Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7095 |
| ensemblid | ENSG00000008952.17 |
| hgncid | 11846 |
| symbol | SEC62 |
| name | SEC62 homolog, preprotein translocation factor |
| refseq_nuc | NM_003262.4 |
| refseq_prot | NP_003253.1 |
| ensembl_nuc | ENST00000337002.9 |
| ensembl_prot | ENSP00000337688.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 169966807 |
| end | 169998373 |
| strand | + |
| ver | v1.2 |
| region | chr3:169966807-169998373 |
| region5000 | chr3:169961807-170003373 |
| regionname0 | SEC62_chr3_169966807_169998373 |
| regionname5000 | SEC62_chr3_169961807_170003373 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 328 | 92 | 46 | 142 | 6 | 40 | 110 | SEC62_chr3_169961807_170003373 | SEC62 | MAERR others(394): Show |
chr3 | 169961807 | 170003373 |
| a0002 | 0/0 | 399 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SEC62_chr3_169961807_170003373 | SEC62 | MAERR others(394): Show |
chr3 | 169961807 | 170003373 |
| a0003 | 0/0 | 399 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | MAERR others(394): Show |
chr3 | 169961807 | 170003373 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 309 | 74 | 45 | 142 | 6 | 40 | SEC62_chr3_169961807_170003373 | SEC62 | ATGGC others(1192): Show |
chr3 | 169961807 | 170003373 | ||
| a0001c0002 | 0/0 | 1197 | 12 | 11 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | ATGGC others(1192): Show |
chr3 | 169961807 | 170003373 | ||
| a0001c0003 | 0/0 | 1197 | 7 | 7 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | ATGGC others(1192): Show |
chr3 | 169961807 | 170003373 | ||
| a0002c0004 | 0/0 | 1197 | 6 | 0 | 0 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | ATGGC others(1192): Show |
chr3 | 169961807 | 170003373 | ||
| a0003c0005 | 0/0 | 1197 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | ATGGC others(1192): Show |
chr3 | 169961807 | 170003373 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6526 | 156 | 35 | 29 | 68 | 4 | 18 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0002 | 0/0 | 6526 | 55 | 9 | 6 | 27 | 2 | 11 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0003 | 0/0 | 6527 | 28 | 0 | 0 | 26 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6522): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0004 | 0/0 | 6528 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6523): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0005 | 0/0 | 6525 | 11 | 8 | 3 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0006 | 0/0 | 6526 | 11 | 0 | 5 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0007 | 0/0 | 6526 | 4 | 0 | 0 | 0 | 0 | 4 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0008 | 0/0 | 6526 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0009 | 0/0 | 6526 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0010 | 0/0 | 6526 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0011 | 0/0 | 6526 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0012 | 0/0 | 6525 | 3 | 0 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0014 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0015 | 0/0 | 6526 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0017 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0018 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0019 | 0/0 | 6527 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCA others(6522): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0020 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0022 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0023 | 0/0 | 6526 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0024 | 0/0 | 6526 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0025 | 0/0 | 6526 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0026 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0027 | 0/0 | 6526 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0028 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0032 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0033 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0034 | 0/0 | 6527 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6522): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0035 | 0/0 | 6527 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6522): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0036 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0037 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0038 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0039 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0040 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0041 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0001t0042 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0002t0004 | 0/0 | 6528 | 10 | 9 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6523): Show |
chr3 | 169961807 | 170003373 |
| a0001c0002t0029 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| a0001c0002t0030 | 0/0 | 6528 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6523): Show |
chr3 | 169961807 | 170003373 |
| a0001c0003t0013 | 0/0 | 6525 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0003t0016 | 0/0 | 6525 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0003t0021 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0001c0003t0031 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6520): Show |
chr3 | 169961807 | 170003373 |
| a0002c0004t0003 | 0/0 | 6527 | 6 | 0 | 0 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6522): Show |
chr3 | 169961807 | 170003373 |
| a0003c0005t0001 | 0/0 | 6526 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | GGGCG others(6521): Show |
chr3 | 169961807 | 170003373 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 35 | 2 | 4 | 23 | 1 | 5 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0003 | 0/0 | 16 | 4 | 2 | 6 | 1 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0039 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0005 | 0/0 | 8 | 1 | 1 | 0 | 2 | 4 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0011 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0002 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0026 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0006g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0006g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0007g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0009g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0011g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0012g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0014g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0015g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0017g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0018g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0019g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0020g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0022g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0023g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0024g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0025g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0026g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0027g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0032g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0033g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0035g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0036g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0038g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0039g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0040g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0041g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0001t0042g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0002t0004g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0002t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0002t0029g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0002t0030g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0003t0013g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0003t0016g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0003t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0001c0003t0031g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0002c0004t0003g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0002c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| a0003c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01081 | hp2 | a0001 | c0001 | t0025 | g0121 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01106 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01167 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01243 | hp1 | a0001 | c0001 | t0027 | g0003 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01884 | hp2 | a0001 | c0001 | t0037 | g0032 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02015 | hp1 | a0001 | c0001 | t0026 | g0090 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0080 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02451 | hp1 | a0001 | c0003 | t0016 | g0031 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0015 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02622 | hp1 | a0001 | c0003 | t0016 | g0031 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0027 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02896 | hp2 | a0001 | c0001 | t0036 | g0063 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02922 | hp2 | a0001 | c0001 | t0041 | g0015 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0087 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0084 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0034 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03098 | hp2 | a0001 | c0002 | t0030 | g0079 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03130 | hp2 | a0001 | c0002 | t0029 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0076 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03209 | hp1 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03453 | hp1 | a0001 | c0003 | t0031 | g0078 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03453 | hp2 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03491 | hp2 | a0001 | c0001 | t0024 | g0092 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03516 | hp1 | a0001 | c0001 | t0040 | g0074 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03540 | hp1 | a0001 | c0001 | t0039 | g0069 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03579 | hp2 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03710 | hp1 | a0001 | c0001 | t0023 | g0059 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0015 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03927 | hp1 | a0001 | c0001 | t0012 | g0015 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0005 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18945 | hp1 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18947 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18954 | hp1 | a0001 | c0001 | t0019 | g0149 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18959 | hp2 | a0001 | c0001 | t0022 | g0065 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18963 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18968 | hp1 | a0001 | c0001 | t0038 | g0130 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18979 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18998 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19001 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19005 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19030 | hp1 | a0001 | c0001 | t0033 | g0068 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19030 | hp2 | a0001 | c0001 | t0018 | g0034 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19057 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19064 | hp2 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19076 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19077 | hp2 | a0001 | c0001 | t0020 | g0120 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19081 | hp1 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19082 | hp1 | a0002 | c0004 | t0003 | g0151 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19240 | hp1 | a0001 | c0001 | t0032 | g0137 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ASW | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ASW | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | GIH | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02109 | hp1 | a0001 | c0001 | t0017 | g0027 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG02559 | hp2 | a0001 | c0001 | t0035 | g0002 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0088 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA20300 | hp2 | a0001 | c0003 | t0021 | g0086 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA21309 | hp1 | a0001 | c0001 | t0042 | g0106 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0039 | REF | REF | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0093 | REF | REF | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169992826 | G | C | 1 | a0003 | 2 | HG01106.hp1 HG01167.hp1 |
missense_variant | MODERATE | c.963G>C | p.Glu321Asp | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 979/6526 | 963/1200 | 321/399 | chr3 | 169992826 | |||
| chr3:169993051 | T | G | 1 | a0002 | 6 | NA18979.hp1 NA18998.hp1 NA19001.hp1 others(3): Show |
missense_variant | MODERATE | c.1188T>G | p.His396Gln | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1204/6526 | 1188/1200 | 396/399 | chr3 | 169993051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169975646 | C | G | 1 | a0001c0002 | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.75C>G | p.Ala25Ala | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/8 | 91/6526 | 75/1200 | 25/399 | chr3 | 169975646 | |||
| chr3:169982737 | C | G | 1 | a0001c0003 | 7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
synonymous_variant | LOW | c.282C>G | p.Ala94Ala | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/8 | 298/6526 | 282/1200 | 94/399 | chr3 | 169982737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169966811 | G | A | 1 | a0001c0001t0019 | 1 | NA18954.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/8 | 12 | chr3 | 169966811 | ||||||
| chr3:169993242 | G | T | 1 | a0001c0001t0007 | 4 | HG03017.hp2 HG03704.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*179G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 179 | chr3 | 169993242 | ||||||
| chr3:169993310 | T | C | 1 | a0001c0001t0020 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 247 | chr3 | 169993310 | ||||||
| chr3:169993709 | G | A | 1 | a0001c0003t0021 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*646G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 646 | chr3 | 169993709 | ||||||
| chr3:169993773 | G | A | 1 | a0001c0001t0008 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 710 | chr3 | 169993773 | ||||||
| chr3:169993920 | C | A | 1 | a0001c0001t0022 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 857 | chr3 | 169993920 | ||||||
| chr3:169994033 | C | T | 1 | a0001c0001t0042 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*970C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 970 | chr3 | 169994033 | ||||||
| chr3:169994223 | G | T | 1 | a0001c0001t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1160 | chr3 | 169994223 | ||||||
| chr3:169994441 | A | G | 1 | a0001c0001t0018 | 2 | HG03041.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1378A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1378 | chr3 | 169994441 | ||||||
| chr3:169994521 | C | T | 1 | a0001c0001t0040 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1458 | chr3 | 169994521 | ||||||
| chr3:169994623 | A | G | 1 | a0001c0001t0039 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1560A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1560 | chr3 | 169994623 | ||||||
| chr3:169994642 | C | T | 1 | a0001c0003t0013 | 3 | HG03209.hp1 HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1579C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1579 | chr3 | 169994642 | ||||||
| chr3:169994770 | A | G | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(9): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1707A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1707 | chr3 | 169994770 | ||||||
| chr3:169995247 | T | C | 1 | a0001c0001t0011 | 3 | HG03195.hp1 HG03471.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2184T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2184 | chr3 | 169995247 | ||||||
| chr3:169995506 | A | G | 1 | a0001c0001t0036 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2443A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2443 | chr3 | 169995506 | ||||||
| chr3:169995624 | A | AT | 5 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0034 others(2): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2571dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2572 | INFO_REALIGN_3_PRIME | chr3 | 169995624 | |||||
| chr3:169995634 | T | A | 1 | a0001c0001t0037 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2571T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2571 | chr3 | 169995634 | ||||||
| chr3:169995694 | AC | A | 1 | a0001c0001t0012 | 3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2632 | chr3 | 169995694 | ||||||
| chr3:169995695 | C | T | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2632C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2632 | chr3 | 169995695 | ||||||
| chr3:169995696 | G | T | 1 | a0001c0001t0012 | 3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2633G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2633 | chr3 | 169995696 | ||||||
| chr3:169995887 | T | C | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2824 | chr3 | 169995887 | ||||||
| chr3:169995888 | G | T | 6 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0032 others(3): Show |
38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2825G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2825 | chr3 | 169995888 | ||||||
| chr3:169995889 | C | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2826C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2826 | chr3 | 169995889 | ||||||
| chr3:169995890 | C | G | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2827 | chr3 | 169995890 | ||||||
| chr3:169995896 | G | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2833G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2833 | chr3 | 169995896 | ||||||
| chr3:169995898 | A | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2835 | chr3 | 169995898 | ||||||
| chr3:169995899 | G | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2836 | chr3 | 169995899 | ||||||
| chr3:169995944 | A | G | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2881A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2881 | chr3 | 169995944 | ||||||
| chr3:169995976 | A | G | 3 | a0001c0003t0013 a0001c0003t0021 a0001c0003t0031 |
5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2913A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2913 | chr3 | 169995976 | ||||||
| chr3:169996006 | CA | C | 6 | a0001c0001t0005 a0001c0001t0039 a0001c0003t0013 others(3): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2950delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2950 | INFO_REALIGN_3_PRIME | chr3 | 169996006 | |||||
| chr3:169996208 | A | G | 4 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0029 others(1): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3145A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3145 | chr3 | 169996208 | ||||||
| chr3:169996305 | C | G | 1 | a0001c0001t0028 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3242C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3242 | chr3 | 169996305 | ||||||
| chr3:169996353 | C | T | 3 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0012 |
17 | HG01261.hp1 HG01934.hp1 HG01952.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3290C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3290 | chr3 | 169996353 | ||||||
| chr3:169996354 | A | G | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*3291A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3291 | chr3 | 169996354 | ||||||
| chr3:169996363 | C | T | 1 | a0001c0001t0017 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3300C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3300 | chr3 | 169996363 | ||||||
| chr3:169996515 | C | T | 1 | a0001c0003t0016 | 2 | HG02451.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3452C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3452 | chr3 | 169996515 | ||||||
| chr3:169996562 | C | T | 1 | a0001c0001t0038 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3499C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3499 | chr3 | 169996562 | ||||||
| chr3:169996605 | G | C | 1 | a0001c0001t0032 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3542 | chr3 | 169996605 | ||||||
| chr3:169996777 | G | A | 1 | a0001c0001t0023 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3714G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3714 | chr3 | 169996777 | ||||||
| chr3:169996781 | G | A | 2 | a0001c0001t0005 a0001c0001t0039 |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3718G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3718 | chr3 | 169996781 | ||||||
| chr3:169996939 | G | A | 1 | a0001c0001t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3876 | chr3 | 169996939 | ||||||
| chr3:169996942 | C | T | 1 | a0001c0001t0020 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3879C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3879 | chr3 | 169996942 | ||||||
| chr3:169997013 | T | C | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(9): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3950T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3950 | chr3 | 169997013 | ||||||
| chr3:169997176 | G | A | 1 | a0001c0001t0009 | 3 | NA18947.hp1 NA18984.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4113G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4113 | chr3 | 169997176 | ||||||
| chr3:169997281 | G | A | 1 | a0001c0001t0024 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4218G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4218 | chr3 | 169997281 | ||||||
| chr3:169997313 | A | G | 1 | a0001c0002t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4250A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4250 | chr3 | 169997313 | ||||||
| chr3:169997459 | G | GTT | 3 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0030 |
12 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4403_*4404dupTT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4405 | INFO_REALIGN_3_PRIME | chr3 | 169997459 | |||||
| chr3:169997460 | T | G | 7 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0039 others(4): Show |
20 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4397T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4397 | chr3 | 169997460 | ||||||
| chr3:169997542 | T | A | 1 | a0001c0001t0005 | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4479T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4479 | chr3 | 169997542 | ||||||
| chr3:169997747 | C | T | 1 | a0001c0001t0015 | 2 | NA19057.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4684C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4684 | chr3 | 169997747 | ||||||
| chr3:169997849 | T | C | 1 | a0001c0001t0005 | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4786T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4786 | chr3 | 169997849 | ||||||
| chr3:169997897 | C | T | 1 | a0001c0001t0027 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4834C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4834 | chr3 | 169997897 | ||||||
| chr3:169997939 | A | G | 1 | a0001c0001t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4876A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4876 | chr3 | 169997939 | ||||||
| chr3:169997945 | A | G | 1 | a0001c0001t0010 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4882A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4882 | chr3 | 169997945 | ||||||
| chr3:169998011 | T | C | 1 | a0001c0003t0016 | 2 | HG02451.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4948T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4948 | chr3 | 169998011 | ||||||
| chr3:169998248 | A | G | 1 | a0001c0001t0014 | 2 | HG02965.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5185A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 5185 | chr3 | 169998248 | ||||||
| chr3:169998356 | T | A | 1 | a0001c0001t0026 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5293T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 5293 | chr3 | 169998356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:169966899 | G | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(34): Show |
87 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.36+41G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169966899 | |||||||
| chr3:169966954 | AGGTGGGG others(3): Show |
A | 19 | a0001c0001t0001g0139 a0001c0001t0003g0002 a0001c0001t0003g0016 others(16): Show |
38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.36+110_36+119delGG others(8): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169966954 | ||||||
| chr3:169967027 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.36+169G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967027 | |||||||
| chr3:169967027 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.36+169G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967027 | |||||||
| chr3:169967090 | A | T | 1 | a0001c0001t0010g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.36+232A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967090 | |||||||
| chr3:169967286 | G | A | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.36+428G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967286 | |||||||
| chr3:169967319 | A | G | 1 | a0001c0001t0022g0065 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.36+461A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967319 | |||||||
| chr3:169967412 | T | C | 1 | a0001c0002t0004g0030 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.36+554T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967412 | |||||||
| chr3:169967493 | C | T | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+635C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967493 | |||||||
| chr3:169967494 | G | T | 7 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+636G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967494 | |||||||
| chr3:169967525 | T | C | 1 | a0001c0001t0005g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36+667T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967525 | |||||||
| chr3:169967586 | G | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(89): Show |
182 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.36+728G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967586 | |||||||
| chr3:169967620 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0018g0034 |
5 | HG02257.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+762T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967620 | |||||||
| chr3:169967691 | C | T | 1 | a0001c0001t0011g0088 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.36+833C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967691 | |||||||
| chr3:169967859 | T | C | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.36+1001T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967859 | |||||||
| chr3:169967881 | C | CT | 53 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(50): Show |
105 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.36+1034dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169967881 | ||||||
| chr3:169967989 | A | G | 2 | a0001c0001t0010g0087 a0001c0003t0021g0086 |
2 | HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.36+1131A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967989 | |||||||
| chr3:169967998 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.36+1140A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967998 | |||||||
| chr3:169968349 | G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.36+1491G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968349 | |||||||
| chr3:169968535 | CA | C | 55 | a0001c0001t0001g0057 a0001c0001t0001g0132 a0001c0001t0002g0004 others(52): Show |
116 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.36+1690delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169968535 | ||||||
| chr3:169968567 | T | G | 1 | a0001c0001t0005g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36+1709T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968567 | |||||||
| chr3:169968605 | T | C | 1 | a0001c0001t0003g0144 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.36+1747T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968605 | |||||||
| chr3:169968652 | A | G | 4 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 others(1): Show |
5 | HG02109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+1794A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968652 | |||||||
| chr3:169969049 | A | G | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+2191A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969049 | |||||||
| chr3:169969217 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.36+2359G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969217 | |||||||
| chr3:169969439 | A | G | 7 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(4): Show |
7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+2581A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969439 | |||||||
| chr3:169969489 | A | G | 2 | a0001c0001t0006g0008 a0001c0001t0008g0018 |
9 | HG01261.hp1 HG01934.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.36+2631A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969489 | |||||||
| chr3:169969515 | GC | G | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.36+2659delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169969515 | ||||||
| chr3:169969566 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0089 a0001c0001t0026g0090 |
4 | HG02015.hp1 HG02135.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2708G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969566 | |||||||
| chr3:169969591 | C | T | 20 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(17): Show |
39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.36+2733C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969591 | |||||||
| chr3:169969592 | G | A | 7 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+2734G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969592 | |||||||
| chr3:169969649 | TC | T | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.36+2792delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969649 | |||||||
| chr3:169969795 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.36+2937C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969795 | |||||||
| chr3:169969819 | A | G | 25 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(22): Show |
51 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.36+2961A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969819 | |||||||
| chr3:169969845 | T | C | 2 | a0001c0001t0003g0145 a0001c0001t0003g0146 |
2 | NA18940.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.36+2987T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969845 | |||||||
| chr3:169970119 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+3261T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970119 | |||||||
| chr3:169970202 | C | T | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+3344C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970202 | |||||||
| chr3:169970230 | T | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.36+3372T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970230 | |||||||
| chr3:169970291 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.36+3433A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970291 | |||||||
| chr3:169970542 | A | G | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.36+3684A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970542 | |||||||
| chr3:169970579 | C | T | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.36+3721C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970579 | |||||||
| chr3:169970740 | C | T | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.36+3882C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970740 | |||||||
| chr3:169970799 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0017g0027 a0001c0001t0040g0074 |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+3941T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970799 | |||||||
| chr3:169971011 | G | A | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.36+4153G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971011 | |||||||
| chr3:169971068 | C | CT | 11 | a0001c0001t0001g0126 a0001c0001t0002g0056 a0001c0001t0002g0131 others(8): Show |
15 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.36+4227dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169971068 | ||||||
| chr3:169971068 | CT | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
16 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.36+4227delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169971068 | ||||||
| chr3:169971130 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.36+4272A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971130 | |||||||
| chr3:169971376 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | NA18948.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-4232A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971376 | |||||||
| chr3:169971399 | A | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.37-4209A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971399 | |||||||
| chr3:169971419 | A | C | 12 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(9): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.37-4189A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971419 | |||||||
| chr3:169971564 | G | A | 65 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
137 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.37-4044G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971564 | |||||||
| chr3:169971592 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0017g0027 a0001c0001t0040g0074 |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-4016C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971592 | |||||||
| chr3:169971899 | T | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3709T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971899 | |||||||
| chr3:169971989 | G | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3619G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971989 | |||||||
| chr3:169972005 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG00735.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.37-3603A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972005 | |||||||
| chr3:169972166 | G | A | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3442G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972166 | |||||||
| chr3:169972197 | T | C | 1 | a0001c0001t0024g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.37-3411T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972197 | |||||||
| chr3:169972301 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37-3307G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972301 | |||||||
| chr3:169972356 | A | T | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-3252A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972356 | |||||||
| chr3:169972385 | A | G | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37-3223A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972385 | |||||||
| chr3:169972404 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.37-3204C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972404 | |||||||
| chr3:169972580 | C | CT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(56): Show |
132 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.37-3008dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | ||||||
| chr3:169972580 | C | CTT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0023 others(25): Show |
54 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.37-3009_37-3008dup others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | ||||||
| chr3:169972580 | CT | C | 7 | a0001c0001t0002g0075 a0001c0001t0003g0140 a0001c0001t0007g0082 others(4): Show |
10 | HG02451.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.37-3008delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | ||||||
| chr3:169972602 | T | G | 20 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(17): Show |
39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.37-3006T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972602 | |||||||
| chr3:169972672 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.37-2936C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972672 | |||||||
| chr3:169972749 | ATT | A | 8 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(5): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-2854_37-2853del others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972749 | ||||||
| chr3:169972797 | G | A | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-2811G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972797 | |||||||
| chr3:169972871 | G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37-2737G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972871 | |||||||
| chr3:169972923 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.37-2685C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972923 | |||||||
| chr3:169972971 | C | A | 1 | a0001c0001t0005g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.37-2637C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972971 | |||||||
| chr3:169973057 | A | T | 1 | a0001c0001t0025g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.37-2551A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973057 | |||||||
| chr3:169973270 | A | T | 1 | a0001c0001t0002g0021 | 3 | HG02258.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.37-2338A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973270 | |||||||
| chr3:169973307 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.37-2301A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973307 | |||||||
| chr3:169973577 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.37-2031C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973577 | |||||||
| chr3:169973645 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.37-1963A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973645 | |||||||
| chr3:169973662 | C | CA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0111 others(3): Show |
7 | HG00544.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-1930dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | ||||||
| chr3:169973662 | C | CAA | 22 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(19): Show |
48 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.37-1931_37-1930dup others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | ||||||
| chr3:169973662 | CA | C | 12 | a0001c0001t0002g0055 a0001c0001t0002g0071 a0001c0001t0005g0026 others(9): Show |
16 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.37-1930delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | ||||||
| chr3:169973887 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.37-1721C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973887 | |||||||
| chr3:169974095 | A | G | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-1513A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974095 | |||||||
| chr3:169974097 | A | T | 12 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(9): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.37-1511A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974097 | |||||||
| chr3:169974282 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0113 a0001c0001t0004g0070 |
8 | HG00639.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-1326T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974282 | |||||||
| chr3:169974317 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.37-1291A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974317 | |||||||
| chr3:169974347 | A | G | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-1261A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974347 | |||||||
| chr3:169974649 | A | T | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(74): Show |
156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.37-959A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974649 | |||||||
| chr3:169974835 | CCTT | C | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-770_37-768delTC others(1): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169974835 | ||||||
| chr3:169975003 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.37-605G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975003 | |||||||
| chr3:169975056 | G | A | 3 | a0001c0001t0011g0076 a0001c0001t0011g0077 a0001c0001t0011g0088 |
3 | HG03195.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.37-552G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975056 | |||||||
| chr3:169975084 | C | T | 3 | a0001c0002t0004g0030 a0001c0002t0004g0080 a0001c0002t0030g0079 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-524C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975084 | |||||||
| chr3:169975103 | A | G | 1 | a0001c0002t0030g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.37-505A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975103 | |||||||
| chr3:169975123 | A | T | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.37-485A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975123 | |||||||
| chr3:169975126 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.37-482C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975126 | |||||||
| chr3:169975222 | A | C | 3 | a0001c0002t0004g0030 a0001c0002t0004g0080 a0001c0002t0030g0079 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-386A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975222 | |||||||
| chr3:169975229 | C | T | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-379C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975229 | |||||||
| chr3:169975280 | C | CA | 36 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0115 others(33): Show |
81 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.37-310dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169975280 | ||||||
| chr3:169975341 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0036g0063 |
3 | HG02615.hp2 HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.37-267A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975341 | |||||||
| chr3:169975443 | C | T | 19 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(16): Show |
38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-165C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975443 | |||||||
| chr3:169975511 | A | G | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-97A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975511 | |||||||
| chr3:169975555 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0033g0068 |
2 | NA19030.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.37-53G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975555 | |||||||
| chr3:169975885 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.145+169A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169975885 | |||||||
| chr3:169975987 | G | A | 6 | a0001c0001t0003g0016 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
9 | NA18961.hp1 NA18969.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+271G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169975987 | |||||||
| chr3:169976005 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0032g0137 |
2 | NA18977.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+289A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976005 | |||||||
| chr3:169976027 | A | G | 1 | a0001c0001t0003g0150 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.145+311A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976027 | |||||||
| chr3:169976130 | C | T | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.145+414C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976130 | |||||||
| chr3:169976194 | C | T | 1 | a0001c0001t0042g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.145+478C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976194 | |||||||
| chr3:169976206 | A | G | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.145+490A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976206 | |||||||
| chr3:169976215 | A | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02965.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.145+499A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976215 | |||||||
| chr3:169976263 | G | T | 1 | a0001c0003t0031g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.145+547G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976263 | |||||||
| chr3:169976264 | C | T | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.145+548C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976264 | |||||||
| chr3:169976338 | A | T | 7 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(4): Show |
7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-608A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976338 | |||||||
| chr3:169976374 | G | GA | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.146-562dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169976374 | ||||||
| chr3:169976609 | C | G | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.146-337C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976609 | |||||||
| chr3:169977222 | T | TTATACTT others(319): Show |
4 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+180_251+181ins others(326): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169977222 | ||||||
| chr3:169977415 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.251+364G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977415 | |||||||
| chr3:169977437 | C | T | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+386C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977437 | |||||||
| chr3:169977631 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0017g0027 a0001c0001t0040g0074 |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+580T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977631 | |||||||
| chr3:169977774 | T | C | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.251+723T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977774 | |||||||
| chr3:169977798 | A | AT | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+751dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169977798 | ||||||
| chr3:169977799 | T | A | 4 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0135 others(1): Show |
7 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.251+748T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977799 | |||||||
| chr3:169977853 | G | C | 1 | a0001c0001t0010g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.251+802G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977853 | |||||||
| chr3:169977980 | T | C | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.251+929T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977980 | |||||||
| chr3:169978075 | C | T | 1 | a0001c0001t0025g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.251+1024C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978075 | |||||||
| chr3:169978095 | A | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+1044A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978095 | |||||||
| chr3:169978104 | C | T | 8 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(5): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+1053C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978104 | |||||||
| chr3:169978134 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.251+1083C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978134 | |||||||
| chr3:169978235 | C | G | 1 | a0001c0003t0031g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.251+1184C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978235 | |||||||
| chr3:169978236 | G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.251+1185G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978236 | |||||||
| chr3:169978417 | G | T | 1 | a0001c0001t0005g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.251+1366G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978417 | |||||||
| chr3:169978430 | G | A | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(74): Show |
156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.251+1379G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978430 | |||||||
| chr3:169978555 | A | G | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+1504A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978555 | |||||||
| chr3:169978587 | G | A | 1 | a0001c0001t0005g0135 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.251+1536G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978587 | |||||||
| chr3:169978616 | C | G | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.251+1565C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978616 | |||||||
| chr3:169978745 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+1694C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978745 | |||||||
| chr3:169978785 | A | T | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.251+1734A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978785 | |||||||
| chr3:169979134 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.251+2083G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979134 | |||||||
| chr3:169979195 | A | T | 1 | a0001c0001t0020g0120 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.251+2144A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979195 | |||||||
| chr3:169979237 | A | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.251+2186A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979237 | |||||||
| chr3:169979296 | C | T | 1 | a0001c0001t0040g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+2245C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979296 | |||||||
| chr3:169979588 | A | G | 66 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(63): Show |
138 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.251+2537A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979588 | |||||||
| chr3:169979845 | A | G | 12 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(9): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+2794A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979845 | |||||||
| chr3:169979888 | A | G | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.252-2819A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979888 | |||||||
| chr3:169979998 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.252-2709A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979998 | |||||||
| chr3:169980081 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.252-2626G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980081 | |||||||
| chr3:169980111 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-2596T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980111 | |||||||
| chr3:169980274 | A | G | 4 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0135 others(1): Show |
7 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-2433A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980274 | |||||||
| chr3:169980320 | G | A | 4 | a0001c0003t0013g0022 a0001c0003t0016g0031 a0001c0003t0021g0086 others(1): Show |
7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-2387G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980320 | |||||||
| chr3:169980355 | CAG | C | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(37): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.252-2347_252-2346d others(4): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169980355 | ||||||
| chr3:169980699 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(37): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.252-2008G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980699 | |||||||
| chr3:169980795 | G | A | 3 | a0001c0003t0013g0022 a0001c0003t0021g0086 a0001c0003t0031g0078 |
5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-1912G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980795 | |||||||
| chr3:169980952 | T | C | 81 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(78): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-1755T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980952 | |||||||
| chr3:169980969 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.252-1738A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980969 | |||||||
| chr3:169981004 | A | G | 1 | a0001c0001t0011g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252-1703A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981004 | |||||||
| chr3:169981144 | G | A | 81 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(78): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-1563G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981144 | |||||||
| chr3:169981395 | A | T | 1 | a0001c0001t0019g0149 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.252-1312A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981395 | |||||||
| chr3:169981521 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.252-1186G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981521 | |||||||
| chr3:169981534 | G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.252-1173G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981534 | |||||||
| chr3:169981661 | C | A | 4 | a0001c0003t0013g0022 a0001c0003t0016g0031 a0001c0003t0021g0086 others(1): Show |
7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-1046C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981661 | |||||||
| chr3:169981726 | G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.252-981G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981726 | |||||||
| chr3:169981727 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.252-980G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981727 | |||||||
| chr3:169981967 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.252-740G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981967 | |||||||
| chr3:169982042 | A | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-665A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982042 | |||||||
| chr3:169982090 | AT | A | 3 | a0001c0003t0013g0022 a0001c0003t0021g0086 a0001c0003t0031g0078 |
5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-616delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982090 | |||||||
| chr3:169982124 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0119 |
2 | HG01109.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.252-583A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982124 | |||||||
| chr3:169982216 | C | G | 81 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(78): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-491C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982216 | |||||||
| chr3:169982316 | T | C | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.252-391T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982316 | |||||||
| chr3:169982366 | G | A | 1 | a0001c0001t0002g0013 | 4 | NA18957.hp2 NA18961.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-341G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982366 | |||||||
| chr3:169982608 | T | C | 8 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(5): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-99T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982608 | |||||||
| chr3:169982669 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.252-38A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982669 | |||||||
| chr3:169982673 | G | T | 8 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(5): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-34G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982673 | |||||||
| chr3:169982686 | C | A | 7 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-21C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982686 | |||||||
| chr3:169982991 | G | A | 6 | a0001c0001t0004g0070 a0001c0002t0004g0006 a0001c0002t0004g0030 others(3): Show |
13 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.456+80G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/7 | chr3 | 169982991 | |||||||
| chr3:169983082 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.457-79T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/7 | chr3 | 169983082 | |||||||
| chr3:169983375 | A | G | 1 | a0001c0001t0003g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.549+122A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983375 | |||||||
| chr3:169983667 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.549+414A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983667 | |||||||
| chr3:169983690 | G | C | 81 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(78): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.549+437G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983690 | |||||||
| chr3:169983885 | A | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.549+632A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983885 | |||||||
| chr3:169984044 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(7): Show |
22 | HG00280.hp2 HG00438.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.549+791C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984044 | |||||||
| chr3:169984477 | C | T | 2 | a0001c0002t0004g0006 a0001c0002t0029g0006 |
8 | HG01243.hp2 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+1224C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984477 | |||||||
| chr3:169984555 | C | T | 1 | a0001c0001t0040g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.550-1250C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984555 | |||||||
| chr3:169984627 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0064 |
7 | NA18944.hp1 NA18946.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-1178A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984627 | |||||||
| chr3:169984877 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.550-928T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984877 | |||||||
| chr3:169984924 | A | G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(37): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.550-881A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984924 | |||||||
| chr3:169984971 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.550-834C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984971 | |||||||
| chr3:169985058 | G | A | 12 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(9): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.550-747G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985058 | |||||||
| chr3:169985145 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.550-660C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985145 | |||||||
| chr3:169985167 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.550-638A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985167 | |||||||
| chr3:169985296 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0101 |
7 | HG00140.hp2 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-509C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985296 | |||||||
| chr3:169985351 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0118 |
5 | HG00741.hp2 HG02280.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-454C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985351 | |||||||
| chr3:169985423 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-382G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985423 | |||||||
| chr3:169985447 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-358G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985447 | |||||||
| chr3:169985485 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18959.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.550-320G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985485 | |||||||
| chr3:169985556 | T | A | 7 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-249T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985556 | |||||||
| chr3:169985883 | A | C | 15 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0013 others(12): Show |
37 | HG00597.hp1 HG01257.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.610+18A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985883 | |||||||
| chr3:169985890 | A | G | 3 | a0001c0001t0002g0073 a0001c0001t0017g0027 a0001c0001t0040g0074 |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+25A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985890 | |||||||
| chr3:169985929 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+64A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985929 | |||||||
| chr3:169986085 | G | A | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.610+220G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986085 | |||||||
| chr3:169986110 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610+245A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986110 | |||||||
| chr3:169986140 | A | G | 1 | a0001c0001t0001g0020 | 3 | HG02572.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.610+275A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986140 | |||||||
| chr3:169986153 | A | G | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610+288A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986153 | |||||||
| chr3:169986246 | A | G | 1 | a0001c0001t0002g0028 | 2 | NA18946.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.610+381A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986246 | |||||||
| chr3:169986268 | G | A | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.610+403G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986268 | |||||||
| chr3:169986542 | T | TA | 4 | a0001c0003t0013g0022 a0001c0003t0016g0031 a0001c0003t0021g0086 others(1): Show |
7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.610+684dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 169986542 | ||||||
| chr3:169986543 | A | T | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.610+678A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986543 | |||||||
| chr3:169986567 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.610+702C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986567 | |||||||
| chr3:169986567 | C | T | 1 | a0001c0001t0018g0034 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.610+702C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986567 | |||||||
| chr3:169986615 | T | C | 15 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0013 others(12): Show |
37 | HG00597.hp1 HG01257.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.610+750T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986615 | |||||||
| chr3:169986712 | T | C | 1 | a0001c0001t0001g0040 | 2 | NA18948.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.610+847T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986712 | |||||||
| chr3:169986764 | G | A | 77 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(74): Show |
156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.610+899G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986764 | |||||||
| chr3:169986859 | G | A | 2 | a0001c0001t0006g0014 a0001c0001t0006g0054 |
5 | HG02056.hp2 HG02155.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+994G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986859 | |||||||
| chr3:169986887 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.610+1022C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986887 | |||||||
| chr3:169986924 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.610+1059G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986924 | |||||||
| chr3:169987065 | G | GA | 2 | a0001c0001t0002g0011 a0001c0001t0002g0056 |
6 | HG01257.hp2 HG01258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-1163dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 169987065 | ||||||
| chr3:169987230 | C | G | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.611-1010C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987230 | |||||||
| chr3:169987256 | G | A | 20 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(17): Show |
39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.611-984G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987256 | |||||||
| chr3:169987283 | G | A | 7 | a0001c0001t0005g0026 a0001c0001t0005g0043 a0001c0001t0005g0044 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.611-957G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987283 | |||||||
| chr3:169987305 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0060 |
4 | HG01099.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-935A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987305 | |||||||
| chr3:169987581 | G | A | 2 | a0001c0001t0005g0044 a0001c0001t0005g0134 |
3 | HG02055.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.611-659G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987581 | |||||||
| chr3:169987913 | G | A | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(77): Show |
159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.611-327G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987913 | |||||||
| chr3:169987951 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.611-289G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987951 | |||||||
| chr3:169987987 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.611-253T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987987 | |||||||
| chr3:169988150 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.611-90G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169988150 | |||||||
| chr3:169988395 | G | A | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+36G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988395 | |||||||
| chr3:169988398 | G | A | 3 | a0001c0002t0004g0030 a0001c0002t0004g0080 a0001c0002t0030g0079 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+39G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988398 | |||||||
| chr3:169988770 | A | G | 1 | a0001c0001t0025g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.730+411A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988770 | |||||||
| chr3:169989002 | A | G | 3 | a0001c0002t0004g0030 a0001c0002t0004g0080 a0001c0002t0030g0079 |
4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+643A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989002 | |||||||
| chr3:169989034 | A | C | 5 | a0001c0002t0004g0006 a0001c0002t0004g0030 a0001c0002t0004g0080 others(2): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.730+675A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989034 | |||||||
| chr3:169989072 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+713A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989072 | |||||||
| chr3:169989109 | TTAGAGGC others(9): Show |
T | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.730+751_730+766del others(16): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989109 | |||||||
| chr3:169989126 | C | A | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.730+767C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989126 | |||||||
| chr3:169989223 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.730+864A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989223 | |||||||
| chr3:169989255 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0064 |
7 | NA18944.hp1 NA18946.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+896G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989255 | |||||||
| chr3:169989288 | C | CCCAGGCT others(403): Show |
94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989288 | ||||||
| chr3:169989288 | C | CCTAGGCT others(403): Show |
3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+930_730+931ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989288 | ||||||
| chr3:169989290 | C | CAGGCTGA others(403): Show |
1 | a0001c0001t0008g0018 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | ||||||
| chr3:169989290 | C | CAGGCTGG others(403): Show |
25 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(22): Show |
51 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | ||||||
| chr3:169989290 | C | CAGGCTGG others(403): Show |
39 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(36): Show |
83 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | ||||||
| chr3:169989362 | G | A | 1 | a0001c0001t0032g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+1003G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989362 | |||||||
| chr3:169989424 | C | T | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.730+1065C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989424 | |||||||
| chr3:169989425 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.730+1066T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989425 | |||||||
| chr3:169989641 | T | A | 1 | a0001c0001t0005g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.730+1282T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989641 | |||||||
| chr3:169989744 | C | T | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.730+1385C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989744 | |||||||
| chr3:169989792 | T | A | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.730+1433T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989792 | |||||||
| chr3:169989845 | T | G | 81 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(78): Show |
160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.730+1486T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989845 | |||||||
| chr3:169989944 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1585G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989944 | |||||||
| chr3:169989978 | TATATATG others(8): Show |
T | 1 | a0001c0001t0003g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.730+1633_730+1647d others(17): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989978 | ||||||
| chr3:169990000 | GATATATC others(8): Show |
G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(37): Show |
86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.730+1652_730+1666d others(17): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169990000 | ||||||
| chr3:169990002 | TATATC | T | 7 | a0001c0001t0001g0009 a0001c0001t0010g0087 a0001c0002t0004g0006 others(4): Show |
14 | HG01123.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.730+1647_730+1651d others(7): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169990002 | ||||||
| chr3:169990051 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730+1692A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990051 | |||||||
| chr3:169990166 | A | G | 1 | a0001c0001t0005g0026 | 3 | HG01167.hp2 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.730+1807A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990166 | |||||||
| chr3:169990313 | A | G | 1 | a0001c0001t0042g0106 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.730+1954A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990313 | |||||||
| chr3:169990488 | G | A | 1 | a0001c0003t0021g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.731-2106G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990488 | |||||||
| chr3:169990503 | A | G | 18 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0138 others(15): Show |
37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.731-2091A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990503 | |||||||
| chr3:169990646 | A | G | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.731-1948A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990646 | |||||||
| chr3:169990696 | A | C | 1 | a0001c0001t0003g0141 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.731-1898A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990696 | |||||||
| chr3:169990743 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.731-1851C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990743 | |||||||
| chr3:169990846 | C | T | 3 | a0001c0003t0013g0022 a0001c0003t0021g0086 a0001c0003t0031g0078 |
5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1748C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990846 | |||||||
| chr3:169991094 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.731-1500C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991094 | |||||||
| chr3:169991192 | A | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1402A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991192 | |||||||
| chr3:169991316 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.731-1278G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991316 | |||||||
| chr3:169991700 | C | T | 1 | a0001c0001t0008g0018 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.731-894C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991700 | |||||||
| chr3:169991732 | A | G | 3 | a0001c0001t0010g0066 a0001c0001t0010g0072 a0001c0001t0010g0087 |
3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.731-862A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991732 | |||||||
| chr3:169991754 | G | C | 7 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0075 others(4): Show |
7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-840G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991754 | |||||||
| chr3:169992002 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.731-592C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992002 | |||||||
| chr3:169992137 | A | G | 1 | a0001c0001t0026g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.731-457A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992137 | |||||||
| chr3:169992311 | G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.731-283G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992311 | |||||||
| chr3:169992324 | A | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(34): Show |
82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.731-270A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992324 | |||||||
| chr3:169992575 | G | T | 65 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(62): Show |
137 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.731-19G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992575 |