Cobalamin Intron Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
LMBRD1chr67050166070501661rs9446161+TG/Tintron51000GENOMES,BL,SC_SNP,SSMP,TISHKOFF,20.074146
LMBRD1chr67038905370389054rs9454867+AA/Gintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_SNP,SSMP,TISHKOFF,20.120104
LMBRD1chr67038980970389810rs9454868+CA/Cintron81000GENOMES,AFFY,HGSV,KRIBB_YJKIM,PERLEGEN,SC_SNP,SSMP,TISHKOFF,20.071921
LMBRD1chr67042053870420539rs9454873+CC/Tintron51000GENOMES,BL,SC_SNP,SSMP,TISHKOFF,20.93652
LMBRD1chr67042662070426621rs9454876+GA/Gintron31000GENOMES,SC_SNP,SSMP,20.071649
LMBRD1chr67042792270427923rs9454877+GA/Gintron31000GENOMES,ILLUMINA-UK,SC_SNP,20.026944
LMBRD1chr67043575170435752rs9454878+GG/Tintron31000GENOMES,SC_SNP,TISHKOFF,20.989899
LMBRD1chr67045544570455446rs9454880+GA/Gintron61000GENOMES,BL,GMI,SC_SNP,SSMP,TISHKOFF,20.069006
LMBRD1chr67045678270456783rs9454881+GA/Gintron71000GENOMES,BL,GMI,PERLEGEN,SC_SNP,SSMP,TISHKOFF,20.07069
LMBRD1chr67045834470458345rs9454882+GA/Gintron31000GENOMES,SC_SNP,TISHKOFF,20.06664
LMBRD1chr67046879070468791rs9454887+AA/Gintron71000GENOMES,BL,GMI,PERLEGEN,SC_SNP,SSMP,TISHKOFF,20.930417
LMBRD1chr67047511970475120rs9454889+CA/Cintron61000GENOMES,BL,GMI,SC_SNP,SSMP,TISHKOFF,20.068612
LMBRD1chr67048930770489308rs9454890+AA/Gintron61000GENOMES,BL,GMI,SC_SNP,SSMP,TISHKOFF,20.931782
LMBRD1chr67049421270494213rs9454892+CC/Tintron81000GENOMES,BL,GMI,ILLUMINA,PERLEGEN,SC_SNP,SSMP,TISHKOFF,20.903791
LMBRD1chr67049606070496061rs9454893+CC/Tintron81000GENOMES,BL,GMI,HGSV,PJP,SC_SNP,SSMP,TISHKOFF,20.930556
MUTchr64940079449400795rs9463480+GG/Tintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,SC_SNP,SSMP,TISHKOFF,20.69151
MUTchr64940706849407069rs9463482+TC/Tintron101000GENOMES,ABI,BCMHGSC_JDW,BL,GMI,HGSV,PJP,SC_SNP,SSMP,TISHKOFF,20.516971
MUTchr64940984749409848rs9463483+TA/Tintron101000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,GMI,PJP,SC_SNP,SSMP,20.309937
MTRchr1236996116236996117rs946403+TC/Tintron181000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,TSC-CSHL,YUSUKE,20.44869
MUTchr64940948649409487rs9473555+GC/Gintron131000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,PJP,SC_SNP,SSMP,20.30698
MUTchr64940973649409737rs9473557+TC/Tintron121000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,CLINSEQ_SNP,ENSEMBL,GMI,PJP,SC_SNP,SI_EXO,SSMP,20.33005
MUTchr64942284749422848rs9473559+TA/Tintron61000GENOMES,BCMHGSC_JDW,BGI,GMI,SC_SNP,SSMP,20.236593
MUTchr64942791749427918rs9473560+AA/Gintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,PJP,SC_SNP,SSMP,TISHKOFF,20.681941
MUTchr64942875449428755rs9473561+GA/Gintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.320478
MTRchr1236980503236980504rs955516+TA/Tintron101000GENOMES,BCMHGSC_JDW,BUSHMAN,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,TSC-CSHL,20.360908
LMBRD1chr67041332770413328rs960144-TA/Gintron191000GENOMES,ABI,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,YUSUKE,20.462882
CUBNchr101701209717012098rs9633766+CC/Tintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,20.58477
CUBNchr101709478417094785rs9663167+AA/Gintron71000GENOMES,BUSHMAN,GMI,HGSV,PJP,SC_SNP,WI_SSAHASNP,20.820642
CUBNchr101709960417099605rs9664265+CC/Tintron51000GENOMES,COMPLETE_GENOMICS,SSAHASNP,TISHKOFF,WI_SSAHASNP,20.977982
CUBNchr101709464817094649rs9664321+CC/Tintron51000GENOMES,COMPLETE_GENOMICS,HGSV,TISHKOFF,WI_SSAHASNP,20.977106
CUBNchr101709467417094675rs9664323+CA/Cintron101000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,HGSV,KRIBB_YJKIM,PJP,SC_SNP,TISHKOFF,WI_SSAHASNP,20.069818
CUBNchr101710417217104173rs9665553+GA/Gintron231000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP20.792917
CUBNchr101703395317033954rs9733534+GA/C/Gintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_SNP,SSAHASNP,SSMP,20.785779
LMBRD1chr67039164970391650rs980587-CA/Gintron121000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSMP,TSC-CSHL,WI_SSAHASNP,20.128666
CUBNchr101701556017015561rs9888018+GC/Gintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.037456
LMBRD1chr67048121970481220rs991973+CC/Tintron121000GENOMES,ABI,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,ILLUMINA-UK,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.897692
MMABchr12110004996110004997rs9919738+GA/Gintron101000GENOMES,BCM_SSAHASNP,COMPLETE_GENOMICS,GMI,ILLUMINA,PJP,RSG_JCVI,SC_SNP,SSMP,TISHKOFF,20.332569
LMBRD1chr67048126670481267rs991974+GG/Tintron131000GENOMES,ABI,AFFY,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,TSC-CSHL,20.856082
CUBNchr101713590717135908rs994714-AC/Tintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SEQUENOM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.544987
CUBNchr101713586617135867rs994715-GC/Tintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.10111
CUBNchr101698784016987841rs9971057+CC/Tintron61000GENOMES,HGSV,ILLUMINA-UK,PJP,TISHKOFF,WUGSC_SSAHASNP,20.980734
MMAAchr4146569256146569257rs9990503+TC/Tintron71000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,WI_SSAHASNP,20.123168
MMAAchr4146542024146542025rs9998804+TA/Tintron31000GENOMES,BUSHMAN,WI_SSAHASNP,20.012844