemissense191000GENOMES,BCM-HGSC-SUB,BL,BUSHMAN,EGP_SNPS,EXOME_CHIP,GMI,ILLUMINA,LEE,MGC_GENOME_DIFF,NHLBI-ESP,PHARMGKB_AB_DME,PHARMGKB_PMT,SEQUENOM,SNP500CANCER,SSMP,TISHKOFF,WIAF-CSNP,YUSUKE,20.723404
PORchr77561530075615301rs56256515+TC/Tsinglemissense3EXOME_CHIP,NHLBI-ESP,XBZ4050KLSIC,20.020202
SLC25A32chr8104417044104417045rs17803441+CC/Tsingleintron,ncRNA,missense91000GENOMES,AFFY,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,20.952397
SLC25A32chr8104427358104427359rs3134295+AA/CsinglencRNA,missense,untranslated-5251000GENOMES,AFFY,BCM-HGSC-SUB,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,EXOME_CHIP,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,KYUGEN,NHLBI-ESP,PERLEGEN,PJP,SC_JCM,SEATTLESEQ,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.537010
SLC52A2chr8145577898145577899rs116055973+CC/Tsingleintron,ncRNA,missense21000GENOMES,TISHKOFF,20.982578
SLC52A2chr8145579703145579704rs61747069+TC/Tsinglenear-gene-5,missense2CORNELL,NHLBI-ESP,20.016667
SLC52A2chr8145579791145579792rs2272665+CA/Csinglenear-gene-5,missense3ILLUMINA,KRIBB_YJKIM,YUSUKE,20.017913
SLC52A2chr8145579961145579962rs77494279+CC/Tsinglenear-gene-5,missense3CLINSEQ_SNP,ENSEMBL,EXOME_CHIP,20.932166
SLC52A2chr8145580534145580535rs61746974+CC/Gsinglenear-gene-5,missense91000GENOMES,CLINSEQ_SNP,CORNELL,EXOME_CHIP,GOLDSTEINLAB,ILLUMINA,NHLBI-ESP,SEATTLESEQ,TISHKOFF,20.935919
SLC52A2chr8145581949145581950rs200282665+CC/Gsinglenear-gene-5,missense21000GENOMES,NHLBI-ESP,20.985308
AIFM1chrX129281845129281846rs61730894+CC/Tsingleintron,missense1CORNELL,20.987179