Item | Value |
---|---|
geneid | 55454 |
ensemblid | ENSG00000169826.8 |
hgncid | 24292 |
symbol | CSGALNACT2 |
name | chondroitin sulfate N-acetylgalactosaminyltransferase 2 |
refseq_nuc | NM_018590.5 |
refseq_prot | NP_061060.3 |
ensembl_nuc | ENST00000374466.4 |
ensembl_prot | ENSP00000363590.3 |
mane_status | MANE Select |
chr | chr10 |
start | 43138445 |
end | 43185302 |
strand | + |
ver | v1.2 |
region | chr10:43138445-43185302 |
region5000 | chr10:43133445-43190302 |
regionname0 | CSGALNACT2_chr10_43138445_43185302 |
regionname5000 | CSGALNACT2_chr10_43133445_43190302 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 542 | 323 | 86 | 55 | 139 | 9 | 33 | 107 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | MPRRG others(537): Show |
chr10 | 43133445 | 43190302 |
a0002 | 0/1 | 542 | 66 | 1 | 17 | 33 | 5 | 9 | 25 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | MPRRG others(537): Show |
chr10 | 43133445 | 43190302 |
a0003 | 0/0 | 542 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | MPRRG others(537): Show |
chr10 | 43133445 | 43190302 |
a0004 | 0/0 | 542 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | MPRRG others(537): Show |
chr10 | 43133445 | 43190302 |
a0005 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | MPRRG others(537): Show |
chr10 | 43133445 | 43190302 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1626 | 312 | 83 | 52 | 138 | 9 | 29 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0001c0003 | 0/0 | 1626 | 7 | 1 | 2 | 0 | 0 | 4 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0001c0006 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0001c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0001c0009 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0002c0002 | 0/1 | 1626 | 66 | 1 | 17 | 33 | 5 | 9 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0003c0004 | 0/0 | 1626 | 5 | 4 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0004c0005 | 0/0 | 1626 | 3 | 2 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 | ||
a0005c0008 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | ATGCC others(1621): Show |
chr10 | 43133445 | 43190302 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3765 | 78 | 35 | 10 | 19 | 6 | 8 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0002 | 1/0 | 3765 | 97 | 1 | 14 | 70 | 1 | 10 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0003 | 0/0 | 3765 | 42 | 13 | 13 | 10 | 2 | 4 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0004 | 0/0 | 3766 | 38 | 0 | 0 | 34 | 0 | 4 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3761): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0005 | 0/0 | 3765 | 13 | 10 | 3 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0006 | 0/0 | 3765 | 11 | 11 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0007 | 0/0 | 3765 | 10 | 1 | 7 | 0 | 0 | 2 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0009 | 0/0 | 3765 | 6 | 4 | 2 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0010 | 0/0 | 3765 | 6 | 0 | 1 | 5 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0011 | 0/0 | 3765 | 4 | 3 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0012 | 0/0 | 3765 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0013 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0016 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0017 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0018 | 0/0 | 3765 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0019 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0001t0020 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0003t0008 | 0/0 | 3765 | 7 | 1 | 2 | 0 | 0 | 4 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0006t0005 | 0/0 | 3765 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0001c0007t0004 | 0/0 | 3766 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3761): Show |
chr10 | 43133445 | 43190302 |
a0001c0009t0001 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0002c0002t0001 | 0/1 | 3765 | 64 | 0 | 16 | 33 | 5 | 9 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0002c0002t0014 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0002c0002t0015 | 0/0 | 3765 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0003c0004t0001 | 0/0 | 3765 | 5 | 4 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0004c0005t0001 | 0/0 | 3765 | 3 | 2 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
a0005c0008t0001 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | CTCTC others(3760): Show |
chr10 | 43133445 | 43190302 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0002 | 1/0 | 10 | 0 | 3 | 4 | 0 | 2 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0008 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0003 | 0/0 | 9 | 4 | 2 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0007g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0007g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0009g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0011g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0012g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0013g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0018g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0019g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0001t0020g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0003t0008g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0006t0005g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0007t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0001c0009t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0001 | 0/0 | 12 | 0 | 5 | 4 | 1 | 2 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0002c0002t0015g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0003c0004t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0003c0004t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0003c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0004c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0004c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0004c0005t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
a0005c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0183 | EUR | GBR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0149 | EUR | GBR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0172 | EUR | GBR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | FIN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00735 | hp2 | a0001 | c0001 | t0011 | g0036 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00738 | hp1 | a0002 | c0002 | t0015 | g0157 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01099 | hp2 | a0003 | c0004 | t0001 | g0022 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01106 | hp2 | a0001 | c0006 | t0005 | g0035 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0096 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0019 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01168 | hp1 | a0001 | c0001 | t0018 | g0248 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01192 | hp2 | a0001 | c0003 | t0008 | g0275 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0253 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01361 | hp1 | a0001 | c0003 | t0008 | g0271 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0122 | EUR | IBS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01934 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01981 | hp2 | a0001 | c0001 | t0007 | g0015 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0049 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CDX | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CDX | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CDX | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CDX | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02273 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02273 | hp2 | a0001 | c0001 | t0010 | g0103 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02572 | hp1 | a0005 | c0008 | t0001 | g0139 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02602 | hp1 | a0001 | c0003 | t0008 | g0272 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02630 | hp1 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0298 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0265 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0187 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0180 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02897 | hp2 | a0003 | c0004 | t0001 | g0022 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02976 | hp2 | a0004 | c0005 | t0001 | g0252 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03017 | hp1 | a0001 | c0003 | t0008 | g0273 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0311 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03041 | hp1 | a0002 | c0002 | t0014 | g0150 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03130 | hp1 | a0001 | c0003 | t0008 | g0274 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0267 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0036 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03239 | hp1 | a0001 | c0003 | t0008 | g0276 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0288 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03579 | hp1 | a0001 | c0001 | t0019 | g0270 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0062 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03688 | hp2 | a0001 | c0003 | t0008 | g0277 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0308 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | STU | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18522 | hp1 | a0004 | c0005 | t0001 | g0251 | AFR | YRI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18522 | hp2 | a0003 | c0004 | t0001 | g0023 | AFR | YRI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18747 | hp2 | a0001 | c0001 | t0010 | g0104 | EAS | CHB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0262 | AFR | YRI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0257 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0258 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19005 | hp2 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19043 | hp1 | a0001 | c0009 | t0001 | g0281 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0266 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19055 | hp2 | a0001 | c0007 | t0004 | g0290 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ASW | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20129 | hp2 | a0003 | c0004 | t0001 | g0023 | AFR | ASW | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0144 | EUR | TSI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0231 | EUR | TSI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | GIH | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0069 | SAS | GIH | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02109 | hp1 | a0001 | c0006 | t0005 | g0035 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | MSL | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | USA | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | LWK | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0169 | REF | REF | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | CSGALNACT2_chr10_43133445_43190302 | CSGALNACT2 | chr10 | 43133445 | 43190302 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:43158721 | A | G | 1 | a0005 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.668A>G | p.Tyr223Cys | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/8 | 1044/3765 | 668/1629 | 223/542 | chr10 | 43158721 | |||
chr10:43175951 | G | A | 1 | a0003 | 5 | HG01099.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1255G>A | p.Val419Ile | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/8 | 1631/3765 | 1255/1629 | 419/542 | chr10 | 43175951 | |||
chr10:43183348 | C | T | 1 | a0002 | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
missense_variant | MODERATE | c.1435C>T | p.Pro479Ser | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1811/3765 | 1435/1629 | 479/542 | chr10 | 43183348 | |||
chr10:43183493 | C | T | 1 | a0004 | 3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.1580C>T | p.Thr527Met | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1956/3765 | 1580/1629 | 527/542 | chr10 | 43183493 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:43155197 | G | C | 1 | a0001c0006 | 2 | HG01106.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.48G>C | p.Leu16Leu | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/8 | 424/3765 | 48/1629 | 16/542 | chr10 | 43155197 | |||
chr10:43155392 | A | G | 1 | a0001c0009 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.243A>G | p.Gln81Gln | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/8 | 619/3765 | 243/1629 | 81/542 | chr10 | 43155392 | |||
chr10:43155467 | C | T | 1 | a0001c0003 | 7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
synonymous_variant | LOW | c.318C>T | p.Gly106Gly | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/8 | 694/3765 | 318/1629 | 106/542 | chr10 | 43155467 | |||
chr10:43158746 | A | G | 1 | a0001c0003 | 7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
synonymous_variant | LOW | c.693A>G | p.Thr231Thr | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/8 | 1069/3765 | 693/1629 | 231/542 | chr10 | 43158746 | |||
chr10:43158905 | A | T | 1 | a0001c0007 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.852A>T | p.Ala284Ala | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/8 | 1228/3765 | 852/1629 | 284/542 | chr10 | 43158905 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:43138467 | C | CG | 2 | a0001c0001t0004 a0001c0007t0004 |
39 | HG00544.hp2 HG02155.hp1 HG02602.hp2 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-349dupG | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/8 | 16677 | INFO_REALIGN_3_PRIME | chr10 | 43138467 | |||||
chr10:43138492 | C | G | 1 | a0001c0003t0008 | 7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-329C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/8 | 16658 | chr10 | 43138492 | ||||||
chr10:43138541 | C | A | 1 | a0001c0001t0012 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-280C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/8 | 16609 | chr10 | 43138541 | ||||||
chr10:43155094 | T | C | 1 | a0001c0001t0009 | 6 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-56T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/8 | 56 | chr10 | 43155094 | ||||||
chr10:43183558 | G | A | 1 | a0001c0001t0006 | 11 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 16 | chr10 | 43183558 | ||||||
chr10:43183602 | T | A | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*60T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 60 | chr10 | 43183602 | ||||||
chr10:43183603 | T | C | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*61T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 61 | chr10 | 43183603 | ||||||
chr10:43183604 | C | A | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 62 | chr10 | 43183604 | ||||||
chr10:43183605 | T | C | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 63 | chr10 | 43183605 | ||||||
chr10:43183606 | A | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 64 | chr10 | 43183606 | ||||||
chr10:43183609 | T | A | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 67 | chr10 | 43183609 | ||||||
chr10:43183610 | C | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 68 | chr10 | 43183610 | ||||||
chr10:43183612 | A | G | 2 | a0001c0001t0011 a0001c0001t0020 |
5 | HG00735.hp2 HG02886.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 70 | chr10 | 43183612 | ||||||
chr10:43183616 | G | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 74 | chr10 | 43183616 | ||||||
chr10:43183725 | T | C | 1 | a0002c0002t0014 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 183 | chr10 | 43183725 | ||||||
chr10:43183923 | C | G | 1 | a0001c0001t0019 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 381 | chr10 | 43183923 | ||||||
chr10:43183937 | C | T | 1 | a0001c0001t0018 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 395 | chr10 | 43183937 | ||||||
chr10:43183942 | T | C | 1 | a0002c0002t0015 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 400 | chr10 | 43183942 | ||||||
chr10:43184138 | G | A | 1 | a0001c0001t0007 | 10 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*596G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 596 | chr10 | 43184138 | ||||||
chr10:43184347 | T | C | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(3): Show |
67 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*805T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 805 | chr10 | 43184347 | ||||||
chr10:43184352 | T | G | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*810T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 810 | chr10 | 43184352 | ||||||
chr10:43184576 | C | T | 2 | a0001c0001t0011 a0001c0001t0013 |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1034 | chr10 | 43184576 | ||||||
chr10:43184780 | G | A | 1 | a0001c0003t0008 | 7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1238G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1238 | chr10 | 43184780 | ||||||
chr10:43184872 | T | G | 1 | a0001c0001t0016 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1330 | chr10 | 43184872 | ||||||
chr10:43184968 | C | A | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1426C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1426 | chr10 | 43184968 | ||||||
chr10:43185089 | A | G | 1 | a0001c0001t0017 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1547 | chr10 | 43185089 | ||||||
chr10:43185101 | C | T | 1 | a0001c0001t0010 | 6 | HG02273.hp2 NA18747.hp2 NA18940.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1559C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1559 | chr10 | 43185101 | ||||||
chr10:43185229 | A | C | 2 | a0001c0001t0005 a0001c0006t0005 |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1687A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 8/8 | 1687 | chr10 | 43185229 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:43138592 | C | T | 1 | a0001c0001t0012g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-254+25C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43138592 | |||||||
chr10:43138624 | G | A | 2 | a0001c0001t0010g0045 a0001c0001t0010g0046 |
2 | NA18991.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-254+57G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43138624 | |||||||
chr10:43138793 | T | G | 1 | a0002c0002t0001g0047 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-254+226T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43138793 | |||||||
chr10:43138822 | C | T | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.-254+255C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43138822 | |||||||
chr10:43139196 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-254+629G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43139196 | |||||||
chr10:43139556 | A | G | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-254+989A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43139556 | |||||||
chr10:43139572 | T | G | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-254+1005T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43139572 | |||||||
chr10:43139580 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-254+1013C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43139580 | |||||||
chr10:43139634 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+1067A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43139634 | |||||||
chr10:43140010 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-254+1443A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140010 | |||||||
chr10:43140026 | T | C | 1 | a0001c0001t0017g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-254+1459T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140026 | |||||||
chr10:43140054 | C | T | 2 | a0001c0001t0003g0268 a0001c0001t0003g0269 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-254+1487C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140054 | |||||||
chr10:43140265 | A | G | 4 | a0001c0001t0001g0310 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
6 | HG02155.hp1 HG02523.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-254+1698A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140265 | |||||||
chr10:43140456 | C | T | 3 | a0001c0001t0011g0266 a0001c0001t0011g0267 a0001c0001t0013g0265 |
3 | HG02809.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-254+1889C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140456 | |||||||
chr10:43140615 | A | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-254+2048A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140615 | |||||||
chr10:43140666 | A | G | 1 | a0001c0001t0009g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-254+2099A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140666 | |||||||
chr10:43140692 | C | T | 3 | a0001c0001t0011g0266 a0001c0001t0011g0267 a0001c0001t0013g0265 |
3 | HG02809.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-254+2125C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140692 | |||||||
chr10:43140733 | G | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-254+2166G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140733 | |||||||
chr10:43140734 | C | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+2167C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140734 | |||||||
chr10:43140751 | A | G | 3 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0005g0261 |
3 | HG03098.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-254+2184A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140751 | |||||||
chr10:43140763 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-254+2196T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43140763 | |||||||
chr10:43141016 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+2449A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141016 | |||||||
chr10:43141286 | C | T | 2 | a0001c0001t0010g0257 a0001c0001t0010g0258 |
2 | NA18940.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-254+2719C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141286 | |||||||
chr10:43141348 | G | T | 1 | a0001c0003t0008g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-254+2781G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141348 | |||||||
chr10:43141351 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-254+2784G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141351 | |||||||
chr10:43141352 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-254+2785G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141352 | |||||||
chr10:43141379 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-254+2812G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141379 | |||||||
chr10:43141406 | C | CG | 231 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-254+2842dupG | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141406 | ||||||
chr10:43141414 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+2847A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141414 | |||||||
chr10:43141497 | G | T | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0278 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-254+2930G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141497 | |||||||
chr10:43141554 | C | G | 3 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 |
3 | NA18955.hp2 NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-254+2987C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141554 | |||||||
chr10:43141572 | AG | A | 132 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(129): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-254+3007delG | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141572 | ||||||
chr10:43141594 | A | G | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-254+3027A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141594 | |||||||
chr10:43141624 | C | CA | 6 | a0001c0001t0001g0185 a0001c0001t0002g0188 a0001c0001t0002g0189 others(3): Show |
6 | HG01261.hp1 HG02004.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.-254+3084dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141624 | ||||||
chr10:43141624 | CA | C | 63 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0056 others(60): Show |
75 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.-254+3084delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141624 | ||||||
chr10:43141624 | CAA | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(123): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-254+3083_-254+308 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141624 | ||||||
chr10:43141624 | CAAA | C | 39 | a0001c0001t0001g0054 a0001c0001t0001g0084 a0001c0001t0001g0085 others(36): Show |
45 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-254+3082_-254+308 others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43141624 | ||||||
chr10:43141690 | C | G | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-254+3123C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141690 | |||||||
chr10:43141782 | G | C | 1 | a0001c0001t0004g0286 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-254+3215G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141782 | |||||||
chr10:43141948 | A | G | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-254+3381A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43141948 | |||||||
chr10:43142048 | C | T | 3 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0172 |
3 | HG00140.hp2 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-254+3481C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142048 | |||||||
chr10:43142166 | T | A | 112 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0121 others(109): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-254+3599T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142166 | |||||||
chr10:43142170 | CTTT | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0165 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+3606_-254+360 others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43142170 | ||||||
chr10:43142204 | G | GTTTA | 8 | a0001c0001t0005g0259 a0001c0003t0008g0271 a0001c0003t0008g0272 others(5): Show |
8 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-254+3657_-254+366 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43142204 | ||||||
chr10:43142298 | G | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-254+3731G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142298 | |||||||
chr10:43142318 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-254+3751T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142318 | |||||||
chr10:43142328 | C | T | 1 | a0002c0002t0001g0012 | 3 | HG00621.hp1 NA18989.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-254+3761C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142328 | |||||||
chr10:43142480 | G | T | 1 | a0002c0002t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-254+3913G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142480 | |||||||
chr10:43142482 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+3915A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142482 | |||||||
chr10:43142492 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-254+3925G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142492 | |||||||
chr10:43142562 | A | G | 5 | a0001c0001t0003g0126 a0001c0001t0011g0036 a0001c0001t0011g0266 others(2): Show |
6 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-254+3995A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142562 | |||||||
chr10:43142603 | A | G | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-254+4036A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142603 | |||||||
chr10:43142677 | G | A | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-254+4110G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142677 | |||||||
chr10:43142733 | A | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-254+4166A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142733 | |||||||
chr10:43142751 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-254+4184A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142751 | |||||||
chr10:43142931 | C | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00621.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-254+4364C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43142931 | |||||||
chr10:43143032 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-254+4465A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43143032 | |||||||
chr10:43143353 | C | G | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.-254+4786C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43143353 | |||||||
chr10:43143377 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-254+4810T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43143377 | |||||||
chr10:43143385 | A | T | 5 | a0001c0001t0005g0179 a0001c0001t0005g0259 a0001c0001t0005g0260 others(2): Show |
6 | HG01106.hp2 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-254+4818A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43143385 | |||||||
chr10:43143493 | A | ATG | 41 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0056 others(38): Show |
52 | HG00423.hp2 HG00597.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.-254+4969_-254+497 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | A | ATGTG | 34 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0052 others(31): Show |
41 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.-254+4967_-254+497 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | A | ATGTGTG | 11 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0082 others(8): Show |
11 | HG01081.hp2 HG01243.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-254+4965_-254+497 others(10): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATG | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0057 others(86): Show |
123 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-254+4969_-254+497 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTG | A | 43 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(40): Show |
58 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-254+4967_-254+497 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTGTG | A | 9 | a0001c0001t0001g0165 a0001c0001t0002g0188 a0001c0001t0003g0093 others(6): Show |
9 | HG01192.hp2 HG01361.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-254+4965_-254+497 others(10): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTGTGT others(1): Show |
A | 19 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(16): Show |
22 | HG01099.hp2 HG01167.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.-254+4963_-254+497 others(12): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0005g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-254+4961_-254+497 others(14): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0002g0196 a0001c0001t0019g0270 |
2 | HG03579.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-254+4957_-254+497 others(18): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143493 | ATGTGTGT others(11): Show |
A | 1 | a0002c0002t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-254+4953_-254+497 others(22): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143493 | ||||||
chr10:43143544 | TAATA | T | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.-254+4980_-254+498 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43143544 | ||||||
chr10:43143830 | T | C | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-254+5263T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43143830 | |||||||
chr10:43144564 | G | T | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-254+5997G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43144564 | |||||||
chr10:43144565 | GT | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-254+6007delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43144565 | ||||||
chr10:43144692 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-254+6125A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43144692 | |||||||
chr10:43144841 | A | G | 1 | a0002c0002t0001g0160 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-254+6274A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43144841 | |||||||
chr10:43144878 | A | C | 1 | a0002c0002t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-254+6311A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43144878 | |||||||
chr10:43144921 | T | C | 7 | a0001c0001t0001g0185 a0001c0001t0011g0036 a0001c0001t0011g0266 others(4): Show |
8 | HG00735.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-254+6354T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43144921 | |||||||
chr10:43145027 | A | G | 4 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0159 others(1): Show |
6 | HG02451.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-254+6460A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145027 | |||||||
chr10:43145099 | G | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
61 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-254+6532G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145099 | |||||||
chr10:43145336 | A | G | 2 | a0001c0001t0001g0024 a0005c0008t0001g0139 |
3 | HG01978.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-254+6769A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145336 | |||||||
chr10:43145374 | T | C | 5 | a0001c0001t0009g0019 a0001c0001t0009g0088 a0001c0001t0009g0096 others(2): Show |
6 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-254+6807T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145374 | |||||||
chr10:43145410 | C | CT | 164 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-254+6867dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43145410 | ||||||
chr10:43145410 | C | CTT | 38 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0135 others(35): Show |
47 | HG00544.hp2 HG00741.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-254+6866_-254+686 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43145410 | ||||||
chr10:43145410 | CT | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0129 a0001c0001t0001g0130 others(18): Show |
23 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(20): Show |
intron_variant | MODIFIER | c.-254+6867delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43145410 | ||||||
chr10:43145410 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-254+6856_-254+686 others(16): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43145410 | ||||||
chr10:43145414 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-254+6847T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145414 | |||||||
chr10:43145462 | C | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0278 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-254+6895C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145462 | |||||||
chr10:43145466 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
61 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-254+6899C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145466 | |||||||
chr10:43145581 | T | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(221): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-254+7014T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145581 | |||||||
chr10:43145610 | G | A | 15 | a0001c0001t0002g0007 a0001c0001t0002g0037 a0001c0001t0002g0189 others(12): Show |
19 | HG00423.hp1 HG00621.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-254+7043G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145610 | |||||||
chr10:43145695 | C | T | 1 | a0001c0006t0005g0035 | 2 | HG01106.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-254+7128C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145695 | |||||||
chr10:43145719 | A | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0165 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-254+7152A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145719 | |||||||
chr10:43145897 | A | C | 1 | a0001c0001t0002g0233 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-254+7330A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145897 | |||||||
chr10:43145939 | T | C | 6 | a0001c0001t0010g0045 a0001c0001t0010g0046 a0001c0001t0010g0103 others(3): Show |
6 | HG02273.hp2 NA18747.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.-254+7372T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43145939 | |||||||
chr10:43146056 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-254+7489G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146056 | |||||||
chr10:43146146 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-254+7579G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146146 | |||||||
chr10:43146273 | TG | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0127 others(5): Show |
10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-254+7707delG | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146273 | |||||||
chr10:43146667 | A | G | 231 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-254+8100A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146667 | |||||||
chr10:43146725 | G | C | 231 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-254+8158G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146725 | |||||||
chr10:43146730 | C | CT | 6 | a0001c0001t0002g0213 a0001c0001t0003g0119 a0001c0001t0005g0013 others(3): Show |
8 | HG00741.hp2 HG01192.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-253-8153dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146730 | ||||||
chr10:43146730 | CT | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
66 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-253-8153delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146730 | ||||||
chr10:43146963 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0004g0297 a0001c0001t0004g0298 a0001c0001t0004g0299 others(4): Show |
7 | HG02602.hp1 HG02602.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-7915_-253-790 others(12): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0310 a0001c0001t0004g0284 a0001c0001t0004g0288 others(5): Show |
8 | HG01192.hp2 HG02523.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-253-7916_-253-790 others(13): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0004g0043 a0001c0001t0004g0308 a0001c0003t0008g0273 |
4 | HG03017.hp1 HG04199.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-253-7917_-253-790 others(14): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0004g0009 a0001c0001t0004g0044 a0001c0001t0004g0282 others(5): Show |
12 | HG02155.hp1 NA18941.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.-253-7918_-253-790 others(15): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(5): Show |
11 | a0001c0001t0004g0042 a0001c0001t0004g0283 a0001c0001t0004g0285 others(8): Show |
12 | NA18949.hp1 NA18961.hp2 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.-253-7919_-253-790 others(16): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-253-7921_-253-790 others(18): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0294 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-253-7925_-253-790 others(22): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0004g0305 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-253-7926_-253-790 others(23): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146963 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0017g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-253-7928_-253-790 others(25): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146963 | ||||||
chr10:43146978 | TTTTTTTT others(7): Show |
T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0166 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-253-7918_-253-790 others(18): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146978 | |||||||
chr10:43146979 | TTTTTTTT others(6): Show |
T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0185 |
2 | HG03239.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-253-7917_-253-790 others(17): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146979 | |||||||
chr10:43146980 | TTTTTTTT others(5): Show |
T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
68 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-253-7916_-253-790 others(16): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146980 | |||||||
chr10:43146982 | TTTTTTTT others(3): Show |
T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0168 a0001c0001t0001g0263 others(1): Show |
5 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-253-7914_-253-790 others(14): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146982 | |||||||
chr10:43146984 | TTTTTTGT others(1): Show |
T | 44 | a0001c0001t0003g0003 a0001c0001t0003g0021 a0001c0001t0003g0090 others(41): Show |
53 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-253-7912_-253-790 others(12): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146984 | |||||||
chr10:43146985 | TTTTTGTG | T | 21 | a0001c0001t0003g0087 a0001c0001t0003g0089 a0001c0001t0003g0119 others(18): Show |
29 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.-253-7911_-253-790 others(11): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146985 | |||||||
chr10:43146988 | TTG | T | 74 | a0001c0001t0001g0130 a0001c0001t0002g0002 a0001c0001t0002g0007 others(71): Show |
92 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.-253-7906_-253-790 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146988 | ||||||
chr10:43146989 | TG | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0014 others(15): Show |
19 | HG00438.hp1 HG01358.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-253-7907delG | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146989 | |||||||
chr10:43146989 | TGTG | T | 51 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(48): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-253-7906_-253-790 others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43146989 | ||||||
chr10:43146990 | G | T | 49 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0278 others(46): Show |
55 | HG00544.hp2 HG01192.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-253-7907G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146990 | |||||||
chr10:43146992 | G | T | 136 | a0001c0001t0001g0130 a0001c0001t0001g0165 a0001c0001t0001g0186 others(133): Show |
166 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.-253-7905G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43146992 | |||||||
chr10:43147015 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-253-7882G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147015 | |||||||
chr10:43147136 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
61 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-253-7761C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147136 | |||||||
chr10:43147143 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-253-7754T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147143 | |||||||
chr10:43147175 | C | T | 2 | a0001c0001t0007g0004 a0001c0001t0007g0062 |
6 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-253-7722C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147175 | |||||||
chr10:43147186 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-253-7711G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147186 | |||||||
chr10:43147226 | C | T | 1 | a0001c0001t0005g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-253-7671C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147226 | |||||||
chr10:43147343 | GTTA | G | 224 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(221): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-253-7548_-253-754 others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43147343 | ||||||
chr10:43147362 | C | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-253-7535C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147362 | |||||||
chr10:43147714 | T | A | 1 | a0002c0002t0001g0142 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-253-7183T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43147714 | |||||||
chr10:43147782 | C | CT | 46 | a0001c0001t0002g0232 a0001c0001t0002g0245 a0001c0001t0003g0003 others(43): Show |
56 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-253-7096dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43147782 | ||||||
chr10:43147782 | CT | C | 14 | a0001c0001t0002g0222 a0001c0001t0002g0249 a0001c0001t0004g0300 others(11): Show |
14 | HG01192.hp2 HG01361.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-253-7096delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43147782 | ||||||
chr10:43148002 | G | T | 5 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(2): Show |
6 | HG00735.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-253-6895G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148002 | |||||||
chr10:43148018 | A | G | 45 | a0002c0002t0001g0001 a0002c0002t0001g0012 a0002c0002t0001g0020 others(42): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-253-6879A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148018 | |||||||
chr10:43148149 | T | G | 1 | a0001c0001t0013g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-253-6748T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148149 | |||||||
chr10:43148241 | C | A | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-253-6656C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148241 | |||||||
chr10:43148241 | C | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-253-6656C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148241 | |||||||
chr10:43148250 | A | G | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.-253-6647A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148250 | |||||||
chr10:43148294 | G | T | 1 | a0001c0001t0010g0046 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-253-6603G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148294 | |||||||
chr10:43148301 | T | C | 1 | a0002c0002t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-253-6596T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148301 | |||||||
chr10:43148581 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-6316A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148581 | |||||||
chr10:43148693 | T | C | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.-253-6204T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148693 | |||||||
chr10:43148726 | C | T | 2 | a0002c0002t0001g0156 a0002c0002t0001g0160 |
2 | NA18999.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-253-6171C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148726 | |||||||
chr10:43148951 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-253-5946G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43148951 | |||||||
chr10:43149091 | T | C | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-253-5806T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149091 | |||||||
chr10:43149144 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-253-5753G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149144 | |||||||
chr10:43149214 | C | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-5683C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149214 | |||||||
chr10:43149247 | G | A | 14 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(11): Show |
17 | HG01099.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-253-5650G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149247 | |||||||
chr10:43149308 | A | T | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-253-5589A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149308 | |||||||
chr10:43149338 | C | T | 4 | a0001c0001t0001g0131 a0003c0004t0001g0022 a0003c0004t0001g0023 others(1): Show |
6 | HG01099.hp2 HG01167.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-253-5559C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149338 | |||||||
chr10:43149376 | C | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-253-5521C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149376 | |||||||
chr10:43149445 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-253-5452G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149445 | |||||||
chr10:43149507 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-253-5390T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149507 | |||||||
chr10:43149616 | T | A | 1 | a0002c0002t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-253-5281T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149616 | |||||||
chr10:43149642 | A | G | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-253-5255A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149642 | |||||||
chr10:43149796 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-253-5101G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149796 | |||||||
chr10:43149799 | G | A | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-253-5098G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149799 | |||||||
chr10:43149828 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-253-5069G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149828 | |||||||
chr10:43149839 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-253-5058G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149839 | |||||||
chr10:43149939 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-253-4958T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149939 | |||||||
chr10:43149999 | G | A | 133 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(130): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-253-4898G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43149999 | |||||||
chr10:43150021 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-253-4876C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150021 | |||||||
chr10:43150023 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-253-4874C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150023 | |||||||
chr10:43150030 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-253-4867G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150030 | |||||||
chr10:43150054 | C | T | 185 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-253-4843C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150054 | |||||||
chr10:43150141 | A | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0078 others(1): Show |
4 | HG03239.hp2 HG03831.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-253-4756A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150141 | |||||||
chr10:43150318 | A | T | 1 | a0001c0001t0002g0231 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-253-4579A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150318 | |||||||
chr10:43150354 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-4543G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150354 | |||||||
chr10:43150406 | C | T | 231 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-253-4491C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150406 | |||||||
chr10:43150495 | A | G | 1 | a0002c0002t0001g0140 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-253-4402A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150495 | |||||||
chr10:43150813 | T | A | 185 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-253-4084T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150813 | |||||||
chr10:43150987 | C | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-253-3910C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43150987 | |||||||
chr10:43151027 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-253-3870C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151027 | |||||||
chr10:43151064 | A | T | 1 | a0001c0001t0002g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-253-3833A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151064 | |||||||
chr10:43151094 | A | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-3803A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151094 | |||||||
chr10:43151191 | G | C | 16 | a0001c0001t0002g0014 a0001c0001t0002g0190 a0001c0001t0002g0214 others(13): Show |
18 | HG00673.hp1 NA18950.hp1 NA18955.hp2 others(15): Show |
intron_variant | MODIFIER | c.-253-3706G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151191 | |||||||
chr10:43151265 | T | C | 2 | a0001c0001t0003g0106 a0001c0001t0003g0120 |
2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-253-3632T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151265 | |||||||
chr10:43151632 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-253-3265A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151632 | |||||||
chr10:43151707 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-253-3190G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151707 | |||||||
chr10:43151810 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-3087G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151810 | |||||||
chr10:43151879 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-253-3018T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151879 | |||||||
chr10:43151912 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-253-2985A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151912 | |||||||
chr10:43151998 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-253-2899C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151998 | |||||||
chr10:43151999 | G | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-253-2898G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43151999 | |||||||
chr10:43152424 | T | TAACA | 231 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-253-2473_-253-247 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152424 | |||||||
chr10:43152518 | T | C | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-253-2379T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152518 | |||||||
chr10:43152718 | T | C | 2 | a0001c0001t0004g0284 a0001c0001t0004g0297 |
2 | NA18984.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-253-2179T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152718 | |||||||
chr10:43152719 | T | G | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-253-2178T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152719 | |||||||
chr10:43152773 | G | T | 185 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-253-2124G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152773 | |||||||
chr10:43152994 | A | G | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00621.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-253-1903A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43152994 | |||||||
chr10:43153087 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-253-1810G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153087 | |||||||
chr10:43153191 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-253-1706C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153191 | |||||||
chr10:43153196 | G | T | 1 | a0001c0001t0006g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-253-1701G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153196 | |||||||
chr10:43153208 | G | A | 5 | a0001c0001t0003g0097 a0001c0001t0003g0099 a0001c0001t0003g0107 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-253-1689G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153208 | |||||||
chr10:43153220 | A | C | 1 | a0002c0002t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-253-1677A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153220 | |||||||
chr10:43153228 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-253-1669G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153228 | |||||||
chr10:43153313 | C | T | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-253-1584C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153313 | |||||||
chr10:43153334 | C | CAAAAAAA others(3): Show |
214 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(211): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-253-1562_-253-155 others(14): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43153334 | ||||||
chr10:43153334 | C | CAAAAAAA others(4): Show |
8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0096 others(5): Show |
8 | HG01071.hp2 HG01109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-253-1553_-253-155 others(15): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43153334 | ||||||
chr10:43153334 | C | CAAAAAAA others(6): Show |
4 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(1): Show |
4 | HG01361.hp1 HG02602.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-253-1553_-253-155 others(17): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43153334 | ||||||
chr10:43153334 | C | CAAAAAAA others(7): Show |
3 | a0001c0003t0008g0274 a0001c0003t0008g0275 a0001c0003t0008g0276 |
3 | HG01192.hp2 HG03130.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-253-1553_-253-155 others(18): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43153334 | ||||||
chr10:43153430 | G | T | 1 | a0002c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-253-1467G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153430 | |||||||
chr10:43153496 | T | TA | 6 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(3): Show |
6 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-253-1400dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43153496 | ||||||
chr10:43153499 | C | A | 1 | a0001c0003t0008g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-253-1398C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153499 | |||||||
chr10:43153712 | C | G | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-253-1185C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153712 | |||||||
chr10:43153863 | A | G | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-253-1034A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43153863 | |||||||
chr10:43154088 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0208 |
2 | NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-253-809A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154088 | |||||||
chr10:43154115 | T | G | 48 | a0001c0001t0001g0121 a0001c0001t0001g0132 a0001c0001t0003g0003 others(45): Show |
58 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-253-782T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154115 | |||||||
chr10:43154175 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-253-722G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154175 | |||||||
chr10:43154229 | G | C | 1 | a0001c0001t0002g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-253-668G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154229 | |||||||
chr10:43154345 | C | T | 1 | a0001c0001t0004g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-253-552C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154345 | |||||||
chr10:43154438 | A | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-253-459A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154438 | |||||||
chr10:43154605 | T | C | 2 | a0001c0001t0003g0100 a0001c0001t0016g0109 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-253-292T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154605 | |||||||
chr10:43154625 | G | A | 2 | a0001c0001t0001g0185 a0001c0009t0001g0281 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-253-272G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | chr10 | 43154625 | |||||||
chr10:43154726 | C | CA | 14 | a0001c0001t0001g0033 a0001c0001t0001g0078 a0001c0001t0001g0127 others(11): Show |
15 | HG01192.hp2 HG01361.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-253-156dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43154726 | ||||||
chr10:43154726 | CA | C | 31 | a0001c0001t0001g0077 a0001c0001t0001g0186 a0001c0001t0001g0310 others(28): Show |
37 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(34): Show |
intron_variant | MODIFIER | c.-253-156delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 43154726 | ||||||
chr10:43155816 | G | A | 1 | a0002c0002t0001g0148 | 1 | HG03831.hp1 | splice_region_variant&intron_variant | LOW | c.661+6G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43155816 | |||||||
chr10:43156159 | G | A | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+349G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156159 | |||||||
chr10:43156181 | A | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+371A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156181 | |||||||
chr10:43156250 | A | G | 1 | a0001c0001t0005g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.661+440A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156250 | |||||||
chr10:43156381 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+571G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156381 | |||||||
chr10:43156709 | A | G | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.661+899A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156709 | |||||||
chr10:43156715 | G | T | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.661+905G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156715 | |||||||
chr10:43156762 | A | G | 3 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 |
3 | NA18955.hp2 NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.661+952A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156762 | |||||||
chr10:43156782 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.661+972C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156782 | |||||||
chr10:43156803 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0166 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+993C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156803 | |||||||
chr10:43156883 | G | A | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+1073G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156883 | |||||||
chr10:43156890 | G | A | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+1080G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156890 | |||||||
chr10:43156939 | C | T | 53 | a0001c0001t0001g0121 a0001c0001t0003g0003 a0001c0001t0003g0021 others(50): Show |
68 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.661+1129C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156939 | |||||||
chr10:43156997 | C | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.661+1187C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43156997 | |||||||
chr10:43157064 | C | G | 112 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0121 others(109): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.661+1254C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157064 | |||||||
chr10:43157117 | ACT | A | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+1310_661+1311d others(4): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43157117 | ||||||
chr10:43157204 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.661+1394T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157204 | |||||||
chr10:43157208 | ATAAC | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+1402_661+1405d others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43157208 | ||||||
chr10:43157241 | T | G | 5 | a0002c0002t0001g0026 a0002c0002t0001g0047 a0002c0002t0001g0138 others(2): Show |
6 | NA18953.hp1 NA18967.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+1431T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157241 | |||||||
chr10:43157253 | A | G | 5 | a0002c0002t0001g0026 a0002c0002t0001g0047 a0002c0002t0001g0138 others(2): Show |
6 | NA18953.hp1 NA18967.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+1443A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157253 | |||||||
chr10:43157312 | T | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.662-1403T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157312 | |||||||
chr10:43157366 | C | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662-1349C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157366 | |||||||
chr10:43157520 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662-1195C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157520 | |||||||
chr10:43157544 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.662-1171C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157544 | |||||||
chr10:43157726 | G | A | 7 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(4): Show |
9 | HG00741.hp2 HG01192.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.662-989G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157726 | |||||||
chr10:43157740 | T | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-975T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157740 | |||||||
chr10:43157797 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.662-918G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157797 | |||||||
chr10:43157895 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.662-820G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157895 | |||||||
chr10:43157954 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.662-761G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43157954 | |||||||
chr10:43158022 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.662-693C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158022 | |||||||
chr10:43158026 | T | TA | 20 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0001g0073 others(17): Show |
20 | HG00733.hp2 HG01099.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.662-666dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43158026 | ||||||
chr10:43158026 | T | TAA | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-667_662-666dup others(2): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43158026 | ||||||
chr10:43158026 | TA | T | 36 | a0001c0001t0001g0131 a0001c0001t0001g0168 a0001c0001t0001g0185 others(33): Show |
42 | HG00544.hp2 HG01167.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-666delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43158026 | ||||||
chr10:43158122 | A | G | 1 | a0001c0001t0005g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.662-593A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158122 | |||||||
chr10:43158177 | C | A | 2 | a0001c0003t0008g0274 a0001c0003t0008g0275 |
2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.662-538C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158177 | |||||||
chr10:43158189 | C | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.662-526C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158189 | |||||||
chr10:43158191 | G | C | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.662-524G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158191 | |||||||
chr10:43158191 | GAT | G | 229 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.662-511_662-510del others(2): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43158191 | ||||||
chr10:43158193 | T | G | 2 | a0002c0002t0001g0183 a0002c0002t0001g0184 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.662-522T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158193 | |||||||
chr10:43158299 | G | C | 1 | a0002c0002t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.662-416G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158299 | |||||||
chr10:43158375 | T | G | 1 | a0002c0002t0001g0154 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.662-340T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158375 | |||||||
chr10:43158399 | ATTTC | A | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.662-312_662-309del others(4): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 43158399 | ||||||
chr10:43158536 | C | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-179C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158536 | |||||||
chr10:43158550 | C | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-165C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158550 | |||||||
chr10:43158558 | T | C | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662-157T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 2/7 | chr10 | 43158558 | |||||||
chr10:43159049 | A | G | 1 | a0002c0002t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.878+118A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159049 | |||||||
chr10:43159067 | T | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.878+136T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159067 | |||||||
chr10:43159110 | T | C | 59 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.878+179T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159110 | |||||||
chr10:43159263 | A | G | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.878+332A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159263 | |||||||
chr10:43159305 | A | AT | 6 | a0001c0003t0008g0272 a0001c0003t0008g0273 a0001c0003t0008g0274 others(3): Show |
6 | HG01192.hp2 HG02602.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.878+385dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 43159305 | ||||||
chr10:43159335 | A | G | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.878+404A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159335 | |||||||
chr10:43159631 | A | AT | 4 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0166 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.878+701dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 43159631 | ||||||
chr10:43159712 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.878+781A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43159712 | |||||||
chr10:43160096 | A | T | 1 | a0005c0008t0001g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.879-398A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43160096 | |||||||
chr10:43160122 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.879-372G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43160122 | |||||||
chr10:43160172 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879-322T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43160172 | |||||||
chr10:43160249 | G | A | 185 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.879-245G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43160249 | |||||||
chr10:43160428 | G | A | 1 | a0001c0001t0010g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.879-66G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 3/7 | chr10 | 43160428 | |||||||
chr10:43160776 | C | T | 1 | a0002c0002t0001g0147 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.980+181C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43160776 | |||||||
chr10:43160946 | C | T | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.980+351C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43160946 | |||||||
chr10:43160971 | T | A | 1 | a0001c0001t0016g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.980+376T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43160971 | |||||||
chr10:43161027 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.980+432A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161027 | |||||||
chr10:43161067 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.980+472G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161067 | |||||||
chr10:43161236 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.980+641A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161236 | |||||||
chr10:43161633 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.980+1038A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161633 | |||||||
chr10:43161793 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.980+1198G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161793 | |||||||
chr10:43161815 | C | G | 1 | a0001c0001t0002g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.980+1220C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43161815 | |||||||
chr10:43162033 | T | G | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.980+1438T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162033 | |||||||
chr10:43162092 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0060 others(2): Show |
7 | HG02145.hp2 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+1497A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162092 | |||||||
chr10:43162149 | C | T | 2 | a0002c0002t0001g0028 a0002c0002t0001g0152 |
3 | NA18994.hp1 NA19058.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.980+1554C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162149 | |||||||
chr10:43162279 | G | C | 1 | a0001c0001t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.981-1587G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162279 | |||||||
chr10:43162280 | A | G | 3 | a0001c0001t0002g0219 a0001c0001t0002g0241 a0001c0001t0002g0247 |
3 | HG02683.hp2 HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.981-1586A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162280 | |||||||
chr10:43162363 | T | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.981-1503T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162363 | |||||||
chr10:43162521 | A | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.981-1345A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162521 | |||||||
chr10:43162644 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.981-1222A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162644 | |||||||
chr10:43162675 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.981-1191G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162675 | |||||||
chr10:43162783 | C | G | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.981-1083C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162783 | |||||||
chr10:43162817 | T | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.981-1049T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162817 | |||||||
chr10:43162823 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.981-1043A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162823 | |||||||
chr10:43162928 | C | T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0116 |
2 | HG01361.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.981-938C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43162928 | |||||||
chr10:43163045 | C | T | 2 | a0003c0004t0001g0022 a0003c0004t0001g0180 |
3 | HG01099.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.981-821C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163045 | |||||||
chr10:43163056 | G | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0175 others(1): Show |
6 | HG00741.hp2 HG01192.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.981-810G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163056 | |||||||
chr10:43163104 | CTTTGAGA others(8): Show |
C | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.981-756_981-742del others(15): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 43163104 | ||||||
chr10:43163205 | A | G | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.981-661A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163205 | |||||||
chr10:43163219 | C | T | 1 | a0002c0002t0001g0161 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.981-647C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163219 | |||||||
chr10:43163302 | C | G | 1 | a0001c0001t0004g0282 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.981-564C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163302 | |||||||
chr10:43163474 | A | C | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.981-392A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163474 | |||||||
chr10:43163516 | T | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.981-350T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163516 | |||||||
chr10:43163633 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.981-233A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163633 | |||||||
chr10:43163645 | C | T | 2 | a0004c0005t0001g0251 a0004c0005t0001g0252 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.981-221C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163645 | |||||||
chr10:43163687 | A | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(13): Show |
23 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.981-179A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163687 | |||||||
chr10:43163813 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.981-53A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 4/7 | chr10 | 43163813 | |||||||
chr10:43164088 | C | T | 188 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1159+44C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164088 | |||||||
chr10:43164330 | G | T | 1 | a0001c0001t0004g0295 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1159+286G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164330 | |||||||
chr10:43164430 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1159+386T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164430 | |||||||
chr10:43164586 | C | G | 1 | a0002c0002t0001g0161 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1159+542C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164586 | |||||||
chr10:43164644 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1159+600T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164644 | |||||||
chr10:43164845 | CA | C | 11 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0278 others(8): Show |
11 | HG01070.hp2 HG01099.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+818delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 43164845 | ||||||
chr10:43164944 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1159+900C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164944 | |||||||
chr10:43164994 | C | T | 1 | a0001c0001t0005g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1159+950C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43164994 | |||||||
chr10:43165067 | C | G | 6 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(3): Show |
11 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159+1023C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165067 | |||||||
chr10:43165190 | A | T | 6 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(3): Show |
11 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159+1146A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165190 | |||||||
chr10:43165371 | C | CA | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+1339dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 43165371 | ||||||
chr10:43165379 | A | G | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.1159+1335A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165379 | |||||||
chr10:43165412 | T | G | 8 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(5): Show |
8 | HG01192.hp2 HG01243.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1368T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165412 | |||||||
chr10:43165514 | G | T | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1159+1470G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165514 | |||||||
chr10:43165547 | C | T | 6 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(3): Show |
6 | HG01361.hp1 HG02602.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1457C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165547 | |||||||
chr10:43165766 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-1238G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165766 | |||||||
chr10:43165779 | C | T | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.1160-1225C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165779 | |||||||
chr10:43165788 | G | A | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.1160-1216G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165788 | |||||||
chr10:43165936 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-1068C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43165936 | |||||||
chr10:43166172 | T | C | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1160-832T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166172 | |||||||
chr10:43166344 | C | T | 8 | a0001c0001t0002g0037 a0001c0001t0002g0198 a0001c0001t0002g0199 others(5): Show |
9 | HG02135.hp1 HG02155.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-660C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166344 | |||||||
chr10:43166388 | G | C | 233 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1160-616G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166388 | |||||||
chr10:43166433 | T | G | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1160-571T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166433 | |||||||
chr10:43166443 | A | G | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-561A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166443 | |||||||
chr10:43166476 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1160-528G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166476 | |||||||
chr10:43166811 | G | C | 3 | a0001c0001t0011g0266 a0001c0001t0011g0267 a0001c0001t0013g0265 |
3 | HG02809.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1160-193G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166811 | |||||||
chr10:43166951 | A | T | 5 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(2): Show |
6 | HG00735.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-53A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 5/7 | chr10 | 43166951 | |||||||
chr10:43167137 | G | A | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1254+39G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167137 | |||||||
chr10:43167270 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1254+172A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167270 | |||||||
chr10:43167294 | C | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+196C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167294 | |||||||
chr10:43167323 | TTTAGGTC others(18): Show |
T | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1254+227_1254+251d others(27): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43167323 | ||||||
chr10:43167356 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+258A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167356 | |||||||
chr10:43167357 | T | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+259T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167357 | |||||||
chr10:43167358 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+260G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167358 | |||||||
chr10:43167360 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+262G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167360 | |||||||
chr10:43167361 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+263G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167361 | |||||||
chr10:43167367 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+269G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167367 | |||||||
chr10:43167370 | C | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+272C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167370 | |||||||
chr10:43167380 | T | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+282T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167380 | |||||||
chr10:43167385 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+287G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167385 | |||||||
chr10:43167386 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+288C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167386 | |||||||
chr10:43167395 | A | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+297A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167395 | |||||||
chr10:43167397 | T | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+299T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167397 | |||||||
chr10:43167400 | T | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+302T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167400 | |||||||
chr10:43167401 | A | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+303A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167401 | |||||||
chr10:43167402 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+304C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167402 | |||||||
chr10:43167404 | A | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+306A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167404 | |||||||
chr10:43167748 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1254+650C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167748 | |||||||
chr10:43167792 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+694G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167792 | |||||||
chr10:43167812 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(46): Show |
64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1254+714A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167812 | |||||||
chr10:43167879 | A | T | 43 | a0002c0002t0001g0001 a0002c0002t0001g0012 a0002c0002t0001g0020 others(40): Show |
62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1254+781A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43167879 | |||||||
chr10:43167986 | ATAAAG | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1254+891_1254+895d others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43167986 | ||||||
chr10:43168049 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02055.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1254+951A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168049 | |||||||
chr10:43168191 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1254+1093G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168191 | |||||||
chr10:43168195 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1254+1097G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168195 | |||||||
chr10:43168217 | T | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+1119T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168217 | |||||||
chr10:43168312 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1254+1214G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168312 | |||||||
chr10:43168550 | G | A | 1 | a0002c0002t0015g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1254+1452G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168550 | |||||||
chr10:43168585 | G | C | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1254+1487G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168585 | |||||||
chr10:43168598 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+1500G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168598 | |||||||
chr10:43168673 | G | GAC | 11 | a0001c0001t0002g0007 a0001c0001t0002g0189 a0001c0001t0002g0191 others(8): Show |
14 | HG01081.hp1 HG01123.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1254+1610_1254+161 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GAC | G | 5 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0003t0008g0272 others(2): Show |
5 | HG02602.hp1 HG03017.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+1610_1254+161 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GACAC | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0003t0008g0274 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+1608_1254+161 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GACACAC | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1254+1606_1254+161 others(10): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GACACACA others(1): Show |
G | 70 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0127 others(67): Show |
90 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1254+1604_1254+161 others(12): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GACACACA others(5): Show |
G | 1 | a0001c0001t0003g0116 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1254+1600_1254+161 others(16): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168673 | GACACACA others(11): Show |
G | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.1254+1594_1254+161 others(22): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43168673 | ||||||
chr10:43168792 | A | G | 1 | a0001c0001t0009g0098 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1254+1694A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168792 | |||||||
chr10:43168896 | C | T | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1254+1798C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168896 | |||||||
chr10:43168904 | G | A | 1 | a0001c0001t0009g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1254+1806G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168904 | |||||||
chr10:43168945 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1254+1847G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168945 | |||||||
chr10:43168988 | T | C | 6 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+1890T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43168988 | |||||||
chr10:43169071 | T | TGTGCATG others(3): Show |
1 | a0001c0001t0001g0058 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1254+1973_1254+197 others(14): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169071 | |||||||
chr10:43169098 | T | G | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1254+2000T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169098 | |||||||
chr10:43169125 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1254+2027C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169125 | |||||||
chr10:43169142 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1254+2044T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169142 | |||||||
chr10:43169286 | C | A | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+2188C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169286 | |||||||
chr10:43169367 | A | C | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0278 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+2269A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169367 | |||||||
chr10:43169386 | A | C | 1 | a0001c0001t0005g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1254+2288A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169386 | |||||||
chr10:43169751 | GA | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0080 others(1): Show |
6 | HG00423.hp2 HG00609.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+2654delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169751 | |||||||
chr10:43169833 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1254+2735G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169833 | |||||||
chr10:43169931 | A | C | 1 | a0001c0001t0001g0016 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1254+2833A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43169931 | |||||||
chr10:43170294 | A | G | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1254+3196A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170294 | |||||||
chr10:43170302 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1254+3204A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170302 | |||||||
chr10:43170309 | G | A | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0278 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+3211G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170309 | |||||||
chr10:43170360 | A | G | 47 | a0001c0001t0001g0121 a0001c0001t0003g0003 a0001c0001t0003g0021 others(44): Show |
57 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1254+3262A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170360 | |||||||
chr10:43170410 | T | G | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+3312T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170410 | |||||||
chr10:43170551 | A | G | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0278 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+3453A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170551 | |||||||
chr10:43170568 | C | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1254+3470C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170568 | |||||||
chr10:43170716 | A | G | 1 | a0002c0002t0001g0158 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1254+3618A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170716 | |||||||
chr10:43170747 | G | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+3649G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170747 | |||||||
chr10:43170874 | G | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(22): Show |
32 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1254+3776G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43170874 | |||||||
chr10:43171036 | T | A | 1 | a0001c0001t0002g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1254+3938T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171036 | |||||||
chr10:43171119 | C | G | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4021C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171119 | |||||||
chr10:43171129 | T | TAATAGTT others(7): Show |
1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4031_1254+403 others(18): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171129 | |||||||
chr10:43171131 | C | A | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4033C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171131 | |||||||
chr10:43171132 | T | C | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4034T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171132 | |||||||
chr10:43171175 | T | C | 132 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(129): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1254+4077T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171175 | |||||||
chr10:43171203 | A | G | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4105A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171203 | |||||||
chr10:43171205 | A | T | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4107A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171205 | |||||||
chr10:43171206 | C | T | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4108C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171206 | |||||||
chr10:43171207 | A | T | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4109A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171207 | |||||||
chr10:43171210 | A | T | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4112A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171210 | |||||||
chr10:43171214 | C | A | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4116C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171214 | |||||||
chr10:43171216 | C | A | 1 | a0001c0001t0011g0267 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+4118C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171216 | |||||||
chr10:43171319 | G | T | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1254+4221G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171319 | |||||||
chr10:43171354 | C | CT | 15 | a0001c0001t0002g0228 a0001c0001t0002g0238 a0001c0001t0005g0013 others(12): Show |
18 | HG00741.hp2 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1254+4271dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43171354 | ||||||
chr10:43171424 | C | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+4326C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171424 | |||||||
chr10:43171457 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1254+4359A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171457 | |||||||
chr10:43171580 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02723.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1255-4371T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171580 | |||||||
chr10:43171646 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1255-4305C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171646 | |||||||
chr10:43171950 | G | A | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1255-4001G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171950 | |||||||
chr10:43171989 | T | C | 1 | a0001c0001t0005g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1255-3962T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43171989 | |||||||
chr10:43172041 | C | T | 2 | a0001c0001t0002g0199 a0001c0001t0002g0204 |
2 | NA18941.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1255-3910C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172041 | |||||||
chr10:43172044 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1255-3907C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172044 | |||||||
chr10:43172289 | G | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1255-3662G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172289 | |||||||
chr10:43172322 | AAAG | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1255-3628_1255-362 others(7): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172322 | |||||||
chr10:43172593 | CTG | C | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1255-3355_1255-335 others(6): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43172593 | ||||||
chr10:43172710 | G | T | 1 | a0001c0001t0002g0196 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1255-3241G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172710 | |||||||
chr10:43172727 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1255-3224T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172727 | |||||||
chr10:43172738 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1255-3213C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172738 | |||||||
chr10:43172808 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0208 |
2 | NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1255-3143G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172808 | |||||||
chr10:43172950 | G | A | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1255-3001G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172950 | |||||||
chr10:43172968 | C | T | 3 | a0002c0002t0001g0149 a0002c0002t0001g0170 a0002c0002t0001g0171 |
3 | HG00140.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1255-2983C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43172968 | |||||||
chr10:43173065 | G | A | 1 | a0001c0003t0008g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1255-2886G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173065 | |||||||
chr10:43173148 | G | T | 12 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
15 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1255-2803G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173148 | |||||||
chr10:43173214 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1255-2737G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173214 | |||||||
chr10:43173278 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1255-2673A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173278 | |||||||
chr10:43173513 | G | A | 5 | a0002c0002t0001g0026 a0002c0002t0001g0047 a0002c0002t0001g0138 others(2): Show |
6 | NA18953.hp1 NA18967.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-2438G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173513 | |||||||
chr10:43173627 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1255-2324T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173627 | |||||||
chr10:43173704 | A | ATAAT | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-2245_1255-224 others(8): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43173704 | ||||||
chr10:43173742 | G | C | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1255-2209G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173742 | |||||||
chr10:43173976 | C | G | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1255-1975C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43173976 | |||||||
chr10:43174387 | C | T | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-1564C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174387 | |||||||
chr10:43174408 | G | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1255-1543G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174408 | |||||||
chr10:43174449 | A | T | 1 | a0001c0001t0002g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1255-1502A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174449 | |||||||
chr10:43174528 | T | G | 1 | a0001c0001t0004g0301 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1255-1423T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174528 | |||||||
chr10:43174591 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1255-1360C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174591 | |||||||
chr10:43174750 | A | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(11): Show |
17 | HG01099.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1255-1201A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174750 | |||||||
chr10:43174853 | C | G | 3 | a0004c0005t0001g0251 a0004c0005t0001g0252 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1255-1098C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174853 | |||||||
chr10:43174971 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1255-980A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43174971 | |||||||
chr10:43175231 | C | T | 1 | a0001c0001t0007g0004 | 5 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-720C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175231 | |||||||
chr10:43175246 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0016g0109 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1255-705C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175246 | |||||||
chr10:43175283 | A | G | 39 | a0001c0001t0001g0186 a0001c0001t0001g0263 a0001c0001t0001g0264 others(36): Show |
45 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(42): Show |
intron_variant | MODIFIER | c.1255-668A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175283 | |||||||
chr10:43175357 | C | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1255-594C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175357 | |||||||
chr10:43175886 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1255-65C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175886 | |||||||
chr10:43175930 | GT | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
splice_region_variant&intron_variant | LOW | c.1255-8delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43175930 | ||||||
chr10:43175930 | GTT | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0165 others(3): Show |
7 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1255-9_1255-8delTT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 43175930 | ||||||
chr10:43175932 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1255-19T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175932 | |||||||
chr10:43175935 | T | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-16T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 6/7 | chr10 | 43175935 | |||||||
chr10:43176048 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1336+16A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176048 | |||||||
chr10:43176158 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1336+126G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176158 | |||||||
chr10:43176419 | A | AT | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1336+394dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43176419 | ||||||
chr10:43176554 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0054 |
3 | HG00099.hp1 HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1336+522C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176554 | |||||||
chr10:43176668 | C | T | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1336+636C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176668 | |||||||
chr10:43176700 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1336+668G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176700 | |||||||
chr10:43176755 | C | T | 1 | a0001c0001t0005g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1336+723C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43176755 | |||||||
chr10:43177076 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0127 a0001c0001t0001g0166 |
4 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336+1044G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177076 | |||||||
chr10:43177113 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336+1081C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177113 | |||||||
chr10:43177328 | G | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1336+1296G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177328 | |||||||
chr10:43177337 | G | A | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1336+1305G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177337 | |||||||
chr10:43177408 | A | G | 1 | a0002c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1336+1376A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177408 | |||||||
chr10:43177650 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1336+1618T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177650 | |||||||
chr10:43177689 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1336+1657T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177689 | |||||||
chr10:43177888 | T | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG00673.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1336+1856T>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43177888 | |||||||
chr10:43178234 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1336+2202C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178234 | |||||||
chr10:43178283 | G | T | 226 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1336+2251G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178283 | |||||||
chr10:43178361 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1336+2329G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178361 | |||||||
chr10:43178389 | G | A | 188 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1336+2357G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178389 | |||||||
chr10:43178394 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1336+2362G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178394 | |||||||
chr10:43178397 | C | G | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+2365C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178397 | |||||||
chr10:43178398 | A | G | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1336+2366A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178398 | |||||||
chr10:43178490 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1336+2458A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178490 | |||||||
chr10:43178541 | A | C | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1336+2509A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178541 | |||||||
chr10:43178553 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1336+2521G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178553 | |||||||
chr10:43178618 | C | CA | 34 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0074 others(31): Show |
34 | HG01070.hp2 HG01123.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1336+2604dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43178618 | ||||||
chr10:43178714 | G | A | 2 | a0001c0001t0003g0097 a0001c0001t0019g0270 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1336+2682G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178714 | |||||||
chr10:43178945 | A | G | 1 | a0002c0002t0001g0164 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1336+2913A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178945 | |||||||
chr10:43178955 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1336+2923G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178955 | |||||||
chr10:43178992 | T | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1336+2960T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43178992 | |||||||
chr10:43179249 | G | GT | 17 | a0001c0001t0001g0166 a0001c0001t0002g0188 a0001c0001t0002g0193 others(14): Show |
18 | HG00735.hp1 HG01109.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1336+3233dupT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43179249 | ||||||
chr10:43179249 | G | T | 1 | a0002c0002t0001g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1336+3217G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179249 | |||||||
chr10:43179249 | GT | G | 8 | a0001c0001t0001g0168 a0001c0001t0002g0199 a0001c0001t0002g0239 others(5): Show |
9 | HG00735.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1336+3233delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43179249 | ||||||
chr10:43179270 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0004c0005t0001g0253 |
3 | HG01243.hp1 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1336+3238G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179270 | |||||||
chr10:43179383 | G | A | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1336+3351G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179383 | |||||||
chr10:43179389 | GT | G | 8 | a0001c0001t0001g0131 a0001c0003t0008g0271 a0001c0003t0008g0272 others(5): Show |
8 | HG01167.hp2 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336+3368delT | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43179389 | ||||||
chr10:43179465 | G | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1336+3433G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179465 | |||||||
chr10:43179467 | C | T | 3 | a0001c0001t0002g0221 a0001c0001t0002g0225 a0001c0001t0002g0240 |
3 | NA18994.hp2 NA19068.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1336+3435C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179467 | |||||||
chr10:43179485 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1336+3453C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179485 | |||||||
chr10:43179639 | C | T | 2 | a0001c0003t0008g0274 a0001c0003t0008g0275 |
2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1336+3607C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179639 | |||||||
chr10:43179643 | G | A | 1 | a0001c0001t0019g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1337-3607G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179643 | |||||||
chr10:43179962 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337-3288T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179962 | |||||||
chr10:43179970 | C | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1337-3280C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179970 | |||||||
chr10:43179978 | C | G | 1 | a0002c0002t0001g0140 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1337-3272C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179978 | |||||||
chr10:43179978 | C | T | 2 | a0001c0003t0008g0274 a0001c0003t0008g0275 |
2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1337-3272C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43179978 | |||||||
chr10:43180008 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1337-3242G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180008 | |||||||
chr10:43180223 | T | C | 234 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(231): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1337-3027T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180223 | |||||||
chr10:43180229 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1337-3021G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180229 | |||||||
chr10:43180273 | C | T | 188 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1337-2977C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180273 | |||||||
chr10:43180439 | G | C | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337-2811G>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180439 | |||||||
chr10:43180902 | C | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02723.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1337-2348C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180902 | |||||||
chr10:43180906 | T | G | 1 | a0002c0002t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1337-2344T>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180906 | |||||||
chr10:43180967 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1337-2283A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43180967 | |||||||
chr10:43181038 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1337-2212C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181038 | |||||||
chr10:43181404 | C | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337-1846C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181404 | |||||||
chr10:43181636 | G | A | 1 | a0001c0001t0005g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1337-1614G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181636 | |||||||
chr10:43181651 | A | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0128 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1337-1599A>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181651 | |||||||
chr10:43181811 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1337-1439G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181811 | |||||||
chr10:43181834 | G | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1337-1416G>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181834 | |||||||
chr10:43181881 | A | AAGACCAG others(1433): Show |
1 | a0001c0001t0001g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1444): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1433): Show |
1 | a0001c0001t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1444): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1432): Show |
36 | a0001c0001t0001g0186 a0001c0001t0001g0278 a0001c0001t0001g0279 others(33): Show |
42 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(39): Show |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1443): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1432): Show |
1 | a0001c0001t0004g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1443): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
1 | a0001c0001t0001g0131 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
1 | a0001c0001t0005g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
1 | a0001c0001t0012g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
122 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(119): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
46 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
11 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0174 others(8): Show |
14 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1430): Show |
1 | a0001c0001t0001g0018 | 2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1429): Show |
3 | a0001c0001t0006g0159 a0002c0002t0001g0181 a0002c0002t0014g0150 |
3 | HG01168.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1440): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGACCAG others(1429): Show |
1 | a0001c0001t0007g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1337-1367_1337-136 others(1440): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181881 | A | AAGGCCAG others(1430): Show |
7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337-1367_1337-136 others(1441): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43181881 | ||||||
chr10:43181898 | G | A | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1337-1352G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43181898 | |||||||
chr10:43182260 | T | C | 2 | a0002c0002t0001g0095 a0002c0002t0001g0136 |
2 | NA18966.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1337-990T>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182260 | |||||||
chr10:43182438 | C | G | 1 | a0001c0001t0010g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1337-812C>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182438 | |||||||
chr10:43182456 | A | G | 1 | a0001c0001t0020g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1337-794A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182456 | |||||||
chr10:43182607 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1337-643G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182607 | |||||||
chr10:43182626 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1337-624A>G | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182626 | |||||||
chr10:43182654 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1337-596G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182654 | |||||||
chr10:43182675 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(46): Show |
64 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1337-575C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182675 | |||||||
chr10:43182715 | C | CA | 21 | a0001c0001t0001g0055 a0001c0001t0001g0135 a0001c0001t0003g0089 others(18): Show |
25 | HG00741.hp2 HG01106.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1337-520dupA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43182715 | ||||||
chr10:43182749 | C | T | 33 | a0001c0001t0001g0310 a0001c0001t0004g0009 a0001c0001t0004g0042 others(30): Show |
39 | HG00544.hp2 HG02155.hp1 HG02523.hp1 others(36): Show |
intron_variant | MODIFIER | c.1337-501C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182749 | |||||||
chr10:43182750 | G | A | 3 | a0002c0002t0001g0149 a0002c0002t0001g0170 a0002c0002t0001g0171 |
3 | HG00140.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1337-500G>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182750 | |||||||
chr10:43182789 | C | T | 4 | a0001c0001t0011g0036 a0001c0001t0011g0266 a0001c0001t0011g0267 others(1): Show |
5 | HG00735.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1337-461C>T | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182789 | |||||||
chr10:43182884 | AAC | A | 7 | a0001c0003t0008g0271 a0001c0003t0008g0272 a0001c0003t0008g0273 others(4): Show |
7 | HG01192.hp2 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1337-364_1337-363d others(4): Show |
CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43182884 | ||||||
chr10:43182886 | C | A | 10 | a0001c0001t0001g0033 a0001c0001t0001g0077 a0001c0001t0001g0081 others(7): Show |
11 | HG01891.hp2 HG01928.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1337-364C>A | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182886 | |||||||
chr10:43182886 | CA | C | 239 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(236): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1337-353delA | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 43182886 | ||||||
chr10:43182887 | A | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0077 a0001c0001t0001g0081 others(14): Show |
18 | HG01192.hp2 HG01361.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1337-363A>C | CSGALNACT2 | ENSG00000169826.8 | transcript | ENST00000374466.4 | protein_coding | 7/7 | chr10 | 43182887 |