Item | Value |
---|---|
geneid | 54682 |
ensemblid | ENSG00000111261.14 |
hgncid | 25505 |
symbol | MANSC1 |
name | MANSC domain containing 1 |
refseq_nuc | NM_018050.4 |
refseq_prot | NP_060520.2 |
ensembl_nuc | ENST00000535902.6 |
ensembl_prot | ENSP00000438205.1 |
mane_status | MANE Select |
chr | chr12 |
start | 12326056 |
end | 12350242 |
strand | - |
ver | v1.2 |
region | chr12:12326056-12350242 |
region5000 | chr12:12321056-12355242 |
regionname0 | MANSC1_chr12_12326056_12350242 |
regionname5000 | MANSC1_chr12_12321056_12355242 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 431 | 293 | 49 | 59 | 151 | 8 | 24 | 112 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0002 | 0/0 | 431 | 21 | 0 | 7 | 8 | 4 | 2 | 7 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0003 | 0/0 | 431 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0004 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0005 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0006 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(426): Show |
chr12 | 12321056 | 12355242 |
a0007 | 0/0 | 139 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | MFFGG others(134): Show |
chr12 | 12321056 | 12355242 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1293 | 144 | 20 | 20 | 90 | 2 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0002 | 0/1 | 1293 | 129 | 21 | 37 | 53 | 6 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0004 | 0/0 | 1293 | 8 | 0 | 0 | 8 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0005 | 0/0 | 1293 | 7 | 6 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0008 | 0/0 | 1293 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0009 | 0/0 | 1293 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0001c0014 | 0/0 | 1293 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0002c0003 | 0/0 | 1293 | 18 | 0 | 7 | 5 | 4 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0002c0007 | 0/0 | 1293 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0003c0006 | 0/0 | 1293 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0004c0013 | 0/0 | 1293 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0005c0012 | 0/0 | 1293 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0006c0010 | 0/0 | 1293 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1288): Show |
chr12 | 12321056 | 12355242 | ||
a0007c0011 | 0/0 | 1309 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ATGTT others(1304): Show |
chr12 | 12321056 | 12355242 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5538 | 26 | 0 | 3 | 22 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0003 | 0/0 | 5539 | 20 | 0 | 3 | 16 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0005 | 0/0 | 5541 | 10 | 4 | 0 | 6 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0010 | 0/0 | 5540 | 5 | 2 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0014 | 0/0 | 5536 | 4 | 0 | 2 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0015 | 0/0 | 5539 | 5 | 0 | 1 | 3 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0016 | 0/0 | 5532 | 5 | 0 | 2 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0017 | 0/0 | 5537 | 4 | 0 | 1 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0018 | 0/0 | 5537 | 4 | 0 | 2 | 1 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0021 | 0/0 | 5537 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0022 | 0/0 | 5537 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0024 | 0/0 | 5522 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5517): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0025 | 0/0 | 5542 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0029 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0030 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0038 | 0/0 | 5522 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5517): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0039 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0040 | 0/0 | 5543 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0041 | 0/0 | 5538 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0044 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0054 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0062 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0065 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0066 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0068 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0079 | 0/0 | 5545 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5540): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0080 | 0/0 | 5543 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0081 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0098 | 0/0 | 5526 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5521): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0099 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5517): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0100 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0101 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0102 | 1/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0103 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0104 | 0/0 | 5534 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0105 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0106 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0107 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0108 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0109 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0110 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0111 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0112 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0113 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0114 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0116 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0117 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0118 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5539): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0119 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5540): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0120 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5541): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0121 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0122 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0124 | 0/0 | 5535 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0125 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5525): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0129 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0130 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0131 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0001t0133 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0001 | 0/0 | 5539 | 30 | 0 | 9 | 14 | 1 | 6 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0004 | 0/0 | 5537 | 12 | 0 | 2 | 7 | 2 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0007 | 0/0 | 5541 | 7 | 0 | 0 | 7 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0008 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0009 | 0/0 | 5535 | 3 | 0 | 2 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0011 | 0/0 | 5537 | 5 | 0 | 0 | 4 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0012 | 0/0 | 5539 | 5 | 0 | 4 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0013 | 0/1 | 5541 | 3 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0019 | 0/0 | 5543 | 4 | 1 | 1 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0020 | 0/0 | 5532 | 4 | 0 | 4 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0023 | 0/0 | 5540 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0027 | 0/0 | 5535 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0028 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0031 | 0/0 | 5543 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0032 | 0/0 | 5536 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0033 | 0/0 | 5538 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0035 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0036 | 0/0 | 5538 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0037 | 0/0 | 5543 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0045 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0046 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0047 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5525): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0052 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0053 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0056 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0057 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0059 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0060 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0061 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0063 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0064 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0067 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0069 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0070 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0071 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0072 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0073 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0074 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0075 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0076 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0077 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5539): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0078 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0082 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5540): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0083 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5540): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0085 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0086 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0087 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5525): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0088 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0089 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0091 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0092 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0093 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0094 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0001c0002t0096 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0004t0008 | 0/0 | 5537 | 5 | 0 | 0 | 5 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0001c0004t0034 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0004t0095 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5540): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0026 | 0/0 | 5534 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0050 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5525): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0051 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0055 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5529): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0058 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0001c0005t0084 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0001c0008t0013 | 0/0 | 5541 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5536): Show |
chr12 | 12321056 | 12355242 |
a0001c0009t0048 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0001c0009t0049 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5526): Show |
chr12 | 12321056 | 12355242 |
a0001c0014t0090 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0006 | 0/0 | 5529 | 8 | 0 | 4 | 0 | 3 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5524): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0021 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5532): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0042 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0043 | 0/0 | 5535 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0044 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5534): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0126 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5524): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0127 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5527): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0128 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5526): Show |
chr12 | 12321056 | 12355242 |
a0002c0003t0132 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0002c0007t0009 | 0/0 | 5535 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5530): Show |
chr12 | 12321056 | 12355242 |
a0003c0006t0002 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5533): Show |
chr12 | 12321056 | 12355242 |
a0003c0006t0010 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5535): Show |
chr12 | 12321056 | 12355242 |
a0003c0006t0014 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5531): Show |
chr12 | 12321056 | 12355242 |
a0003c0006t0025 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5537): Show |
chr12 | 12321056 | 12355242 |
a0004c0013t0115 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5538): Show |
chr12 | 12321056 | 12355242 |
a0005c0012t0097 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5539): Show |
chr12 | 12321056 | 12355242 |
a0006c0010t0042 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5528): Show |
chr12 | 12321056 | 12355242 |
a0007c0011t0123 | 0/0 | 5548 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | ACTTG others(5543): Show |
chr12 | 12321056 | 12355242 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0014g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0015g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0015g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0015g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0015g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0016g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0016g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0016g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0017g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0017g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0017g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0018g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0018g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0018g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0021g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0021g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0022g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0024g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0024g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0025g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0025g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0029g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0030g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0030g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0038g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0039g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0039g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0040g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0040g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0041g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0044g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0054g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0062g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0065g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0066g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0068g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0079g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0080g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0081g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0098g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0099g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0100g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0101g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0102g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0103g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0104g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0105g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0106g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0107g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0108g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0109g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0110g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0111g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0112g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0113g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0114g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0116g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0117g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0118g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0119g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0120g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0121g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0122g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0124g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0125g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0129g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0130g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0131g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0001t0133g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0001 | 0/0 | 9 | 0 | 4 | 3 | 0 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0011g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0011g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0011g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0012g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0012g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0013g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0013g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0013g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0019g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0019g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0019g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0020g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0027g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0027g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0028g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0028g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0031g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0031g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0032g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0032g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0033g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0035g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0035g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0036g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0037g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0037g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0045g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0046g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0047g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0052g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0053g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0056g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0057g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0059g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0060g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0061g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0063g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0064g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0067g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0069g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0070g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0071g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0072g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0073g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0074g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0075g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0076g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0077g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0078g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0082g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0083g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0085g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0086g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0087g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0088g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0089g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0091g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0092g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0093g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0094g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0002t0096g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0004t0008g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0004t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0004t0034g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0004t0095g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0026g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0050g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0051g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0055g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0058g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0005t0084g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0008t0013g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0009t0048g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0009t0049g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0001c0014t0090g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0006g0003 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0021g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0021g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0042g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0043g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0043g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0044g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0126g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0127g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0128g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0003t0132g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0002c0007t0009g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0003c0006t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0003c0006t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0003c0006t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0003c0006t0025g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0004c0013t0115g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0005c0012t0097g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0006c0010t0042g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
a0007c0011t0123g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0003 | t0127 | g0065 | EUR | GBR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0022 | EUR | GBR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00280 | hp1 | a0001 | c0001 | t0018 | g0031 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00280 | hp2 | a0001 | c0002 | t0060 | g0057 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0028 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0036 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00408 | hp1 | a0001 | c0002 | t0007 | g0143 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00408 | hp2 | a0001 | c0001 | t0017 | g0040 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00423 | hp1 | a0001 | c0002 | t0083 | g0157 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00423 | hp2 | a0001 | c0001 | t0068 | g0192 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0179 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00438 | hp2 | a0001 | c0001 | t0025 | g0048 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00597 | hp1 | a0001 | c0002 | t0007 | g0134 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00597 | hp2 | a0003 | c0006 | t0002 | g0188 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00609 | hp1 | a0001 | c0001 | t0065 | g0236 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00609 | hp2 | a0001 | c0002 | t0082 | g0132 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00621 | hp1 | a0001 | c0001 | t0133 | g0087 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00639 | hp1 | a0001 | c0002 | t0061 | g0058 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00639 | hp2 | a0001 | c0002 | t0013 | g0166 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00642 | hp2 | a0001 | c0002 | t0020 | g0004 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00673 | hp1 | a0001 | c0001 | t0131 | g0233 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00673 | hp2 | a0003 | c0006 | t0025 | g0210 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00733 | hp1 | a0001 | c0002 | t0012 | g0012 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00733 | hp2 | a0001 | c0002 | t0063 | g0113 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00735 | hp1 | a0002 | c0003 | t0006 | g0070 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00735 | hp2 | a0002 | c0003 | t0006 | g0003 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00741 | hp1 | a0001 | c0002 | t0012 | g0156 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01069 | hp1 | a0001 | c0002 | t0027 | g0054 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01069 | hp2 | a0001 | c0002 | t0012 | g0012 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01081 | hp1 | a0001 | c0002 | t0059 | g0055 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01081 | hp2 | a0001 | c0002 | t0037 | g0129 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01099 | hp2 | a0001 | c0002 | t0032 | g0110 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01109 | hp1 | a0001 | c0002 | t0094 | g0099 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01109 | hp2 | a0002 | c0003 | t0006 | g0064 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01167 | hp1 | a0001 | c0002 | t0020 | g0004 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01167 | hp2 | a0001 | c0001 | t0038 | g0032 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01168 | hp1 | a0001 | c0002 | t0075 | g0164 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01168 | hp2 | a0001 | c0001 | t0018 | g0173 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0031 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01169 | hp2 | a0001 | c0001 | t0038 | g0032 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01243 | hp2 | a0001 | c0001 | t0129 | g0232 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01255 | hp1 | a0001 | c0002 | t0077 | g0167 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01255 | hp2 | a0002 | c0003 | t0128 | g0068 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01256 | hp1 | a0001 | c0002 | t0020 | g0004 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01258 | hp2 | a0001 | c0002 | t0020 | g0004 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01261 | hp1 | a0002 | c0003 | t0132 | g0066 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01261 | hp2 | a0001 | c0001 | t0079 | g0150 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01346 | hp1 | a0001 | c0002 | t0027 | g0056 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01361 | hp1 | a0001 | c0002 | t0013 | g0155 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01361 | hp2 | a0002 | c0003 | t0126 | g0067 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01433 | hp1 | a0001 | c0002 | t0009 | g0104 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01433 | hp2 | a0001 | c0008 | t0013 | g0027 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0147 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01516 | hp1 | a0002 | c0003 | t0006 | g0003 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01516 | hp2 | a0001 | c0002 | t0037 | g0091 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01517 | hp1 | a0001 | c0002 | t0004 | g0151 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01517 | hp2 | a0002 | c0003 | t0006 | g0003 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01884 | hp1 | a0001 | c0002 | t0093 | g0096 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01891 | hp1 | a0001 | c0009 | t0049 | g0176 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01891 | hp2 | a0001 | c0005 | t0051 | g0183 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01934 | hp1 | a0001 | c0005 | t0026 | g0088 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01934 | hp2 | a0001 | c0001 | t0081 | g0231 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01943 | hp1 | a0001 | c0001 | t0017 | g0040 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01943 | hp2 | a0001 | c0002 | t0004 | g0028 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01952 | hp1 | a0001 | c0002 | t0032 | g0170 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0037 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01981 | hp2 | a0001 | c0001 | t0130 | g0222 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02004 | hp1 | a0001 | c0002 | t0012 | g0012 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02004 | hp2 | a0001 | c0001 | t0014 | g0026 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02027 | hp1 | a0001 | c0001 | t0054 | g0235 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02027 | hp2 | a0001 | c0001 | t0104 | g0050 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02056 | hp1 | a0001 | c0001 | t0030 | g0219 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02056 | hp2 | a0001 | c0001 | t0066 | g0045 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02071 | hp1 | a0004 | c0013 | t0115 | g0213 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02071 | hp2 | a0001 | c0001 | t0108 | g0051 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02080 | hp2 | a0001 | c0002 | t0072 | g0168 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02083 | hp1 | a0001 | c0002 | t0007 | g0169 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02083 | hp2 | a0001 | c0001 | t0110 | g0194 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02129 | hp2 | a0001 | c0001 | t0014 | g0189 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02132 | hp1 | a0001 | c0001 | t0015 | g0190 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02135 | hp1 | a0001 | c0001 | t0016 | g0239 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02135 | hp2 | a0003 | c0006 | t0010 | g0187 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02145 | hp1 | a0001 | c0005 | t0055 | g0089 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02145 | hp2 | a0001 | c0002 | t0089 | g0094 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02148 | hp1 | a0001 | c0002 | t0070 | g0106 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02148 | hp2 | a0001 | c0002 | t0036 | g0030 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02155 | hp1 | a0001 | c0002 | t0074 | g0119 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02155 | hp2 | a0001 | c0001 | t0017 | g0228 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02165 | hp2 | a0001 | c0002 | t0031 | g0171 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02257 | hp1 | a0005 | c0012 | t0097 | g0078 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02257 | hp2 | a0001 | c0002 | t0092 | g0098 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02258 | hp1 | a0001 | c0001 | t0101 | g0218 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02258 | hp2 | a0001 | c0001 | t0117 | g0202 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02273 | hp1 | a0001 | c0001 | t0014 | g0026 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02273 | hp2 | a0001 | c0001 | t0016 | g0238 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02293 | hp2 | a0001 | c0002 | t0009 | g0160 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02451 | hp1 | a0001 | c0002 | t0096 | g0100 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02451 | hp2 | a0001 | c0002 | t0091 | g0081 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02615 | hp1 | a0001 | c0002 | t0019 | g0029 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02615 | hp2 | a0001 | c0009 | t0048 | g0159 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02622 | hp1 | a0001 | c0002 | t0035 | g0095 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02622 | hp2 | a0001 | c0001 | t0120 | g0203 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02647 | hp1 | a0001 | c0001 | t0024 | g0174 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02647 | hp2 | a0001 | c0002 | t0053 | g0146 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02723 | hp1 | a0001 | c0005 | t0058 | g0076 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02723 | hp2 | a0001 | c0002 | t0085 | g0079 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02818 | hp1 | a0001 | c0002 | t0033 | g0020 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02818 | hp2 | a0001 | c0001 | t0121 | g0244 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02922 | hp1 | a0001 | c0001 | t0100 | g0084 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02922 | hp2 | a0001 | c0001 | t0114 | g0092 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02970 | hp1 | a0001 | c0001 | t0099 | g0185 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG02970 | hp2 | a0001 | c0002 | t0088 | g0093 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03041 | hp1 | a0001 | c0001 | t0103 | g0086 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03041 | hp2 | a0001 | c0001 | t0024 | g0033 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03139 | hp1 | a0001 | c0002 | t0086 | g0080 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03139 | hp2 | a0001 | c0002 | t0033 | g0020 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03195 | hp2 | a0001 | c0002 | t0045 | g0043 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03209 | hp1 | a0001 | c0001 | t0024 | g0033 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03209 | hp2 | a0001 | c0005 | t0050 | g0182 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03225 | hp1 | a0001 | c0002 | t0023 | g0135 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03225 | hp2 | a0001 | c0002 | t0047 | g0216 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03239 | hp2 | a0001 | c0001 | t0118 | g0205 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03492 | hp1 | a0001 | c0002 | t0046 | g0116 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03516 | hp2 | a0001 | c0005 | t0026 | g0090 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03540 | hp1 | a0001 | c0001 | t0105 | g0184 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03540 | hp2 | a0001 | c0002 | t0078 | g0248 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03579 | hp1 | a0001 | c0001 | t0111 | g0061 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03579 | hp2 | a0001 | c0002 | t0023 | g0077 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03654 | hp1 | a0001 | c0002 | t0011 | g0118 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03669 | hp1 | a0001 | c0002 | t0052 | g0121 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03669 | hp2 | a0001 | c0001 | t0044 | g0247 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03710 | hp1 | a0001 | c0001 | t0021 | g0246 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03831 | hp1 | a0002 | c0003 | t0044 | g0072 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03927 | hp1 | a0001 | c0001 | t0109 | g0153 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG03927 | hp2 | a0001 | c0001 | t0015 | g0217 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04115 | hp1 | a0001 | c0002 | t0031 | g0152 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04115 | hp2 | a0001 | c0001 | t0106 | g0211 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04184 | hp2 | a0001 | c0001 | t0112 | g0198 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04199 | hp2 | a0001 | c0001 | t0124 | g0136 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04204 | hp1 | a0001 | c0001 | t0080 | g0241 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04204 | hp2 | a0002 | c0003 | t0006 | g0063 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04228 | hp1 | a0001 | c0008 | t0013 | g0027 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG04228 | hp2 | a0001 | c0001 | t0014 | g0191 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18612 | hp1 | a0001 | c0002 | t0028 | g0133 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18747 | hp2 | a0002 | c0003 | t0043 | g0062 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18906 | hp1 | a0001 | c0002 | t0087 | g0175 | AFR | YRI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18943 | hp1 | a0001 | c0001 | t0022 | g0225 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18943 | hp2 | a0002 | c0007 | t0009 | g0008 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18944 | hp2 | a0002 | c0007 | t0009 | g0008 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18945 | hp1 | a0001 | c0001 | t0119 | g0177 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18947 | hp1 | a0006 | c0010 | t0042 | g0075 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18947 | hp2 | a0001 | c0002 | t0011 | g0142 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18949 | hp1 | a0001 | c0004 | t0008 | g0127 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18949 | hp2 | a0001 | c0001 | t0039 | g0242 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18950 | hp2 | a0001 | c0002 | t0019 | g0103 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18951 | hp2 | a0001 | c0004 | t0034 | g0023 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18957 | hp1 | a0001 | c0002 | t0056 | g0162 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18957 | hp2 | a0001 | c0001 | t0021 | g0207 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18959 | hp1 | a0001 | c0004 | t0034 | g0023 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18959 | hp2 | a0001 | c0002 | t0011 | g0124 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18960 | hp1 | a0001 | c0001 | t0122 | g0046 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18961 | hp2 | a0001 | c0001 | t0022 | g0039 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18962 | hp1 | a0001 | c0001 | t0029 | g0041 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0181 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18963 | hp1 | a0002 | c0007 | t0009 | g0008 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18963 | hp2 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18966 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18966 | hp2 | a0001 | c0001 | t0025 | g0049 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18973 | hp2 | a0001 | c0002 | t0064 | g0105 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18977 | hp1 | a0001 | c0002 | t0019 | g0145 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18977 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18978 | hp2 | a0001 | c0002 | t0008 | g0139 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18979 | hp1 | a0001 | c0002 | t0004 | g0131 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18981 | hp1 | a0001 | c0002 | t0011 | g0141 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18981 | hp2 | a0001 | c0001 | t0017 | g0234 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18986 | hp1 | a0001 | c0002 | t0007 | g0120 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18991 | hp1 | a0001 | c0001 | t0098 | g0237 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18991 | hp2 | a0007 | c0011 | t0123 | g0223 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18992 | hp1 | a0001 | c0002 | t0069 | g0083 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18992 | hp2 | a0001 | c0002 | t0007 | g0021 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18993 | hp1 | a0001 | c0002 | t0011 | g0138 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18994 | hp1 | a0001 | c0001 | t0062 | g0221 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18995 | hp2 | a0001 | c0002 | t0076 | g0165 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18997 | hp1 | a0001 | c0001 | t0016 | g0149 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18997 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18998 | hp1 | a0001 | c0002 | t0073 | g0229 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA18998 | hp2 | a0002 | c0003 | t0042 | g0074 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19004 | hp2 | a0001 | c0002 | t0007 | g0021 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19005 | hp1 | a0001 | c0001 | t0022 | g0039 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19005 | hp2 | a0001 | c0002 | t0028 | g0117 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19007 | hp1 | a0001 | c0001 | t0015 | g0034 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19010 | hp2 | a0001 | c0001 | t0113 | g0196 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19011 | hp1 | a0001 | c0001 | t0015 | g0034 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19011 | hp2 | a0001 | c0001 | t0016 | g0037 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19012 | hp2 | a0001 | c0002 | t0071 | g0163 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19057 | hp1 | a0001 | c0001 | t0041 | g0016 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19060 | hp1 | a0002 | c0003 | t0021 | g0069 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19060 | hp2 | a0001 | c0002 | t0012 | g0060 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19062 | hp1 | a0001 | c0001 | t0116 | g0053 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19062 | hp2 | a0001 | c0002 | t0067 | g0161 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19064 | hp2 | a0001 | c0002 | t0008 | g0224 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19065 | hp1 | a0003 | c0006 | t0014 | g0204 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19066 | hp1 | a0002 | c0003 | t0021 | g0071 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19067 | hp2 | a0001 | c0002 | t0009 | g0122 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19068 | hp2 | a0002 | c0003 | t0043 | g0073 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19074 | hp1 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19077 | hp1 | a0001 | c0001 | t0018 | g0230 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19077 | hp2 | a0001 | c0001 | t0010 | g0208 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19078 | hp1 | a0001 | c0002 | t0007 | g0137 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19079 | hp2 | a0001 | c0001 | t0039 | g0199 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19080 | hp2 | a0001 | c0001 | t0041 | g0016 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19081 | hp2 | a0001 | c0001 | t0107 | g0052 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19082 | hp1 | a0001 | c0002 | t0057 | g0140 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19082 | hp2 | a0001 | c0001 | t0040 | g0193 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19084 | hp1 | a0001 | c0001 | t0040 | g0197 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19084 | hp2 | a0001 | c0001 | t0030 | g0226 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19085 | hp2 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19086 | hp2 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19088 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19091 | hp1 | a0001 | c0001 | t0029 | g0041 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA19091 | hp2 | a0001 | c0004 | t0095 | g0128 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20129 | hp1 | a0001 | c0002 | t0023 | g0097 | AFR | ASW | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20129 | hp2 | a0001 | c0001 | t0125 | g0240 | AFR | ASW | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20752 | hp1 | a0002 | c0003 | t0006 | g0003 | EUR | TSI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20752 | hp2 | a0001 | c0002 | t0036 | g0030 | EUR | TSI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20905 | hp1 | a0001 | c0002 | t0004 | g0172 | SAS | GIH | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20905 | hp2 | a0001 | c0014 | t0090 | g0126 | SAS | GIH | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01123 | hp1 | a0001 | c0002 | t0019 | g0029 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
HG01123 | hp2 | a0002 | c0003 | t0006 | g0003 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | USA | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA20300 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | USA | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA21309 | hp1 | a0001 | c0005 | t0084 | g0082 | AFR | LWK | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
NA21309 | hp2 | a0001 | c0002 | t0035 | g0101 | AFR | LWK | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
homoSapiens | chm13v2 | a0001 | c0002 | t0013 | g0154 | REF | REF | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
homoSapiens | grch38p0 | a0001 | c0001 | t0102 | g0085 | REF | REF | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:12330086 | G | A | 1 | a0004 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1237C>T | p.Arg413Cys | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1502/5532 | 1237/1296 | 413/431 | chr12 | 12330086 | |||
chr12:12330200 | T | A | 1 | a0003 | 4 | HG00597.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
missense_variant | MODERATE | c.1123A>T | p.Asn375Tyr | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1388/5532 | 1123/1296 | 375/431 | chr12 | 12330200 | |||
chr12:12330299 | A | G | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1024T>C | p.Ser342Pro | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1289/5532 | 1024/1296 | 342/431 | chr12 | 12330299 | |||
chr12:12330917 | G | GTCTATGG others(9): Show |
1 | a0007 | 1 | NA18991.hp2 | frameshift_variant&stop_gained | HIGH | c.405_406insATTGAAAG others(8): Show |
p.Pro136fs | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 670/5532 | 405/1296 | 135/431 | chr12 | 12330917 | |||
chr12:12330937 | T | A | 1 | a0006 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.386A>T | p.Asn129Ile | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 651/5532 | 386/1296 | 129/431 | chr12 | 12330937 | |||
chr12:12343152 | C | T | 2 | a0002 a0006 |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
missense_variant | MODERATE | c.163G>A | p.Val55Ile | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/4 | 428/5532 | 163/1296 | 55/431 | chr12 | 12343152 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:12330096 | C | T | 1 | a0001c0008 | 2 | HG01433.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.1227G>A | p.Ser409Ser | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1492/5532 | 1227/1296 | 409/431 | chr12 | 12330096 | |||
chr12:12330341 | G | A | 8 | a0001c0002 a0001c0004 a0001c0005 others(5): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
synonymous_variant | LOW | c.982C>T | p.Leu328Leu | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1247/5532 | 982/1296 | 328/431 | chr12 | 12330341 | |||
chr12:12330384 | C | T | 1 | a0001c0005 | 7 | HG01891.hp2 HG01934.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.939G>A | p.Ser313Ser | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1204/5532 | 939/1296 | 313/431 | chr12 | 12330384 | |||
chr12:12330779 | A | G | 7 | a0001c0002 a0001c0004 a0001c0005 others(4): Show |
150 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(147): Show |
synonymous_variant | LOW | c.544T>C | p.Leu182Leu | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 809/5532 | 544/1296 | 182/431 | chr12 | 12330779 | |||
chr12:12338421 | T | C | 1 | a0001c0014 | 1 | NA20905.hp2 | splice_region_variant&synonymous_variant | LOW | c.363A>G | p.Thr121Thr | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/4 | 628/5532 | 363/1296 | 121/431 | chr12 | 12338421 | |||
chr12:12343219 | C | T | 1 | a0001c0004 | 8 | NA18949.hp1 NA18951.hp2 NA18959.hp1 others(5): Show |
synonymous_variant | LOW | c.96G>A | p.Lys32Lys | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/4 | 361/5532 | 96/1296 | 32/431 | chr12 | 12343219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:12326183 | C | T | 1 | a0001c0001t0022 | 3 | NA18943.hp1 NA18961.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3844G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3844 | chr12 | 12326183 | ||||||
chr12:12326201 | T | C | 1 | a0001c0002t0061 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3826A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3826 | chr12 | 12326201 | ||||||
chr12:12326206 | C | T | 1 | a0001c0001t0117 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3821G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3821 | chr12 | 12326206 | ||||||
chr12:12326234 | C | T | 1 | a0001c0002t0028 | 2 | NA18612.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3793G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3793 | chr12 | 12326234 | ||||||
chr12:12326316 | C | T | 75 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0016 others(72): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*3711G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3711 | chr12 | 12326316 | ||||||
chr12:12326550 | A | T | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3477T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3477 | chr12 | 12326550 | ||||||
chr12:12326603 | G | GT | 6 | a0001c0001t0106 a0001c0001t0108 a0001c0001t0113 others(3): Show |
6 | HG01168.hp1 HG02071.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3423dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3423 | chr12 | 12326603 | ||||||
chr12:12326603 | G | GTT | 20 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0022 others(17): Show |
52 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3422_*3423dupAA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3423 | chr12 | 12326603 | ||||||
chr12:12326611 | T | G | 8 | a0001c0001t0111 a0001c0001t0112 a0001c0002t0089 others(5): Show |
15 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3416A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3416 | chr12 | 12326611 | ||||||
chr12:12326614 | G | T | 1 | a0001c0001t0029 | 2 | NA18962.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3413C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3413 | chr12 | 12326614 | ||||||
chr12:12326628 | G | GT | 76 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0015 others(73): Show |
204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*3398dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3398 | chr12 | 12326628 | ||||||
chr12:12326628 | G | GTT | 7 | a0001c0001t0108 a0001c0001t0129 a0001c0002t0064 others(4): Show |
7 | HG00140.hp1 HG01168.hp1 HG01243.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3397_*3398dupAA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3398 | chr12 | 12326628 | ||||||
chr12:12326661 | G | A | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3366C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3366 | chr12 | 12326661 | ||||||
chr12:12326903 | C | T | 22 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0022 others(19): Show |
54 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3124G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3124 | chr12 | 12326903 | ||||||
chr12:12327015 | G | A | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3012C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3012 | chr12 | 12327015 | ||||||
chr12:12327071 | A | T | 1 | a0001c0002t0063 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2956T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2956 | chr12 | 12327071 | ||||||
chr12:12327100 | A | G | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2927T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2927 | chr12 | 12327100 | ||||||
chr12:12327108 | C | T | 32 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(29): Show |
71 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2919G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2919 | chr12 | 12327108 | ||||||
chr12:12327115 | T | C | 23 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0022 others(20): Show |
55 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2912A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2912 | chr12 | 12327115 | ||||||
chr12:12327154 | C | T | 24 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0022 others(21): Show |
56 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2873G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2873 | chr12 | 12327154 | ||||||
chr12:12327359 | G | A | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2668C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2668 | chr12 | 12327359 | ||||||
chr12:12327371 | G | T | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2656 | chr12 | 12327371 | ||||||
chr12:12327426 | T | C | 23 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0022 others(20): Show |
55 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2601A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2601 | chr12 | 12327426 | ||||||
chr12:12327959 | TGTCTTAA others(4): Show |
T | 1 | a0001c0001t0098 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057_*2067delGCAA others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2057 | chr12 | 12327959 | ||||||
chr12:12327971 | T | C | 1 | a0001c0001t0105 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2056A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2056 | chr12 | 12327971 | ||||||
chr12:12328152 | CT | C | 9 | a0001c0002t0035 a0001c0002t0078 a0001c0002t0093 others(6): Show |
17 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1874delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1874 | chr12 | 12328152 | ||||||
chr12:12328203 | T | A | 1 | a0001c0002t0069 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1824 | chr12 | 12328203 | ||||||
chr12:12328204 | C | G | 1 | a0001c0002t0069 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1823 | chr12 | 12328204 | ||||||
chr12:12328216 | T | C | 8 | a0001c0001t0125 a0001c0005t0026 a0001c0005t0050 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1811A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1811 | chr12 | 12328216 | ||||||
chr12:12328282 | G | A | 2 | a0001c0002t0060 a0001c0002t0061 |
2 | HG00280.hp2 HG00639.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1745 | chr12 | 12328282 | ||||||
chr12:12328310 | C | T | 26 | a0001c0001t0062 a0001c0001t0103 a0001c0002t0008 others(23): Show |
47 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1717G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1717 | chr12 | 12328310 | ||||||
chr12:12328342 | C | T | 1 | a0001c0002t0073 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1685 | chr12 | 12328342 | ||||||
chr12:12328343 | G | A | 13 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(10): Show |
42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1684C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1684 | chr12 | 12328343 | ||||||
chr12:12328362 | C | T | 59 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(56): Show |
154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1665 | chr12 | 12328362 | ||||||
chr12:12328402 | G | A | 8 | a0001c0001t0131 a0001c0002t0011 a0001c0002t0012 others(5): Show |
19 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1625C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1625 | chr12 | 12328402 | ||||||
chr12:12328406 | G | A | 2 | a0001c0005t0050 a0001c0005t0051 |
2 | HG01891.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1621C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1621 | chr12 | 12328406 | ||||||
chr12:12328417 | C | T | 1 | a0001c0002t0053 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1610 | chr12 | 12328417 | ||||||
chr12:12328526 | G | A | 13 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(10): Show |
42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1501C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1501 | chr12 | 12328526 | ||||||
chr12:12328547 | C | T | 39 | a0001c0001t0099 a0001c0001t0109 a0001c0001t0121 others(36): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1480G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1480 | chr12 | 12328547 | ||||||
chr12:12328594 | C | T | 7 | a0001c0005t0026 a0001c0005t0050 a0001c0005t0051 others(4): Show |
8 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1433G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1433 | chr12 | 12328594 | ||||||
chr12:12328619 | A | G | 90 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(87): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1408T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1408 | chr12 | 12328619 | ||||||
chr12:12328662 | A | C | 1 | a0001c0001t0111 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1365T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1365 | chr12 | 12328662 | ||||||
chr12:12328680 | T | C | 42 | a0001c0001t0107 a0001c0001t0109 a0001c0001t0116 others(39): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1347A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1347 | chr12 | 12328680 | ||||||
chr12:12328712 | G | A | 13 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(10): Show |
42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1315C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1315 | chr12 | 12328712 | ||||||
chr12:12328852 | T | G | 4 | a0001c0002t0027 a0001c0002t0059 a0001c0002t0060 others(1): Show |
5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1175A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1175 | chr12 | 12328852 | ||||||
chr12:12328856 | C | G | 5 | a0001c0001t0122 a0001c0002t0027 a0001c0002t0059 others(2): Show |
6 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1171G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1171 | chr12 | 12328856 | ||||||
chr12:12328857 | G | A | 12 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(9): Show |
40 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1170C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1170 | chr12 | 12328857 | ||||||
chr12:12328857 | G | C | 1 | a0001c0001t0122 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1170C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1170 | chr12 | 12328857 | ||||||
chr12:12328861 | G | A | 3 | a0001c0002t0057 a0001c0002t0073 a0001c0002t0074 |
3 | HG02155.hp1 NA18998.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1166C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1166 | chr12 | 12328861 | ||||||
chr12:12328875 | C | T | 1 | a0001c0001t0125 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1152G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1152 | chr12 | 12328875 | ||||||
chr12:12328880 | T | C | 104 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(101): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1147A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1147 | chr12 | 12328880 | ||||||
chr12:12328880 | T | G | 1 | a0001c0002t0067 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1147 | chr12 | 12328880 | ||||||
chr12:12328890 | A | G | 1 | a0001c0002t0067 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1137 | chr12 | 12328890 | ||||||
chr12:12328936 | C | T | 7 | a0001c0005t0026 a0001c0005t0050 a0001c0005t0051 others(4): Show |
8 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1091 | chr12 | 12328936 | ||||||
chr12:12328981 | C | T | 1 | a0001c0001t0110 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1046 | chr12 | 12328981 | ||||||
chr12:12328984 | T | TCA | 24 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0022 others(21): Show |
44 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1041_*1042dupTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACA | 26 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0018 others(23): Show |
70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1039_*1042dupTGTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACACA | 29 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0030 others(26): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1042dupTGTG others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACACAC others(1): Show |
21 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0021 others(18): Show |
46 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1042dupTGTG others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACACAC others(3): Show |
17 | a0001c0001t0025 a0001c0001t0040 a0001c0001t0044 others(14): Show |
24 | HG00438.hp2 HG00673.hp2 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1042dupTGTG others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACACAC others(5): Show |
5 | a0001c0001t0118 a0001c0001t0119 a0001c0002t0082 others(2): Show |
5 | HG00423.hp1 HG00609.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1042dupTGTG others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | T | TCACACAC others(7): Show |
1 | a0001c0001t0120 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029_*1042dupTGTG others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | ||||||
chr12:12328984 | TCA | T | 5 | a0001c0002t0047 a0001c0002t0087 a0001c0005t0050 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1041_*1042delTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1041 | chr12 | 12328984 | ||||||
chr12:12328984 | TCACACAC others(3): Show |
T | 3 | a0001c0001t0024 a0001c0001t0038 a0001c0001t0099 |
6 | HG01167.hp2 HG01169.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1042delTGTG others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1033 | chr12 | 12328984 | ||||||
chr12:12328988 | A | T | 2 | a0001c0009t0048 a0001c0009t0049 |
2 | HG01891.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1039T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1039 | chr12 | 12328988 | ||||||
chr12:12329027 | A | C | 2 | a0001c0002t0085 a0001c0002t0086 |
2 | HG02723.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1000T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1000 | chr12 | 12329027 | ||||||
chr12:12329257 | A | G | 1 | a0001c0002t0047 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*770T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 770 | chr12 | 12329257 | ||||||
chr12:12329329 | G | A | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*698C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 698 | chr12 | 12329329 | ||||||
chr12:12329514 | T | C | 43 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0044 others(40): Show |
73 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*513A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 513 | chr12 | 12329514 | ||||||
chr12:12329607 | C | A | 1 | a0001c0001t0098 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 420 | chr12 | 12329607 | ||||||
chr12:12329765 | T | G | 1 | a0001c0001t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 262 | chr12 | 12329765 | ||||||
chr12:12329824 | C | T | 1 | a0001c0001t0038 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 203 | chr12 | 12329824 | ||||||
chr12:12329849 | G | A | 2 | a0001c0001t0041 a0001c0001t0122 |
3 | NA18960.hp1 NA19057.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*178C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 178 | chr12 | 12329849 | ||||||
chr12:12329869 | A | G | 104 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(101): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*158T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 158 | chr12 | 12329869 | ||||||
chr12:12329886 | C | A | 18 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0044 others(15): Show |
32 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 141 | chr12 | 12329886 | ||||||
chr12:12329922 | C | T | 1 | a0001c0002t0046 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 105 | chr12 | 12329922 | ||||||
chr12:12329942 | CCTG | C | 20 | a0001c0001t0016 a0001c0001t0021 a0001c0001t0044 others(17): Show |
34 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*84delCAG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 82 | chr12 | 12329942 | ||||||
chr12:12350123 | A | C | 1 | a0001c0002t0045 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/4 | 6809 | chr12 | 12350123 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:12330993 | G | A | 174 | a0001c0001t0002g0245 a0001c0001t0003g0002 a0001c0001t0003g0015 others(171): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.365-35C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12330993 | |||||||
chr12:12331007 | C | T | 4 | a0001c0005t0026g0088 a0001c0005t0026g0090 a0001c0005t0055g0089 others(1): Show |
4 | HG01934.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-49G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331007 | |||||||
chr12:12331202 | G | A | 21 | a0001c0001t0002g0245 a0001c0001t0021g0207 a0001c0001t0021g0246 others(18): Show |
27 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.365-244C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331202 | |||||||
chr12:12331392 | C | T | 82 | a0001c0001t0112g0198 a0001c0001t0133g0087 a0001c0002t0001g0001 others(79): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.365-434G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331392 | |||||||
chr12:12331483 | C | T | 1 | a0001c0002t0019g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.365-525G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331483 | |||||||
chr12:12331484 | G | A | 1 | a0001c0002t0053g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365-526C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331484 | |||||||
chr12:12331486 | A | T | 136 | a0001c0001t0002g0245 a0001c0001t0021g0207 a0001c0001t0021g0246 others(133): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.365-528T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331486 | |||||||
chr12:12331535 | T | G | 1 | a0001c0002t0047g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-577A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331535 | |||||||
chr12:12331635 | G | A | 1 | a0001c0002t0053g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365-677C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331635 | |||||||
chr12:12331656 | T | A | 58 | a0001c0001t0002g0245 a0001c0001t0021g0207 a0001c0001t0021g0246 others(55): Show |
73 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.365-698A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331656 | |||||||
chr12:12331670 | A | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0022 others(75): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.365-712T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331670 | |||||||
chr12:12331715 | G | A | 77 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0022 others(74): Show |
101 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.365-757C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331715 | |||||||
chr12:12331717 | G | A | 1 | a0001c0001t0103g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.365-759C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331717 | |||||||
chr12:12331728 | C | T | 35 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(32): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.365-770G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331728 | |||||||
chr12:12331744 | T | C | 1 | a0001c0002t0067g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.365-786A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331744 | |||||||
chr12:12331836 | G | T | 1 | a0001c0002t0001g0109 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365-878C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331836 | |||||||
chr12:12331882 | A | C | 1 | a0001c0002t0067g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.365-924T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331882 | |||||||
chr12:12331957 | C | T | 151 | a0001c0001t0002g0059 a0001c0001t0003g0002 a0001c0001t0003g0015 others(148): Show |
201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.365-999G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331957 | |||||||
chr12:12332139 | A | G | 1 | a0001c0001t0100g0084 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.365-1181T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332139 | |||||||
chr12:12332178 | G | A | 2 | a0001c0009t0048g0159 a0001c0009t0049g0176 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.365-1220C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332178 | |||||||
chr12:12332237 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.365-1279G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332237 | |||||||
chr12:12332358 | T | C | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1400A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332358 | |||||||
chr12:12332417 | G | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1459C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332417 | |||||||
chr12:12332514 | G | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1556C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332514 | |||||||
chr12:12332589 | C | T | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.365-1631G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332589 | |||||||
chr12:12332621 | G | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1663C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332621 | |||||||
chr12:12332623 | C | T | 1 | a0001c0002t0047g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-1665G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332623 | |||||||
chr12:12332664 | G | A | 1 | a0001c0002t0052g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.365-1706C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332664 | |||||||
chr12:12332665 | C | T | 67 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(64): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.365-1707G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332665 | |||||||
chr12:12332768 | C | G | 1 | a0001c0002t0019g0145 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.365-1810G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332768 | |||||||
chr12:12332873 | A | G | 1 | a0001c0002t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.365-1915T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332873 | |||||||
chr12:12332947 | C | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1989G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332947 | |||||||
chr12:12333044 | A | AATATATA others(5): Show |
16 | a0001c0001t0021g0207 a0002c0003t0006g0003 a0002c0003t0006g0063 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.365-2098_365-2087d others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333044 | |||||||
chr12:12333044 | A | AATATATA others(9): Show |
2 | a0001c0001t0124g0136 a0002c0003t0043g0073 |
2 | HG04199.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.365-2102_365-2087d others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333044 | |||||||
chr12:12333142 | G | A | 1 | a0001c0001t0005g0195 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.365-2184C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333142 | |||||||
chr12:12333150 | A | G | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2192T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333150 | |||||||
chr12:12333299 | A | G | 125 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(122): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.365-2341T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333299 | |||||||
chr12:12333329 | G | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2371C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333329 | |||||||
chr12:12333494 | C | G | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2536G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333494 | |||||||
chr12:12333505 | C | T | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.365-2547G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333505 | |||||||
chr12:12333510 | C | T | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2552G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333510 | |||||||
chr12:12333598 | A | C | 3 | a0001c0005t0026g0088 a0001c0005t0026g0090 a0001c0005t0055g0089 |
3 | HG01934.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.365-2640T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333598 | |||||||
chr12:12333991 | G | C | 1 | a0001c0002t0007g0021 | 2 | NA18992.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.365-3033C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333991 | |||||||
chr12:12334014 | C | T | 35 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(32): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.365-3056G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334014 | |||||||
chr12:12334055 | C | A | 1 | a0001c0002t0011g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.365-3097G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334055 | |||||||
chr12:12334073 | A | AC | 9 | a0001c0001t0133g0087 a0001c0002t0008g0139 a0001c0005t0026g0088 others(6): Show |
9 | HG00621.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-3116dupG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334073 | |||||||
chr12:12334073 | AC | A | 16 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.365-3116delG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334073 | |||||||
chr12:12334078 | C | A | 7 | a0001c0001t0005g0014 a0001c0001t0005g0180 a0001c0001t0005g0186 others(4): Show |
10 | NA18986.hp2 NA18994.hp2 NA19007.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3120G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334078 | |||||||
chr12:12334079 | C | T | 7 | a0001c0001t0005g0014 a0001c0001t0005g0180 a0001c0001t0005g0186 others(4): Show |
10 | NA18986.hp2 NA18994.hp2 NA19007.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3121G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334079 | |||||||
chr12:12334114 | C | G | 1 | a0001c0002t0001g0102 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.365-3156G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334114 | |||||||
chr12:12334131 | T | C | 2 | a0002c0003t0006g0070 a0002c0003t0126g0067 |
2 | HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.365-3173A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334131 | |||||||
chr12:12334162 | A | C | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-3204T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334162 | |||||||
chr12:12334211 | C | T | 1 | a0001c0004t0008g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.365-3253G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334211 | |||||||
chr12:12334215 | G | A | 1 | a0002c0003t0021g0071 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.365-3257C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334215 | |||||||
chr12:12334227 | C | A | 3 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0080g0241 |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-3269G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334227 | |||||||
chr12:12334288 | GA | G | 54 | a0001c0001t0002g0035 a0001c0001t0002g0059 a0001c0001t0029g0041 others(51): Show |
73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.365-3331delT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334288 | |||||||
chr12:12334315 | A | C | 2 | a0001c0009t0048g0159 a0001c0009t0049g0176 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.365-3357T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334315 | |||||||
chr12:12334365 | T | C | 2 | a0001c0001t0015g0190 a0001c0001t0015g0217 |
2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.365-3407A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334365 | |||||||
chr12:12334511 | A | T | 1 | a0001c0001t0125g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.365-3553T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334511 | |||||||
chr12:12334513 | G | A | 18 | a0001c0001t0021g0207 a0001c0001t0124g0136 a0002c0003t0006g0003 others(15): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-3555C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334513 | |||||||
chr12:12334517 | G | A | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.365-3559C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334517 | |||||||
chr12:12334619 | C | T | 1 | a0001c0002t0009g0160 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.365-3661G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334619 | |||||||
chr12:12334634 | C | T | 1 | a0001c0002t0094g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.365-3676G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334634 | |||||||
chr12:12334736 | T | C | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.364+3684A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334736 | |||||||
chr12:12334746 | C | T | 55 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(52): Show |
78 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.364+3674G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334746 | |||||||
chr12:12334764 | A | G | 35 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(32): Show |
52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.364+3656T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334764 | |||||||
chr12:12334948 | C | A | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+3472G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334948 | |||||||
chr12:12334956 | G | A | 1 | a0001c0002t0027g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.364+3464C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334956 | |||||||
chr12:12335085 | C | T | 1 | a0001c0002t0063g0113 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.364+3335G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335085 | |||||||
chr12:12335133 | T | C | 42 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(39): Show |
59 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.364+3287A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335133 | |||||||
chr12:12335211 | G | A | 2 | a0001c0001t0010g0148 a0001c0001t0039g0242 |
2 | NA18949.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.364+3209C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335211 | |||||||
chr12:12335262 | G | T | 1 | a0001c0002t0001g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364+3158C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335262 | |||||||
chr12:12335319 | G | A | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364+3101C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335319 | |||||||
chr12:12335339 | C | CTTT | 79 | a0001c0001t0002g0059 a0001c0001t0109g0153 a0001c0002t0001g0001 others(76): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.364+3078_364+3080d others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335339 | |||||||
chr12:12335339 | CT | C | 6 | a0001c0001t0024g0033 a0001c0001t0024g0174 a0001c0001t0038g0032 others(3): Show |
8 | HG01167.hp2 HG01169.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+3080delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335339 | |||||||
chr12:12335343 | T | C | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+3077A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335343 | |||||||
chr12:12335358 | C | T | 85 | a0001c0001t0002g0059 a0001c0001t0109g0153 a0001c0002t0001g0001 others(82): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.364+3062G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335358 | |||||||
chr12:12335380 | G | A | 1 | a0001c0009t0049g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364+3040C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335380 | |||||||
chr12:12335389 | A | G | 4 | a0001c0002t0032g0110 a0001c0002t0032g0170 a0001c0002t0036g0030 others(1): Show |
5 | HG01099.hp2 HG01952.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+3031T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335389 | |||||||
chr12:12335416 | C | T | 81 | a0001c0001t0002g0059 a0001c0001t0109g0153 a0001c0002t0001g0001 others(78): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.364+3004G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335416 | |||||||
chr12:12335525 | G | C | 169 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(166): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.364+2895C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335525 | |||||||
chr12:12335586 | G | A | 1 | a0001c0001t0030g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.364+2834C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335586 | |||||||
chr12:12335735 | A | G | 208 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(205): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.364+2685T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335735 | |||||||
chr12:12335853 | T | A | 149 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(146): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.364+2567A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335853 | |||||||
chr12:12335855 | A | T | 23 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0047 others(20): Show |
27 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.364+2565T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335855 | |||||||
chr12:12335888 | C | A | 52 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(49): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.364+2532G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335888 | |||||||
chr12:12335911 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0243 |
2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.364+2509C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335911 | |||||||
chr12:12335958 | G | A | 1 | a0001c0002t0007g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.364+2462C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335958 | |||||||
chr12:12335967 | G | A | 5 | a0001c0001t0002g0017 a0001c0001t0104g0050 a0001c0001t0107g0052 others(2): Show |
6 | HG00621.hp2 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+2453C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335967 | |||||||
chr12:12336012 | A | G | 53 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(50): Show |
76 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.364+2408T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336012 | |||||||
chr12:12336059 | C | T | 1 | a0001c0002t0004g0010 | 3 | NA18944.hp1 NA18977.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.364+2361G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336059 | |||||||
chr12:12336184 | G | A | 52 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(49): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.364+2236C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336184 | |||||||
chr12:12336252 | C | T | 1 | a0001c0009t0049g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364+2168G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336252 | |||||||
chr12:12336593 | C | G | 149 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(146): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.364+1827G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336593 | |||||||
chr12:12336614 | C | T | 1 | a0002c0003t0021g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.364+1806G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336614 | |||||||
chr12:12336671 | C | T | 79 | a0001c0001t0002g0059 a0001c0002t0001g0001 a0001c0002t0001g0009 others(76): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.364+1749G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336671 | |||||||
chr12:12336743 | G | T | 2 | a0001c0001t0015g0190 a0001c0001t0015g0217 |
2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.364+1677C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336743 | |||||||
chr12:12337115 | CA | C | 58 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(55): Show |
81 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.364+1304delT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337115 | |||||||
chr12:12337115 | CAAA | C | 149 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(146): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.364+1302_364+1304d others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337115 | |||||||
chr12:12337141 | G | A | 1 | a0001c0002t0012g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.364+1279C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337141 | |||||||
chr12:12337231 | C | G | 3 | a0001c0001t0024g0174 a0001c0002t0087g0175 a0001c0009t0049g0176 |
3 | HG01891.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364+1189G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337231 | |||||||
chr12:12337255 | C | T | 1 | a0001c0001t0099g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364+1165G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337255 | |||||||
chr12:12337256 | G | A | 1 | a0001c0002t0009g0122 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.364+1164C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337256 | |||||||
chr12:12337374 | G | A | 66 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(63): Show |
82 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.364+1046C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337374 | |||||||
chr12:12337421 | C | T | 1 | a0001c0002t0011g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.364+999G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337421 | |||||||
chr12:12337422 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG00140.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.364+998C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337422 | |||||||
chr12:12337466 | C | T | 67 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(64): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.364+954G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337466 | |||||||
chr12:12337469 | G | T | 1 | a0001c0001t0133g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.364+951C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337469 | |||||||
chr12:12337512 | G | C | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+908C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337512 | |||||||
chr12:12337516 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(34): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.364+904C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337516 | |||||||
chr12:12337532 | T | G | 2 | a0001c0001t0125g0240 a0001c0002t0035g0101 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.364+888A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337532 | |||||||
chr12:12337539 | C | T | 1 | a0001c0002t0069g0083 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.364+881G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337539 | |||||||
chr12:12337619 | G | T | 4 | a0001c0001t0024g0033 a0001c0001t0038g0032 a0001c0001t0099g0185 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+801C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337619 | |||||||
chr12:12337953 | A | G | 1 | a0001c0002t0083g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.364+467T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337953 | |||||||
chr12:12337980 | G | A | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.364+440C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337980 | |||||||
chr12:12338047 | T | C | 1 | a0002c0003t0128g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.364+373A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338047 | |||||||
chr12:12338117 | T | C | 1 | a0001c0002t0004g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.364+303A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338117 | |||||||
chr12:12338334 | T | C | 15 | a0001c0001t0003g0002 a0001c0001t0003g0038 a0001c0001t0003g0042 others(12): Show |
27 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.364+86A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338334 | |||||||
chr12:12338890 | A | AAC | 61 | a0001c0001t0133g0087 a0001c0002t0001g0001 a0001c0002t0001g0022 others(58): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.224-332_224-331dup others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACAC | 73 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(70): Show |
93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.224-334_224-331dup others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACAC | 6 | a0001c0001t0002g0047 a0001c0001t0014g0191 a0001c0001t0015g0190 others(3): Show |
6 | HG00438.hp2 HG02132.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-336_224-331dup others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(3): Show |
30 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(27): Show |
46 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.224-340_224-331dup others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(5): Show |
3 | a0001c0001t0130g0222 a0001c0002t0073g0229 a0001c0005t0084g0082 |
3 | HG01981.hp2 NA18998.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.224-342_224-331dup others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(7): Show |
1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.224-344_224-331dup others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(9): Show |
9 | a0001c0001t0125g0240 a0001c0002t0047g0216 a0001c0009t0049g0176 others(6): Show |
15 | HG00735.hp1 HG00735.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.224-346_224-331dup others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(11): Show |
9 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0024g0174 others(6): Show |
10 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.224-348_224-331dup others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(13): Show |
2 | a0001c0002t0087g0175 a0002c0003t0006g0063 |
2 | HG04204.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.224-350_224-331dup others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | AACACACA others(15): Show |
2 | a0001c0001t0080g0241 a0002c0003t0042g0074 |
2 | HG04204.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.224-352_224-331dup others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | A | ACACACAC others(4): Show |
1 | a0001c0001t0017g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.224-331_224-330ins others(11): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338890 | AACACAC | A | 2 | a0001c0001t0024g0033 a0001c0001t0038g0032 |
4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-336_224-331del others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | |||||||
chr12:12338903 | A | T | 2 | a0001c0001t0024g0033 a0001c0001t0038g0032 |
4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-343T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338903 | |||||||
chr12:12338917 | A | ACACACAC others(17): Show |
1 | a0002c0003t0043g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.224-358_224-357ins others(24): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338917 | |||||||
chr12:12338949 | C | T | 1 | a0001c0001t0014g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.224-389G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338949 | |||||||
chr12:12338956 | A | T | 3 | a0001c0001t0024g0174 a0001c0002t0087g0175 a0001c0009t0049g0176 |
3 | HG01891.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224-396T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338956 | |||||||
chr12:12339080 | G | C | 3 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0080g0241 |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-520C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339080 | |||||||
chr12:12339351 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0108 |
3 | HG00558.hp2 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.224-791G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339351 | |||||||
chr12:12339450 | T | C | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.224-890A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339450 | |||||||
chr12:12339473 | G | C | 1 | a0001c0001t0099g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224-913C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339473 | |||||||
chr12:12339531 | G | C | 1 | a0001c0001t0099g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224-971C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339531 | |||||||
chr12:12339531 | G | T | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.224-971C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339531 | |||||||
chr12:12339547 | T | G | 1 | a0001c0002t0023g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224-987A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339547 | |||||||
chr12:12339719 | T | C | 1 | a0001c0002t0087g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224-1159A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339719 | |||||||
chr12:12339891 | C | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(34): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.224-1331G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339891 | |||||||
chr12:12340156 | C | T | 1 | a0001c0001t0125g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224-1596G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340156 | |||||||
chr12:12340401 | T | A | 1 | a0001c0002t0094g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224-1841A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340401 | |||||||
chr12:12340969 | C | T | 6 | a0001c0002t0035g0095 a0001c0002t0035g0101 a0001c0002t0088g0093 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+2123G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340969 | |||||||
chr12:12341150 | C | T | 54 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(51): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.223+1942G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341150 | |||||||
chr12:12341157 | C | T | 1 | a0001c0002t0082g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223+1935G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341157 | |||||||
chr12:12341309 | C | A | 1 | a0001c0002t0087g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.223+1783G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341309 | |||||||
chr12:12341357 | C | A | 1 | a0001c0002t0082g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223+1735G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341357 | |||||||
chr12:12341460 | A | C | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1632T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341460 | |||||||
chr12:12341476 | A | G | 1 | a0001c0002t0013g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.223+1616T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341476 | |||||||
chr12:12341497 | G | A | 5 | a0001c0001t0002g0047 a0001c0001t0025g0048 a0001c0001t0025g0049 others(2): Show |
6 | HG00438.hp2 NA18960.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+1595C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341497 | |||||||
chr12:12341502 | G | A | 69 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(66): Show |
85 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.223+1590C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341502 | |||||||
chr12:12341538 | G | T | 1 | a0001c0002t0011g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223+1554C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341538 | |||||||
chr12:12341670 | G | A | 1 | a0001c0005t0026g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.223+1422C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341670 | |||||||
chr12:12341682 | G | C | 3 | a0001c0002t0037g0091 a0001c0002t0037g0129 a0001c0014t0090g0126 |
3 | HG01081.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223+1410C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341682 | |||||||
chr12:12341689 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0206 a0001c0001t0002g0209 others(2): Show |
8 | HG02074.hp1 HG02074.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1403C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341689 | |||||||
chr12:12341711 | G | C | 1 | a0001c0002t0011g0124 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223+1381C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341711 | |||||||
chr12:12341777 | A | G | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1315T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341777 | |||||||
chr12:12341816 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.223+1276G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341816 | |||||||
chr12:12341827 | T | C | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1265A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341827 | |||||||
chr12:12341884 | C | T | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1208G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341884 | |||||||
chr12:12341939 | C | G | 4 | a0001c0001t0133g0087 a0001c0005t0026g0088 a0001c0005t0026g0090 others(1): Show |
4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1153G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341939 | |||||||
chr12:12341958 | CTCCG | C | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1130_223+1133d others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341958 | |||||||
chr12:12342016 | C | T | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223+1076G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342016 | |||||||
chr12:12342063 | C | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(34): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.223+1029G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342063 | |||||||
chr12:12342109 | A | G | 1 | a0001c0002t0047g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.223+983T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342109 | |||||||
chr12:12342156 | T | C | 71 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(68): Show |
87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.223+936A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342156 | |||||||
chr12:12342239 | G | C | 1 | a0001c0002t0001g0125 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.223+853C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342239 | |||||||
chr12:12342333 | T | C | 2 | a0001c0002t0035g0101 a0001c0002t0096g0100 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.223+759A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342333 | |||||||
chr12:12342366 | C | T | 1 | a0003c0006t0002g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.223+726G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342366 | |||||||
chr12:12342574 | GTGTTTTT others(1): Show |
G | 23 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0042 others(20): Show |
36 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.223+510_223+517del others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342574 | |||||||
chr12:12342576 | GTTTTTTT others(3): Show |
G | 1 | a0002c0003t0043g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223+506_223+515del others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342576 | |||||||
chr12:12342576 | GTTTTTTT others(4): Show |
G | 15 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(12): Show |
21 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+505_223+515del others(11): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342576 | |||||||
chr12:12342577 | T | G | 2 | a0001c0002t0085g0079 a0001c0002t0086g0080 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.223+515A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342577 | |||||||
chr12:12342577 | TTTTTTTG | T | 12 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0003g0220 others(9): Show |
16 | HG00280.hp1 HG00323.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.223+508_223+514del others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342577 | |||||||
chr12:12342579 | TTTTTG | T | 17 | a0001c0001t0002g0059 a0001c0001t0014g0191 a0001c0001t0038g0032 others(14): Show |
19 | HG00408.hp1 HG00544.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.223+508_223+512del others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342579 | |||||||
chr12:12342580 | TTTTG | T | 119 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(116): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.223+508_223+511del others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342580 | |||||||
chr12:12342581 | TTTG | T | 25 | a0001c0001t0002g0007 a0001c0001t0024g0174 a0001c0001t0099g0185 others(22): Show |
27 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.223+508_223+510del others(3): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342581 | |||||||
chr12:12342582 | TTG | T | 30 | a0001c0001t0005g0019 a0001c0001t0005g0186 a0001c0001t0100g0084 others(27): Show |
34 | HG00621.hp1 HG00642.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.223+508_223+509del others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342582 | |||||||
chr12:12342583 | TG | T | 4 | a0001c0001t0005g0018 a0001c0002t0023g0077 a0001c0002t0035g0101 others(1): Show |
5 | HG02451.hp1 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+508delC | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342583 | |||||||
chr12:12342584 | G | T | 6 | a0001c0001t0005g0019 a0001c0001t0103g0086 a0001c0001t0111g0061 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+508C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342584 | |||||||
chr12:12342591 | T | G | 1 | a0002c0003t0043g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223+501A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342591 | |||||||
chr12:12342592 | T | G | 16 | a0001c0001t0002g0209 a0002c0003t0006g0003 a0002c0003t0006g0063 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+500A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342592 | |||||||
chr12:12342593 | T | G | 1 | a0001c0001t0106g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+499A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342593 | |||||||
chr12:12342594 | T | G | 1 | a0003c0006t0025g0210 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.223+498A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342594 | |||||||
chr12:12342596 | T | G | 2 | a0001c0001t0005g0186 a0003c0006t0010g0187 |
2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.223+496A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342596 | |||||||
chr12:12342597 | T | G | 62 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(59): Show |
76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.223+495A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342597 | |||||||
chr12:12342601 | T | G | 2 | a0001c0001t0106g0211 a0001c0001t0116g0053 |
2 | HG04115.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.223+491A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342601 | |||||||
chr12:12342602 | T | G | 4 | a0001c0001t0002g0212 a0001c0001t0002g0214 a0001c0001t0002g0243 others(1): Show |
4 | HG02071.hp1 NA19056.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+490A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342602 | |||||||
chr12:12342704 | G | A | 1 | a0001c0002t0031g0171 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.223+388C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342704 | |||||||
chr12:12342741 | A | T | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+351T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342741 | |||||||
chr12:12342837 | A | G | 209 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(206): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.223+255T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342837 | |||||||
chr12:12342839 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.223+253A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342839 | |||||||
chr12:12342841 | G | A | 2 | a0001c0001t0125g0240 a0001c0002t0045g0043 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.223+251C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342841 | |||||||
chr12:12342991 | C | T | 3 | a0001c0002t0037g0091 a0001c0002t0037g0129 a0001c0014t0090g0126 |
3 | HG01081.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223+101G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342991 | |||||||
chr12:12343025 | C | T | 78 | a0001c0001t0002g0059 a0001c0002t0001g0001 a0001c0002t0001g0009 others(75): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.223+67G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12343025 | |||||||
chr12:12343077 | G | T | 4 | a0001c0001t0133g0087 a0001c0005t0026g0088 a0001c0005t0026g0090 others(1): Show |
4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+15C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12343077 | |||||||
chr12:12343475 | C | T | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-100-61G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343475 | |||||||
chr12:12343537 | C | A | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-123G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343537 | |||||||
chr12:12343564 | T | C | 1 | a0001c0001t0101g0218 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-100-150A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343564 | |||||||
chr12:12343625 | C | A | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-100-211G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343625 | |||||||
chr12:12343690 | G | A | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-276C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343690 | |||||||
chr12:12343701 | A | G | 17 | a0001c0001t0121g0244 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-287T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343701 | |||||||
chr12:12343706 | T | A | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-100-292A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343706 | |||||||
chr12:12343738 | C | T | 1 | a0001c0002t0011g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-100-324G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343738 | |||||||
chr12:12343824 | A | G | 71 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(68): Show |
87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-100-410T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343824 | |||||||
chr12:12343964 | T | A | 4 | a0001c0004t0008g0006 a0001c0004t0008g0127 a0001c0004t0034g0023 others(1): Show |
8 | NA18949.hp1 NA18951.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.-100-550A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343964 | |||||||
chr12:12344001 | G | A | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-587C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344001 | |||||||
chr12:12344043 | G | A | 1 | a0001c0002t0007g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-100-629C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344043 | |||||||
chr12:12344229 | T | C | 4 | a0001c0001t0133g0087 a0001c0005t0026g0088 a0001c0005t0026g0090 others(1): Show |
4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-815A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344229 | |||||||
chr12:12344232 | A | G | 1 | a0001c0001t0010g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-100-818T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344232 | |||||||
chr12:12344289 | G | T | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-875C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344289 | |||||||
chr12:12344366 | C | T | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-952G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344366 | |||||||
chr12:12344399 | T | C | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-985A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344399 | |||||||
chr12:12344419 | T | C | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1005A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344419 | |||||||
chr12:12344461 | C | T | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-1047G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344461 | |||||||
chr12:12344471 | A | G | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-1057T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344471 | |||||||
chr12:12344475 | C | CT | 6 | a0001c0001t0005g0180 a0001c0001t0018g0031 a0001c0001t0018g0173 others(3): Show |
7 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1062dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344475 | |||||||
chr12:12344475 | CT | C | 35 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(32): Show |
51 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-100-1062delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344475 | |||||||
chr12:12344545 | C | T | 2 | a0001c0002t0020g0004 a0001c0002t0032g0110 |
5 | HG00642.hp2 HG01099.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-100-1131G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344545 | |||||||
chr12:12344568 | C | T | 1 | a0001c0001t0038g0032 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-100-1154G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344568 | |||||||
chr12:12344599 | A | C | 1 | a0001c0002t0001g0109 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-100-1185T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344599 | |||||||
chr12:12344686 | A | G | 17 | a0001c0005t0084g0082 a0002c0003t0006g0003 a0002c0003t0006g0063 others(14): Show |
23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-1272T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344686 | |||||||
chr12:12344703 | A | G | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1289T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344703 | |||||||
chr12:12344712 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0108 |
3 | HG00558.hp2 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-100-1298G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344712 | |||||||
chr12:12344913 | T | G | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-1499A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344913 | |||||||
chr12:12344915 | CCATATAT others(3): Show |
C | 1 | a0001c0002t0053g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-100-1511_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344915 | |||||||
chr12:12344916 | C | CAT | 49 | a0001c0001t0002g0011 a0001c0001t0002g0035 a0001c0001t0002g0144 others(46): Show |
51 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-100-1504_-100-150 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATAT | 25 | a0001c0001t0003g0002 a0001c0001t0003g0038 a0001c0001t0003g0042 others(22): Show |
26 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.-100-1506_-100-150 others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATAT | 22 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0003g0002 others(19): Show |
26 | HG01168.hp1 HG01346.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.-100-1508_-100-150 others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(1): Show |
24 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0059 others(21): Show |
27 | HG00544.hp1 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100-1510_-100-150 others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(3): Show |
19 | a0001c0001t0002g0047 a0001c0001t0003g0002 a0001c0001t0003g0015 others(16): Show |
19 | HG00408.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.-100-1512_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(5): Show |
10 | a0001c0001t0002g0214 a0001c0001t0003g0002 a0001c0001t0003g0015 others(7): Show |
10 | HG01358.hp2 HG01952.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-100-1514_-100-150 others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(7): Show |
1 | a0001c0002t0069g0083 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-100-1516_-100-150 others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(9): Show |
2 | a0001c0001t0066g0045 a0001c0004t0008g0006 |
2 | HG02056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-100-1518_-100-150 others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(11): Show |
1 | a0001c0001t0081g0231 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-100-1520_-100-150 others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | C | CATATATA others(17): Show |
1 | a0001c0002t0012g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-100-1526_-100-150 others(28): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CAT | C | 21 | a0001c0001t0005g0019 a0001c0001t0010g0208 a0001c0001t0014g0026 others(18): Show |
21 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-100-1504_-100-150 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATAT | C | 18 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0209 others(15): Show |
20 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-100-1506_-100-150 others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATAT | C | 10 | a0001c0001t0002g0200 a0001c0001t0010g0201 a0001c0001t0018g0031 others(7): Show |
10 | HG00621.hp1 HG01069.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-1508_-100-150 others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(1): Show |
C | 7 | a0001c0001t0003g0015 a0001c0001t0005g0018 a0001c0001t0024g0033 others(4): Show |
7 | HG02257.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1510_-100-150 others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(3): Show |
C | 6 | a0001c0001t0125g0240 a0001c0002t0007g0143 a0001c0002t0012g0012 others(3): Show |
6 | HG00408.hp1 HG00741.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-100-1512_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(5): Show |
C | 6 | a0001c0002t0056g0162 a0001c0002t0067g0161 a0001c0002t0071g0163 others(3): Show |
7 | HG01255.hp2 NA18943.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1514_-100-150 others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(7): Show |
C | 4 | a0002c0003t0006g0003 a0002c0003t0006g0064 a0002c0003t0006g0070 others(1): Show |
7 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-1516_-100-150 others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(9): Show |
C | 5 | a0002c0003t0006g0063 a0002c0003t0126g0067 a0002c0003t0127g0065 others(2): Show |
5 | HG00140.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-1518_-100-150 others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(11): Show |
C | 8 | a0001c0001t0015g0217 a0001c0001t0016g0239 a0002c0003t0021g0069 others(5): Show |
8 | HG02135.hp1 HG03927.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.-100-1520_-100-150 others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(13): Show |
C | 1 | a0001c0002t0035g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-100-1522_-100-150 others(24): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(15): Show |
C | 13 | a0001c0001t0002g0017 a0001c0001t0005g0014 a0001c0001t0005g0180 others(10): Show |
16 | HG00621.hp2 HG01243.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-1524_-100-150 others(26): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(17): Show |
C | 7 | a0001c0001t0003g0220 a0001c0002t0035g0101 a0001c0002t0088g0093 others(4): Show |
7 | HG01884.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-1526_-100-150 others(28): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(23): Show |
C | 1 | a0001c0002t0061g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-100-1532_-100-150 others(34): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344916 | CATATATA others(25): Show |
C | 1 | a0001c0005t0058g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-1534_-100-150 others(36): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | |||||||
chr12:12344938 | T | TATATATA others(3): Show |
2 | a0001c0002t0037g0091 a0001c0002t0037g0129 |
2 | HG01081.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-100-1525_-100-152 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344938 | |||||||
chr12:12345023 | A | G | 1 | a0001c0005t0084g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1609T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345023 | |||||||
chr12:12345044 | G | A | 1 | a0001c0005t0058g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-1630C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345044 | |||||||
chr12:12345117 | C | G | 70 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(67): Show |
86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-100-1703G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345117 | |||||||
chr12:12345117 | C | T | 1 | a0001c0001t0111g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-100-1703G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345117 | |||||||
chr12:12345215 | G | A | 34 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(31): Show |
50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-1801C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345215 | |||||||
chr12:12345291 | G | A | 3 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0080g0241 |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-1877C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345291 | |||||||
chr12:12345320 | C | CA | 118 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(115): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-100-1907dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345320 | |||||||
chr12:12345320 | C | CAA | 6 | a0001c0001t0015g0217 a0001c0001t0018g0173 a0001c0001t0107g0052 others(3): Show |
6 | HG01168.hp2 HG01981.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-100-1908_-100-190 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345320 | |||||||
chr12:12345462 | A | T | 6 | a0001c0002t0023g0077 a0001c0002t0023g0135 a0001c0002t0085g0079 others(3): Show |
6 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-100-2048T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345462 | |||||||
chr12:12345470 | G | A | 1 | a0001c0001t0016g0239 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-100-2056C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345470 | |||||||
chr12:12345760 | T | C | 1 | a0001c0001t0101g0218 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-100-2346A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345760 | |||||||
chr12:12345820 | T | C | 1 | a0001c0001t0114g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100-2406A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345820 | |||||||
chr12:12345949 | A | C | 2 | a0001c0001t0024g0033 a0001c0001t0038g0032 |
4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-2535T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345949 | |||||||
chr12:12346062 | A | G | 1 | a0001c0005t0058g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-2648T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346062 | |||||||
chr12:12346089 | C | T | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-2675G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346089 | |||||||
chr12:12346100 | C | T | 1 | a0001c0001t0030g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-100-2686G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346100 | |||||||
chr12:12346146 | G | A | 34 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(31): Show |
50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-2732C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346146 | |||||||
chr12:12346160 | C | A | 1 | a0001c0001t0002g0035 | 2 | HG00558.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-100-2746G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346160 | |||||||
chr12:12346183 | GAATGGCA others(12): Show |
G | 34 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(31): Show |
50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-2788_-100-277 others(23): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346183 | |||||||
chr12:12346197 | C | CTG | 124 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(121): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-100-2784_-100-278 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346197 | |||||||
chr12:12346245 | T | C | 3 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0080g0241 |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-2831A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346245 | |||||||
chr12:12346258 | G | A | 1 | a0001c0002t0045g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-100-2844C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346258 | |||||||
chr12:12346265 | C | T | 3 | a0001c0001t0119g0177 a0001c0002t0011g0141 a0001c0002t0011g0142 |
3 | NA18945.hp1 NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-100-2851G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346265 | |||||||
chr12:12346266 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(34): Show |
54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-100-2852C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346266 | |||||||
chr12:12346270 | C | CA | 30 | a0001c0001t0025g0049 a0001c0002t0001g0024 a0001c0002t0007g0134 others(27): Show |
38 | HG00140.hp1 HG00597.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-2857dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346270 | |||||||
chr12:12346298 | A | G | 2 | a0001c0001t0109g0153 a0001c0001t0124g0136 |
2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-100-2884T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346298 | |||||||
chr12:12346490 | A | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(31): Show |
50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-3076T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346490 | |||||||
chr12:12346538 | A | G | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-3124T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346538 | |||||||
chr12:12346650 | T | G | 1 | a0001c0002t0023g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-100-3236A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346650 | |||||||
chr12:12346659 | AT | A | 3 | a0002c0003t0042g0074 a0002c0003t0043g0073 a0006c0010t0042g0075 |
3 | NA18947.hp1 NA18998.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-100-3246delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346659 | |||||||
chr12:12346914 | G | A | 2 | a0001c0002t0094g0099 a0001c0009t0049g0176 |
2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-101+3164C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346914 | |||||||
chr12:12346966 | G | GT | 8 | a0001c0001t0003g0220 a0001c0001t0030g0219 a0001c0001t0062g0221 others(5): Show |
8 | HG01517.hp1 HG01981.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-101+3111dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346966 | |||||||
chr12:12346975 | T | A | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-101+3103A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346975 | |||||||
chr12:12346999 | C | T | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-101+3079G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346999 | |||||||
chr12:12347066 | T | C | 29 | a0001c0001t0109g0153 a0001c0001t0121g0244 a0001c0002t0001g0158 others(26): Show |
35 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-101+3012A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347066 | |||||||
chr12:12347080 | C | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0036 others(31): Show |
50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-101+2998G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347080 | |||||||
chr12:12347177 | C | A | 1 | a0001c0002t0004g0172 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-101+2901G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347177 | |||||||
chr12:12347266 | C | T | 1 | a0001c0001t0121g0244 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-101+2812G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347266 | |||||||
chr12:12347290 | A | C | 1 | a0001c0001t0016g0149 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-101+2788T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347290 | |||||||
chr12:12347323 | G | A | 16 | a0002c0003t0006g0003 a0002c0003t0006g0063 a0002c0003t0006g0064 others(13): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-101+2755C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347323 | |||||||
chr12:12347348 | C | T | 10 | a0001c0001t0002g0059 a0001c0002t0001g0009 a0001c0002t0001g0024 others(7): Show |
14 | HG00741.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101+2730G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347348 | |||||||
chr12:12347422 | G | T | 157 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(154): Show |
202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-101+2656C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347422 | |||||||
chr12:12347663 | T | C | 70 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(67): Show |
86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-101+2415A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347663 | |||||||
chr12:12347896 | T | TA | 29 | a0001c0001t0109g0153 a0001c0001t0121g0244 a0001c0002t0001g0158 others(26): Show |
35 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-101+2181dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347896 | |||||||
chr12:12347950 | C | T | 75 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(72): Show |
91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-101+2128G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347950 | |||||||
chr12:12347978 | G | A | 2 | a0001c0002t0035g0101 a0001c0002t0096g0100 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-101+2100C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347978 | |||||||
chr12:12348185 | A | G | 3 | a0001c0001t0018g0031 a0001c0001t0018g0173 a0001c0001t0080g0241 |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+1893T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348185 | |||||||
chr12:12348265 | G | A | 142 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(139): Show |
181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.-101+1813C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348265 | |||||||
chr12:12348267 | A | G | 1 | a0001c0001t0111g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-101+1811T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348267 | |||||||
chr12:12348370 | T | C | 2 | a0001c0002t0011g0141 a0001c0002t0011g0142 |
2 | NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-101+1708A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348370 | |||||||
chr12:12348477 | G | A | 1 | a0001c0002t0053g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-101+1601C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348477 | |||||||
chr12:12348717 | C | CA | 84 | a0001c0001t0002g0011 a0001c0001t0002g0059 a0001c0001t0010g0148 others(81): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-101+1360dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | |||||||
chr12:12348717 | C | CAA | 107 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0017 others(104): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-101+1359_-101+136 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | |||||||
chr12:12348717 | C | CAAA | 6 | a0001c0001t0002g0243 a0001c0001t0003g0042 a0001c0001t0039g0242 others(3): Show |
7 | HG02132.hp2 HG02818.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101+1358_-101+136 others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | |||||||
chr12:12348736 | A | G | 5 | a0001c0001t0002g0047 a0001c0001t0025g0048 a0001c0001t0025g0049 others(2): Show |
6 | HG00438.hp2 NA18960.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-101+1342T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348736 | |||||||
chr12:12348957 | C | T | 1 | a0001c0002t0012g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-101+1121G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348957 | |||||||
chr12:12349067 | G | A | 142 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0013 others(139): Show |
181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.-101+1011C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349067 | |||||||
chr12:12349083 | A | C | 1 | a0001c0001t0002g0059 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-101+995T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349083 | |||||||
chr12:12349216 | C | T | 5 | a0001c0002t0027g0054 a0001c0002t0027g0056 a0001c0002t0059g0055 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101+862G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349216 | |||||||
chr12:12349220 | G | T | 10 | a0001c0001t0002g0017 a0001c0001t0002g0047 a0001c0001t0025g0048 others(7): Show |
12 | HG00438.hp2 HG00621.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-101+858C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349220 | |||||||
chr12:12349566 | A | G | 2 | a0001c0001t0003g0044 a0001c0001t0066g0045 |
2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.-101+512T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349566 | |||||||
chr12:12349984 | C | A | 3 | a0001c0001t0002g0245 a0001c0001t0021g0246 a0001c0001t0044g0247 |
3 | HG03654.hp2 HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-101+94G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349984 | |||||||
chr12:12350070 | C | A | 1 | a0001c0002t0078g0248 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.-101+8G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12350070 |