Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 843 |
| ensemblid | ENSG00000003400.16 |
| hgncid | 1500 |
| symbol | CASP10 |
| name | caspase 10 |
| refseq_nuc | NM_032977.4 |
| refseq_prot | NP_116759.2 |
| ensembl_nuc | ENST00000286186.11 |
| ensembl_prot | ENSP00000286186.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 201183141 |
| end | 201221665 |
| strand | + |
| ver | v1.2 |
| region | chr2:201183141-201221665 |
| region5000 | chr2:201178141-201226665 |
| regionname0 | CASP10_chr2_201183141_201221665 |
| regionname5000 | CASP10_chr2_201178141_201226665 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 522 | 218 | 63 | 40 | 82 | 3 | 29 | 54 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0002 | 0/1 | 522 | 91 | 24 | 24 | 27 | 6 | 9 | 19 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0003 | 0/0 | 522 | 6 | 0 | 3 | 0 | 2 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0004 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(532): Show |
chr2 | 201178141 | 201226665 |
| a0005 | 0/0 | 522 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0006 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0007 | 0/0 | 522 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0008 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0009 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| a0010 | 0/0 | 522 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | MKSQG others(517): Show |
chr2 | 201178141 | 201226665 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1566 | 197 | 45 | 39 | 81 | 2 | 29 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0001c0003 | 0/0 | 1566 | 14 | 11 | 1 | 1 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0001c0005 | 0/0 | 1566 | 4 | 4 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0001c0006 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0001c0014 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0002c0002 | 0/1 | 1566 | 90 | 24 | 24 | 27 | 5 | 9 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0002c0007 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0003c0004 | 0/0 | 1566 | 6 | 0 | 3 | 0 | 2 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0004c0013 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1606): Show |
chr2 | 201178141 | 201226665 | ||
| a0005c0015 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0006c0008 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0007c0009 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0008c0011 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0009c0010 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 | ||
| a0010c0012 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | ATGAA others(1561): Show |
chr2 | 201178141 | 201226665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5668 | 148 | 17 | 37 | 63 | 2 | 28 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0003 | 0/0 | 5669 | 16 | 16 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5664): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0004 | 0/0 | 5669 | 11 | 0 | 2 | 9 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5664): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0005 | 0/0 | 5670 | 6 | 6 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5665): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0010 | 0/0 | 5668 | 4 | 0 | 0 | 4 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0011 | 0/0 | 5668 | 3 | 3 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0013 | 0/0 | 5668 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0014 | 0/0 | 5668 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0015 | 0/0 | 5667 | 2 | 1 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0021 | 0/0 | 5668 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0027 | 0/0 | 5668 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0001t0028 | 0/0 | 5668 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0001 | 0/0 | 5668 | 4 | 3 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0007 | 0/0 | 5666 | 5 | 3 | 1 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5661): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0018 | 0/0 | 5667 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0019 | 0/0 | 5666 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5661): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0020 | 0/0 | 5668 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0022 | 0/0 | 5668 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0003t0023 | 0/0 | 5668 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0005t0009 | 0/0 | 5668 | 4 | 4 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0001c0006t0012 | 0/0 | 5667 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0001c0014t0017 | 0/0 | 5667 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0001 | 0/0 | 5668 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0002 | 0/1 | 5667 | 75 | 18 | 20 | 23 | 5 | 8 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0006 | 0/0 | 5668 | 6 | 0 | 3 | 2 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0008 | 0/0 | 5667 | 5 | 5 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0024 | 0/0 | 5667 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0025 | 0/0 | 5667 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0002t0026 | 0/0 | 5667 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0002c0007t0002 | 0/0 | 5667 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0003c0004t0002 | 0/0 | 5667 | 6 | 0 | 3 | 0 | 2 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0004c0013t0016 | 0/0 | 5680 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5675): Show |
chr2 | 201178141 | 201226665 |
| a0005c0015t0002 | 0/0 | 5667 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0006c0008t0005 | 0/0 | 5670 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5665): Show |
chr2 | 201178141 | 201226665 |
| a0007c0009t0001 | 0/0 | 5668 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5663): Show |
chr2 | 201178141 | 201226665 |
| a0008c0011t0003 | 0/0 | 5669 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5664): Show |
chr2 | 201178141 | 201226665 |
| a0009c0010t0002 | 0/0 | 5667 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| a0010c0012t0002 | 0/0 | 5667 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | AGTTT others(5662): Show |
chr2 | 201178141 | 201226665 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 2 | 6 | 0 | 7 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0013g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0014g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0027g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0001t0028g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0019g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0022g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0003t0023g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0005t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0005t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0005t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0006t0012g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0001c0014t0017g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0002 | 0/0 | 7 | 0 | 0 | 3 | 1 | 3 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0003 | 0/0 | 6 | 0 | 3 | 1 | 2 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0004 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0008g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0002t0026g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0002c0007t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0003c0004t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0003c0004t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0003c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0004c0013t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0005c0015t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0006c0008t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0007c0009t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0008c0011t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0009c0010t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| a0010c0012t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | GBR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00140 | hp1 | a0003 | c0004 | t0002 | g0002 | EUR | GBR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0206 | EUR | FIN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00323 | hp2 | a0002 | c0007 | t0002 | g0129 | EUR | FIN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00609 | hp1 | a0002 | c0002 | t0006 | g0037 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00642 | hp2 | a0002 | c0002 | t0026 | g0209 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0184 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0178 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01070 | hp2 | a0003 | c0004 | t0002 | g0041 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01071 | hp1 | a0003 | c0004 | t0002 | g0041 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0179 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01106 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01109 | hp2 | a0002 | c0002 | t0006 | g0213 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01261 | hp2 | a0001 | c0003 | t0007 | g0171 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01361 | hp2 | a0002 | c0002 | t0006 | g0189 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01496 | hp2 | a0002 | c0002 | t0006 | g0194 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01884 | hp1 | a0004 | c0013 | t0016 | g0173 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01884 | hp2 | a0001 | c0014 | t0017 | g0174 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01891 | hp2 | a0002 | c0002 | t0008 | g0007 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02015 | hp2 | a0001 | c0001 | t0021 | g0117 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02027 | hp1 | a0002 | c0002 | t0025 | g0010 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02055 | hp2 | a0001 | c0003 | t0023 | g0063 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02145 | hp1 | a0001 | c0003 | t0018 | g0060 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0072 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02148 | hp1 | a0005 | c0015 | t0002 | g0003 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | CDX | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | CDX | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0183 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PEL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0214 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02630 | hp1 | a0001 | c0005 | t0009 | g0019 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0076 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02683 | hp1 | a0001 | c0001 | t0015 | g0067 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02717 | hp1 | a0001 | c0005 | t0009 | g0069 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02723 | hp1 | a0002 | c0002 | t0008 | g0007 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02723 | hp2 | a0001 | c0003 | t0019 | g0176 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02818 | hp1 | a0001 | c0005 | t0009 | g0019 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02818 | hp2 | a0002 | c0002 | t0008 | g0007 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02895 | hp1 | a0001 | c0005 | t0009 | g0044 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02896 | hp1 | a0001 | c0003 | t0007 | g0059 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02965 | hp2 | a0001 | c0006 | t0012 | g0018 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0227 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03098 | hp2 | a0006 | c0008 | t0005 | g0012 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03130 | hp1 | a0001 | c0003 | t0007 | g0061 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0225 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03225 | hp2 | a0002 | c0002 | t0008 | g0007 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03516 | hp1 | a0001 | c0003 | t0007 | g0062 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0077 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03654 | hp1 | a0007 | c0009 | t0001 | g0015 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0187 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0199 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04115 | hp1 | a0002 | c0002 | t0006 | g0202 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0220 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04199 | hp2 | a0003 | c0004 | t0002 | g0198 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | YRI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0007 | AFR | YRI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | CHB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | YRI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0028 | AFR | YRI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18945 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18964 | hp1 | a0001 | c0001 | t0010 | g0167 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18980 | hp1 | a0001 | c0001 | t0027 | g0133 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18989 | hp1 | a0001 | c0001 | t0028 | g0020 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19005 | hp1 | a0001 | c0001 | t0014 | g0005 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19043 | hp2 | a0008 | c0011 | t0003 | g0045 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19057 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0097 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19078 | hp1 | a0002 | c0002 | t0006 | g0200 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19084 | hp2 | a0009 | c0010 | t0002 | g0218 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20752 | hp1 | a0003 | c0004 | t0002 | g0226 | EUR | TSI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20752 | hp2 | a0001 | c0003 | t0007 | g0172 | EUR | TSI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0221 | EUR | TSI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20805 | hp2 | a0010 | c0012 | t0002 | g0177 | EUR | TSI | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02109 | hp1 | a0001 | c0003 | t0022 | g0175 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| HG06807 | hp2 | a0001 | c0006 | t0012 | g0018 | AFR | USA | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | USA | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA20300 | hp2 | a0002 | c0002 | t0024 | g0003 | AFR | USA | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA21309 | hp1 | a0001 | c0003 | t0020 | g0064 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0188 | REF | REF | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0147 | REF | REF | CASP10_chr2_201178141_201226665 | CASP10 | chr2 | 201178141 | 201226665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201186072 | A | G | 1 | a0007 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.295A>G | p.Lys99Glu | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/10 | 470/5668 | 295/1569 | 99/522 | chr2 | 201186072 | |||
| chr2:201187798 | T | C | 1 | a0009 | 1 | NA19084.hp2 | missense_variant&splice_region_variant | MODERATE | c.440T>C | p.Met147Thr | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/10 | 615/5668 | 440/1569 | 147/522 | chr2 | 201187798 | |||
| chr2:201205957 | C | T | 1 | a0005 | 1 | HG02148.hp1 | missense_variant | MODERATE | c.797C>T | p.Ser266Phe | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/10 | 972/5668 | 797/1569 | 266/522 | chr2 | 201205957 | |||
| chr2:201209375 | G | A | 1 | a0003 | 6 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
missense_variant | MODERATE | c.1228G>A | p.Val410Ile | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/10 | 1403/5668 | 1228/1569 | 410/522 | chr2 | 201209375 | |||
| chr2:201209484 | A | G | 1 | a0010 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1337A>G | p.Tyr446Cys | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/10 | 1512/5668 | 1337/1569 | 446/522 | chr2 | 201209484 | |||
| chr2:201217590 | A | G | 1 | a0006 | 1 | HG03098.hp2 | missense_variant&splice_region_variant | MODERATE | c.1418A>G | p.His473Arg | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1593/5668 | 1418/1569 | 473/522 | chr2 | 201217590 | |||
| chr2:201217635 | G | GTCGAAGA others(38): Show |
1 | a0004 | 1 | HG01884.hp1 | conservative_inframe_insertion | MODERATE | c.1465_1509dupCGAAGA others(39): Show |
p.Arg489_Pro503dup | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1685/5668 | 1510/1569 | 504/522 | INFO_REALIGN_3_PRIME | chr2 | 201217635 | ||
| chr2:201217730 | C | T | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1558C>T | p.Leu520Phe | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1733/5668 | 1558/1569 | 520/522 | chr2 | 201217730 | |||
| chr2:201217736 | T | A | 5 | a0002 a0003 a0005 others(2): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
missense_variant | MODERATE | c.1564T>A | p.Leu522Ile | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1739/5668 | 1564/1569 | 522/522 | chr2 | 201217736 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201185954 | A | G | 11 | a0001c0003 a0001c0005 a0001c0006 others(8): Show |
121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
synonymous_variant | LOW | c.177A>G | p.Ser59Ser | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/10 | 352/5668 | 177/1569 | 59/522 | chr2 | 201185954 | |||
| chr2:201193076 | A | C | 1 | a0001c0006 | 2 | HG02965.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.534A>C | p.Val178Val | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/10 | 709/5668 | 534/1569 | 178/522 | chr2 | 201193076 | |||
| chr2:201209215 | G | T | 1 | a0001c0005 | 4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1068G>T | p.Leu356Leu | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/10 | 1243/5668 | 1068/1569 | 356/522 | chr2 | 201209215 | |||
| chr2:201209443 | C | T | 2 | a0001c0014 a0004c0013 |
2 | HG01884.hp1 HG01884.hp2 |
synonymous_variant | LOW | c.1296C>T | p.Ala432Ala | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/10 | 1471/5668 | 1296/1569 | 432/522 | chr2 | 201209443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201218018 | G | A | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0007 others(8): Show |
39 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*277G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 277 | chr2 | 201218018 | ||||||
| chr2:201218026 | G | A | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0007 others(8): Show |
39 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 285 | chr2 | 201218026 | ||||||
| chr2:201218036 | C | T | 1 | a0001c0003t0019 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 295 | chr2 | 201218036 | ||||||
| chr2:201218108 | G | C | 1 | a0002c0002t0008 | 5 | HG01891.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*367G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 367 | chr2 | 201218108 | ||||||
| chr2:201218395 | C | T | 1 | a0001c0001t0028 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 654 | chr2 | 201218395 | ||||||
| chr2:201218406 | G | A | 1 | a0001c0001t0013 | 2 | HG03041.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*665G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 665 | chr2 | 201218406 | ||||||
| chr2:201218556 | C | T | 2 | a0001c0003t0007 a0001c0003t0018 |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 815 | chr2 | 201218556 | ||||||
| chr2:201218587 | A | G | 1 | a0001c0001t0027 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 846 | chr2 | 201218587 | ||||||
| chr2:201219261 | C | T | 6 | a0001c0003t0007 a0001c0003t0018 a0001c0003t0019 others(3): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1520C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1520 | chr2 | 201219261 | ||||||
| chr2:201219458 | G | A | 2 | a0001c0014t0017 a0004c0013t0016 |
2 | HG01884.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1717G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1717 | chr2 | 201219458 | ||||||
| chr2:201219534 | C | A | 1 | a0001c0003t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1793C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1793 | chr2 | 201219534 | ||||||
| chr2:201219661 | G | C | 4 | a0001c0001t0003 a0001c0001t0005 a0006c0008t0005 others(1): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1920G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1920 | chr2 | 201219661 | ||||||
| chr2:201219696 | G | A | 1 | a0001c0003t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1955 | chr2 | 201219696 | ||||||
| chr2:201219700 | T | A | 1 | a0001c0001t0014 | 2 | NA19005.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1959T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1959 | chr2 | 201219700 | ||||||
| chr2:201219705 | C | CT | 4 | a0001c0001t0003 a0001c0001t0004 a0002c0002t0006 others(1): Show |
34 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1982dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1983 | INFO_REALIGN_3_PRIME | chr2 | 201219705 | |||||
| chr2:201219705 | C | CTT | 2 | a0001c0001t0005 a0006c0008t0005 |
7 | HG02572.hp1 HG02886.hp1 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1981_*1982dupTT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1983 | INFO_REALIGN_3_PRIME | chr2 | 201219705 | |||||
| chr2:201219705 | CT | C | 3 | a0001c0001t0015 a0001c0003t0007 a0001c0003t0019 |
8 | HG01261.hp2 HG02145.hp2 HG02683.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1982delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 1982 | INFO_REALIGN_3_PRIME | chr2 | 201219705 | |||||
| chr2:201219932 | G | A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2191G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2191 | chr2 | 201219932 | ||||||
| chr2:201220030 | A | C | 1 | a0002c0002t0026 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2289A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2289 | chr2 | 201220030 | ||||||
| chr2:201220328 | TG | T | 17 | a0001c0003t0007 a0001c0003t0018 a0001c0003t0019 others(14): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2594delG | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2594 | INFO_REALIGN_3_PRIME | chr2 | 201220328 | |||||
| chr2:201220329 | G | T | 1 | a0002c0002t0001 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2588 | chr2 | 201220329 | ||||||
| chr2:201220343 | A | G | 1 | a0001c0005t0009 | 4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2602 | chr2 | 201220343 | ||||||
| chr2:201220359 | G | A | 1 | a0001c0001t0011 | 3 | HG02647.hp1 HG03130.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2618G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2618 | chr2 | 201220359 | ||||||
| chr2:201220430 | A | G | 1 | a0001c0001t0011 | 3 | HG02647.hp1 HG03130.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2689A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2689 | chr2 | 201220430 | ||||||
| chr2:201220478 | G | A | 1 | a0001c0005t0009 | 4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2737G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2737 | chr2 | 201220478 | ||||||
| chr2:201220498 | A | G | 4 | a0001c0001t0003 a0001c0001t0005 a0006c0008t0005 others(1): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2757A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2757 | chr2 | 201220498 | ||||||
| chr2:201220499 | T | C | 1 | a0002c0002t0024 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2758T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2758 | chr2 | 201220499 | ||||||
| chr2:201220501 | G | C | 1 | a0001c0014t0017 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2760G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2760 | chr2 | 201220501 | ||||||
| chr2:201220572 | C | T | 2 | a0001c0003t0020 a0001c0003t0023 |
2 | HG02055.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2831C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 2831 | chr2 | 201220572 | ||||||
| chr2:201220812 | G | A | 1 | a0001c0001t0010 | 4 | HG00558.hp2 NA18945.hp2 NA18964.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3071G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3071 | chr2 | 201220812 | ||||||
| chr2:201221254 | A | G | 1 | a0001c0003t0022 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3513A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3513 | chr2 | 201221254 | ||||||
| chr2:201221398 | A | C | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3657A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3657 | chr2 | 201221398 | ||||||
| chr2:201221399 | A | T | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3658A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3658 | chr2 | 201221399 | ||||||
| chr2:201221408 | G | T | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3667G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3667 | chr2 | 201221408 | ||||||
| chr2:201221434 | A | T | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3693A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3693 | chr2 | 201221434 | ||||||
| chr2:201221436 | T | G | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3695T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3695 | chr2 | 201221436 | ||||||
| chr2:201221441 | T | G | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3700T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3700 | chr2 | 201221441 | ||||||
| chr2:201221442 | G | C | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3701G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3701 | chr2 | 201221442 | ||||||
| chr2:201221445 | A | C | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3704A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3704 | chr2 | 201221445 | ||||||
| chr2:201221446 | A | C | 1 | a0001c0001t0021 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3705A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3705 | chr2 | 201221446 | ||||||
| chr2:201221447 | ATTCCTTC others(25): Show |
A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3708_*3739delTCCT others(28): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3708 | INFO_REALIGN_3_PRIME | chr2 | 201221447 | |||||
| chr2:201221480 | T | G | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3739T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3739 | chr2 | 201221480 | ||||||
| chr2:201221482 | C | A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3741C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3741 | chr2 | 201221482 | ||||||
| chr2:201221483 | C | G | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3742C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3742 | chr2 | 201221483 | ||||||
| chr2:201221486 | A | T | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3745A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3745 | chr2 | 201221486 | ||||||
| chr2:201221487 | G | A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3746G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3746 | chr2 | 201221487 | ||||||
| chr2:201221492 | C | A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3751C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3751 | chr2 | 201221492 | ||||||
| chr2:201221518 | C | A | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3777C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3777 | chr2 | 201221518 | ||||||
| chr2:201221525 | A | C | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3784A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3784 | chr2 | 201221525 | ||||||
| chr2:201221526 | C | T | 1 | a0004c0013t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3785C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3785 | chr2 | 201221526 | ||||||
| chr2:201221533 | C | T | 1 | a0001c0005t0009 | 4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3792C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3792 | chr2 | 201221533 | ||||||
| chr2:201221603 | C | T | 1 | a0002c0002t0025 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3862C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3862 | chr2 | 201221603 | ||||||
| chr2:201221607 | C | A | 1 | a0001c0014t0017 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3866C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 10/10 | 3866 | chr2 | 201221607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201183400 | C | T | 69 | a0001c0003t0001g0185 a0001c0003t0001g0207 a0002c0002t0001g0201 others(66): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-8+92C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183400 | |||||||
| chr2:201183421 | T | G | 1 | a0010c0012t0002g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8+113T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183421 | |||||||
| chr2:201183496 | C | T | 6 | a0001c0003t0007g0171 a0001c0003t0007g0172 a0001c0003t0019g0176 others(3): Show |
6 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+188C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183496 | |||||||
| chr2:201183586 | G | A | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8+278G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183586 | |||||||
| chr2:201183678 | A | T | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8+370A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183678 | |||||||
| chr2:201183732 | T | C | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-8+424T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183732 | |||||||
| chr2:201183844 | G | A | 19 | a0001c0001t0001g0053 a0001c0001t0003g0011 a0001c0001t0003g0046 others(16): Show |
23 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8+536G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183844 | |||||||
| chr2:201183856 | C | CTTTA | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG03017.hp2 HG03834.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+578_-8+581dupTT others(2): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 201183856 | ||||||
| chr2:201183856 | CTTTA | C | 70 | a0001c0001t0001g0070 a0001c0003t0001g0185 a0001c0003t0001g0207 others(67): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-8+578_-8+581delTT others(2): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 201183856 | ||||||
| chr2:201183856 | CTTTATTT others(1): Show |
C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0065 others(28): Show |
35 | HG02055.hp2 HG02145.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.-8+574_-8+581delTT others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 201183856 | ||||||
| chr2:201183856 | CTTTATTT others(5): Show |
C | 8 | a0001c0003t0001g0042 a0001c0003t0001g0043 a0001c0003t0007g0171 others(5): Show |
8 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+570_-8+581delTT others(10): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 201183856 | ||||||
| chr2:201183859 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-8+551T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183859 | |||||||
| chr2:201183860 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-8+552A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183860 | |||||||
| chr2:201183909 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8+601G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183909 | |||||||
| chr2:201183966 | G | A | 1 | a0001c0001t0011g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-8+658G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201183966 | |||||||
| chr2:201184096 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0015g0072 |
3 | HG02145.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-8+788G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184096 | |||||||
| chr2:201184130 | AC | A | 32 | a0001c0001t0001g0053 a0001c0001t0003g0011 a0001c0001t0003g0046 others(29): Show |
36 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8+823delC | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184130 | |||||||
| chr2:201184604 | G | A | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7-1167G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184604 | |||||||
| chr2:201184607 | A | G | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-1164A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184607 | |||||||
| chr2:201184886 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-7-885C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184886 | |||||||
| chr2:201184919 | T | C | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-852T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201184919 | |||||||
| chr2:201185082 | C | A | 2 | a0002c0002t0002g0178 a0002c0002t0002g0179 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-7-689C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201185082 | |||||||
| chr2:201185280 | A | C | 1 | a0002c0002t0002g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-7-491A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201185280 | |||||||
| chr2:201185303 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-7-468G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201185303 | |||||||
| chr2:201185430 | G | A | 10 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(7): Show |
10 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-341G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201185430 | |||||||
| chr2:201185729 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-7-42C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 1/9 | chr2 | 201185729 | |||||||
| chr2:201186133 | G | T | 20 | a0001c0001t0001g0053 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
25 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.347+9G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201186133 | |||||||
| chr2:201186386 | C | T | 1 | a0003c0004t0002g0226 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.347+262C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201186386 | |||||||
| chr2:201186480 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347+356C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201186480 | |||||||
| chr2:201186997 | G | A | 3 | a0001c0001t0011g0071 a0001c0001t0011g0076 a0001c0001t0011g0077 |
3 | HG02647.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.348-709G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201186997 | |||||||
| chr2:201187058 | G | A | 1 | a0010c0012t0002g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.348-648G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187058 | |||||||
| chr2:201187226 | G | A | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348-480G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187226 | |||||||
| chr2:201187300 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348-406C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187300 | |||||||
| chr2:201187443 | T | A | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.348-263T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187443 | |||||||
| chr2:201187567 | C | A | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.348-139C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187567 | |||||||
| chr2:201187582 | A | C | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.348-124A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 2/9 | chr2 | 201187582 | |||||||
| chr2:201187894 | A | G | 38 | a0001c0001t0001g0053 a0001c0001t0003g0011 a0001c0001t0003g0033 others(35): Show |
45 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.441+95A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201187894 | |||||||
| chr2:201187922 | G | A | 3 | a0002c0002t0002g0180 a0002c0002t0002g0181 a0002c0002t0002g0182 |
3 | HG02155.hp2 NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.441+123G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201187922 | |||||||
| chr2:201188020 | A | C | 20 | a0001c0001t0001g0053 a0001c0001t0003g0011 a0001c0001t0003g0033 others(17): Show |
25 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.441+221A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188020 | |||||||
| chr2:201188031 | C | T | 16 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(13): Show |
18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+232C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188031 | |||||||
| chr2:201188270 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.441+471C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188270 | |||||||
| chr2:201188571 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.441+772G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188571 | |||||||
| chr2:201188642 | G | A | 1 | a0002c0002t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+843G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188642 | |||||||
| chr2:201188669 | C | T | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441+870C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188669 | |||||||
| chr2:201188720 | G | C | 1 | a0002c0002t0002g0184 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.441+921G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188720 | |||||||
| chr2:201188743 | T | C | 2 | a0001c0001t0001g0079 a0001c0003t0001g0185 |
2 | HG02155.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.441+944T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188743 | |||||||
| chr2:201188797 | T | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | NA18979.hp1 NA18989.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+998T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188797 | |||||||
| chr2:201188799 | A | T | 3 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 |
3 | HG00544.hp2 HG02015.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.441+1000A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201188799 | |||||||
| chr2:201188872 | A | AT | 7 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(4): Show |
7 | HG00099.hp2 HG01099.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+1088dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201188872 | ||||||
| chr2:201188872 | AT | A | 15 | a0001c0001t0001g0080 a0001c0003t0007g0059 a0001c0003t0007g0061 others(12): Show |
17 | HG01168.hp1 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.441+1088delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201188872 | ||||||
| chr2:201189124 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.441+1325G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189124 | |||||||
| chr2:201189177 | T | C | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1378T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189177 | |||||||
| chr2:201189270 | AT | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(179): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.441+1487delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201189270 | ||||||
| chr2:201189275 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441+1476T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189275 | |||||||
| chr2:201189544 | G | T | 3 | a0002c0002t0002g0178 a0002c0002t0002g0179 a0002c0002t0002g0221 |
3 | HG01069.hp1 HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.441+1745G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189544 | |||||||
| chr2:201189562 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18971.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.441+1763T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189562 | |||||||
| chr2:201189596 | C | G | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.441+1797C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189596 | |||||||
| chr2:201189752 | C | G | 1 | a0002c0002t0002g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.441+1953C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189752 | |||||||
| chr2:201189951 | G | A | 9 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(6): Show |
10 | HG01261.hp2 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+2152G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201189951 | |||||||
| chr2:201190225 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.441+2426G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201190225 | |||||||
| chr2:201190589 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(43): Show |
66 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.442-2395C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201190589 | |||||||
| chr2:201190785 | G | T | 1 | a0001c0001t0015g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.442-2199G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201190785 | |||||||
| chr2:201190785 | GT | G | 16 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(13): Show |
18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-2190delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201190785 | ||||||
| chr2:201190849 | A | AATT | 10 | a0001c0001t0001g0070 a0001c0003t0007g0059 a0001c0003t0007g0061 others(7): Show |
11 | HG01261.hp2 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-2110_442-2108d others(5): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201190849 | ||||||
| chr2:201190849 | A | AATTATT | 2 | a0001c0003t0018g0060 a0001c0006t0012g0018 |
3 | HG02145.hp1 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.442-2113_442-2108d others(8): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201190849 | ||||||
| chr2:201191131 | G | A | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-1853G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201191131 | |||||||
| chr2:201191268 | T | G | 1 | a0008c0011t0003g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-1716T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201191268 | |||||||
| chr2:201191290 | C | T | 1 | a0002c0007t0002g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.442-1694C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201191290 | |||||||
| chr2:201191629 | T | C | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442-1355T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201191629 | |||||||
| chr2:201192394 | A | AAAT | 35 | a0001c0001t0001g0083 a0001c0001t0001g0110 a0001c0001t0001g0164 others(32): Show |
49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.442-561_442-559dup others(3): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201192394 | ||||||
| chr2:201192394 | A | AAATAAT | 6 | a0001c0005t0009g0069 a0002c0002t0002g0035 a0002c0002t0002g0036 others(3): Show |
8 | HG01255.hp2 HG01358.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-564_442-559dup others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201192394 | ||||||
| chr2:201192394 | A | AAATAATA others(5): Show |
1 | a0002c0002t0002g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.442-570_442-559dup others(12): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201192394 | ||||||
| chr2:201192394 | AAAT | A | 33 | a0001c0001t0001g0070 a0001c0001t0003g0011 a0001c0001t0003g0033 others(30): Show |
40 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.442-561_442-559del others(3): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 201192394 | ||||||
| chr2:201192764 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.442-220A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201192764 | |||||||
| chr2:201192768 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.442-216A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201192768 | |||||||
| chr2:201192900 | A | G | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.442-84A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201192900 | |||||||
| chr2:201192952 | A | C | 1 | a0002c0002t0002g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442-32A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 3/9 | chr2 | 201192952 | |||||||
| chr2:201193243 | T | C | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.577+124T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201193243 | |||||||
| chr2:201193382 | A | G | 6 | a0001c0001t0005g0012 a0001c0001t0005g0055 a0001c0001t0005g0056 others(3): Show |
7 | HG02572.hp1 HG02886.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+263A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201193382 | |||||||
| chr2:201193508 | C | CGTG | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.577+390_577+392dup others(3): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201193508 | ||||||
| chr2:201194000 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.577+881C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201194000 | |||||||
| chr2:201194087 | T | TTG | 10 | a0001c0001t0001g0014 a0001c0001t0001g0084 a0001c0001t0001g0111 others(7): Show |
12 | HG00735.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.577+1002_577+1003d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | T | TTGTG | 3 | a0001c0001t0001g0134 a0001c0003t0001g0042 a0001c0003t0001g0043 |
3 | HG02486.hp2 HG03486.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.577+1000_577+1003d others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | TTG | T | 33 | a0001c0001t0001g0029 a0001c0001t0001g0078 a0001c0001t0001g0106 others(30): Show |
45 | HG00280.hp2 HG01070.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.577+1002_577+1003d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | TTGTG | T | 22 | a0001c0001t0001g0107 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
26 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.577+1000_577+1003d others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | TTGTGTG | T | 46 | a0001c0006t0012g0018 a0002c0002t0001g0201 a0002c0002t0002g0002 others(43): Show |
68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.577+998_577+1003de others(7): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | TTGTGTGT others(3): Show |
T | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.577+994_577+1003de others(11): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194087 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.577+992_577+1003de others(13): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201194087 | ||||||
| chr2:201194137 | A | G | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.577+1018A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201194137 | |||||||
| chr2:201194221 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.577+1102C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201194221 | |||||||
| chr2:201194380 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.577+1261G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201194380 | |||||||
| chr2:201194597 | CAT | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0105 others(3): Show |
8 | HG00642.hp1 HG00735.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-1244_578-1243d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201194597 | |||||||
| chr2:201195168 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.578-674T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201195168 | |||||||
| chr2:201195309 | C | T | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.578-533C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201195309 | |||||||
| chr2:201195363 | C | T | 11 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(8): Show |
12 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.578-479C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201195363 | |||||||
| chr2:201195542 | T | TAA | 104 | a0001c0001t0001g0151 a0001c0001t0003g0011 a0001c0001t0003g0033 others(101): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.578-298_578-297dup others(2): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 201195542 | ||||||
| chr2:201195553 | T | C | 2 | a0001c0001t0003g0033 a0001c0001t0003g0163 |
3 | HG02970.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.578-289T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 4/9 | chr2 | 201195553 | |||||||
| chr2:201196097 | C | T | 37 | a0002c0002t0001g0201 a0002c0002t0002g0002 a0002c0002t0002g0003 others(34): Show |
53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.684+149C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196097 | |||||||
| chr2:201196103 | G | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | HG02071.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.684+155G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196103 | |||||||
| chr2:201196327 | C | G | 35 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(32): Show |
42 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.684+379C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196327 | |||||||
| chr2:201196682 | A | T | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.684+734A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196682 | |||||||
| chr2:201196905 | G | C | 1 | a0002c0002t0002g0192 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.684+957G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196905 | |||||||
| chr2:201196947 | T | C | 16 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(13): Show |
18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+999T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201196947 | |||||||
| chr2:201197059 | C | T | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.684+1111C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197059 | |||||||
| chr2:201197142 | T | TTTAAAAT others(338): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.684+1209_684+1210i others(347): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201197142 | ||||||
| chr2:201197142 | T | TTTAAAAT others(339): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0166 |
2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.684+1209_684+1210i others(348): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201197142 | ||||||
| chr2:201197149 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02523.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.684+1201T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197149 | |||||||
| chr2:201197304 | C | T | 1 | a0002c0002t0002g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.684+1356C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197304 | |||||||
| chr2:201197306 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.684+1358A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197306 | |||||||
| chr2:201197435 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+1487C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197435 | |||||||
| chr2:201197482 | G | A | 1 | a0001c0001t0003g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.684+1534G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197482 | |||||||
| chr2:201197666 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0161 a0001c0001t0013g0028 |
4 | HG02622.hp2 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1718C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197666 | |||||||
| chr2:201197870 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.684+1922T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197870 | |||||||
| chr2:201197969 | C | T | 1 | a0002c0002t0006g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.684+2021C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201197969 | |||||||
| chr2:201198136 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0125 a0001c0001t0001g0153 others(1): Show |
4 | HG02735.hp1 HG03017.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+2188C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198136 | |||||||
| chr2:201198206 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.684+2258A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198206 | |||||||
| chr2:201198225 | CT | C | 7 | a0001c0001t0001g0073 a0001c0001t0001g0114 a0001c0001t0001g0136 others(4): Show |
7 | HG00639.hp2 HG02683.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.684+2293delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201198225 | ||||||
| chr2:201198437 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.684+2489C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198437 | |||||||
| chr2:201198510 | C | T | 7 | a0001c0003t0001g0207 a0002c0002t0002g0017 a0002c0002t0002g0186 others(4): Show |
13 | HG01891.hp2 HG02615.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.684+2562C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198510 | |||||||
| chr2:201198520 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.684+2572C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198520 | |||||||
| chr2:201198539 | C | CT | 64 | a0001c0001t0001g0100 a0001c0001t0001g0108 a0001c0001t0001g0144 others(61): Show |
85 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.684+2610dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201198539 | ||||||
| chr2:201198539 | C | CTT | 39 | a0001c0003t0019g0176 a0001c0003t0022g0175 a0001c0005t0009g0019 others(36): Show |
56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.684+2609_684+2610d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201198539 | ||||||
| chr2:201198627 | G | A | 16 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(13): Show |
18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+2679G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198627 | |||||||
| chr2:201198685 | C | A | 1 | a0001c0003t0001g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.684+2737C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198685 | |||||||
| chr2:201198838 | C | T | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.684+2890C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198838 | |||||||
| chr2:201198943 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.684+2995A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201198943 | |||||||
| chr2:201199056 | A | G | 1 | a0002c0002t0002g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.684+3108A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199056 | |||||||
| chr2:201199270 | A | G | 2 | a0001c0003t0019g0176 a0001c0003t0022g0175 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.684+3322A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199270 | |||||||
| chr2:201199272 | A | C | 1 | a0002c0002t0001g0201 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.684+3324A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199272 | |||||||
| chr2:201199294 | C | T | 1 | a0001c0014t0017g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.684+3346C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199294 | |||||||
| chr2:201199437 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.684+3489G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199437 | |||||||
| chr2:201199569 | CT | C | 36 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(33): Show |
39 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.684+3644delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201199569 | ||||||
| chr2:201199569 | CTT | C | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+3643_684+3644d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201199569 | ||||||
| chr2:201199569 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0002g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.684+3635_684+3644d others(12): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201199569 | ||||||
| chr2:201199573 | T | C | 2 | a0001c0003t0019g0176 a0001c0003t0022g0175 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.684+3625T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199573 | |||||||
| chr2:201199593 | G | T | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.684+3645G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199593 | |||||||
| chr2:201199680 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.684+3732T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199680 | |||||||
| chr2:201199784 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02523.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.684+3836A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199784 | |||||||
| chr2:201199931 | T | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0050 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.685-3799T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201199931 | |||||||
| chr2:201200013 | G | T | 3 | a0002c0002t0002g0010 a0002c0002t0002g0039 a0002c0002t0025g0010 |
6 | HG00741.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-3717G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200013 | |||||||
| chr2:201200043 | C | T | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-3687C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200043 | |||||||
| chr2:201200276 | C | T | 4 | a0001c0001t0004g0098 a0001c0001t0010g0027 a0001c0001t0010g0097 others(1): Show |
5 | HG00558.hp2 NA18945.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-3454C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200276 | |||||||
| chr2:201200442 | G | A | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.685-3288G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200442 | |||||||
| chr2:201200577 | C | T | 2 | a0002c0002t0002g0186 a0002c0002t0008g0007 |
6 | HG01891.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-3153C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200577 | |||||||
| chr2:201200595 | C | T | 3 | a0001c0001t0011g0071 a0001c0001t0011g0076 a0001c0001t0011g0077 |
3 | HG02647.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685-3135C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200595 | |||||||
| chr2:201200605 | C | T | 1 | a0001c0001t0021g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.685-3125C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200605 | |||||||
| chr2:201200609 | A | G | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.685-3121A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200609 | |||||||
| chr2:201200617 | C | A | 1 | a0001c0001t0011g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.685-3113C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200617 | |||||||
| chr2:201200648 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.685-3082A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200648 | |||||||
| chr2:201200730 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685-3000G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200730 | |||||||
| chr2:201200739 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.685-2991C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200739 | |||||||
| chr2:201200938 | A | G | 33 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(30): Show |
40 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.685-2792A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200938 | |||||||
| chr2:201200972 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18981.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.685-2758C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201200972 | |||||||
| chr2:201201107 | G | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.685-2623G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201107 | |||||||
| chr2:201201125 | A | G | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.685-2605A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201125 | |||||||
| chr2:201201199 | G | A | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.685-2531G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201199 | |||||||
| chr2:201201218 | T | A | 3 | a0001c0003t0019g0176 a0001c0003t0022g0175 a0001c0006t0012g0018 |
4 | HG02109.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2512T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201218 | |||||||
| chr2:201201220 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18944.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.685-2510T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201220 | |||||||
| chr2:201201401 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(39): Show |
62 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.685-2329G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201401 | |||||||
| chr2:201201473 | A | AAC | 11 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0078 others(8): Show |
13 | HG01261.hp2 HG02717.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.685-2236_685-2235d others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201201473 | ||||||
| chr2:201201473 | A | AACAC | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0003t0018g0060 |
3 | HG02071.hp1 HG02145.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.685-2238_685-2235d others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201201473 | ||||||
| chr2:201201584 | G | A | 35 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0003g0011 others(32): Show |
42 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.685-2146G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201584 | |||||||
| chr2:201201812 | T | A | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.685-1918T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201812 | |||||||
| chr2:201201945 | G | C | 2 | a0001c0003t0001g0042 a0001c0003t0001g0043 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.685-1785G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201201945 | |||||||
| chr2:201202006 | G | A | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.685-1724G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202006 | |||||||
| chr2:201202071 | C | T | 5 | a0002c0002t0002g0204 a0002c0002t0002g0205 a0002c0002t0002g0215 others(2): Show |
5 | HG02040.hp1 NA18959.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-1659C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202071 | |||||||
| chr2:201202146 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0002c0002t0002g0225 |
3 | HG03225.hp1 HG04184.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.685-1584C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202146 | |||||||
| chr2:201202432 | G | C | 1 | a0001c0005t0009g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.685-1298G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202432 | |||||||
| chr2:201202435 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.685-1295C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202435 | |||||||
| chr2:201202553 | G | C | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685-1177G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202553 | |||||||
| chr2:201202632 | C | T | 1 | a0001c0001t0013g0028 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.685-1098C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202632 | |||||||
| chr2:201202893 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.685-837C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202893 | |||||||
| chr2:201202990 | A | G | 1 | a0002c0002t0026g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.685-740A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201202990 | |||||||
| chr2:201203043 | T | C | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.685-687T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203043 | |||||||
| chr2:201203155 | T | A | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.685-575T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203155 | |||||||
| chr2:201203307 | T | C | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.685-423T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203307 | |||||||
| chr2:201203308 | C | T | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.685-422C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203308 | |||||||
| chr2:201203308 | CT | C | 83 | a0001c0001t0001g0091 a0001c0001t0001g0137 a0001c0001t0001g0146 others(80): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.685-406delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 201203308 | ||||||
| chr2:201203369 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.685-361C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203369 | |||||||
| chr2:201203441 | G | A | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-289G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203441 | |||||||
| chr2:201203570 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0082 others(2): Show |
6 | HG00438.hp2 HG00544.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-160G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203570 | |||||||
| chr2:201203604 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.685-126G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203604 | |||||||
| chr2:201203710 | C | T | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-20C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203710 | |||||||
| chr2:201203711 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.685-19C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 5/9 | chr2 | 201203711 | |||||||
| chr2:201203849 | G | A | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.721+83G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201203849 | |||||||
| chr2:201204036 | C | T | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.721+270C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204036 | |||||||
| chr2:201204132 | G | A | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.721+366G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204132 | |||||||
| chr2:201204350 | C | T | 1 | a0001c0003t0019g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.721+584C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204350 | |||||||
| chr2:201204351 | AT | A | 5 | a0001c0003t0019g0176 a0001c0003t0022g0175 a0001c0006t0012g0018 others(2): Show |
6 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.721+594delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 201204351 | ||||||
| chr2:201204372 | T | C | 2 | a0001c0014t0017g0174 a0004c0013t0016g0173 |
2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.721+606T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204372 | |||||||
| chr2:201204579 | G | A | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.721+813G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204579 | |||||||
| chr2:201204636 | G | A | 1 | a0002c0002t0002g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.721+870G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201204636 | |||||||
| chr2:201205155 | A | G | 11 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(8): Show |
12 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.722-727A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205155 | |||||||
| chr2:201205208 | TTTTTC | T | 4 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 others(1): Show |
5 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.722-654_722-650del others(5): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 201205208 | ||||||
| chr2:201205228 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(9): Show |
15 | HG00323.hp1 HG01070.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.722-640dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 201205228 | ||||||
| chr2:201205277 | T | G | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.722-605T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205277 | |||||||
| chr2:201205317 | C | T | 2 | a0002c0002t0002g0038 a0002c0002t0002g0228 |
3 | HG03927.hp2 NA18943.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.722-565C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205317 | |||||||
| chr2:201205523 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.722-359G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205523 | |||||||
| chr2:201205668 | A | G | 1 | a0009c0010t0002g0218 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.722-214A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205668 | |||||||
| chr2:201205695 | C | A | 1 | a0001c0006t0012g0018 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.722-187C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205695 | |||||||
| chr2:201205866 | G | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-16G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 6/9 | chr2 | 201205866 | |||||||
| chr2:201205995 | C | T | 29 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(26): Show |
35 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.813+22C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201205995 | |||||||
| chr2:201206012 | A | T | 107 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0003g0011 others(104): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.813+39A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206012 | |||||||
| chr2:201206041 | G | A | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.813+68G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206041 | |||||||
| chr2:201206096 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.813+123C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206096 | |||||||
| chr2:201206124 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.813+151C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206124 | |||||||
| chr2:201206440 | A | G | 1 | a0002c0002t0002g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.813+467A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206440 | |||||||
| chr2:201206584 | C | A | 18 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(15): Show |
23 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.813+611C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206584 | |||||||
| chr2:201206598 | G | GTA | 4 | a0001c0001t0001g0024 a0001c0006t0012g0018 a0001c0014t0017g0174 others(1): Show |
6 | HG01884.hp1 HG01884.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+638_813+639dup others(2): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201206598 | ||||||
| chr2:201206598 | G | GTATA | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+636_813+639dup others(4): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201206598 | ||||||
| chr2:201206611 | T | C | 7 | a0001c0003t0001g0207 a0002c0002t0002g0017 a0002c0002t0002g0186 others(4): Show |
13 | HG01891.hp2 HG02615.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.813+638T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206611 | |||||||
| chr2:201206621 | C | CAT | 2 | a0001c0005t0009g0019 a0001c0005t0009g0044 |
3 | HG02630.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.813+657_813+658dup others(2): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201206621 | ||||||
| chr2:201206836 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.813+863C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206836 | |||||||
| chr2:201206842 | T | C | 3 | a0001c0003t0019g0176 a0001c0003t0022g0175 a0001c0006t0012g0018 |
4 | HG02109.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+869T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206842 | |||||||
| chr2:201206938 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.813+965A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206938 | |||||||
| chr2:201206958 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG04184.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.813+985A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201206958 | |||||||
| chr2:201207011 | AT | A | 4 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+1042delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201207011 | ||||||
| chr2:201207361 | C | T | 1 | a0002c0002t0002g0038 | 2 | HG03927.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.814-714C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207361 | |||||||
| chr2:201207405 | G | T | 3 | a0001c0003t0019g0176 a0001c0003t0022g0175 a0001c0006t0012g0018 |
4 | HG02109.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-670G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207405 | |||||||
| chr2:201207476 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0122 a0001c0005t0009g0019 others(2): Show |
7 | HG00423.hp1 HG02071.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-599C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207476 | |||||||
| chr2:201207578 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.814-497G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207578 | |||||||
| chr2:201207734 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.814-341G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207734 | |||||||
| chr2:201207756 | C | CA | 6 | a0001c0001t0001g0065 a0001c0001t0001g0109 a0001c0001t0001g0111 others(3): Show |
6 | HG01261.hp2 HG01981.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-304dupA | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201207756 | ||||||
| chr2:201207756 | CA | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
11 | HG01069.hp2 HG01192.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.814-304delA | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 201207756 | ||||||
| chr2:201207851 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.814-224C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207851 | |||||||
| chr2:201207852 | G | A | 1 | a0002c0002t0002g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.814-223G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207852 | |||||||
| chr2:201207912 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.814-163G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 7/9 | chr2 | 201207912 | |||||||
| chr2:201208250 | A | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.922+67A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208250 | |||||||
| chr2:201208426 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.922+243C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208426 | |||||||
| chr2:201208509 | A | G | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.922+326A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208509 | |||||||
| chr2:201208558 | G | A | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.922+375G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208558 | |||||||
| chr2:201208753 | A | T | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-317A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208753 | |||||||
| chr2:201208759 | A | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.923-311A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208759 | |||||||
| chr2:201208846 | T | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-224T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208846 | |||||||
| chr2:201208921 | G | T | 1 | a0002c0002t0002g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.923-149G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201208921 | |||||||
| chr2:201209041 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(9): Show |
15 | HG00323.hp1 HG01070.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.923-13dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 201209041 | ||||||
| chr2:201209041 | CT | C | 6 | a0001c0001t0001g0141 a0001c0001t0010g0097 a0001c0003t0023g0063 others(3): Show |
7 | HG02055.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.923-13delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 201209041 | ||||||
| chr2:201209044 | T | C | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-26T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201209044 | |||||||
| chr2:201209067 | C | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.923-3C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 8/9 | chr2 | 201209067 | |||||||
| chr2:201209805 | A | G | 61 | a0002c0002t0001g0201 a0002c0002t0002g0002 a0002c0002t0002g0003 others(58): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1415+243A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201209805 | |||||||
| chr2:201210125 | C | T | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1415+563C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210125 | |||||||
| chr2:201210126 | G | A | 1 | a0001c0003t0023g0063 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1415+564G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210126 | |||||||
| chr2:201210148 | C | T | 11 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(8): Show |
12 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1415+586C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210148 | |||||||
| chr2:201210182 | T | A | 1 | a0001c0014t0017g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1415+620T>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210182 | |||||||
| chr2:201210196 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1415+634C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210196 | |||||||
| chr2:201210449 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1415+887C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210449 | |||||||
| chr2:201210497 | G | A | 2 | a0001c0003t0019g0176 a0001c0003t0022g0175 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1415+935G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210497 | |||||||
| chr2:201210642 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0122 |
3 | HG00423.hp1 HG02071.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1415+1080C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210642 | |||||||
| chr2:201210769 | A | G | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415+1207A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201210769 | |||||||
| chr2:201211029 | T | C | 69 | a0001c0003t0001g0207 a0002c0002t0001g0201 a0002c0002t0002g0002 others(66): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1415+1467T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211029 | |||||||
| chr2:201211112 | G | A | 1 | a0002c0002t0002g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1415+1550G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211112 | |||||||
| chr2:201211225 | C | T | 6 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415+1663C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211225 | |||||||
| chr2:201211258 | C | G | 19 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(16): Show |
24 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.1415+1696C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211258 | |||||||
| chr2:201211442 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415+1880G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211442 | |||||||
| chr2:201211464 | A | T | 11 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(8): Show |
12 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1415+1902A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211464 | |||||||
| chr2:201211725 | T | C | 39 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0003g0011 others(36): Show |
46 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.1415+2163T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211725 | |||||||
| chr2:201211985 | C | T | 1 | a0001c0001t0005g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1415+2423C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201211985 | |||||||
| chr2:201212299 | G | A | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1415+2737G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201212299 | |||||||
| chr2:201212494 | T | C | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1415+2932T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201212494 | |||||||
| chr2:201212499 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1415+2937G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201212499 | |||||||
| chr2:201212890 | A | G | 61 | a0002c0002t0001g0201 a0002c0002t0002g0002 a0002c0002t0002g0003 others(58): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1415+3328A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201212890 | |||||||
| chr2:201213111 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1415+3549A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213111 | |||||||
| chr2:201213119 | G | A | 1 | a0001c0003t0018g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1415+3557G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213119 | |||||||
| chr2:201213190 | T | C | 33 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(30): Show |
40 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1415+3628T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213190 | |||||||
| chr2:201213207 | C | G | 1 | a0001c0001t0027g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1415+3645C>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213207 | |||||||
| chr2:201213261 | A | C | 1 | a0001c0001t0001g0032 | 2 | HG00423.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1415+3699A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213261 | |||||||
| chr2:201213516 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18944.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1415+3954G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213516 | |||||||
| chr2:201213622 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416-3966G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213622 | |||||||
| chr2:201213628 | G | C | 2 | a0001c0014t0017g0174 a0004c0013t0016g0173 |
2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1416-3960G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213628 | |||||||
| chr2:201213744 | C | T | 1 | a0002c0002t0002g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1416-3844C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213744 | |||||||
| chr2:201213771 | G | A | 108 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0003g0011 others(105): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1416-3817G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213771 | |||||||
| chr2:201213832 | G | A | 2 | a0001c0003t0019g0176 a0001c0006t0012g0018 |
3 | HG02723.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1416-3756G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213832 | |||||||
| chr2:201213908 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1416-3680G>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201213908 | |||||||
| chr2:201214275 | A | G | 10 | a0001c0003t0007g0059 a0001c0003t0007g0061 a0001c0003t0007g0062 others(7): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1416-3313A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214275 | |||||||
| chr2:201214467 | A | G | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416-3121A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214467 | |||||||
| chr2:201214469 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1416-3119G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214469 | |||||||
| chr2:201214523 | G | A | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416-3065G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214523 | |||||||
| chr2:201214810 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416-2778T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214810 | |||||||
| chr2:201214847 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1416-2741C>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201214847 | |||||||
| chr2:201215042 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1416-2546T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215042 | |||||||
| chr2:201215043 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1416-2545C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215043 | |||||||
| chr2:201215141 | A | C | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1416-2447A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215141 | |||||||
| chr2:201215176 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1416-2412T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215176 | |||||||
| chr2:201215180 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1416-2408T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215180 | |||||||
| chr2:201215206 | C | T | 3 | a0001c0005t0009g0019 a0001c0005t0009g0044 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416-2382C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215206 | |||||||
| chr2:201215210 | G | A | 1 | a0002c0002t0002g0221 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1416-2378G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215210 | |||||||
| chr2:201215211 | G | GT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0074 a0001c0001t0001g0119 others(5): Show |
8 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-2352dupT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | G | GTTTTTTT others(3): Show |
2 | a0001c0005t0009g0044 a0001c0014t0017g0174 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1416-2361_1416-235 others(14): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | G | GTTTTTTT others(4): Show |
3 | a0001c0003t0019g0176 a0001c0005t0009g0019 a0001c0005t0009g0069 |
4 | HG02630.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416-2362_1416-235 others(15): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | G | GTTTTTTT others(5): Show |
2 | a0001c0003t0007g0171 a0001c0003t0007g0172 |
2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1416-2363_1416-235 others(16): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1416-2377G>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215211 | |||||||
| chr2:201215211 | GT | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1416-2352delT | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | GTT | G | 7 | a0001c0001t0001g0125 a0001c0001t0003g0163 a0001c0001t0004g0162 others(4): Show |
7 | HG01981.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416-2353_1416-235 others(6): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | GTTT | G | 4 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0034 others(1): Show |
8 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-2354_1416-235 others(7): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215211 | GTTTTT | G | 10 | a0001c0001t0001g0100 a0001c0001t0003g0046 a0001c0001t0003g0047 others(7): Show |
11 | HG01433.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-2356_1416-235 others(9): Show |
CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 201215211 | ||||||
| chr2:201215587 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(194): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1416-2001A>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215587 | |||||||
| chr2:201215757 | A | T | 1 | a0002c0002t0002g0183 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1416-1831A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215757 | |||||||
| chr2:201215771 | T | C | 1 | a0001c0003t0022g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1416-1817T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215771 | |||||||
| chr2:201215787 | G | A | 1 | a0001c0001t0005g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1416-1801G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201215787 | |||||||
| chr2:201216042 | C | T | 1 | a0004c0013t0016g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1416-1546C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201216042 | |||||||
| chr2:201216103 | T | G | 1 | a0003c0004t0002g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1416-1485T>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201216103 | |||||||
| chr2:201216320 | A | G | 10 | a0002c0002t0002g0003 a0002c0002t0002g0183 a0002c0002t0002g0187 others(7): Show |
15 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1416-1268A>G | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201216320 | |||||||
| chr2:201217149 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0003t0001g0042 |
3 | HG02895.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1416-439T>C | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201217149 | |||||||
| chr2:201217363 | C | T | 1 | a0002c0002t0002g0214 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1416-225C>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201217363 | |||||||
| chr2:201217445 | G | A | 1 | a0001c0003t0001g0207 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1416-143G>A | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201217445 | |||||||
| chr2:201217564 | A | T | 2 | a0001c0003t0020g0064 a0001c0003t0023g0063 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1416-24A>T | CASP10 | ENSG00000003400.16 | transcript | ENST00000286186.11 | protein_coding | 9/9 | chr2 | 201217564 |