Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11231 |
| ensemblid | ENSG00000025796.14 |
| hgncid | 21082 |
| symbol | SEC63 |
| name | SEC63 homolog, protein translocation regulator |
| refseq_nuc | NM_007214.5 |
| refseq_prot | NP_009145.1 |
| ensembl_nuc | ENST00000369002.9 |
| ensembl_prot | ENSP00000357998.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 107867756 |
| end | 107958208 |
| strand | - |
| ver | v1.2 |
| region | chr6:107867756-107958208 |
| region5000 | chr6:107862756-107963208 |
| regionname0 | SEC63_chr6_107867756_107958208 |
| regionname5000 | SEC63_chr6_107862756_107963208 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 760 | 328 | 92 | 56 | 146 | 9 | 23 | 114 | SEC63_chr6_107862756_107963208 | SEC63 | MAGQQ others(755): Show |
chr6 | 107862756 | 107963208 |
| a0002 | 0/0 | 760 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | MAGQQ others(755): Show |
chr6 | 107862756 | 107963208 |
| a0003 | 0/0 | 760 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | MAGQQ others(755): Show |
chr6 | 107862756 | 107963208 |
| a0004 | 0/0 | 760 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | MAGQQ others(755): Show |
chr6 | 107862756 | 107963208 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2280 | 214 | 74 | 46 | 70 | 6 | 18 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0002 | 1/1 | 2280 | 105 | 14 | 10 | 72 | 3 | 4 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0003 | 0/0 | 2280 | 3 | 3 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0006 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0008 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0009 | 0/0 | 2280 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0010 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0011 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0001c0012 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0002c0004 | 0/0 | 2280 | 2 | 0 | 0 | 0 | 0 | 2 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0003c0007 | 0/0 | 2280 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 | ||
| a0004c0005 | 0/0 | 2280 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | ATGGC others(2275): Show |
chr6 | 107862756 | 107963208 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6422 | 116 | 13 | 39 | 46 | 4 | 14 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0003 | 0/0 | 6422 | 21 | 8 | 2 | 7 | 2 | 2 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0006 | 0/0 | 6422 | 13 | 13 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0007 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0008 | 0/0 | 6424 | 6 | 6 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6419): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0009 | 0/0 | 6425 | 6 | 6 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6420): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0010 | 0/0 | 6422 | 6 | 1 | 0 | 5 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0012 | 0/0 | 6423 | 4 | 4 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0014 | 0/0 | 6427 | 3 | 3 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6422): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0016 | 0/0 | 6424 | 3 | 3 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6419): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0017 | 0/0 | 6426 | 3 | 3 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6421): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0019 | 0/0 | 6425 | 2 | 2 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6420): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0020 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6419): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0021 | 0/0 | 6423 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0022 | 0/0 | 6428 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6423): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0023 | 0/0 | 6423 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0024 | 0/0 | 6422 | 2 | 2 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0027 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6423): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0029 | 0/0 | 6425 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6420): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0030 | 0/0 | 6423 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0031 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6426): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0032 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6423): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0033 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6422): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0034 | 0/0 | 6423 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0035 | 0/0 | 6423 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0036 | 0/0 | 6423 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0037 | 0/0 | 6422 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0038 | 0/0 | 6422 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0039 | 0/0 | 6422 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0040 | 0/0 | 6423 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6418): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0041 | 0/0 | 6422 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0043 | 0/0 | 6422 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0044 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0045 | 0/0 | 6422 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0046 | 0/0 | 6422 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0047 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0001t0048 | 0/0 | 6422 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0001 | 0/0 | 6422 | 2 | 0 | 0 | 0 | 2 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0002 | 0/0 | 6430 | 31 | 1 | 2 | 28 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0004 | 1/0 | 6430 | 21 | 0 | 2 | 18 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0005 | 0/0 | 6434 | 18 | 1 | 4 | 10 | 1 | 2 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6429): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0007 | 0/0 | 6422 | 7 | 5 | 2 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0011 | 0/0 | 6433 | 6 | 0 | 0 | 6 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6428): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0013 | 0/0 | 6431 | 4 | 0 | 0 | 4 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6426): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0015 | 0/0 | 6433 | 4 | 4 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6428): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0018 | 0/0 | 6430 | 3 | 0 | 0 | 2 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0025 | 0/0 | 6431 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6426): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0026 | 0/0 | 6430 | 2 | 2 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0028 | 0/0 | 6430 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0049 | 0/0 | 6430 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6425): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0050 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6427): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0051 | 0/1 | 6435 | 1 | 0 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6430): Show |
chr6 | 107862756 | 107963208 |
| a0001c0002t0052 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6428): Show |
chr6 | 107862756 | 107963208 |
| a0001c0003t0006 | 0/0 | 6422 | 3 | 3 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0006t0001 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0008t0001 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0009t0001 | 0/0 | 6422 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0010t0001 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0001c0011t0014 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6422): Show |
chr6 | 107862756 | 107963208 |
| a0001c0012t0001 | 0/0 | 6422 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0002c0004t0003 | 0/0 | 6422 | 2 | 0 | 0 | 0 | 0 | 2 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0003c0007t0042 | 0/0 | 6422 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6417): Show |
chr6 | 107862756 | 107963208 |
| a0004c0005t0005 | 0/0 | 6434 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | CTCTC others(6429): Show |
chr6 | 107862756 | 107963208 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0014g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0014g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0014g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0016g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0017g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0017g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0017g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0019g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0020g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0021g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0021g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0022g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0023g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0023g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0024g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0027g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0029g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0030g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0032g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0033g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0034g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0035g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0036g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0037g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0038g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0039g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0040g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0041g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0043g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0044g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0045g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0046g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0047g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0001t0048g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0011g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0011g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0013g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0013g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0013g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0015g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0018g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0018g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0018g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0025g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0025g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0026g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0026g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0028g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0049g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0050g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0051g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0002t0052g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0003t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0003t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0003t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0011t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0001c0012t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0002c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0002c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0003c0007t0042g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| a0004c0005t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0007 | t0042 | g0320 | EUR | GBR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | GBR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0199 | EUR | FIN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00408 | hp1 | a0001 | c0002 | t0025 | g0288 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00408 | hp2 | a0001 | c0012 | t0001 | g0321 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00558 | hp1 | a0001 | c0010 | t0001 | g0116 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00621 | hp2 | a0001 | c0002 | t0011 | g0195 | EAS | CHS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00735 | hp1 | a0001 | c0002 | t0005 | g0193 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG00741 | hp2 | a0001 | c0002 | t0005 | g0181 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01099 | hp1 | a0001 | c0001 | t0043 | g0065 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01167 | hp2 | a0001 | c0002 | t0007 | g0052 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0048 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01169 | hp2 | a0001 | c0001 | t0034 | g0124 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01243 | hp2 | a0001 | c0001 | t0039 | g0141 | AMR | PUR | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0024 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01256 | hp2 | a0001 | c0002 | t0005 | g0008 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01258 | hp2 | a0001 | c0002 | t0005 | g0008 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01346 | hp1 | a0001 | c0001 | t0037 | g0251 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0128 | EUR | IBS | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01884 | hp1 | a0001 | c0001 | t0033 | g0313 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01891 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0093 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG01993 | hp2 | a0001 | c0002 | t0004 | g0043 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02004 | hp1 | a0001 | c0001 | t0041 | g0064 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0287 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02027 | hp2 | a0001 | c0006 | t0001 | g0157 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02055 | hp2 | a0001 | c0002 | t0007 | g0054 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02071 | hp1 | a0001 | c0008 | t0001 | g0152 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02145 | hp2 | a0001 | c0011 | t0014 | g0205 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | CDX | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02257 | hp1 | a0001 | c0001 | t0030 | g0179 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0317 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0286 | AMR | PEL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0315 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02572 | hp1 | a0001 | c0001 | t0045 | g0216 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0316 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0097 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02622 | hp2 | a0001 | c0002 | t0015 | g0200 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02630 | hp2 | a0001 | c0002 | t0015 | g0311 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02717 | hp2 | a0001 | c0001 | t0032 | g0314 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02723 | hp1 | a0001 | c0001 | t0046 | g0167 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02723 | hp2 | a0001 | c0003 | t0006 | g0218 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0175 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02809 | hp2 | a0001 | c0002 | t0015 | g0309 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0051 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02818 | hp2 | a0001 | c0003 | t0006 | g0204 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0053 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0209 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0049 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0047 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0177 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0318 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0056 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0046 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0176 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03139 | hp1 | a0001 | c0002 | t0026 | g0230 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03195 | hp1 | a0001 | c0001 | t0031 | g0096 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0312 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0012 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0319 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03486 | hp1 | a0001 | c0002 | t0015 | g0201 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0220 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03492 | hp2 | a0002 | c0004 | t0003 | g0171 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0094 | AFR | ESN | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0050 | AFR | GWD | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03579 | hp1 | a0001 | c0001 | t0024 | g0057 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03688 | hp1 | a0001 | c0002 | t0049 | g0289 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03688 | hp2 | a0002 | c0004 | t0003 | g0159 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03831 | hp2 | a0001 | c0002 | t0018 | g0058 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03927 | hp1 | a0001 | c0002 | t0005 | g0190 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04184 | hp2 | a0001 | c0001 | t0038 | g0086 | SAS | BEB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04199 | hp1 | a0001 | c0001 | t0048 | g0078 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04204 | hp1 | a0001 | c0002 | t0005 | g0006 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04204 | hp2 | a0001 | c0009 | t0001 | g0275 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG04228 | hp2 | a0004 | c0005 | t0005 | g0182 | SAS | STU | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18522 | hp2 | a0001 | c0002 | t0026 | g0229 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0197 | EAS | CHB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0095 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18941 | hp1 | a0001 | c0001 | t0023 | g0103 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18945 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18948 | hp2 | a0001 | c0001 | t0047 | g0073 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0006 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18949 | hp2 | a0001 | c0001 | t0036 | g0068 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18950 | hp2 | a0001 | c0002 | t0005 | g0198 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18951 | hp1 | a0001 | c0002 | t0005 | g0183 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18952 | hp1 | a0001 | c0002 | t0011 | g0189 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18952 | hp2 | a0001 | c0001 | t0044 | g0145 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18953 | hp1 | a0001 | c0002 | t0013 | g0035 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18953 | hp2 | a0001 | c0001 | t0022 | g0135 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18957 | hp2 | a0001 | c0002 | t0011 | g0005 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18961 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18962 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18967 | hp1 | a0001 | c0001 | t0035 | g0085 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18967 | hp2 | a0001 | c0002 | t0005 | g0196 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18983 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18984 | hp1 | a0001 | c0001 | t0021 | g0203 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18986 | hp1 | a0001 | c0002 | t0011 | g0005 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18987 | hp1 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18987 | hp2 | a0001 | c0002 | t0005 | g0184 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18988 | hp2 | a0001 | c0002 | t0013 | g0002 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18989 | hp1 | a0001 | c0002 | t0013 | g0029 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18991 | hp2 | a0001 | c0001 | t0023 | g0133 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18992 | hp2 | a0001 | c0002 | t0011 | g0187 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0192 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19004 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19012 | hp1 | a0001 | c0002 | t0013 | g0002 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19012 | hp2 | a0001 | c0001 | t0040 | g0082 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19030 | hp1 | a0001 | c0001 | t0029 | g0207 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19055 | hp1 | a0001 | c0001 | t0022 | g0132 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19055 | hp2 | a0001 | c0002 | t0052 | g0194 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19060 | hp1 | a0001 | c0002 | t0005 | g0186 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19062 | hp2 | a0001 | c0002 | t0018 | g0060 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19064 | hp1 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19064 | hp2 | a0001 | c0002 | t0005 | g0191 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19067 | hp1 | a0001 | c0001 | t0021 | g0228 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0023 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19080 | hp1 | a0001 | c0002 | t0028 | g0038 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19081 | hp1 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19088 | hp2 | a0001 | c0002 | t0011 | g0188 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19089 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0185 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19091 | hp2 | a0001 | c0002 | t0025 | g0305 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ASW | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0079 | EUR | TSI | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0020 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0178 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02559 | hp1 | a0001 | c0002 | t0050 | g0310 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03471 | hp1 | a0001 | c0001 | t0027 | g0017 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | USA | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18955 | hp1 | a0001 | c0002 | t0018 | g0180 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA18955 | hp2 | a0001 | c0001 | t0010 | g0088 | EAS | JPT | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | USA | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | USA | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA21309 | hp1 | a0001 | c0002 | t0005 | g0174 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0051 | g0202 | REF | REF | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0037 | REF | REF | SEC63_chr6_107862756_107963208 | SEC63 | chr6 | 107862756 | 107963208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:107876571 | G | A | 1 | a0003 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2027C>T | p.Thr676Ile | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/21 | 2226/6430 | 2027/2283 | 676/760 | chr6 | 107876571 | |||
| chr6:107881195 | G | C | 1 | a0004 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1889C>G | p.Thr630Ser | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/21 | 2088/6430 | 1889/2283 | 630/760 | chr6 | 107881195 | |||
| chr6:107893490 | C | T | 1 | a0002 | 2 | HG03492.hp2 HG03688.hp2 |
missense_variant | MODERATE | c.1666G>A | p.Val556Ile | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/21 | 1865/6430 | 1666/2283 | 556/760 | chr6 | 107893490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:107897655 | T | G | 1 | a0001c0008 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1434A>C | p.Thr478Thr | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/21 | 1633/6430 | 1434/2283 | 478/760 | chr6 | 107897655 | |||
| chr6:107901404 | A | G | 1 | a0001c0006 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1323T>C | p.Ser441Ser | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/21 | 1522/6430 | 1323/2283 | 441/760 | chr6 | 107901404 | |||
| chr6:107901449 | G | A | 1 | a0001c0009 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1278C>T | p.Phe426Phe | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/21 | 1477/6430 | 1278/2283 | 426/760 | chr6 | 107901449 | |||
| chr6:107902970 | T | C | 1 | a0001c0010 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1083A>G | p.Ala361Ala | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/21 | 1282/6430 | 1083/2283 | 361/760 | chr6 | 107902970 | |||
| chr6:107908979 | T | C | 1 | a0001c0011 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.681A>G | p.Thr227Thr | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/21 | 880/6430 | 681/2283 | 227/760 | chr6 | 107908979 | |||
| chr6:107912725 | G | A | 10 | a0001c0001 a0001c0003 a0001c0006 others(7): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
synonymous_variant | LOW | c.564C>T | p.Asn188Asn | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/21 | 763/6430 | 564/2283 | 188/760 | chr6 | 107912725 | |||
| chr6:107921886 | T | C | 1 | a0001c0003 | 3 | HG02723.hp2 HG02818.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.363A>G | p.Lys121Lys | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/21 | 562/6430 | 363/2283 | 121/760 | chr6 | 107921886 | |||
| chr6:107957902 | G | A | 1 | a0001c0012 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.108C>T | p.Pro36Pro | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/21 | 307/6430 | 108/2283 | 36/760 | chr6 | 107957902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:107867809 | A | G | 3 | a0001c0001t0010 a0001c0001t0035 a0001c0001t0038 |
8 | HG02717.hp1 HG04184.hp2 NA18950.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3895T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3895 | chr6 | 107867809 | ||||||
| chr6:107868079 | T | A | 1 | a0001c0001t0045 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3625 | chr6 | 107868079 | ||||||
| chr6:107868124 | C | T | 54 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(51): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3580G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3580 | chr6 | 107868124 | ||||||
| chr6:107868129 | T | TGTC | 54 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(51): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3574_*3575insGAC | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3574 | chr6 | 107868129 | ||||||
| chr6:107868207 | T | C | 5 | a0001c0001t0003 a0001c0001t0039 a0001c0001t0040 others(2): Show |
26 | HG00438.hp1 HG00642.hp2 HG01081.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3497A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3497 | chr6 | 107868207 | ||||||
| chr6:107868223 | TA | T | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(48): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*3480delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3480 | chr6 | 107868223 | ||||||
| chr6:107868273 | T | G | 54 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(51): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3431A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3431 | chr6 | 107868273 | ||||||
| chr6:107868282 | C | A | 1 | a0001c0001t0041 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3422G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3422 | chr6 | 107868282 | ||||||
| chr6:107868311 | G | A | 53 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(50): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*3393C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3393 | chr6 | 107868311 | ||||||
| chr6:107868314 | C | T | 1 | a0001c0001t0039 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3390G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3390 | chr6 | 107868314 | ||||||
| chr6:107868370 | G | A | 6 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0016 others(3): Show |
16 | HG01884.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3334C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3334 | chr6 | 107868370 | ||||||
| chr6:107868493 | C | T | 1 | a0001c0001t0038 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3211G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3211 | chr6 | 107868493 | ||||||
| chr6:107868534 | G | A | 1 | a0003c0007t0042 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3170C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3170 | chr6 | 107868534 | ||||||
| chr6:107868561 | G | A | 1 | a0001c0001t0043 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3143C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3143 | chr6 | 107868561 | ||||||
| chr6:107868577 | G | A | 1 | a0001c0001t0033 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3127C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3127 | chr6 | 107868577 | ||||||
| chr6:107868580 | T | C | 1 | a0001c0001t0044 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3124A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 3124 | chr6 | 107868580 | ||||||
| chr6:107868893 | G | A | 3 | a0001c0001t0006 a0001c0001t0045 a0001c0003t0006 |
17 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2811C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2811 | chr6 | 107868893 | ||||||
| chr6:107868902 | A | T | 1 | a0001c0002t0052 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2802T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2802 | chr6 | 107868902 | ||||||
| chr6:107868999 | A | G | 8 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0017 others(5): Show |
17 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2705T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2705 | chr6 | 107868999 | ||||||
| chr6:107869042 | C | T | 47 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(44): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*2662G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2662 | chr6 | 107869042 | ||||||
| chr6:107869080 | A | G | 1 | a0001c0001t0034 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2624T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2624 | chr6 | 107869080 | ||||||
| chr6:107869199 | T | TA | 5 | a0001c0001t0014 a0001c0001t0017 a0001c0001t0032 others(2): Show |
9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2504dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2504 | chr6 | 107869199 | ||||||
| chr6:107869248 | C | T | 1 | a0001c0001t0024 | 2 | HG03041.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2456G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2456 | chr6 | 107869248 | ||||||
| chr6:107869687 | A | G | 1 | a0001c0001t0037 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 2017 | chr6 | 107869687 | ||||||
| chr6:107869767 | TG | T | 1 | a0001c0001t0012 | 4 | HG02630.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1936delC | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1936 | chr6 | 107869767 | ||||||
| chr6:107869772 | G | GT | 5 | a0001c0002t0005 a0001c0002t0013 a0001c0002t0015 others(2): Show |
29 | HG00280.hp2 HG00408.hp1 HG00735.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1931dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1931 | chr6 | 107869772 | ||||||
| chr6:107869772 | GTTTT | G | 4 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0016 others(1): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1928_*1931delAAAA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1928 | chr6 | 107869772 | ||||||
| chr6:107869772 | GTTTTT | G | 9 | a0001c0001t0014 a0001c0001t0021 a0001c0001t0030 others(6): Show |
12 | HG01169.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1931delAAAA others(1): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1927 | chr6 | 107869772 | ||||||
| chr6:107869772 | GTTTTTT | G | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(29): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1926_*1931delAAAA others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1926 | chr6 | 107869772 | ||||||
| chr6:107869777 | T | G | 1 | a0001c0002t0002 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1927 | chr6 | 107869777 | ||||||
| chr6:107869803 | T | C | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(29): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1901A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1901 | chr6 | 107869803 | ||||||
| chr6:107869865 | G | C | 1 | a0001c0001t0024 | 2 | HG03041.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1839C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1839 | chr6 | 107869865 | ||||||
| chr6:107869902 | G | GA | 4 | a0001c0002t0005 a0001c0002t0011 a0001c0002t0052 others(1): Show |
26 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1801dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1801 | chr6 | 107869902 | ||||||
| chr6:107869902 | GA | G | 9 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0017 others(6): Show |
19 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1801delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1801 | chr6 | 107869902 | ||||||
| chr6:107869910 | AAAAC | A | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(36): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1790_*1793delGTTT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1790 | chr6 | 107869910 | ||||||
| chr6:107869999 | C | T | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(55): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1705G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1705 | chr6 | 107869999 | ||||||
| chr6:107870178 | A | G | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(45): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1526T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1526 | chr6 | 107870178 | ||||||
| chr6:107870306 | T | G | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(45): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1398A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1398 | chr6 | 107870306 | ||||||
| chr6:107870526 | A | C | 2 | a0001c0001t0016 a0001c0001t0030 |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1178T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 1178 | chr6 | 107870526 | ||||||
| chr6:107870797 | G | A | 1 | a0001c0001t0048 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 907 | chr6 | 107870797 | ||||||
| chr6:107870843 | T | C | 1 | a0001c0002t0026 | 2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*861A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 861 | chr6 | 107870843 | ||||||
| chr6:107871160 | T | C | 1 | a0001c0001t0047 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*544A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 544 | chr6 | 107871160 | ||||||
| chr6:107871292 | C | T | 1 | a0001c0001t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 412 | chr6 | 107871292 | ||||||
| chr6:107871447 | T | C | 2 | a0001c0001t0048 a0001c0002t0028 |
2 | HG04199.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*257A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 257 | chr6 | 107871447 | ||||||
| chr6:107871512 | A | G | 1 | a0001c0002t0049 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 192 | chr6 | 107871512 | ||||||
| chr6:107871581 | A | T | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(45): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*123T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 21/21 | 123 | chr6 | 107871581 | ||||||
| chr6:107958086 | G | A | 52 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(49): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-77C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/21 | chr6 | 107958086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:107871944 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2140-97G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107871944 | |||||||
| chr6:107872049 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2140-202A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872049 | |||||||
| chr6:107872098 | A | G | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2140-251T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872098 | |||||||
| chr6:107872144 | C | G | 2 | a0001c0001t0016g0176 a0001c0001t0016g0177 |
2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2140-297G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872144 | |||||||
| chr6:107872459 | T | C | 5 | a0001c0001t0003g0106 a0001c0001t0003g0118 a0001c0001t0003g0119 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2139+349A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872459 | |||||||
| chr6:107872461 | A | G | 5 | a0001c0001t0003g0106 a0001c0001t0003g0118 a0001c0001t0003g0119 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2139+347T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872461 | |||||||
| chr6:107872503 | T | TA | 61 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(58): Show |
68 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.2139+304dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872503 | |||||||
| chr6:107872521 | T | C | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2139+287A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872521 | |||||||
| chr6:107872603 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2139+205T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 20/20 | chr6 | 107872603 | |||||||
| chr6:107873037 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2035-125A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873037 | |||||||
| chr6:107873198 | A | G | 8 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0087 others(5): Show |
8 | HG02717.hp1 HG04184.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.2035-286T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873198 | |||||||
| chr6:107873459 | C | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2035-547G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873459 | |||||||
| chr6:107873471 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2035-559C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873471 | |||||||
| chr6:107873632 | T | TA | 198 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2035-721dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873632 | |||||||
| chr6:107873871 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2035-959A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873871 | |||||||
| chr6:107873985 | T | C | 6 | a0001c0002t0002g0010 a0001c0002t0002g0231 a0001c0002t0002g0294 others(3): Show |
7 | NA18939.hp1 NA18946.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.2035-1073A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107873985 | |||||||
| chr6:107874054 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2035-1142C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874054 | |||||||
| chr6:107874316 | C | T | 3 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0004c0005t0005g0182 |
3 | HG02922.hp1 HG03098.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2035-1404G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874316 | |||||||
| chr6:107874321 | A | G | 28 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0127 others(25): Show |
28 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2035-1409T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874321 | |||||||
| chr6:107874322 | C | T | 1 | a0001c0002t0002g0302 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2035-1410G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874322 | |||||||
| chr6:107874328 | C | T | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2035-1416G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874328 | |||||||
| chr6:107874340 | A | G | 7 | a0001c0001t0010g0083 a0001c0001t0010g0087 a0001c0001t0010g0088 others(4): Show |
7 | HG04184.hp2 NA18950.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.2035-1428T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874340 | |||||||
| chr6:107874376 | C | T | 6 | a0001c0001t0009g0093 a0001c0001t0009g0094 a0001c0001t0009g0095 others(3): Show |
6 | HG01891.hp2 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2035-1464G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874376 | |||||||
| chr6:107874398 | T | C | 1 | a0001c0002t0018g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2035-1486A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874398 | |||||||
| chr6:107874400 | A | C | 14 | a0001c0001t0001g0091 a0001c0001t0001g0117 a0001c0001t0001g0246 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035-1488T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874400 | |||||||
| chr6:107874402 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2035-1490C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874402 | |||||||
| chr6:107874408 | C | T | 3 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0002t0005g0191 |
3 | NA18984.hp1 NA19064.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2035-1496G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874408 | |||||||
| chr6:107874411 | A | G | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2035-1499T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874411 | |||||||
| chr6:107874423 | T | C | 7 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2035-1511A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874423 | |||||||
| chr6:107874436 | A | T | 1 | a0001c0001t0022g0132 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2035-1524T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874436 | |||||||
| chr6:107874459 | A | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2035-1547T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874459 | |||||||
| chr6:107874464 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2035-1552G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874464 | |||||||
| chr6:107874469 | G | A | 10 | a0001c0001t0008g0015 a0001c0001t0008g0021 a0001c0001t0008g0022 others(7): Show |
10 | HG01884.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2035-1557C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874469 | |||||||
| chr6:107874476 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2035-1564T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874476 | |||||||
| chr6:107874560 | C | T | 2 | a0001c0002t0002g0235 a0001c0002t0002g0291 |
2 | HG00558.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2035-1648G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874560 | |||||||
| chr6:107874561 | A | T | 8 | a0001c0001t0012g0011 a0001c0001t0012g0012 a0001c0001t0012g0013 others(5): Show |
8 | HG01884.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2035-1649T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874561 | |||||||
| chr6:107874574 | C | T | 1 | a0001c0002t0004g0028 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2035-1662G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874574 | |||||||
| chr6:107874581 | G | C | 194 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.2035-1669C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874581 | |||||||
| chr6:107874595 | C | CA | 60 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0142 others(57): Show |
63 | HG00408.hp1 HG00558.hp2 HG01257.hp1 others(60): Show |
intron_variant | MODIFIER | c.2035-1684dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874595 | |||||||
| chr6:107874595 | CA | C | 25 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0269 others(22): Show |
29 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2035-1684delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874595 | |||||||
| chr6:107874650 | G | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2035-1738C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107874650 | |||||||
| chr6:107875020 | ATTTTGT | A | 11 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0244 others(8): Show |
11 | HG01074.hp1 HG01346.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2034+1538_2034+154 others(10): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875020 | |||||||
| chr6:107875059 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2034+1505A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875059 | |||||||
| chr6:107875100 | C | G | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2034+1464G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875100 | |||||||
| chr6:107875117 | G | T | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034+1447C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875117 | |||||||
| chr6:107875118 | C | A | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034+1446G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875118 | |||||||
| chr6:107875524 | C | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0237 others(41): Show |
45 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.2034+1040G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875524 | |||||||
| chr6:107875553 | C | A | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2034+1011G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107875553 | |||||||
| chr6:107876054 | A | C | 4 | a0001c0002t0002g0236 a0001c0002t0002g0284 a0001c0002t0002g0302 others(1): Show |
4 | NA18968.hp2 NA18984.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+510T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107876054 | |||||||
| chr6:107876064 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2034+500G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107876064 | |||||||
| chr6:107876127 | T | A | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2034+437A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 19/20 | chr6 | 107876127 | |||||||
| chr6:107876670 | C | CAA | 62 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0126 others(59): Show |
63 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.1936-10_1936-9dupT others(1): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876670 | |||||||
| chr6:107876670 | C | CAAA | 144 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1936-11_1936-9dupT others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876670 | |||||||
| chr6:107876670 | C | CAAAA | 14 | a0001c0001t0001g0101 a0001c0001t0001g0137 a0001c0001t0003g0129 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1936-12_1936-9dupT others(3): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876670 | |||||||
| chr6:107876670 | CA | C | 7 | a0001c0001t0017g0316 a0001c0001t0017g0317 a0001c0002t0002g0285 others(4): Show |
8 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1936-9delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876670 | |||||||
| chr6:107876696 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1936-34C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876696 | |||||||
| chr6:107876794 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1936-132T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876794 | |||||||
| chr6:107876848 | T | C | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1936-186A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107876848 | |||||||
| chr6:107877065 | G | A | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1936-403C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877065 | |||||||
| chr6:107877069 | GTGTA | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1936-411_1936-408d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877069 | |||||||
| chr6:107877071 | G | GTATATAT others(3): Show |
52 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0231 others(49): Show |
57 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1936-419_1936-410d others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877071 | G | GTATATAT others(5): Show |
4 | a0001c0002t0002g0290 a0001c0002t0005g0192 a0001c0002t0026g0229 others(1): Show |
4 | HG03139.hp1 NA18522.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-421_1936-410d others(14): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877071 | G | GTGTATAT others(3): Show |
1 | a0001c0002t0002g0232 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1936-410_1936-409i others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877071 | G | GTGTATAT others(5): Show |
1 | a0001c0002t0005g0008 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1936-410_1936-409i others(14): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877071 | G | GTGTATAT others(15): Show |
1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1936-410_1936-409i others(24): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877071 | GTATA | G | 4 | a0001c0001t0024g0056 a0001c0001t0024g0057 a0001c0001t0029g0207 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-413_1936-410d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877071 | |||||||
| chr6:107877073 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1936-411T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877073 | |||||||
| chr6:107877078 | T | TATATATA others(3): Show |
3 | a0001c0002t0002g0010 a0001c0002t0002g0294 a0001c0002t0002g0295 |
4 | NA18939.hp1 NA18946.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-426_1936-417d others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877078 | |||||||
| chr6:107877159 | G | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1936-497C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877159 | |||||||
| chr6:107877192 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1936-530A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877192 | |||||||
| chr6:107877465 | G | A | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1936-803C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877465 | |||||||
| chr6:107877487 | G | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0039 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1936-825C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877487 | |||||||
| chr6:107877656 | G | A | 1 | a0001c0001t0039g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1936-994C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877656 | |||||||
| chr6:107877664 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1936-1002T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877664 | |||||||
| chr6:107877821 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1936-1159G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107877821 | |||||||
| chr6:107878396 | T | C | 16 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0027 others(13): Show |
16 | HG01255.hp2 HG01993.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1936-1734A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878396 | |||||||
| chr6:107878441 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1936-1779C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878441 | |||||||
| chr6:107878642 | A | G | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1936-1980T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878642 | |||||||
| chr6:107878645 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0043g0065 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1936-1983G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878645 | |||||||
| chr6:107878806 | G | A | 4 | a0001c0002t0005g0008 a0001c0002t0005g0181 a0001c0002t0005g0193 others(1): Show |
5 | HG00280.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-2144C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878806 | |||||||
| chr6:107878951 | T | TA | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1935+2197_1935+219 others(5): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107878951 | |||||||
| chr6:107879018 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1935+2131G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879018 | |||||||
| chr6:107879061 | A | G | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1935+2088T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879061 | |||||||
| chr6:107879096 | T | C | 8 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+2053A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879096 | |||||||
| chr6:107879312 | C | T | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1935+1837G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879312 | |||||||
| chr6:107879325 | G | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+1824C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879325 | |||||||
| chr6:107879332 | G | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1935+1817C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879332 | |||||||
| chr6:107879470 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02165.hp1 NA18962.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+1679G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879470 | |||||||
| chr6:107879724 | C | CT | 59 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(56): Show |
67 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1935+1424dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879724 | |||||||
| chr6:107879724 | CT | C | 27 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0001c0001t0006g0209 others(24): Show |
27 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1935+1424delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879724 | |||||||
| chr6:107879724 | CTT | C | 202 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1935+1423_1935+142 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879724 | |||||||
| chr6:107879842 | A | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+1307T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879842 | |||||||
| chr6:107879998 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1935+1151G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107879998 | |||||||
| chr6:107880020 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1935+1129T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880020 | |||||||
| chr6:107880172 | C | G | 32 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(29): Show |
35 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.1935+977G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880172 | |||||||
| chr6:107880240 | G | A | 1 | a0001c0002t0002g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1935+909C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880240 | |||||||
| chr6:107880489 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1935+660G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880489 | |||||||
| chr6:107880503 | G | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1935+646C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880503 | |||||||
| chr6:107880624 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0044g0145 |
2 | NA18952.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1935+525C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880624 | |||||||
| chr6:107880664 | C | T | 30 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(27): Show |
33 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1935+485G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880664 | |||||||
| chr6:107880685 | C | T | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1935+464G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880685 | |||||||
| chr6:107880723 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0048g0078 |
2 | HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1935+426G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880723 | |||||||
| chr6:107880724 | G | A | 1 | a0001c0002t0002g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1935+425C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880724 | |||||||
| chr6:107880798 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0122 |
3 | HG01981.hp2 NA18612.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1935+351T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880798 | |||||||
| chr6:107880973 | G | A | 3 | a0001c0001t0008g0016 a0001c0001t0008g0018 a0001c0001t0027g0017 |
3 | HG02965.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1935+176C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 18/20 | chr6 | 107880973 | |||||||
| chr6:107881456 | C | T | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1834-206G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107881456 | |||||||
| chr6:107881566 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1834-316T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107881566 | |||||||
| chr6:107881943 | T | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1834-693A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107881943 | |||||||
| chr6:107881971 | C | T | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1834-721G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107881971 | |||||||
| chr6:107882395 | T | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1833+593A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882395 | |||||||
| chr6:107882503 | C | G | 1 | a0001c0002t0004g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1833+485G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882503 | |||||||
| chr6:107882516 | T | G | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1833+472A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882516 | |||||||
| chr6:107882593 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0126 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1833+395T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882593 | |||||||
| chr6:107882665 | A | G | 19 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(16): Show |
19 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1833+323T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882665 | |||||||
| chr6:107882736 | C | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1833+252G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882736 | |||||||
| chr6:107882771 | G | A | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1833+217C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882771 | |||||||
| chr6:107882836 | G | A | 3 | a0001c0001t0008g0016 a0001c0001t0008g0018 a0001c0001t0027g0017 |
3 | HG02965.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1833+152C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 17/20 | chr6 | 107882836 | |||||||
| chr6:107883384 | A | G | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1675-238T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883384 | |||||||
| chr6:107883479 | G | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1675-333C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883479 | |||||||
| chr6:107883536 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1675-390A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883536 | |||||||
| chr6:107883611 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1675-465G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883611 | |||||||
| chr6:107883642 | T | TTA | 8 | a0001c0001t0009g0175 a0001c0002t0002g0232 a0001c0002t0002g0233 others(5): Show |
8 | HG00408.hp1 HG00558.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675-498_1675-497d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883642 | |||||||
| chr6:107883647 | T | C | 1 | a0001c0002t0001g0007 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1675-501A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883647 | |||||||
| chr6:107883938 | C | A | 2 | a0001c0002t0015g0200 a0001c0002t0015g0201 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1675-792G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107883938 | |||||||
| chr6:107884078 | C | T | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1675-932G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884078 | |||||||
| chr6:107884098 | A | AAAAC | 189 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1675-956_1675-953d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884098 | |||||||
| chr6:107884201 | C | T | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1675-1055G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884201 | |||||||
| chr6:107884250 | CA | C | 193 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1675-1105delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884250 | |||||||
| chr6:107884407 | C | T | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1675-1261G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884407 | |||||||
| chr6:107884662 | C | T | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1675-1516G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884662 | |||||||
| chr6:107884839 | T | C | 2 | a0001c0002t0002g0235 a0001c0002t0002g0291 |
2 | HG00558.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1675-1693A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884839 | |||||||
| chr6:107884858 | T | A | 2 | a0001c0001t0029g0207 a0001c0011t0014g0205 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1675-1712A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884858 | |||||||
| chr6:107884929 | GA | G | 216 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1675-1784delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107884929 | |||||||
| chr6:107885181 | G | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1675-2035C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885181 | |||||||
| chr6:107885306 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0041g0064 |
2 | HG01496.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1675-2160G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885306 | |||||||
| chr6:107885383 | T | A | 1 | a0001c0002t0004g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1675-2237A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885383 | |||||||
| chr6:107885607 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG02015.hp2 HG02083.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1675-2461A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885607 | |||||||
| chr6:107885634 | A | G | 20 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(17): Show |
20 | HG01074.hp1 HG01346.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1675-2488T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885634 | |||||||
| chr6:107885649 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1675-2503T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885649 | |||||||
| chr6:107885709 | A | C | 1 | a0001c0002t0002g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1675-2563T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885709 | |||||||
| chr6:107885832 | A | G | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1675-2686T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885832 | |||||||
| chr6:107885869 | A | T | 32 | a0001c0001t0003g0128 a0001c0001t0029g0207 a0001c0002t0001g0007 others(29): Show |
36 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1675-2723T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885869 | |||||||
| chr6:107885887 | C | T | 1 | a0001c0002t0005g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1675-2741G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107885887 | |||||||
| chr6:107886007 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1675-2861A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886007 | |||||||
| chr6:107886086 | C | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675-2940G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886086 | |||||||
| chr6:107886106 | G | A | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1675-2960C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886106 | |||||||
| chr6:107886150 | G | C | 1 | a0001c0001t0010g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1675-3004C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886150 | |||||||
| chr6:107886165 | C | T | 3 | a0001c0003t0006g0204 a0001c0003t0006g0218 a0001c0003t0006g0220 |
3 | HG02723.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1675-3019G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886165 | |||||||
| chr6:107886259 | T | C | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675-3113A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886259 | |||||||
| chr6:107886530 | C | T | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675-3384G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886530 | |||||||
| chr6:107886535 | T | A | 1 | a0001c0001t0001g0261 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1675-3389A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886535 | |||||||
| chr6:107886701 | ATTGT | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1675-3559_1675-355 others(8): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886701 | |||||||
| chr6:107886763 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1675-3617A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886763 | |||||||
| chr6:107886842 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0262 |
2 | NA18981.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1675-3696A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886842 | |||||||
| chr6:107886845 | G | GT | 54 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0072 others(51): Show |
54 | HG00558.hp1 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1675-3700dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886845 | |||||||
| chr6:107886845 | G | GTT | 9 | a0001c0001t0008g0015 a0001c0001t0008g0022 a0001c0001t0012g0012 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1675-3701_1675-370 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886845 | |||||||
| chr6:107886845 | GT | G | 61 | a0001c0001t0001g0138 a0001c0001t0001g0264 a0001c0001t0009g0175 others(58): Show |
67 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1675-3700delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886845 | |||||||
| chr6:107886846 | T | G | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1675-3700A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886846 | |||||||
| chr6:107886880 | T | C | 30 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(27): Show |
33 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1675-3734A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107886880 | |||||||
| chr6:107887026 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1675-3880G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887026 | |||||||
| chr6:107887031 | G | A | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1675-3885C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887031 | |||||||
| chr6:107887083 | A | C | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1675-3937T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887083 | |||||||
| chr6:107887208 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1675-4062C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887208 | |||||||
| chr6:107887225 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1675-4079A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887225 | |||||||
| chr6:107887264 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1675-4118G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887264 | |||||||
| chr6:107887283 | A | C | 6 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-4137T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887283 | |||||||
| chr6:107887312 | C | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1675-4166G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887312 | |||||||
| chr6:107887312 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1675-4166G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887312 | |||||||
| chr6:107887431 | A | G | 1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1675-4285T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887431 | |||||||
| chr6:107887491 | T | C | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0019g0046 others(1): Show |
4 | HG01099.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675-4345A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887491 | |||||||
| chr6:107887609 | A | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1675-4463T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887609 | |||||||
| chr6:107887654 | C | A | 1 | a0001c0001t0033g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675-4508G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887654 | |||||||
| chr6:107887654 | C | T | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1675-4508G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887654 | |||||||
| chr6:107887689 | G | A | 1 | a0001c0001t0033g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675-4543C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887689 | |||||||
| chr6:107887691 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1675-4545T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887691 | |||||||
| chr6:107887699 | GTAAC | G | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1675-4557_1675-455 others(8): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887699 | |||||||
| chr6:107887709 | C | T | 10 | a0001c0002t0005g0006 a0001c0002t0005g0185 a0001c0002t0005g0191 others(7): Show |
12 | HG00621.hp2 HG04204.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.1675-4563G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887709 | |||||||
| chr6:107887812 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1675-4666C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107887812 | |||||||
| chr6:107888059 | T | A | 1 | a0001c0002t0005g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1675-4913A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107888059 | |||||||
| chr6:107888349 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1674+5133G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107888349 | |||||||
| chr6:107888398 | G | A | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1674+5084C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107888398 | |||||||
| chr6:107888941 | A | C | 3 | a0001c0001t0006g0222 a0001c0001t0006g0223 a0001c0001t0006g0279 |
3 | HG03453.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1674+4541T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107888941 | |||||||
| chr6:107889203 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1674+4279C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889203 | |||||||
| chr6:107889233 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1674+4249C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889233 | |||||||
| chr6:107889241 | G | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1674+4241C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889241 | |||||||
| chr6:107889551 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1674+3931A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889551 | |||||||
| chr6:107889558 | T | C | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+3924A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889558 | |||||||
| chr6:107889725 | T | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1674+3757A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889725 | |||||||
| chr6:107889830 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1674+3652G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889830 | |||||||
| chr6:107889896 | C | A | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+3586G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107889896 | |||||||
| chr6:107890171 | TAA | T | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1674+3309_1674+331 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107890171 | |||||||
| chr6:107890396 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1674+3086G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107890396 | |||||||
| chr6:107890558 | G | A | 211 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1674+2924C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107890558 | |||||||
| chr6:107890951 | T | C | 1 | a0001c0002t0026g0230 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1674+2531A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107890951 | |||||||
| chr6:107890980 | T | A | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1674+2502A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107890980 | |||||||
| chr6:107891464 | G | A | 1 | a0001c0002t0002g0301 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1674+2018C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107891464 | |||||||
| chr6:107891538 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1674+1944G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107891538 | |||||||
| chr6:107891988 | C | G | 1 | a0001c0002t0007g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1674+1494G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107891988 | |||||||
| chr6:107892275 | G | C | 33 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(30): Show |
36 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.1674+1207C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892275 | |||||||
| chr6:107892329 | T | C | 40 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(37): Show |
44 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1674+1153A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892329 | |||||||
| chr6:107892449 | C | T | 1 | a0001c0001t0024g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1674+1033G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892449 | |||||||
| chr6:107892642 | G | T | 32 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(29): Show |
35 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.1674+840C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892642 | |||||||
| chr6:107892757 | G | C | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1674+725C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892757 | |||||||
| chr6:107892846 | C | T | 6 | a0001c0001t0009g0093 a0001c0001t0009g0094 a0001c0001t0009g0095 others(3): Show |
6 | HG01891.hp2 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1674+636G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892846 | |||||||
| chr6:107892850 | G | C | 1 | a0001c0001t0008g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1674+632C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892850 | |||||||
| chr6:107892909 | C | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1674+573G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107892909 | |||||||
| chr6:107893014 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1674+468G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893014 | |||||||
| chr6:107893026 | T | A | 2 | a0001c0001t0003g0119 a0001c0001t0003g0120 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1674+456A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893026 | |||||||
| chr6:107893107 | T | TAC | 5 | a0001c0002t0004g0034 a0001c0002t0004g0042 a0001c0002t0013g0029 others(2): Show |
5 | NA18955.hp1 NA18962.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1674+373_1674+374d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TAC | T | 3 | a0001c0002t0004g0023 a0001c0002t0004g0044 a0001c0002t0013g0035 |
3 | NA18953.hp1 NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1674+373_1674+374d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACAC | T | 7 | a0001c0001t0007g0045 a0001c0002t0007g0048 a0001c0002t0007g0049 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+371_1674+374d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(1): Show |
T | 28 | a0001c0001t0001g0071 a0001c0001t0001g0111 a0001c0001t0001g0153 others(25): Show |
29 | HG00280.hp2 HG00621.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1674+367_1674+374d others(10): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(3): Show |
T | 95 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0150 others(92): Show |
101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1674+365_1674+374d others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(5): Show |
T | 105 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0067 others(102): Show |
106 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1674+363_1674+374d others(14): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(7): Show |
T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0134 a0001c0001t0001g0140 others(18): Show |
22 | HG00438.hp1 HG01071.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1674+361_1674+374d others(16): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(9): Show |
T | 31 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(28): Show |
31 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(28): Show |
intron_variant | MODIFIER | c.1674+359_1674+374d others(18): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(11): Show |
T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1674+357_1674+374d others(20): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893107 | TACACACA others(15): Show |
T | 4 | a0001c0001t0008g0016 a0001c0001t0027g0017 a0001c0002t0005g0183 others(1): Show |
4 | HG02965.hp1 HG03471.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674+353_1674+374d others(24): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893107 | |||||||
| chr6:107893189 | A | G | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+293T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893189 | |||||||
| chr6:107893259 | T | C | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1674+223A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 16/20 | chr6 | 107893259 | |||||||
| chr6:107893774 | T | C | 1 | a0001c0001t0017g0319 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1500+64A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 15/20 | chr6 | 107893774 | |||||||
| chr6:107894011 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1441-114A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894011 | |||||||
| chr6:107894027 | C | T | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1441-130G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894027 | |||||||
| chr6:107894080 | A | G | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441-183T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894080 | |||||||
| chr6:107894086 | T | C | 1 | a0001c0002t0005g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1441-189A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894086 | |||||||
| chr6:107894157 | A | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1441-260T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894157 | |||||||
| chr6:107894207 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1441-310C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894207 | |||||||
| chr6:107894231 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1441-334T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894231 | |||||||
| chr6:107894283 | G | A | 1 | a0001c0002t0002g0286 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1441-386C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894283 | |||||||
| chr6:107894520 | A | AAT | 289 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(286): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1441-624_1441-623i others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894520 | |||||||
| chr6:107894591 | C | T | 8 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0087 others(5): Show |
8 | HG02717.hp1 HG04184.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-694G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894591 | |||||||
| chr6:107894770 | C | G | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1441-873G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894770 | |||||||
| chr6:107894784 | T | A | 1 | a0001c0001t0021g0203 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1441-887A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894784 | |||||||
| chr6:107894785 | T | A | 288 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(285): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1441-888A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894785 | |||||||
| chr6:107894785 | T | TA | 4 | a0001c0001t0001g0062 a0001c0001t0001g0249 a0001c0001t0001g0278 others(1): Show |
4 | HG01257.hp2 HG01952.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-889dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107894785 | |||||||
| chr6:107895031 | C | T | 1 | a0001c0002t0004g0031 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1441-1134G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895031 | |||||||
| chr6:107895237 | C | A | 2 | a0001c0002t0002g0283 a0001c0002t0002g0297 |
2 | HG02074.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1441-1340G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895237 | |||||||
| chr6:107895555 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1441-1658T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895555 | |||||||
| chr6:107895613 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0034g0124 |
2 | HG00741.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1441-1716T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895613 | |||||||
| chr6:107895849 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1440+1800G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895849 | |||||||
| chr6:107895850 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+1799C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895850 | |||||||
| chr6:107895860 | T | TA | 183 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1440+1788dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895860 | |||||||
| chr6:107895860 | T | TAA | 14 | a0001c0001t0001g0267 a0001c0001t0008g0016 a0001c0001t0008g0018 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1440+1787_1440+178 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895860 | |||||||
| chr6:107895860 | TA | T | 7 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(4): Show |
7 | HG03041.hp2 HG03579.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+1788delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895860 | |||||||
| chr6:107895860 | TAAAAAAA others(3): Show |
T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1440+1779_1440+178 others(14): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895860 | |||||||
| chr6:107895963 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0034g0124 |
2 | HG00741.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1440+1686C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107895963 | |||||||
| chr6:107896017 | T | C | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1440+1632A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896017 | |||||||
| chr6:107896218 | C | A | 1 | a0001c0002t0002g0233 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1440+1431G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896218 | |||||||
| chr6:107896333 | A | G | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1440+1316T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896333 | |||||||
| chr6:107896419 | T | C | 4 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(1): Show |
4 | HG03041.hp2 HG03579.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+1230A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896419 | |||||||
| chr6:107896509 | T | G | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1440+1140A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896509 | |||||||
| chr6:107896567 | C | T | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+1082G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896567 | |||||||
| chr6:107896697 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1440+952C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896697 | |||||||
| chr6:107896768 | G | C | 1 | a0001c0001t0044g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1440+881C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896768 | |||||||
| chr6:107896878 | C | T | 4 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(1): Show |
4 | HG03041.hp2 HG03579.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+771G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107896878 | |||||||
| chr6:107897001 | A | G | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1440+648T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897001 | |||||||
| chr6:107897044 | G | A | 4 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(1): Show |
4 | HG03041.hp2 HG03579.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+605C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897044 | |||||||
| chr6:107897123 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1440+526G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897123 | |||||||
| chr6:107897288 | T | C | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1440+361A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897288 | |||||||
| chr6:107897429 | T | C | 1 | a0001c0001t0019g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1440+220A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897429 | |||||||
| chr6:107897579 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1440+70T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897579 | |||||||
| chr6:107897597 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1440+52T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 14/20 | chr6 | 107897597 | |||||||
| chr6:107897814 | A | C | 1 | a0001c0002t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1358-83T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107897814 | |||||||
| chr6:107897829 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1358-98A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107897829 | |||||||
| chr6:107897859 | T | C | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1358-128A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107897859 | |||||||
| chr6:107897922 | TA | T | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-192delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107897922 | |||||||
| chr6:107898256 | CA | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1358-526delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898256 | |||||||
| chr6:107898256 | CAA | C | 19 | a0001c0001t0001g0240 a0001c0001t0008g0015 a0001c0001t0008g0016 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1358-527_1358-526d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898256 | |||||||
| chr6:107898327 | C | T | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1358-596G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898327 | |||||||
| chr6:107898636 | ATTAT | A | 4 | a0001c0001t0010g0087 a0001c0001t0010g0088 a0001c0001t0010g0089 others(1): Show |
4 | NA18950.hp1 NA18955.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1358-909_1358-906d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898636 | |||||||
| chr6:107898735 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1358-1004A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898735 | |||||||
| chr6:107898795 | GTTC | G | 8 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358-1067_1358-106 others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898795 | |||||||
| chr6:107898923 | T | C | 2 | a0001c0001t0006g0209 a0001c0001t0006g0210 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1358-1192A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898923 | |||||||
| chr6:107898928 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1358-1197G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898928 | |||||||
| chr6:107898945 | G | C | 1 | a0001c0001t0017g0319 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1358-1214C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898945 | |||||||
| chr6:107898968 | G | GTA | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-1239_1358-123 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898968 | |||||||
| chr6:107898984 | C | A | 32 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(29): Show |
35 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.1358-1253G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107898984 | |||||||
| chr6:107899074 | T | C | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-1343A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899074 | |||||||
| chr6:107899166 | T | G | 2 | a0001c0002t0005g0192 a0001c0002t0005g0197 |
2 | NA18612.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1358-1435A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899166 | |||||||
| chr6:107899350 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1358-1619G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899350 | |||||||
| chr6:107899359 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1358-1628G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899359 | |||||||
| chr6:107899400 | C | T | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1358-1669G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899400 | |||||||
| chr6:107899432 | T | G | 1 | a0001c0002t0004g0040 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1358-1701A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899432 | |||||||
| chr6:107899489 | G | T | 17 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(14): Show |
17 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1358-1758C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899489 | |||||||
| chr6:107899592 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1357+1778C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899592 | |||||||
| chr6:107899649 | T | G | 225 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(222): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1357+1721A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899649 | |||||||
| chr6:107899668 | C | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1357+1702G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899668 | |||||||
| chr6:107899712 | G | T | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1357+1658C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899712 | |||||||
| chr6:107899713 | T | C | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1357+1657A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899713 | |||||||
| chr6:107899716 | CA | C | 222 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1357+1653delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899716 | |||||||
| chr6:107899787 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1357+1583G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107899787 | |||||||
| chr6:107900056 | T | C | 317 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(314): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1357+1314A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900056 | |||||||
| chr6:107900164 | G | T | 4 | a0001c0002t0002g0236 a0001c0002t0002g0284 a0001c0002t0002g0302 others(1): Show |
4 | NA18968.hp2 NA18984.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+1206C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900164 | |||||||
| chr6:107900165 | T | G | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1357+1205A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900165 | |||||||
| chr6:107900552 | G | GTAGAAGG others(9): Show |
1 | a0001c0001t0001g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1357+802_1357+817d others(18): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900552 | |||||||
| chr6:107900592 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1357+778C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900592 | |||||||
| chr6:107900697 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1357+673A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900697 | |||||||
| chr6:107900697 | T | C | 1 | a0001c0002t0004g0003 | 2 | HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1357+673A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900697 | |||||||
| chr6:107900733 | A | C | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1357+637T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900733 | |||||||
| chr6:107900746 | A | C | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1357+624T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107900746 | |||||||
| chr6:107901033 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0278 |
2 | HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1357+337T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107901033 | |||||||
| chr6:107901248 | T | C | 33 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(30): Show |
36 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.1357+122A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 13/20 | chr6 | 107901248 | |||||||
| chr6:107901523 | TA | T | 8 | a0001c0001t0009g0093 a0001c0001t0009g0094 a0001c0001t0009g0095 others(5): Show |
8 | HG01891.hp2 HG02622.hp1 HG03041.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1210-7delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901523 | |||||||
| chr6:107901595 | T | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1210-78A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901595 | |||||||
| chr6:107901694 | G | A | 1 | a0001c0001t0009g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1210-177C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901694 | |||||||
| chr6:107901709 | G | C | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1210-192C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901709 | |||||||
| chr6:107901950 | G | A | 11 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1210-433C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901950 | |||||||
| chr6:107901986 | T | C | 2 | a0001c0002t0005g0183 a0001c0002t0005g0184 |
2 | NA18951.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1210-469A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107901986 | |||||||
| chr6:107902052 | C | T | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-535G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107902052 | |||||||
| chr6:107902126 | A | C | 1 | a0001c0001t0030g0179 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1210-609T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107902126 | |||||||
| chr6:107902304 | TTATC | T | 21 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(18): Show |
21 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1209+536_1209+539d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107902304 | |||||||
| chr6:107902445 | T | C | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209+399A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107902445 | |||||||
| chr6:107902554 | TAG | T | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1209+288_1209+289d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 12/20 | chr6 | 107902554 | |||||||
| chr6:107903218 | A | C | 190 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1055-220T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903218 | |||||||
| chr6:107903270 | C | T | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055-272G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903270 | |||||||
| chr6:107903344 | C | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1055-346G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903344 | |||||||
| chr6:107903395 | C | CA | 14 | a0001c0001t0001g0273 a0001c0001t0019g0046 a0001c0001t0019g0047 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1055-398dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903395 | |||||||
| chr6:107903439 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1055-441C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903439 | |||||||
| chr6:107903499 | G | A | 1 | a0001c0002t0002g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1055-501C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903499 | |||||||
| chr6:107903654 | A | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1055-656T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903654 | |||||||
| chr6:107903857 | T | A | 23 | a0001c0001t0003g0061 a0001c0001t0003g0063 a0001c0001t0003g0079 others(20): Show |
23 | HG00438.hp1 HG00642.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1054+772A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903857 | |||||||
| chr6:107903859 | C | T | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+770G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903859 | |||||||
| chr6:107903920 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1054+709G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903920 | |||||||
| chr6:107903991 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1054+638C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107903991 | |||||||
| chr6:107904075 | G | A | 1 | a0001c0009t0001g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1054+554C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904075 | |||||||
| chr6:107904118 | CA | C | 227 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1054+510delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904118 | |||||||
| chr6:107904234 | A | T | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1054+395T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904234 | |||||||
| chr6:107904270 | T | C | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1054+359A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904270 | |||||||
| chr6:107904519 | C | G | 1 | a0004c0005t0005g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1054+110G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904519 | |||||||
| chr6:107904533 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0122 |
3 | HG01981.hp2 NA18612.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1054+96T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904533 | |||||||
| chr6:107904543 | G | C | 5 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0022g0132 others(2): Show |
5 | HG02083.hp1 NA18952.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+86C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904543 | |||||||
| chr6:107904597 | G | C | 4 | a0001c0002t0005g0186 a0001c0002t0011g0187 a0001c0002t0011g0188 others(1): Show |
4 | NA18952.hp1 NA18992.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+32C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 11/20 | chr6 | 107904597 | |||||||
| chr6:107905316 | A | G | 3 | a0001c0002t0004g0032 a0001c0002t0004g0033 a0001c0002t0004g0042 |
3 | NA18981.hp2 NA19005.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.962-595T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107905316 | |||||||
| chr6:107905334 | T | C | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.962-613A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107905334 | |||||||
| chr6:107905383 | C | T | 1 | a0001c0001t0017g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.962-662G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107905383 | |||||||
| chr6:107905858 | GACTT | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.961+586_961+589del others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107905858 | |||||||
| chr6:107906311 | T | A | 1 | a0001c0002t0005g0192 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.961+137A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107906311 | |||||||
| chr6:107906319 | T | G | 45 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0237 others(42): Show |
46 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.961+129A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107906319 | |||||||
| chr6:107906360 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.961+88C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 10/20 | chr6 | 107906360 | |||||||
| chr6:107906658 | G | A | 2 | a0001c0002t0011g0188 a0001c0002t0011g0189 |
2 | NA18952.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.828+25C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 9/20 | chr6 | 107906658 | |||||||
| chr6:107907016 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0125 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.734-239G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907016 | |||||||
| chr6:107907061 | A | G | 1 | a0001c0001t0010g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.734-284T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907061 | |||||||
| chr6:107907235 | T | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.734-458A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907235 | |||||||
| chr6:107907518 | G | A | 1 | a0001c0002t0004g0027 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.734-741C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907518 | |||||||
| chr6:107907543 | T | C | 1 | a0001c0002t0005g0008 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.734-766A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907543 | |||||||
| chr6:107907648 | C | T | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.734-871G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907648 | |||||||
| chr6:107907716 | T | C | 4 | a0001c0002t0005g0186 a0001c0002t0011g0187 a0001c0002t0011g0188 others(1): Show |
4 | NA18952.hp1 NA18992.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-939A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907716 | |||||||
| chr6:107907788 | T | C | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.734-1011A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907788 | |||||||
| chr6:107907796 | A | T | 8 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-1019T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907796 | |||||||
| chr6:107907865 | C | T | 3 | a0001c0003t0006g0204 a0001c0003t0006g0218 a0001c0003t0006g0220 |
3 | HG02723.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.733+1062G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107907865 | |||||||
| chr6:107908299 | A | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.733+628T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908299 | |||||||
| chr6:107908331 | A | G | 1 | a0001c0001t0012g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733+596T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908331 | |||||||
| chr6:107908336 | AT | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.733+590delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908336 | |||||||
| chr6:107908382 | T | C | 1 | a0001c0001t0040g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.733+545A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908382 | |||||||
| chr6:107908526 | C | T | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.733+401G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908526 | |||||||
| chr6:107908559 | T | C | 1 | a0001c0002t0004g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.733+368A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908559 | |||||||
| chr6:107908563 | C | T | 16 | a0001c0002t0004g0023 a0001c0002t0004g0024 a0001c0002t0004g0027 others(13): Show |
16 | HG01255.hp2 HG01993.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.733+364G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908563 | |||||||
| chr6:107908650 | A | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.733+277T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 8/20 | chr6 | 107908650 | |||||||
| chr6:107909081 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.625-46G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909081 | |||||||
| chr6:107909142 | A | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.625-107T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909142 | |||||||
| chr6:107909234 | T | G | 1 | a0001c0002t0025g0305 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.625-199A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909234 | |||||||
| chr6:107909323 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.625-288C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909323 | |||||||
| chr6:107909328 | G | A | 1 | a0001c0001t0017g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-293C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909328 | |||||||
| chr6:107909362 | G | A | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.625-327C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909362 | |||||||
| chr6:107909442 | G | A | 6 | a0001c0001t0009g0093 a0001c0001t0009g0094 a0001c0001t0009g0095 others(3): Show |
6 | HG01891.hp2 HG02622.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-407C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909442 | |||||||
| chr6:107909461 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.625-426G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909461 | |||||||
| chr6:107909946 | A | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.625-911T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107909946 | |||||||
| chr6:107910284 | G | A | 2 | a0001c0002t0005g0008 a0001c0002t0005g0193 |
3 | HG00735.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.624+1062C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910284 | |||||||
| chr6:107910515 | TATATATA others(18): Show |
T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0134 others(6): Show |
10 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+806_624+830del others(25): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910515 | |||||||
| chr6:107910559 | G | A | 2 | a0001c0001t0029g0207 a0001c0011t0014g0205 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.624+787C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910559 | |||||||
| chr6:107910573 | C | T | 10 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(7): Show |
10 | HG00738.hp1 HG01074.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+773G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910573 | |||||||
| chr6:107910589 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.624+757T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910589 | |||||||
| chr6:107910604 | G | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.624+742C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910604 | |||||||
| chr6:107910622 | C | T | 2 | a0001c0001t0032g0314 a0001c0001t0033g0313 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.624+724G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910622 | |||||||
| chr6:107910641 | CAT | C | 3 | a0001c0002t0004g0025 a0001c0002t0004g0039 a0001c0006t0001g0157 |
3 | HG02027.hp2 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.624+703_624+704del others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910641 | |||||||
| chr6:107910649 | A | G | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.624+697T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910649 | |||||||
| chr6:107910687 | CAT | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0105 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+657_624+658del others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910687 | |||||||
| chr6:107910708 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.624+638A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910708 | |||||||
| chr6:107910792 | A | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.624+554T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910792 | |||||||
| chr6:107910985 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.624+361T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910985 | |||||||
| chr6:107910993 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.624+353C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107910993 | |||||||
| chr6:107911038 | G | A | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.624+308C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107911038 | |||||||
| chr6:107911160 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.624+186A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107911160 | |||||||
| chr6:107911169 | G | A | 3 | a0001c0001t0014g0315 a0001c0001t0014g0318 a0001c0002t0002g0292 |
3 | HG02280.hp1 HG03041.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.624+177C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 7/20 | chr6 | 107911169 | |||||||
| chr6:107911421 | A | T | 1 | a0001c0001t0003g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.574-25T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/20 | chr6 | 107911421 | |||||||
| chr6:107911455 | T | A | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-59A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/20 | chr6 | 107911455 | |||||||
| chr6:107911611 | C | T | 1 | a0001c0002t0005g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.574-215G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/20 | chr6 | 107911611 | |||||||
| chr6:107911834 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0160 others(1): Show |
4 | HG00438.hp2 HG00558.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-438C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/20 | chr6 | 107911834 | |||||||
| chr6:107912214 | T | C | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.573+502A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 6/20 | chr6 | 107912214 | |||||||
| chr6:107913096 | A | G | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.514+270T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 5/20 | chr6 | 107913096 | |||||||
| chr6:107913229 | T | C | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.514+137A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 5/20 | chr6 | 107913229 | |||||||
| chr6:107913601 | G | A | 1 | a0001c0001t0010g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.453-174C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107913601 | |||||||
| chr6:107913679 | T | C | 3 | a0001c0001t0017g0319 a0001c0001t0020g0019 a0001c0001t0020g0020 |
3 | HG01891.hp1 HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.453-252A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107913679 | |||||||
| chr6:107913853 | T | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.453-426A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107913853 | |||||||
| chr6:107914076 | G | GT | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.453-650dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914076 | |||||||
| chr6:107914349 | A | G | 1 | a0001c0001t0047g0073 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.453-922T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914349 | |||||||
| chr6:107914378 | A | G | 1 | a0001c0001t0047g0073 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.453-951T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914378 | |||||||
| chr6:107914418 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.453-991A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914418 | |||||||
| chr6:107914740 | T | C | 1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.453-1313A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914740 | |||||||
| chr6:107914928 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.453-1501G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914928 | |||||||
| chr6:107914935 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.453-1508G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107914935 | |||||||
| chr6:107915070 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.453-1643G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915070 | |||||||
| chr6:107915114 | C | A | 1 | a0001c0001t0010g0090 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.453-1687G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915114 | |||||||
| chr6:107915169 | T | C | 1 | a0001c0001t0008g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.453-1742A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915169 | |||||||
| chr6:107915186 | A | G | 2 | a0001c0002t0007g0048 a0001c0002t0007g0052 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.453-1759T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915186 | |||||||
| chr6:107915197 | G | A | 1 | a0001c0001t0008g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.453-1770C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915197 | |||||||
| chr6:107915234 | G | T | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(226): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.453-1807C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915234 | |||||||
| chr6:107915312 | C | T | 3 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 |
3 | HG02486.hp2 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.453-1885G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915312 | |||||||
| chr6:107915409 | C | T | 1 | a0001c0001t0024g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.453-1982G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915409 | |||||||
| chr6:107915561 | A | G | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.453-2134T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915561 | |||||||
| chr6:107915636 | A | T | 1 | a0001c0001t0003g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.453-2209T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915636 | |||||||
| chr6:107915826 | A | C | 1 | a0002c0004t0003g0171 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.453-2399T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107915826 | |||||||
| chr6:107916083 | A | G | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.453-2656T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107916083 | |||||||
| chr6:107916883 | C | T | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.453-3456G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107916883 | |||||||
| chr6:107916898 | T | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.453-3471A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107916898 | |||||||
| chr6:107916920 | A | C | 14 | a0001c0001t0001g0066 a0001c0001t0001g0239 a0001c0001t0001g0249 others(11): Show |
14 | HG00099.hp2 HG00738.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.453-3493T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107916920 | |||||||
| chr6:107917101 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.453-3674A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917101 | |||||||
| chr6:107917135 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.453-3708T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917135 | |||||||
| chr6:107917437 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.453-4010G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917437 | |||||||
| chr6:107917455 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.453-4028A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917455 | |||||||
| chr6:107917641 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.452+4156C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917641 | |||||||
| chr6:107917697 | G | A | 8 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.452+4100C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917697 | |||||||
| chr6:107917713 | A | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(116): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.452+4084T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917713 | |||||||
| chr6:107917752 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.452+4045A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917752 | |||||||
| chr6:107917785 | A | T | 1 | a0001c0001t0008g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.452+4012T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917785 | |||||||
| chr6:107917825 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.452+3972G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917825 | |||||||
| chr6:107917899 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.452+3898G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107917899 | |||||||
| chr6:107918058 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.452+3739C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918058 | |||||||
| chr6:107918165 | T | C | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.452+3632A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918165 | |||||||
| chr6:107918245 | CA | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.452+3551delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918245 | |||||||
| chr6:107918315 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.452+3482G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918315 | |||||||
| chr6:107918333 | C | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.452+3464G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918333 | |||||||
| chr6:107918440 | C | A | 1 | a0001c0001t0016g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.452+3357G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918440 | |||||||
| chr6:107918515 | A | C | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.452+3282T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918515 | |||||||
| chr6:107918647 | G | A | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.452+3150C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918647 | |||||||
| chr6:107918650 | G | A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.452+3147C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918650 | |||||||
| chr6:107918691 | C | CA | 10 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0003g0299 others(7): Show |
10 | HG00642.hp1 HG00642.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.452+3105dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918691 | |||||||
| chr6:107918757 | C | G | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.452+3040G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918757 | |||||||
| chr6:107918903 | CCTT | C | 6 | a0001c0001t0008g0021 a0001c0001t0012g0012 a0001c0001t0017g0317 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.452+2891_452+2893d others(5): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918903 | |||||||
| chr6:107918903 | CCTTT | C | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.452+2890_452+2893d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918903 | |||||||
| chr6:107918903 | CCTTTT | C | 9 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(6): Show |
9 | HG02280.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.452+2889_452+2893d others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918903 | |||||||
| chr6:107918904 | C | CT | 10 | a0001c0001t0001g0101 a0001c0001t0001g0122 a0001c0001t0003g0163 others(7): Show |
11 | HG01981.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452+2892dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918904 | |||||||
| chr6:107918904 | CT | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0067 others(163): Show |
166 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.452+2892delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918904 | |||||||
| chr6:107918904 | CTT | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0253 others(57): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.452+2891_452+2892d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107918904 | |||||||
| chr6:107919081 | T | G | 1 | a0001c0002t0002g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.452+2716A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919081 | |||||||
| chr6:107919383 | G | C | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.452+2414C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919383 | |||||||
| chr6:107919440 | T | C | 1 | a0001c0010t0001g0116 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.452+2357A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919440 | |||||||
| chr6:107919474 | C | T | 10 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.452+2323G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919474 | |||||||
| chr6:107919646 | C | A | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.452+2151G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919646 | |||||||
| chr6:107919679 | G | C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.452+2118C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919679 | |||||||
| chr6:107919738 | C | T | 1 | a0001c0001t0017g0319 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.452+2059G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919738 | |||||||
| chr6:107919809 | A | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.452+1988T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919809 | |||||||
| chr6:107919821 | C | CA | 10 | a0001c0001t0001g0114 a0001c0001t0001g0304 a0001c0001t0007g0045 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.452+1975dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107919821 | |||||||
| chr6:107920024 | C | G | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.452+1773G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920024 | |||||||
| chr6:107920206 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.452+1591C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920206 | |||||||
| chr6:107920227 | T | C | 3 | a0001c0001t0006g0217 a0001c0001t0006g0219 a0001c0001t0045g0216 |
3 | HG02559.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.452+1570A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920227 | |||||||
| chr6:107920239 | T | C | 2 | a0001c0002t0015g0200 a0001c0002t0015g0201 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452+1558A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920239 | |||||||
| chr6:107920261 | A | T | 1 | a0001c0001t0008g0022 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.452+1536T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920261 | |||||||
| chr6:107920325 | C | A | 1 | a0001c0002t0005g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.452+1472G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920325 | |||||||
| chr6:107920377 | G | A | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.452+1420C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920377 | |||||||
| chr6:107920379 | T | C | 1 | a0001c0002t0002g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.452+1418A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920379 | |||||||
| chr6:107920392 | G | A | 1 | a0001c0002t0004g0030 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.452+1405C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920392 | |||||||
| chr6:107920395 | C | T | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.452+1402G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920395 | |||||||
| chr6:107920425 | C | CA | 26 | a0001c0001t0001g0069 a0001c0001t0014g0315 a0001c0001t0017g0317 others(23): Show |
28 | HG00408.hp1 HG00621.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.452+1371dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920425 | |||||||
| chr6:107920425 | C | CAA | 21 | a0001c0001t0010g0084 a0001c0002t0001g0007 a0001c0002t0002g0281 others(18): Show |
23 | HG00280.hp2 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.452+1370_452+1371d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920425 | |||||||
| chr6:107920425 | CA | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.452+1371delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920425 | |||||||
| chr6:107920425 | CAA | C | 22 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(19): Show |
22 | HG01070.hp2 HG01099.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.452+1370_452+1371d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920425 | |||||||
| chr6:107920425 | CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0004g0031 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.452+1356_452+1371d others(18): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920425 | |||||||
| chr6:107920468 | C | T | 1 | a0001c0001t0006g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452+1329G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920468 | |||||||
| chr6:107920469 | G | A | 20 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.452+1328C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920469 | |||||||
| chr6:107920655 | G | A | 6 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.452+1142C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920655 | |||||||
| chr6:107920777 | G | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.452+1020C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920777 | |||||||
| chr6:107920805 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.452+992G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920805 | |||||||
| chr6:107920935 | C | T | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.452+862G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920935 | |||||||
| chr6:107920977 | T | C | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.452+820A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107920977 | |||||||
| chr6:107921032 | A | C | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.452+765T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921032 | |||||||
| chr6:107921154 | G | C | 1 | a0001c0002t0015g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.452+643C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921154 | |||||||
| chr6:107921446 | A | G | 3 | a0001c0001t0003g0106 a0001c0001t0003g0118 a0001c0001t0046g0167 |
3 | HG01081.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.452+351T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921446 | |||||||
| chr6:107921453 | CT | C | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.452+343delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921453 | |||||||
| chr6:107921475 | A | G | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.452+322T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921475 | |||||||
| chr6:107921520 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.452+277G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921520 | |||||||
| chr6:107921592 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.452+205G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 4/20 | chr6 | 107921592 | |||||||
| chr6:107921915 | GAA | G | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0146 others(7): Show |
10 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.340-8_340-7delTT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921915 | |||||||
| chr6:107921915 | GAAA | G | 13 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0003g0079 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG01517.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.340-9_340-7delTTT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921915 | |||||||
| chr6:107921916 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
splice_region_variant&intron_variant | LOW | c.340-7T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921916 | |||||||
| chr6:107921917 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
splice_region_variant&intron_variant | LOW | c.340-8T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921917 | |||||||
| chr6:107921918 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.340-9T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921918 | |||||||
| chr6:107921919 | A | G | 23 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0138 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-10T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921919 | |||||||
| chr6:107921919 | AAC | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(259): Show |
271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.340-12_340-11delGT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921919 | |||||||
| chr6:107921920 | A | G | 23 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0138 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-11T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921920 | |||||||
| chr6:107921920 | AC | A | 8 | a0001c0001t0001g0101 a0001c0001t0001g0307 a0001c0001t0001g0308 others(5): Show |
8 | HG00099.hp2 HG00741.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-12delG | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921920 | |||||||
| chr6:107921921 | C | G | 23 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0001g0138 others(20): Show |
23 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-12G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107921921 | |||||||
| chr6:107922053 | A | C | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.340-144T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922053 | |||||||
| chr6:107922082 | A | ATT | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.340-175_340-174dup others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922082 | |||||||
| chr6:107922296 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0146 |
2 | HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.340-387C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922296 | |||||||
| chr6:107922323 | T | C | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.340-414A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922323 | |||||||
| chr6:107922365 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.340-456C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922365 | |||||||
| chr6:107922567 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.340-658G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922567 | |||||||
| chr6:107922609 | A | T | 1 | a0004c0005t0005g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-700T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922609 | |||||||
| chr6:107922812 | TACAC | T | 17 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(14): Show |
17 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.340-907_340-904del others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922812 | |||||||
| chr6:107922995 | T | TA | 22 | a0001c0001t0001g0069 a0001c0001t0001g0208 a0001c0001t0006g0209 others(19): Show |
22 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-1087dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922995 | |||||||
| chr6:107922995 | TA | T | 13 | a0001c0001t0008g0015 a0001c0001t0010g0083 a0001c0002t0002g0295 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-1087delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107922995 | |||||||
| chr6:107923078 | T | C | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.340-1169A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923078 | |||||||
| chr6:107923184 | C | T | 1 | a0001c0002t0005g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.340-1275G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923184 | |||||||
| chr6:107923218 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1309C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923218 | |||||||
| chr6:107923396 | G | C | 1 | a0001c0001t0003g0128 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.339+1422C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923396 | |||||||
| chr6:107923612 | C | T | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.339+1206G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923612 | |||||||
| chr6:107923692 | A | AT | 27 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0211 others(24): Show |
27 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.339+1125dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923692 | |||||||
| chr6:107923692 | AT | A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.339+1125delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923692 | |||||||
| chr6:107923710 | TG | T | 29 | a0001c0001t0001g0071 a0001c0001t0001g0237 a0001c0001t0001g0266 others(26): Show |
29 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.339+1107delC | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923710 | |||||||
| chr6:107923711 | G | T | 194 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.339+1107C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923711 | |||||||
| chr6:107923810 | G | A | 1 | a0001c0002t0002g0232 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.339+1008C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923810 | |||||||
| chr6:107923812 | T | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.339+1006A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923812 | |||||||
| chr6:107923833 | T | G | 1 | a0001c0001t0006g0221 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.339+985A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923833 | |||||||
| chr6:107923950 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.339+868T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107923950 | |||||||
| chr6:107924146 | C | A | 9 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+672G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924146 | |||||||
| chr6:107924258 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.339+560G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924258 | |||||||
| chr6:107924259 | G | A | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+559C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924259 | |||||||
| chr6:107924431 | A | G | 1 | a0003c0007t0042g0320 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.339+387T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924431 | |||||||
| chr6:107924483 | G | A | 5 | a0001c0001t0001g0131 a0001c0001t0012g0011 a0001c0001t0012g0012 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+335C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924483 | |||||||
| chr6:107924666 | TATA | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.339+149_339+151del others(3): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 3/20 | chr6 | 107924666 | |||||||
| chr6:107925094 | G | A | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.225-162C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925094 | |||||||
| chr6:107925286 | G | C | 1 | a0001c0001t0003g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.225-354C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925286 | |||||||
| chr6:107925453 | A | G | 1 | a0001c0001t0017g0319 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.225-521T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925453 | |||||||
| chr6:107925477 | A | C | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-545T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925477 | |||||||
| chr6:107925546 | A | G | 8 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-614T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925546 | |||||||
| chr6:107925726 | C | G | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-794G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925726 | |||||||
| chr6:107925795 | G | A | 6 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0105 others(3): Show |
6 | HG00621.hp1 HG02027.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-863C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925795 | |||||||
| chr6:107925881 | G | A | 1 | a0001c0002t0004g0043 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.225-949C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925881 | |||||||
| chr6:107925912 | C | T | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-980G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925912 | |||||||
| chr6:107925962 | C | T | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.225-1030G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107925962 | |||||||
| chr6:107926096 | G | A | 6 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-1164C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926096 | |||||||
| chr6:107926121 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225-1189T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926121 | |||||||
| chr6:107926132 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225-1200G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926132 | |||||||
| chr6:107926144 | T | G | 5 | a0001c0001t0003g0106 a0001c0001t0003g0118 a0001c0001t0003g0119 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-1212A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926144 | |||||||
| chr6:107926473 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.225-1541G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926473 | |||||||
| chr6:107926487 | A | T | 1 | a0001c0002t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.225-1555T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926487 | |||||||
| chr6:107926857 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.225-1925T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107926857 | |||||||
| chr6:107927088 | A | G | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.225-2156T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107927088 | |||||||
| chr6:107927186 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(187): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.224+2229G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107927186 | |||||||
| chr6:107927416 | G | A | 2 | a0002c0004t0003g0159 a0002c0004t0003g0171 |
2 | HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.224+1999C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107927416 | |||||||
| chr6:107927725 | TC | T | 3 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 |
3 | HG02486.hp2 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.224+1689delG | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107927725 | |||||||
| chr6:107927981 | C | T | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.224+1434G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107927981 | |||||||
| chr6:107928292 | G | C | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.224+1123C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928292 | |||||||
| chr6:107928382 | A | C | 1 | a0001c0002t0002g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.224+1033T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928382 | |||||||
| chr6:107928399 | G | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.224+1016C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928399 | |||||||
| chr6:107928562 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.224+853G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928562 | |||||||
| chr6:107928803 | T | C | 4 | a0001c0001t0010g0087 a0001c0001t0010g0088 a0001c0001t0010g0089 others(1): Show |
4 | NA18950.hp1 NA18955.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+612A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928803 | |||||||
| chr6:107928870 | G | A | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.224+545C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928870 | |||||||
| chr6:107928926 | C | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.224+489G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107928926 | |||||||
| chr6:107929074 | T | C | 1 | a0001c0001t0012g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.224+341A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107929074 | |||||||
| chr6:107929083 | G | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | NA18957.hp1 NA18973.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+332C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107929083 | |||||||
| chr6:107929310 | T | C | 9 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.224+105A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 2/20 | chr6 | 107929310 | |||||||
| chr6:107929957 | A | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02165.hp1 NA18962.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-443T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107929957 | |||||||
| chr6:107930121 | G | A | 2 | a0001c0001t0032g0314 a0001c0001t0033g0313 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.125-607C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930121 | |||||||
| chr6:107930141 | C | T | 1 | a0001c0002t0002g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.125-627G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930141 | |||||||
| chr6:107930173 | C | CT | 40 | a0001c0001t0001g0153 a0001c0001t0008g0015 a0001c0001t0008g0016 others(37): Show |
40 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.125-660dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | C | CTT | 109 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0067 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.125-661_125-660dup others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | C | CTTT | 68 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0066 others(65): Show |
70 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.125-662_125-660dup others(3): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | C | CTTTT | 7 | a0001c0001t0001g0156 a0001c0001t0001g0252 a0001c0001t0001g0255 others(4): Show |
7 | HG01099.hp2 HG01433.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-663_125-660dup others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | C | CTTTTT | 10 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0212 others(7): Show |
10 | HG02559.hp2 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-664_125-660dup others(5): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | C | CTTTTTT | 7 | a0001c0001t0006g0211 a0001c0001t0006g0219 a0001c0001t0006g0223 others(4): Show |
7 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-665_125-660dup others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930173 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-672_125-660del others(13): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930173 | |||||||
| chr6:107930315 | T | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.125-801A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930315 | |||||||
| chr6:107930332 | C | T | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.125-818G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930332 | |||||||
| chr6:107930393 | C | T | 2 | a0001c0001t0009g0175 a0001c0002t0004g0044 |
2 | HG02809.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.125-879G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930393 | |||||||
| chr6:107930394 | T | C | 1 | a0001c0002t0004g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.125-880A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930394 | |||||||
| chr6:107930397 | G | A | 9 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-883C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930397 | |||||||
| chr6:107930498 | T | C | 1 | a0001c0002t0002g0293 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.125-984A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930498 | |||||||
| chr6:107930527 | A | C | 1 | a0001c0002t0015g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.125-1013T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930527 | |||||||
| chr6:107930694 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-1180C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930694 | |||||||
| chr6:107930863 | T | C | 3 | a0001c0002t0002g0010 a0001c0002t0002g0294 a0001c0002t0002g0295 |
4 | NA18939.hp1 NA18946.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1349A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930863 | |||||||
| chr6:107930927 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-1413T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107930927 | |||||||
| chr6:107931004 | A | G | 1 | a0001c0001t0017g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125-1490T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931004 | |||||||
| chr6:107931111 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-1597G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931111 | |||||||
| chr6:107931265 | C | G | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125-1751G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931265 | |||||||
| chr6:107931290 | C | T | 4 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1776G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931290 | |||||||
| chr6:107931320 | A | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-1806T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931320 | |||||||
| chr6:107931486 | TA | T | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(226): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.125-1973delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931486 | |||||||
| chr6:107931642 | G | A | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.125-2128C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931642 | |||||||
| chr6:107931673 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-2159G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931673 | |||||||
| chr6:107931704 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125-2190C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931704 | |||||||
| chr6:107931749 | CA | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.125-2236delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931749 | |||||||
| chr6:107931777 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.125-2263G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931777 | |||||||
| chr6:107931844 | CA | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.125-2331delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931844 | |||||||
| chr6:107931865 | G | GA | 3 | a0001c0001t0001g0248 a0001c0001t0001g0306 a0001c0001t0037g0251 |
3 | HG01346.hp1 HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.125-2352dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931865 | |||||||
| chr6:107931878 | G | A | 3 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 |
3 | HG02280.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.125-2364C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931878 | |||||||
| chr6:107931918 | T | C | 2 | a0001c0001t0032g0314 a0001c0001t0033g0313 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.125-2404A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107931918 | |||||||
| chr6:107932066 | A | G | 1 | a0001c0002t0002g0232 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.125-2552T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932066 | |||||||
| chr6:107932101 | A | G | 34 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(31): Show |
37 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-2587T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932101 | |||||||
| chr6:107932495 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-2981A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932495 | |||||||
| chr6:107932640 | G | A | 5 | a0001c0001t0001g0226 a0001c0001t0003g0206 a0001c0001t0003g0224 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-3126C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932640 | |||||||
| chr6:107932704 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.125-3190A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932704 | |||||||
| chr6:107932784 | T | C | 34 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(31): Show |
37 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.125-3270A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932784 | |||||||
| chr6:107932827 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-3313A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107932827 | |||||||
| chr6:107933009 | G | A | 1 | a0001c0001t0006g0219 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.125-3495C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933009 | |||||||
| chr6:107933025 | T | C | 7 | a0001c0001t0006g0217 a0001c0001t0006g0219 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-3511A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933025 | |||||||
| chr6:107933029 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-3515T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933029 | |||||||
| chr6:107933134 | G | A | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.125-3620C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933134 | |||||||
| chr6:107933196 | G | A | 1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.125-3682C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933196 | |||||||
| chr6:107933494 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.125-3980T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933494 | |||||||
| chr6:107933669 | T | TCTGCCC | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-4161_125-4156d others(8): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933669 | |||||||
| chr6:107933669 | TCTGCCC | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0019g0046 others(1): Show |
4 | HG02040.hp2 HG02056.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4161_125-4156d others(8): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933669 | |||||||
| chr6:107933767 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-4253A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933767 | |||||||
| chr6:107933769 | T | G | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.125-4255A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933769 | |||||||
| chr6:107933846 | G | A | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.125-4332C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933846 | |||||||
| chr6:107933858 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.125-4344A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933858 | |||||||
| chr6:107933866 | G | A | 1 | a0001c0002t0002g0280 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.125-4352C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933866 | |||||||
| chr6:107933912 | G | A | 1 | a0001c0003t0006g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125-4398C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933912 | |||||||
| chr6:107933990 | C | T | 1 | a0001c0001t0014g0315 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-4476G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107933990 | |||||||
| chr6:107934053 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-4539G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934053 | |||||||
| chr6:107934075 | C | A | 8 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-4561G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934075 | |||||||
| chr6:107934137 | C | T | 4 | a0001c0001t0024g0056 a0001c0001t0024g0057 a0001c0001t0029g0207 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4623G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934137 | |||||||
| chr6:107934141 | A | AC | 34 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0098 others(31): Show |
34 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-4628dupG | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934141 | |||||||
| chr6:107934144 | C | T | 1 | a0001c0001t0046g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125-4630G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934144 | |||||||
| chr6:107934154 | A | G | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4640T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934154 | |||||||
| chr6:107934173 | T | C | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4659A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934173 | |||||||
| chr6:107934178 | A | G | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4664T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934178 | |||||||
| chr6:107934180 | C | T | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4666G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934180 | |||||||
| chr6:107934185 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4671C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934185 | |||||||
| chr6:107934190 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4676C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934190 | |||||||
| chr6:107934193 | C | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4679G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934193 | |||||||
| chr6:107934202 | C | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4688G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934202 | |||||||
| chr6:107934207 | C | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-4693G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934207 | |||||||
| chr6:107934208 | T | C | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4694A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934208 | |||||||
| chr6:107934214 | GCTGCCCA others(256): Show |
G | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4963_125-4701d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934214 | |||||||
| chr6:107934220 | C | CAGTCTGG others(8): Show |
1 | a0001c0001t0001g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.125-4721_125-4707d others(17): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934220 | |||||||
| chr6:107934289 | C | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-4775G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934289 | |||||||
| chr6:107934373 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.125-4859G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934373 | |||||||
| chr6:107934451 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0122 |
3 | HG01981.hp2 NA18612.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.125-4937C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934451 | |||||||
| chr6:107934469 | G | A | 1 | a0001c0002t0002g0290 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.125-4955C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934469 | |||||||
| chr6:107934479 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4965C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934479 | |||||||
| chr6:107934480 | G | A | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4966C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934480 | |||||||
| chr6:107934483 | G | A | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.125-4969C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934483 | |||||||
| chr6:107934485 | T | C | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4971A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934485 | |||||||
| chr6:107934488 | A | ATCTGAGA others(33): Show |
64 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.125-4975_125-4974i others(42): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934488 | |||||||
| chr6:107934488 | A | G | 1 | a0001c0001t0014g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-4974T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934488 | |||||||
| chr6:107934505 | C | A | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-4991G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934505 | |||||||
| chr6:107934515 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5001G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934515 | |||||||
| chr6:107934520 | G | A | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5006C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934520 | |||||||
| chr6:107934523 | G | A | 3 | a0001c0001t0014g0312 a0001c0001t0021g0203 a0001c0001t0021g0228 |
3 | HG03195.hp2 NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.125-5009C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934523 | |||||||
| chr6:107934550 | A | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5036T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934550 | |||||||
| chr6:107934552 | G | A | 1 | a0001c0002t0005g0184 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.125-5038C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934552 | |||||||
| chr6:107934555 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5041A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934555 | |||||||
| chr6:107934563 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-5049T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934563 | |||||||
| chr6:107934567 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.125-5053G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934567 | |||||||
| chr6:107934573 | G | A | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5059C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934573 | |||||||
| chr6:107934579 | G | T | 1 | a0001c0001t0006g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.125-5065C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934579 | |||||||
| chr6:107934586 | G | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5072C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934586 | |||||||
| chr6:107934587 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5073A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934587 | |||||||
| chr6:107934590 | C | A | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5076G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934590 | |||||||
| chr6:107934595 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5081G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934595 | |||||||
| chr6:107934603 | ACCCCGTC others(266): Show |
A | 3 | a0001c0001t0014g0312 a0001c0001t0019g0046 a0001c0001t0019g0047 |
3 | HG02922.hp1 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.125-5362_125-5090d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934603 | |||||||
| chr6:107934609 | TCCGGGAG others(176): Show |
T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5278_125-5096d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934609 | |||||||
| chr6:107934786 | G | A | 2 | a0001c0002t0004g0024 a0001c0002t0004g0043 |
2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.125-5272C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934786 | |||||||
| chr6:107934809 | C | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5295G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934809 | |||||||
| chr6:107934810 | C | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5296G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934810 | |||||||
| chr6:107934814 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5300A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934814 | |||||||
| chr6:107934818 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5304A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934818 | |||||||
| chr6:107934820 | GCCAGCTG others(43): Show |
G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5356_125-5307d others(52): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934820 | |||||||
| chr6:107934835 | T | C | 64 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.125-5321A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934835 | |||||||
| chr6:107934868 | AGCCAGCT others(216): Show |
A | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.125-5577_125-5355d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934868 | |||||||
| chr6:107934875 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5361A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934875 | |||||||
| chr6:107934876 | G | A | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.125-5362C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107934876 | |||||||
| chr6:107935012 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.125-5498G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935012 | |||||||
| chr6:107935031 | G | A | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.125-5517C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935031 | |||||||
| chr6:107935058 | G | A | 2 | a0001c0001t0014g0315 a0001c0001t0014g0318 |
2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.125-5544C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935058 | |||||||
| chr6:107935103 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-5589G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935103 | |||||||
| chr6:107935136 | G | A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.125-5622C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935136 | |||||||
| chr6:107935153 | G | A | 2 | a0001c0002t0002g0296 a0001c0002t0002g0298 |
2 | NA18979.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.125-5639C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935153 | |||||||
| chr6:107935184 | C | A | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-5670G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935184 | |||||||
| chr6:107935210 | A | G | 6 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-5696T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935210 | |||||||
| chr6:107935219 | G | A | 1 | a0001c0002t0004g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.125-5705C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935219 | |||||||
| chr6:107935255 | C | T | 1 | a0001c0002t0025g0288 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.125-5741G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935255 | |||||||
| chr6:107935304 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.125-5790G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935304 | |||||||
| chr6:107935350 | G | A | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125-5836C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935350 | |||||||
| chr6:107935351 | G | C | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-5837C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935351 | |||||||
| chr6:107935374 | G | A | 1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.125-5860C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935374 | |||||||
| chr6:107935392 | G | A | 1 | a0001c0002t0018g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.125-5878C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935392 | |||||||
| chr6:107935476 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.125-5962C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935476 | |||||||
| chr6:107935480 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.125-5966C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935480 | |||||||
| chr6:107935572 | T | C | 32 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(29): Show |
32 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.125-6058A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935572 | |||||||
| chr6:107935613 | A | AC | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.125-6100dupG | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935613 | |||||||
| chr6:107935664 | G | T | 2 | a0001c0001t0001g0306 a0001c0001t0037g0251 |
2 | HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.125-6150C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935664 | |||||||
| chr6:107935737 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.125-6223A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935737 | |||||||
| chr6:107935751 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.125-6237G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935751 | |||||||
| chr6:107935762 | C | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-6248G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935762 | |||||||
| chr6:107935762 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.125-6248G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935762 | |||||||
| chr6:107935766 | A | G | 1 | a0001c0001t0024g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.125-6252T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935766 | |||||||
| chr6:107935788 | A | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-6274T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935788 | |||||||
| chr6:107935791 | AAAAAT | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0019g0046 others(1): Show |
4 | HG01099.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-6282_125-6278d others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935791 | |||||||
| chr6:107935791 | AAAAATAA others(3): Show |
A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.125-6287_125-6278d others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935791 | |||||||
| chr6:107935854 | T | C | 1 | a0001c0001t0010g0089 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.125-6340A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935854 | |||||||
| chr6:107935944 | A | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-6430T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935944 | |||||||
| chr6:107935975 | T | C | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.125-6461A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107935975 | |||||||
| chr6:107936016 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.125-6502G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107936016 | |||||||
| chr6:107936545 | T | TA | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-7032_125-7031i others(3): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107936545 | |||||||
| chr6:107936553 | A | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-7039T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107936553 | |||||||
| chr6:107936586 | C | T | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-7072G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107936586 | |||||||
| chr6:107936608 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-7094T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107936608 | |||||||
| chr6:107937042 | C | G | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.125-7528G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937042 | |||||||
| chr6:107937107 | A | G | 231 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.125-7593T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937107 | |||||||
| chr6:107937123 | A | AT | 7 | a0001c0001t0001g0123 a0001c0001t0019g0046 a0001c0001t0019g0047 others(4): Show |
7 | HG02004.hp2 HG02273.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-7610dupA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937123 | |||||||
| chr6:107937123 | A | ATT | 18 | a0001c0001t0001g0156 a0001c0001t0009g0175 a0001c0001t0012g0011 others(15): Show |
18 | HG01952.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-7611_125-7610d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937123 | |||||||
| chr6:107937123 | A | ATTT | 21 | a0001c0001t0001g0069 a0001c0001t0001g0149 a0001c0001t0001g0150 others(18): Show |
21 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-7612_125-7610d others(5): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937123 | |||||||
| chr6:107937123 | A | ATTTT | 184 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.125-7613_125-7610d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937123 | |||||||
| chr6:107937372 | T | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-7858A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937372 | |||||||
| chr6:107937378 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0125 a0001c0001t0001g0166 |
3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.125-7864C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937378 | |||||||
| chr6:107937418 | G | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-7904C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937418 | |||||||
| chr6:107937492 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.125-7978A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937492 | |||||||
| chr6:107937668 | A | G | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-8154T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937668 | |||||||
| chr6:107937726 | T | C | 44 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0237 others(41): Show |
45 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.125-8212A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937726 | |||||||
| chr6:107937849 | A | G | 3 | a0001c0001t0006g0222 a0001c0001t0006g0223 a0001c0001t0006g0279 |
3 | HG03453.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.125-8335T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107937849 | |||||||
| chr6:107938008 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.125-8494A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938008 | |||||||
| chr6:107938023 | TTTTAG | T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0125 a0001c0001t0001g0164 others(2): Show |
5 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-8514_125-8510d others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938023 | |||||||
| chr6:107938043 | T | C | 7 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-8529A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938043 | |||||||
| chr6:107938121 | A | G | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.125-8607T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938121 | |||||||
| chr6:107938247 | A | ATT | 31 | a0001c0001t0001g0092 a0001c0001t0001g0125 a0001c0001t0001g0126 others(28): Show |
31 | HG01070.hp1 HG01257.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.125-8735_125-8734d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938247 | |||||||
| chr6:107938247 | A | ATTT | 160 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.125-8736_125-8734d others(5): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938247 | |||||||
| chr6:107938247 | A | ATTTT | 13 | a0001c0001t0001g0070 a0001c0001t0001g0098 a0001c0001t0001g0246 others(10): Show |
13 | HG00621.hp1 HG01257.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.125-8737_125-8734d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938247 | |||||||
| chr6:107938247 | AT | A | 59 | a0001c0001t0021g0203 a0001c0002t0001g0007 a0001c0002t0002g0001 others(56): Show |
66 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.125-8734delA | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938247 | |||||||
| chr6:107938319 | C | T | 1 | a0001c0001t0040g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.125-8805G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938319 | |||||||
| chr6:107938413 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-8899T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938413 | |||||||
| chr6:107938465 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.125-8951T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938465 | |||||||
| chr6:107938494 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.125-8980G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938494 | |||||||
| chr6:107938513 | AGGATTAC others(303): Show |
A | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.125-9309_125-9000d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938513 | |||||||
| chr6:107938531 | C | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-9017G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938531 | |||||||
| chr6:107938548 | G | A | 1 | a0001c0002t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.125-9034C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938548 | |||||||
| chr6:107938566 | CTTTTTTT | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0253 a0001c0001t0001g0255 others(2): Show |
6 | HG01106.hp1 HG01255.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-9059_125-9053d others(9): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938566 | |||||||
| chr6:107938568 | T | C | 1 | a0001c0002t0005g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.125-9054A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938568 | |||||||
| chr6:107938572 | T | TC | 8 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0014g0315 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-9059_125-9058i others(3): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938572 | |||||||
| chr6:107938887 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-9373G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107938887 | |||||||
| chr6:107939110 | T | C | 1 | a0001c0001t0020g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.125-9596A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939110 | |||||||
| chr6:107939153 | C | T | 24 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(21): Show |
24 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.125-9639G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939153 | |||||||
| chr6:107939255 | C | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.125-9741G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939255 | |||||||
| chr6:107939518 | G | A | 7 | a0001c0001t0010g0083 a0001c0001t0010g0087 a0001c0001t0010g0088 others(4): Show |
7 | HG04184.hp2 NA18950.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-10004C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939518 | |||||||
| chr6:107939769 | A | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(123): Show |
127 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.125-10255T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939769 | |||||||
| chr6:107939770 | A | T | 1 | a0001c0001t0010g0083 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.125-10256T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939770 | |||||||
| chr6:107939779 | A | T | 1 | a0001c0001t0017g0316 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.125-10265T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939779 | |||||||
| chr6:107939780 | T | A | 18 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.125-10266A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939780 | |||||||
| chr6:107939784 | T | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0003g0063 others(1): Show |
4 | NA18747.hp2 NA18949.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-10270A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939784 | |||||||
| chr6:107939785 | A | T | 9 | a0001c0001t0016g0176 a0001c0001t0016g0177 a0001c0001t0016g0178 others(6): Show |
9 | HG02145.hp2 HG02486.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-10271T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939785 | |||||||
| chr6:107939786 | A | T | 6 | a0001c0001t0021g0203 a0001c0001t0021g0228 a0001c0001t0024g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-10272T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939786 | |||||||
| chr6:107939878 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-10364A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939878 | |||||||
| chr6:107939945 | C | T | 1 | a0002c0004t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.125-10431G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107939945 | |||||||
| chr6:107940071 | C | A | 1 | a0001c0001t0032g0314 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125-10557G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940071 | |||||||
| chr6:107940111 | A | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(226): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.125-10597T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940111 | |||||||
| chr6:107940116 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18939.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.125-10602A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940116 | |||||||
| chr6:107940165 | A | G | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-10651T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940165 | |||||||
| chr6:107940171 | T | G | 37 | a0001c0001t0009g0175 a0001c0001t0014g0312 a0001c0001t0019g0046 others(34): Show |
40 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(37): Show |
intron_variant | MODIFIER | c.125-10657A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940171 | |||||||
| chr6:107940180 | TA | T | 16 | a0001c0001t0001g0226 a0001c0001t0003g0206 a0001c0001t0003g0224 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-10667delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940180 | |||||||
| chr6:107940225 | C | T | 2 | a0001c0002t0005g0183 a0001c0002t0005g0184 |
2 | NA18951.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.125-10711G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940225 | |||||||
| chr6:107940259 | C | T | 35 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0001c0002t0002g0001 others(32): Show |
38 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-10745G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940259 | |||||||
| chr6:107940351 | A | G | 3 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0055 |
3 | HG02615.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125-10837T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940351 | |||||||
| chr6:107940502 | C | A | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-10988G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940502 | |||||||
| chr6:107940528 | G | A | 1 | a0001c0002t0002g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.125-11014C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940528 | |||||||
| chr6:107940600 | CCT | C | 30 | a0001c0001t0014g0312 a0001c0002t0001g0007 a0001c0002t0005g0006 others(27): Show |
34 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.125-11088_125-1108 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940600 | |||||||
| chr6:107940792 | T | TA | 173 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.125-11279dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940792 | |||||||
| chr6:107940834 | T | C | 4 | a0001c0001t0024g0056 a0001c0001t0024g0057 a0001c0001t0029g0207 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-11320A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107940834 | |||||||
| chr6:107941012 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-11498T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941012 | |||||||
| chr6:107941090 | C | T | 8 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0010g0087 others(5): Show |
8 | HG02717.hp1 HG04184.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-11576G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941090 | |||||||
| chr6:107941149 | G | T | 23 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(20): Show |
23 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.125-11635C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941149 | |||||||
| chr6:107941159 | A | G | 64 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.125-11645T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941159 | |||||||
| chr6:107941310 | G | A | 1 | a0001c0001t0029g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-11796C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941310 | |||||||
| chr6:107941352 | C | T | 1 | a0001c0001t0040g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.125-11838G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941352 | |||||||
| chr6:107941371 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.125-11857A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941371 | |||||||
| chr6:107941781 | A | G | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.125-12267T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941781 | |||||||
| chr6:107941855 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.125-12341C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941855 | |||||||
| chr6:107941956 | G | A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.125-12442C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941956 | |||||||
| chr6:107941987 | T | C | 1 | a0001c0002t0004g0003 | 2 | HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.125-12473A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107941987 | |||||||
| chr6:107942130 | T | A | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-12616A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942130 | |||||||
| chr6:107942195 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.125-12681G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942195 | |||||||
| chr6:107942338 | C | G | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.125-12824G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942338 | |||||||
| chr6:107942411 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.125-12897C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942411 | |||||||
| chr6:107942427 | T | G | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.125-12913A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942427 | |||||||
| chr6:107942498 | C | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-12984G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942498 | |||||||
| chr6:107942734 | C | A | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.125-13220G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942734 | |||||||
| chr6:107942736 | C | G | 1 | a0001c0001t0014g0315 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-13222G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942736 | |||||||
| chr6:107942953 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(39): Show |
43 | HG00408.hp2 HG00738.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.125-13439A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107942953 | |||||||
| chr6:107943097 | T | C | 64 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.125-13583A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943097 | |||||||
| chr6:107943116 | C | T | 1 | a0001c0001t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.125-13602G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943116 | |||||||
| chr6:107943255 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.125-13741T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943255 | |||||||
| chr6:107943315 | T | C | 1 | a0001c0001t0003g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.125-13801A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943315 | |||||||
| chr6:107943319 | T | C | 1 | a0001c0011t0014g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125-13805A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943319 | |||||||
| chr6:107943847 | G | A | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.124+14039C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107943847 | |||||||
| chr6:107944063 | C | G | 1 | a0001c0002t0002g0283 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.124+13823G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944063 | |||||||
| chr6:107944514 | A | G | 2 | a0001c0001t0006g0209 a0001c0001t0006g0210 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.124+13372T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944514 | |||||||
| chr6:107944696 | C | CAAAATA | 285 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(282): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.124+13184_124+1318 others(10): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944696 | |||||||
| chr6:107944764 | A | T | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+13122T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944764 | |||||||
| chr6:107944775 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.124+13111T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944775 | |||||||
| chr6:107944842 | T | C | 3 | a0001c0001t0008g0016 a0001c0001t0008g0018 a0001c0001t0027g0017 |
3 | HG02965.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.124+13044A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944842 | |||||||
| chr6:107944844 | G | T | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.124+13042C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944844 | |||||||
| chr6:107944908 | CAAAAATC others(296): Show |
C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+12675_124+1297 others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107944908 | |||||||
| chr6:107945198 | C | CAAAAAAA others(10): Show |
2 | a0001c0002t0007g0049 a0001c0002t0007g0053 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.124+12671_124+1268 others(21): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945198 | |||||||
| chr6:107945198 | C | CAAAAAAA others(11): Show |
5 | a0001c0002t0007g0048 a0001c0002t0007g0050 a0001c0002t0007g0051 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+12670_124+1268 others(22): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945198 | |||||||
| chr6:107945305 | C | CTT | 6 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+12579_124+1258 others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945305 | |||||||
| chr6:107945687 | C | G | 44 | a0001c0001t0001g0208 a0001c0001t0001g0226 a0001c0001t0003g0206 others(41): Show |
44 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.124+12199G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945687 | |||||||
| chr6:107945761 | CCTT | C | 3 | a0001c0001t0014g0315 a0001c0001t0014g0318 a0001c0001t0017g0319 |
3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.124+12122_124+1212 others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945761 | |||||||
| chr6:107945920 | T | TTTTG | 4 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
4 | NA18747.hp2 NA18961.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+11962_124+1196 others(8): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945920 | |||||||
| chr6:107945936 | A | G | 4 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
4 | NA18747.hp2 NA18961.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+11950T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107945936 | |||||||
| chr6:107946083 | T | G | 3 | a0001c0001t0009g0175 a0001c0001t0024g0056 a0001c0001t0024g0057 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+11803A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946083 | |||||||
| chr6:107946219 | G | A | 2 | a0001c0001t0008g0022 a0001c0001t0008g0055 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.124+11667C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946219 | |||||||
| chr6:107946297 | A | G | 64 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.124+11589T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946297 | |||||||
| chr6:107946421 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG01070.hp2 HG01167.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.124+11465G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946421 | |||||||
| chr6:107946760 | T | C | 1 | a0001c0006t0001g0157 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.124+11126A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946760 | |||||||
| chr6:107946774 | C | T | 3 | a0001c0001t0014g0315 a0001c0001t0014g0318 a0001c0001t0017g0319 |
3 | HG02280.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.124+11112G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946774 | |||||||
| chr6:107946940 | G | T | 1 | a0002c0004t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124+10946C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107946940 | |||||||
| chr6:107947050 | T | G | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.124+10836A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947050 | |||||||
| chr6:107947152 | T | G | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.124+10734A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947152 | |||||||
| chr6:107947268 | G | C | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.124+10618C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947268 | |||||||
| chr6:107947447 | C | T | 1 | a0001c0001t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+10439G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947447 | |||||||
| chr6:107947799 | A | C | 1 | a0004c0005t0005g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.124+10087T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947799 | |||||||
| chr6:107947874 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+10012G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947874 | |||||||
| chr6:107947964 | G | A | 2 | a0001c0001t0020g0019 a0001c0001t0020g0020 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.124+9922C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107947964 | |||||||
| chr6:107948555 | G | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(42): Show |
46 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.124+9331C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107948555 | |||||||
| chr6:107948981 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(165): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.124+8905C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107948981 | |||||||
| chr6:107949056 | C | A | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.124+8830G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949056 | |||||||
| chr6:107949202 | T | C | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+8684A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949202 | |||||||
| chr6:107949417 | C | T | 32 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(29): Show |
35 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.124+8469G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949417 | |||||||
| chr6:107949525 | T | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+8361A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949525 | |||||||
| chr6:107949531 | A | C | 1 | a0001c0002t0002g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.124+8355T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949531 | |||||||
| chr6:107949724 | G | A | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.124+8162C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949724 | |||||||
| chr6:107949864 | G | A | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.124+8022C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107949864 | |||||||
| chr6:107950138 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.124+7748C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950138 | |||||||
| chr6:107950240 | TAAACATT others(3): Show |
T | 1 | a0001c0001t0001g0208 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.124+7636_124+7645d others(12): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950240 | |||||||
| chr6:107950367 | T | C | 1 | a0001c0001t0008g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124+7519A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950367 | |||||||
| chr6:107950451 | C | T | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.124+7435G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950451 | |||||||
| chr6:107950480 | A | C | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.124+7406T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950480 | |||||||
| chr6:107950545 | C | T | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+7341G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950545 | |||||||
| chr6:107950563 | T | C | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.124+7323A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950563 | |||||||
| chr6:107950597 | A | G | 1 | a0001c0002t0002g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.124+7289T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950597 | |||||||
| chr6:107950658 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.124+7228C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950658 | |||||||
| chr6:107950739 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+7147C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950739 | |||||||
| chr6:107950894 | C | T | 8 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+6992G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107950894 | |||||||
| chr6:107951040 | G | A | 3 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0055 |
3 | HG02615.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.124+6846C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951040 | |||||||
| chr6:107951042 | A | G | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+6844T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951042 | |||||||
| chr6:107951069 | T | A | 28 | a0001c0001t0001g0208 a0001c0001t0001g0226 a0001c0001t0003g0206 others(25): Show |
28 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.124+6817A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951069 | |||||||
| chr6:107951330 | T | G | 2 | a0001c0001t0021g0203 a0001c0001t0021g0228 |
2 | NA18984.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.124+6556A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951330 | |||||||
| chr6:107951735 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.124+6151C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951735 | |||||||
| chr6:107951749 | T | C | 292 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(289): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.124+6137A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951749 | |||||||
| chr6:107951750 | G | A | 1 | a0001c0001t0006g0221 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124+6136C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951750 | |||||||
| chr6:107951755 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.124+6131T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951755 | |||||||
| chr6:107951860 | A | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02165.hp1 NA18962.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+6026T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951860 | |||||||
| chr6:107951909 | C | A | 1 | a0001c0002t0002g0297 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.124+5977G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951909 | |||||||
| chr6:107951946 | T | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+5940A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951946 | |||||||
| chr6:107951972 | CA | C | 58 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0208 others(55): Show |
58 | HG01243.hp1 HG01516.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.124+5913delT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107951972 | |||||||
| chr6:107952057 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.124+5829G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952057 | |||||||
| chr6:107952201 | A | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+5685T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952201 | |||||||
| chr6:107952286 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.124+5600C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952286 | |||||||
| chr6:107952333 | G | A | 1 | a0002c0004t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124+5553C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952333 | |||||||
| chr6:107952704 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.124+5182C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952704 | |||||||
| chr6:107952968 | T | C | 30 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0231 others(27): Show |
33 | HG00408.hp1 HG00558.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+4918A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107952968 | |||||||
| chr6:107953034 | T | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124+4852A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953034 | |||||||
| chr6:107953157 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+4729C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953157 | |||||||
| chr6:107953217 | G | A | 5 | a0001c0001t0014g0315 a0001c0001t0014g0318 a0001c0001t0017g0316 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+4669C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953217 | |||||||
| chr6:107953239 | G | A | 1 | a0001c0002t0002g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.124+4647C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953239 | |||||||
| chr6:107953472 | GAAGTGAG others(168): Show |
G | 1 | a0001c0002t0004g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.124+4239_124+4413d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953472 | |||||||
| chr6:107953494 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.124+4392C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953494 | |||||||
| chr6:107953532 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG00280.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.124+4354G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953532 | |||||||
| chr6:107953549 | C | T | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+4337G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953549 | |||||||
| chr6:107953569 | T | TG | 46 | a0001c0001t0001g0168 a0001c0001t0001g0208 a0001c0001t0001g0226 others(43): Show |
46 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.124+4316dupC | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953569 | |||||||
| chr6:107953586 | C | T | 4 | a0001c0002t0005g0006 a0001c0002t0005g0191 a0001c0002t0005g0198 others(1): Show |
5 | HG00621.hp2 HG04204.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+4300G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953586 | |||||||
| chr6:107953603 | CGTCCGGG others(266): Show |
C | 1 | a0001c0002t0005g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.124+4010_124+4282d others(2): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953603 | |||||||
| chr6:107953662 | TCTGCCCG others(41): Show |
T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18964.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.124+4176_124+4223d others(50): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953662 | |||||||
| chr6:107953750 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0014g0312 |
2 | HG02602.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.124+4136C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953750 | |||||||
| chr6:107953761 | C | T | 3 | a0001c0001t0008g0016 a0001c0001t0008g0018 a0001c0001t0027g0017 |
3 | HG02965.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.124+4125G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953761 | |||||||
| chr6:107953778 | CGTCCGGG others(91): Show |
C | 61 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(58): Show |
68 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.124+4010_124+4107d others(100): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953778 | |||||||
| chr6:107953807 | C | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124+4079G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953807 | |||||||
| chr6:107953822 | C | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124+4064G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953822 | |||||||
| chr6:107953828 | G | A | 2 | a0001c0001t0017g0316 a0001c0001t0017g0317 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.124+4058C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953828 | |||||||
| chr6:107953881 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.124+4005C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953881 | |||||||
| chr6:107953897 | C | T | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+3989G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953897 | |||||||
| chr6:107953941 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0006g0209 a0001c0001t0006g0210 others(15): Show |
18 | HG02258.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.124+3945G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107953941 | |||||||
| chr6:107954006 | C | T | 1 | a0001c0002t0004g0023 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.124+3880G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954006 | |||||||
| chr6:107954151 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.124+3735A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954151 | |||||||
| chr6:107954181 | T | C | 64 | a0001c0001t0019g0046 a0001c0001t0019g0047 a0001c0002t0001g0007 others(61): Show |
71 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.124+3705A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954181 | |||||||
| chr6:107954225 | G | A | 8 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+3661C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954225 | |||||||
| chr6:107954228 | C | T | 121 | a0001c0001t0001g0062 a0001c0001t0001g0208 a0001c0001t0001g0226 others(118): Show |
128 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.124+3658G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954228 | |||||||
| chr6:107954276 | G | A | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+3610C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954276 | |||||||
| chr6:107954299 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.124+3587T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954299 | |||||||
| chr6:107954327 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.124+3559A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954327 | |||||||
| chr6:107954464 | T | TA | 6 | a0001c0002t0007g0049 a0001c0002t0007g0050 a0001c0002t0007g0051 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+3421dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954464 | |||||||
| chr6:107954480 | A | T | 52 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(49): Show |
53 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.124+3406T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954480 | |||||||
| chr6:107954481 | T | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(49): Show |
53 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.124+3405A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954481 | |||||||
| chr6:107954482 | C | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0238 others(49): Show |
53 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.124+3404G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954482 | |||||||
| chr6:107954482 | C | CA | 194 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0070 others(191): Show |
198 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.124+3403dupT | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954482 | |||||||
| chr6:107954482 | C | CAA | 36 | a0001c0001t0008g0016 a0001c0001t0008g0018 a0001c0001t0008g0021 others(33): Show |
40 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.124+3402_124+3403d others(4): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954482 | |||||||
| chr6:107954655 | C | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124+3231G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954655 | |||||||
| chr6:107954828 | ACAACT | A | 62 | a0001c0002t0001g0007 a0001c0002t0002g0001 a0001c0002t0002g0010 others(59): Show |
69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.124+3053_124+3057d others(7): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954828 | |||||||
| chr6:107954964 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124+2922G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107954964 | |||||||
| chr6:107955154 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.124+2732A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955154 | |||||||
| chr6:107955186 | T | C | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.124+2700A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955186 | |||||||
| chr6:107955288 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124+2598C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955288 | |||||||
| chr6:107955385 | A | T | 1 | a0001c0001t0009g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.124+2501T>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955385 | |||||||
| chr6:107955574 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.124+2312G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955574 | |||||||
| chr6:107955796 | C | G | 29 | a0001c0002t0001g0007 a0001c0002t0005g0006 a0001c0002t0005g0008 others(26): Show |
33 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.124+2090G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955796 | |||||||
| chr6:107955802 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.124+2084C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955802 | |||||||
| chr6:107955882 | C | CTAAA | 42 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(39): Show |
45 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.124+2000_124+2003d others(6): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955882 | |||||||
| chr6:107955882 | C | CTAAATAA others(1): Show |
6 | a0001c0001t0003g0300 a0001c0001t0014g0318 a0001c0001t0017g0319 others(3): Show |
6 | HG02976.hp2 HG03041.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+1996_124+2003d others(10): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955882 | |||||||
| chr6:107955895 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124+1991A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107955895 | |||||||
| chr6:107956083 | C | A | 286 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.124+1803G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956083 | |||||||
| chr6:107956350 | C | T | 3 | a0001c0001t0014g0312 a0001c0001t0032g0314 a0001c0001t0033g0313 |
3 | HG01884.hp1 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.124+1536G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956350 | |||||||
| chr6:107956407 | A | AGCATTAA others(6): Show |
1 | a0001c0001t0001g0059 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124+1466_124+1478d others(15): Show |
SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956407 | |||||||
| chr6:107956433 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.124+1453A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956433 | |||||||
| chr6:107956490 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.124+1396A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956490 | |||||||
| chr6:107956635 | C | T | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.124+1251G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956635 | |||||||
| chr6:107956738 | G | A | 3 | a0001c0001t0009g0175 a0001c0001t0024g0056 a0001c0001t0024g0057 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+1148C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956738 | |||||||
| chr6:107956797 | T | C | 1 | a0001c0002t0025g0305 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.124+1089A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956797 | |||||||
| chr6:107956823 | T | C | 293 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0059 others(290): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.124+1063A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956823 | |||||||
| chr6:107956833 | G | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | HG00099.hp2 HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.124+1053C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956833 | |||||||
| chr6:107956884 | T | C | 2 | a0001c0001t0019g0046 a0001c0001t0019g0047 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.124+1002A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956884 | |||||||
| chr6:107956933 | G | A | 3 | a0001c0002t0015g0309 a0001c0002t0015g0311 a0001c0002t0050g0310 |
3 | HG02559.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.124+953C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107956933 | |||||||
| chr6:107957161 | A | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+725T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957161 | |||||||
| chr6:107957161 | A | G | 17 | a0001c0001t0008g0015 a0001c0001t0008g0016 a0001c0001t0008g0018 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.124+725T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957161 | |||||||
| chr6:107957164 | G | T | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+722C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957164 | |||||||
| chr6:107957165 | A | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+721T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957165 | |||||||
| chr6:107957166 | C | T | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+720G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957166 | |||||||
| chr6:107957168 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+718G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957168 | |||||||
| chr6:107957171 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+715A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957171 | |||||||
| chr6:107957174 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+712G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957174 | |||||||
| chr6:107957175 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+711A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957175 | |||||||
| chr6:107957184 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+702G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957184 | |||||||
| chr6:107957185 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+701G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957185 | |||||||
| chr6:107957186 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+700A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957186 | |||||||
| chr6:107957187 | A | G | 2 | a0001c0001t0009g0175 a0001c0002t0005g0174 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.124+699T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957187 | |||||||
| chr6:107957188 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+698G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957188 | |||||||
| chr6:107957190 | A | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+696T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957190 | |||||||
| chr6:107957193 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+693A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957193 | |||||||
| chr6:107957194 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+692A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957194 | |||||||
| chr6:107957201 | A | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+685T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957201 | |||||||
| chr6:107957202 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+684G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957202 | |||||||
| chr6:107957207 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+679G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957207 | |||||||
| chr6:107957208 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+678A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957208 | |||||||
| chr6:107957211 | A | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+675T>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957211 | |||||||
| chr6:107957214 | C | T | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+672G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957214 | |||||||
| chr6:107957215 | T | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+671A>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957215 | |||||||
| chr6:107957219 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+667A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957219 | |||||||
| chr6:107957222 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+664A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957222 | |||||||
| chr6:107957223 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+663A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957223 | |||||||
| chr6:107957224 | G | C | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+662C>G | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957224 | |||||||
| chr6:107957225 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+661G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957225 | |||||||
| chr6:107957228 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+658A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957228 | |||||||
| chr6:107957229 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+657A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957229 | |||||||
| chr6:107957230 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+656A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957230 | |||||||
| chr6:107957231 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+655A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957231 | |||||||
| chr6:107957232 | T | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+654A>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957232 | |||||||
| chr6:107957233 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+653G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957233 | |||||||
| chr6:107957234 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+652G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957234 | |||||||
| chr6:107957236 | T | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+650A>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957236 | |||||||
| chr6:107957237 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+649G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957237 | |||||||
| chr6:107957238 | A | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+648T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957238 | |||||||
| chr6:107957239 | C | A | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+647G>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957239 | |||||||
| chr6:107957243 | C | G | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+643G>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957243 | |||||||
| chr6:107957246 | G | T | 1 | a0001c0002t0005g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+640C>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957246 | |||||||
| chr6:107957455 | A | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 others(116): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.124+431T>C | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957455 | |||||||
| chr6:107957475 | G | A | 7 | a0001c0002t0007g0048 a0001c0002t0007g0049 a0001c0002t0007g0050 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+411C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957475 | |||||||
| chr6:107957505 | G | A | 1 | a0001c0001t0008g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.124+381C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957505 | |||||||
| chr6:107957792 | G | A | 8 | a0001c0001t0014g0312 a0001c0001t0014g0315 a0001c0001t0014g0318 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+94C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957792 | |||||||
| chr6:107957864 | G | A | 1 | a0003c0007t0042g0320 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.124+22C>T | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957864 | |||||||
| chr6:107957866 | C | T | 2 | a0001c0001t0024g0056 a0001c0001t0024g0057 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124+20G>A | SEC63 | ENSG00000025796.14 | transcript | ENST00000369002.9 | protein_coding | 1/20 | chr6 | 107957866 |