Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84698 |
| ensemblid | ENSG00000180881.21 |
| hgncid | 16471 |
| symbol | CAPS2 |
| name | calcyphosine 2 |
| refseq_nuc | NM_001355024.4 |
| refseq_prot | NP_001341953.2 |
| ensembl_nuc | ENST00000699294.1 |
| ensembl_prot | ENSP00000514274.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 75275979 |
| end | 75330324 |
| strand | - |
| ver | v1.2 |
| region | chr12:75275979-75330324 |
| region5000 | chr12:75270979-75335324 |
| regionname0 | CAPS2_chr12_75275979_75330324 |
| regionname5000 | CAPS2_chr12_75270979_75335324 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 557 | 289 | 69 | 53 | 118 | 10 | 37 | 86 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0002 | 0/0 | 557 | 70 | 12 | 15 | 36 | 5 | 2 | 27 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0003 | 0/0 | 557 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0004 | 0/0 | 557 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0005 | 0/0 | 557 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0006 | 0/0 | 557 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0007 | 0/0 | 557 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0008 | 0/0 | 557 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| a0009 | 0/0 | 557 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | MDLEV others(552): Show |
chr12 | 75270979 | 75335324 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1671 | 280 | 66 | 52 | 115 | 9 | 36 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0001c0003 | 0/0 | 1671 | 6 | 3 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0001c0010 | 0/0 | 1671 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0001c0013 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0001c0014 | 0/0 | 1671 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0002c0002 | 0/0 | 1671 | 63 | 10 | 11 | 36 | 4 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0002c0004 | 0/0 | 1671 | 5 | 0 | 4 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0002c0008 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0003c0006 | 0/0 | 1671 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0004c0007 | 0/0 | 1671 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0005c0005 | 0/0 | 1671 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0006c0009 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0006c0016 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0007c0012 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0008c0015 | 0/0 | 1671 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 | ||
| a0009c0011 | 0/0 | 1671 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | ATGGA others(1666): Show |
chr12 | 75270979 | 75335324 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5071 | 104 | 20 | 24 | 50 | 3 | 7 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0002 | 0/0 | 5071 | 69 | 11 | 4 | 37 | 0 | 17 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0003 | 1/0 | 5072 | 25 | 0 | 16 | 1 | 3 | 4 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5067): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0004 | 0/0 | 5071 | 19 | 13 | 1 | 0 | 2 | 3 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0005 | 0/0 | 5070 | 16 | 0 | 1 | 14 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5065): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0006 | 0/0 | 5071 | 10 | 0 | 0 | 9 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0007 | 0/0 | 5071 | 7 | 7 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0008 | 0/0 | 5071 | 4 | 4 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0009 | 0/1 | 5072 | 4 | 0 | 2 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5067): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0010 | 0/0 | 5070 | 3 | 3 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5065): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0011 | 0/0 | 5071 | 4 | 0 | 2 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0012 | 0/0 | 5071 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0013 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0014 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0018 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0020 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5067): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0021 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5067): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0022 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0024 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0026 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0027 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0029 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0030 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0001t0033 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5063): Show |
chr12 | 75270979 | 75335324 |
| a0001c0003t0001 | 0/0 | 5071 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0003t0002 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0003t0014 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0003t0031 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5063): Show |
chr12 | 75270979 | 75335324 |
| a0001c0003t0032 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5063): Show |
chr12 | 75270979 | 75335324 |
| a0001c0010t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0013t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0001c0014t0002 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0001 | 0/0 | 5071 | 51 | 6 | 10 | 30 | 4 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0002 | 0/0 | 5071 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0003 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5067): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0008 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0010 | 0/0 | 5070 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5065): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0015 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0017 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0019 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0023 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0025 | 0/0 | 5070 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5065): Show |
chr12 | 75270979 | 75335324 |
| a0002c0002t0028 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0004t0001 | 0/0 | 5071 | 5 | 0 | 4 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0002c0008t0001 | 0/0 | 5071 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0003c0006t0016 | 0/0 | 5068 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5063): Show |
chr12 | 75270979 | 75335324 |
| a0004c0007t0001 | 0/0 | 5071 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0005c0005t0002 | 0/0 | 5071 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0006c0009t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0006c0016t0001 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0007c0012t0001 | 0/0 | 5071 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0008c0015t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| a0009c0011t0001 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | GCCGG others(5066): Show |
chr12 | 75270979 | 75335324 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0003g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0009g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0010g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0011g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0012g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0018g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0020g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0021g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0022g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0024g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0026g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0027g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0029g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0030g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0031g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0003t0032g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0010t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0013t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0001c0014t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0006 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0015g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0017g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0019g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0023g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0025g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0002t0028g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0008t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0002c0008t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0003c0006t0016g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0003c0006t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0004c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0004c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0005c0005t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0006c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0006c0016t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0007c0012t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0008c0015t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| a0009c0011t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0114 | EUR | GBR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0160 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00280 | hp2 | a0001 | c0010 | t0001 | g0092 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00738 | hp2 | a0002 | c0004 | t0001 | g0027 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG00741 | hp2 | a0007 | c0012 | t0001 | g0102 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0191 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01168 | hp2 | a0001 | c0001 | t0011 | g0012 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01243 | hp1 | a0003 | c0006 | t0016 | g0295 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0028 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01258 | hp2 | a0002 | c0004 | t0001 | g0028 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01261 | hp2 | a0002 | c0004 | t0001 | g0027 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0130 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0137 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0029 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01516 | hp1 | a0002 | c0004 | t0001 | g0202 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01516 | hp2 | a0008 | c0015 | t0001 | g0171 | EUR | IBS | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01884 | hp1 | a0002 | c0002 | t0010 | g0186 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0103 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0143 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02004 | hp2 | a0001 | c0001 | t0020 | g0239 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02056 | hp2 | a0001 | c0003 | t0032 | g0293 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02083 | hp2 | a0001 | c0013 | t0001 | g0105 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CDX | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02257 | hp2 | a0002 | c0008 | t0001 | g0209 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0222 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02683 | hp2 | a0001 | c0014 | t0002 | g0165 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02717 | hp2 | a0002 | c0008 | t0001 | g0210 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0146 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02735 | hp2 | a0004 | c0007 | t0001 | g0281 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0140 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02818 | hp1 | a0001 | c0001 | t0029 | g0153 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02818 | hp2 | a0001 | c0003 | t0014 | g0059 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02965 | hp1 | a0003 | c0006 | t0016 | g0296 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03017 | hp1 | a0005 | c0005 | t0002 | g0040 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0228 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03195 | hp2 | a0002 | c0002 | t0008 | g0174 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0145 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0285 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0012 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03491 | hp1 | a0005 | c0005 | t0002 | g0040 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0012 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03669 | hp1 | a0004 | c0007 | t0001 | g0280 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0244 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03927 | hp2 | a0009 | c0011 | t0001 | g0063 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04115 | hp1 | a0002 | c0002 | t0025 | g0198 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04184 | hp2 | a0001 | c0001 | t0021 | g0217 | SAS | BEB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18747 | hp1 | a0006 | c0009 | t0001 | g0070 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18747 | hp2 | a0001 | c0001 | t0033 | g0294 | EAS | CHB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18941 | hp2 | a0001 | c0001 | t0024 | g0052 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18942 | hp1 | a0002 | c0002 | t0028 | g0218 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18963 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18985 | hp1 | a0002 | c0002 | t0017 | g0203 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18990 | hp2 | a0001 | c0001 | t0018 | g0075 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19006 | hp1 | a0002 | c0002 | t0023 | g0183 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19010 | hp2 | a0001 | c0001 | t0030 | g0291 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19078 | hp2 | a0002 | c0002 | t0019 | g0205 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19081 | hp1 | a0001 | c0003 | t0031 | g0292 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19087 | hp2 | a0006 | c0016 | t0001 | g0123 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | YRI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0104 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0173 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0176 | EUR | TSI | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02109 | hp1 | a0002 | c0002 | t0015 | g0046 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02559 | hp1 | a0002 | c0002 | t0015 | g0046 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0060 | AFR | USA | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | LWK | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0111 | REF | REF | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0287 | REF | REF | CAPS2_chr12_75270979_75335324 | CAPS2 | chr12 | 75270979 | 75335324 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75289632 | C | G | 1 | a0003 | 2 | HG01243.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.1270G>C | p.Val424Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/17 | 1757/5072 | 1270/1674 | 424/557 | chr12 | 75289632 | |||
| chr12:75293259 | C | T | 1 | a0007 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.1039G>A | p.Asp347Asn | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/17 | 1526/5072 | 1039/1674 | 347/557 | chr12 | 75293259 | |||
| chr12:75298772 | A | G | 2 | a0004 a0009 |
3 | HG02735.hp2 HG03669.hp1 HG03927.hp2 |
missense_variant | MODERATE | c.845T>C | p.Val282Ala | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/17 | 1332/5072 | 845/1674 | 282/557 | chr12 | 75298772 | |||
| chr12:75312889 | T | G | 1 | a0008 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.504A>C | p.Lys168Asn | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/17 | 991/5072 | 504/1674 | 168/557 | chr12 | 75312889 | |||
| chr12:75316434 | A | G | 1 | a0006 | 2 | NA18747.hp1 NA19087.hp2 |
missense_variant&splice_region_variant | MODERATE | c.355T>C | p.Cys119Arg | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/17 | 842/5072 | 355/1674 | 119/557 | chr12 | 75316434 | |||
| chr12:75321550 | C | A | 2 | a0002 a0004 |
72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
missense_variant | MODERATE | c.204G>T | p.Leu68Phe | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/17 | 691/5072 | 204/1674 | 68/557 | chr12 | 75321550 | |||
| chr12:75321574 | A | T | 1 | a0005 | 2 | HG03017.hp1 HG03491.hp1 |
missense_variant&splice_region_variant | MODERATE | c.180T>A | p.Asp60Glu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/17 | 667/5072 | 180/1674 | 60/557 | chr12 | 75321574 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75289725 | A | G | 1 | a0001c0013 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1177T>C | p.Leu393Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/17 | 1664/5072 | 1177/1674 | 393/557 | chr12 | 75289725 | |||
| chr12:75299911 | C | T | 2 | a0001c0010 a0002c0004 |
6 | HG00280.hp2 HG00738.hp2 HG01256.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.666G>A | p.Lys222Lys | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/17 | 1153/5072 | 666/1674 | 222/557 | chr12 | 75299911 | |||
| chr12:75304768 | T | C | 1 | a0001c0014 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.654A>G | p.Leu218Leu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/17 | 1141/5072 | 654/1674 | 218/557 | chr12 | 75304768 | |||
| chr12:75304855 | C | T | 2 | a0001c0003 a0003c0006 |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
synonymous_variant | LOW | c.567G>A | p.Glu189Glu | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/17 | 1054/5072 | 567/1674 | 189/557 | chr12 | 75304855 | |||
| chr12:75323198 | G | A | 2 | a0002c0008 a0006c0016 |
3 | HG02257.hp2 HG02717.hp2 NA19087.hp2 |
synonymous_variant | LOW | c.156C>T | p.Ser52Ser | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/17 | 643/5072 | 156/1674 | 52/557 | chr12 | 75323198 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75275986 | T | TA | 1 | a0001c0001t0009 | 3 | HG01109.hp2 HG01952.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2903_*2904insT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2903 | chr12 | 75275986 | ||||||
| chr12:75276003 | A | C | 1 | a0001c0001t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2887T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2887 | chr12 | 75276003 | ||||||
| chr12:75276048 | C | A | 2 | a0001c0001t0013 a0001c0003t0031 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2842G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2842 | chr12 | 75276048 | ||||||
| chr12:75276229 | T | A | 1 | a0002c0002t0023 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2661A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2661 | chr12 | 75276229 | ||||||
| chr12:75276667 | T | G | 2 | a0001c0001t0008 a0002c0002t0008 |
5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2223A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2223 | chr12 | 75276667 | ||||||
| chr12:75276733 | G | A | 1 | a0001c0001t0021 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2157C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2157 | chr12 | 75276733 | ||||||
| chr12:75276769 | G | C | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
123 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2121C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2121 | chr12 | 75276769 | ||||||
| chr12:75276783 | C | T | 1 | a0001c0001t0030 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 2107 | chr12 | 75276783 | ||||||
| chr12:75276938 | T | C | 1 | a0001c0001t0024 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1952 | chr12 | 75276938 | ||||||
| chr12:75277186 | C | T | 2 | a0001c0001t0010 a0002c0002t0010 |
4 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1704G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1704 | chr12 | 75277186 | ||||||
| chr12:75277210 | CT | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1679delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1679 | chr12 | 75277210 | ||||||
| chr12:75277210 | CTT | C | 4 | a0001c0001t0005 a0001c0001t0010 a0002c0002t0010 others(1): Show |
21 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1678_*1679delAA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1678 | chr12 | 75277210 | ||||||
| chr12:75277326 | T | A | 2 | a0001c0001t0014 a0001c0003t0014 |
2 | HG02818.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1564A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1564 | chr12 | 75277326 | ||||||
| chr12:75277342 | C | T | 1 | a0003c0006t0016 | 2 | HG01243.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1548G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1548 | chr12 | 75277342 | ||||||
| chr12:75277491 | T | C | 2 | a0001c0001t0004 a0001c0001t0011 |
23 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1399 | chr12 | 75277491 | ||||||
| chr12:75277519 | A | T | 1 | a0001c0001t0020 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1371 | chr12 | 75277519 | ||||||
| chr12:75277603 | A | G | 1 | a0002c0002t0019 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1287 | chr12 | 75277603 | ||||||
| chr12:75277880 | A | G | 2 | a0001c0001t0013 a0001c0003t0031 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1010T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 1010 | chr12 | 75277880 | ||||||
| chr12:75278051 | T | C | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 839 | chr12 | 75278051 | ||||||
| chr12:75278092 | G | A | 1 | a0001c0001t0011 | 4 | HG01168.hp2 HG01361.hp1 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 798 | chr12 | 75278092 | ||||||
| chr12:75278158 | G | T | 1 | a0001c0001t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 732 | chr12 | 75278158 | ||||||
| chr12:75278159 | G | T | 1 | a0001c0001t0012 | 2 | HG01496.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*731C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 731 | chr12 | 75278159 | ||||||
| chr12:75278397 | T | A | 3 | a0001c0001t0006 a0001c0001t0030 a0001c0001t0033 |
12 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*493A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 493 | chr12 | 75278397 | ||||||
| chr12:75278434 | C | T | 1 | a0001c0001t0018 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*456G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 456 | chr12 | 75278434 | ||||||
| chr12:75278606 | C | T | 1 | a0002c0002t0017 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 284 | chr12 | 75278606 | ||||||
| chr12:75278645 | T | G | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 245 | chr12 | 75278645 | ||||||
| chr12:75278833 | T | C | 1 | a0002c0002t0028 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 57 | chr12 | 75278833 | ||||||
| chr12:75278883 | T | C | 2 | a0001c0001t0007 a0001c0001t0029 |
8 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 17/17 | 7 | chr12 | 75278883 | ||||||
| chr12:75329979 | T | C | 1 | a0001c0001t0030 | 1 | NA19010.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | chr12 | 75329979 | |||||||
| chr12:75330099 | T | C | 1 | a0002c0002t0015 | 2 | HG02109.hp1 HG02559.hp1 |
5_prime_UTR_variant | MODIFIER | c.-262A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | 3601 | chr12 | 75330099 | ||||||
| chr12:75330286 | ACCT | A | 4 | a0001c0001t0033 a0001c0003t0031 a0001c0003t0032 others(1): Show |
5 | HG01243.hp1 HG02056.hp2 HG02965.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-452_-450delAGG | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/17 | 3789 | chr12 | 75330286 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:75279325 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1499-260A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279325 | |||||||
| chr12:75279413 | T | C | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-348A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279413 | |||||||
| chr12:75279515 | C | G | 1 | a0002c0002t0001g0030 | 2 | HG02071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1499-450G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279515 | |||||||
| chr12:75279599 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1499-534T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279599 | |||||||
| chr12:75279758 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1499-693G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279758 | |||||||
| chr12:75279967 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(11): Show |
18 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1499-902A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279967 | |||||||
| chr12:75279996 | C | T | 1 | a0001c0001t0004g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1499-931G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75279996 | |||||||
| chr12:75280177 | G | C | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1112C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280177 | |||||||
| chr12:75280254 | G | T | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1189C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280254 | |||||||
| chr12:75280287 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0226 |
3 | HG02647.hp2 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1499-1222C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280287 | |||||||
| chr12:75280547 | T | C | 1 | a0002c0002t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1499-1482A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280547 | |||||||
| chr12:75280565 | G | GAA | 5 | a0001c0010t0001g0092 a0002c0004t0001g0027 a0002c0004t0001g0028 others(2): Show |
7 | HG00280.hp2 HG00738.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-1502_1499-150 others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280565 | |||||||
| chr12:75280638 | G | A | 1 | a0001c0013t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1499-1573C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280638 | |||||||
| chr12:75280655 | A | C | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-1590T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75280655 | |||||||
| chr12:75281028 | T | G | 9 | a0001c0001t0007g0128 a0001c0001t0007g0152 a0001c0001t0007g0154 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498+1223A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281028 | |||||||
| chr12:75281215 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1498+1036C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281215 | |||||||
| chr12:75281225 | A | C | 1 | a0006c0016t0001g0123 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1498+1026T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281225 | |||||||
| chr12:75281319 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1498+932A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281319 | |||||||
| chr12:75281407 | A | G | 1 | a0002c0002t0008g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1498+844T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281407 | |||||||
| chr12:75281414 | G | T | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1498+837C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281414 | |||||||
| chr12:75281549 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498+702A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281549 | |||||||
| chr12:75281894 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1498+357A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281894 | |||||||
| chr12:75281993 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0156 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1498+258T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75281993 | |||||||
| chr12:75282050 | A | G | 1 | a0001c0001t0024g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1498+201T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 16/16 | chr12 | 75282050 | |||||||
| chr12:75282380 | T | C | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1402-33A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282380 | |||||||
| chr12:75282460 | C | A | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1402-113G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282460 | |||||||
| chr12:75282475 | C | A | 1 | a0001c0001t0004g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1402-128G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282475 | |||||||
| chr12:75282518 | C | T | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0138 others(2): Show |
7 | HG01168.hp2 HG01361.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402-171G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282518 | |||||||
| chr12:75282536 | G | A | 88 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(85): Show |
118 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1402-189C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282536 | |||||||
| chr12:75282826 | A | G | 1 | a0001c0001t0012g0131 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1402-479T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282826 | |||||||
| chr12:75282866 | A | C | 1 | a0001c0003t0002g0018 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1402-519T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75282866 | |||||||
| chr12:75283509 | C | G | 1 | a0001c0003t0002g0018 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1402-1162G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283509 | |||||||
| chr12:75283619 | G | C | 3 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1402-1272C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283619 | |||||||
| chr12:75283654 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1401+1307T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283654 | |||||||
| chr12:75283655 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1401+1306T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75283655 | |||||||
| chr12:75284057 | G | A | 1 | a0002c0002t0001g0175 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1401+904C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284057 | |||||||
| chr12:75284234 | T | A | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1401+727A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284234 | |||||||
| chr12:75284239 | C | A | 3 | a0001c0001t0002g0275 a0001c0001t0014g0145 a0001c0003t0014g0059 |
3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1401+722G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284239 | |||||||
| chr12:75284404 | T | C | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1401+557A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284404 | |||||||
| chr12:75284435 | T | C | 4 | a0001c0001t0002g0038 a0001c0001t0002g0254 a0001c0001t0002g0257 others(1): Show |
5 | HG02683.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401+526A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284435 | |||||||
| chr12:75284688 | G | A | 6 | a0001c0001t0001g0149 a0001c0001t0001g0156 a0001c0001t0001g0226 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1401+273C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284688 | |||||||
| chr12:75284754 | T | C | 1 | a0001c0003t0032g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1401+207A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284754 | |||||||
| chr12:75284788 | T | C | 1 | a0001c0003t0002g0018 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1401+173A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284788 | |||||||
| chr12:75284800 | G | A | 7 | a0001c0001t0002g0208 a0001c0001t0002g0219 a0001c0001t0002g0220 others(4): Show |
7 | HG01496.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1401+161C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 15/16 | chr12 | 75284800 | |||||||
| chr12:75285232 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1282-152G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285232 | |||||||
| chr12:75285245 | G | T | 3 | a0001c0001t0002g0275 a0001c0001t0014g0145 a0001c0003t0014g0059 |
3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-165C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285245 | |||||||
| chr12:75285462 | G | A | 1 | a0002c0002t0001g0178 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1282-382C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75285462 | |||||||
| chr12:75286001 | T | C | 1 | a0001c0001t0007g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1282-921A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286001 | |||||||
| chr12:75286148 | AAAT | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1282-1071_1282-106 others(7): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286148 | |||||||
| chr12:75286367 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1282-1287A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286367 | |||||||
| chr12:75286454 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1282-1374T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286454 | |||||||
| chr12:75286553 | G | T | 4 | a0001c0001t0008g0043 a0001c0001t0008g0284 a0001c0001t0008g0285 others(1): Show |
5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-1473C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286553 | |||||||
| chr12:75286895 | A | G | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-1815T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286895 | |||||||
| chr12:75286973 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1282-1893A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75286973 | |||||||
| chr12:75287155 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1282-2075T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287155 | |||||||
| chr12:75287158 | G | T | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1282-2078C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287158 | |||||||
| chr12:75287258 | C | T | 3 | a0001c0001t0002g0275 a0001c0001t0014g0145 a0001c0003t0014g0059 |
3 | HG02280.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1282-2178G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287258 | |||||||
| chr12:75287537 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1281+2084A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287537 | |||||||
| chr12:75287600 | G | A | 4 | a0001c0001t0008g0043 a0001c0001t0008g0284 a0001c0001t0008g0285 others(1): Show |
5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2021C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287600 | |||||||
| chr12:75287945 | T | A | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1281+1676A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75287945 | |||||||
| chr12:75288008 | G | C | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1281+1613C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288008 | |||||||
| chr12:75288200 | G | C | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1281+1421C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288200 | |||||||
| chr12:75288226 | G | T | 63 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0216 others(60): Show |
80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1281+1395C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288226 | |||||||
| chr12:75288327 | C | G | 1 | a0001c0001t0003g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1281+1294G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288327 | |||||||
| chr12:75288423 | C | G | 1 | a0001c0001t0007g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1281+1198G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288423 | |||||||
| chr12:75288927 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1281+694G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288927 | |||||||
| chr12:75288983 | G | C | 9 | a0001c0001t0005g0001 a0001c0001t0005g0034 a0001c0001t0005g0051 others(6): Show |
16 | HG01257.hp2 NA18960.hp2 NA18965.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281+638C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75288983 | |||||||
| chr12:75289016 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
234 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1281+605A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289016 | |||||||
| chr12:75289058 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1281+563A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289058 | |||||||
| chr12:75289167 | A | C | 4 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0001t0021g0217 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+454T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289167 | |||||||
| chr12:75289190 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
2 | HG02074.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1281+431A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289190 | |||||||
| chr12:75289234 | C | T | 69 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(66): Show |
94 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1281+387G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 14/16 | chr12 | 75289234 | |||||||
| chr12:75289803 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1127-28T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289803 | |||||||
| chr12:75289853 | A | C | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1127-78T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289853 | |||||||
| chr12:75289946 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1127-171G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75289946 | |||||||
| chr12:75290223 | A | C | 1 | a0001c0003t0002g0018 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1127-448T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290223 | |||||||
| chr12:75290331 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1127-556G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290331 | |||||||
| chr12:75290369 | C | T | 1 | a0005c0005t0002g0040 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1127-594G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290369 | |||||||
| chr12:75290442 | A | G | 1 | a0002c0002t0001g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1127-667T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290442 | |||||||
| chr12:75290466 | A | G | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1127-691T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290466 | |||||||
| chr12:75290546 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1127-771C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290546 | |||||||
| chr12:75290654 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1127-879C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290654 | |||||||
| chr12:75290761 | A | T | 3 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1126+983T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290761 | |||||||
| chr12:75290935 | C | A | 1 | a0001c0001t0002g0233 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+809G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290935 | |||||||
| chr12:75290936 | A | AAAAAAAA others(3): Show |
4 | a0001c0001t0006g0098 a0001c0001t0013g0140 a0001c0001t0013g0146 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+798_1126+807d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | |||||||
| chr12:75290936 | A | AAAAAAAA others(2): Show |
177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1126+807_1126+808i others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | |||||||
| chr12:75290936 | A | C | 1 | a0001c0001t0002g0233 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+808T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75290936 | |||||||
| chr12:75291155 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1126+589T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291155 | |||||||
| chr12:75291294 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1126+450C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291294 | |||||||
| chr12:75291454 | C | G | 1 | a0001c0001t0002g0277 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1126+290G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291454 | |||||||
| chr12:75291480 | C | CAT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0074 others(23): Show |
33 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+262_1126+263d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | C | CATAT | 8 | a0001c0001t0001g0061 a0001c0001t0001g0087 a0001c0001t0001g0094 others(5): Show |
8 | HG00280.hp2 HG00544.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+260_1126+263d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CAT | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(35): Show |
53 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1126+262_1126+263d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATAT | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0066 others(30): Show |
37 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1126+260_1126+263d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATAT | C | 48 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0072 others(45): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1126+258_1126+263d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATATA others(1): Show |
C | 44 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0049 others(41): Show |
55 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1126+256_1126+263d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATATA others(3): Show |
C | 28 | a0001c0001t0001g0048 a0001c0001t0001g0099 a0001c0001t0002g0208 others(25): Show |
33 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126+254_1126+263d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATATA others(5): Show |
C | 17 | a0001c0001t0001g0107 a0001c0001t0001g0289 a0001c0001t0002g0232 others(14): Show |
19 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1126+252_1126+263d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0134 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1126+250_1126+263d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291480 | CATATATA others(9): Show |
C | 2 | a0001c0001t0003g0168 a0001c0001t0004g0129 |
2 | HG01993.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1126+248_1126+263d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291480 | |||||||
| chr12:75291509 | A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1126+234_1126+235i others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291509 | |||||||
| chr12:75291523 | A | G | 3 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1126+221T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291523 | |||||||
| chr12:75291533 | A | T | 3 | a0001c0001t0004g0024 a0001c0001t0004g0166 a0001c0001t0004g0167 |
4 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+211T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291533 | |||||||
| chr12:75291538 | G | GTA | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(95): Show |
128 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1126+204_1126+205d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291538 | |||||||
| chr12:75291566 | AGTATATA others(1): Show |
A | 3 | a0001c0001t0003g0093 a0001c0001t0003g0113 a0001c0001t0003g0114 |
3 | HG00140.hp2 HG00639.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1126+170_1126+177d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291566 | |||||||
| chr12:75291567 | G | GTA | 33 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0053 others(30): Show |
35 | HG00544.hp2 HG00609.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1126+175_1126+176d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | G | GTATA | 24 | a0001c0001t0001g0009 a0001c0001t0002g0007 a0001c0001t0002g0015 others(21): Show |
28 | HG00673.hp1 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+173_1126+176d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | G | GTATATA | 7 | a0001c0001t0001g0048 a0001c0001t0001g0086 a0001c0001t0002g0007 others(4): Show |
9 | HG00438.hp1 HG00621.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126+171_1126+176d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0045 a0001c0001t0002g0221 a0001c0001t0002g0235 others(1): Show |
4 | HG02129.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+169_1126+176d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | G | GTATATAT others(3): Show |
2 | a0001c0001t0002g0269 a0002c0002t0001g0178 |
2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1126+167_1126+176d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | G | GTATATAT others(7): Show |
1 | a0002c0002t0001g0032 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1126+163_1126+176d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTA | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0132 others(34): Show |
41 | HG00323.hp1 HG00738.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1126+175_1126+176d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATA | G | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0172 others(22): Show |
27 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1126+173_1126+176d others(6): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATA | G | 9 | a0001c0001t0001g0149 a0001c0001t0001g0163 a0001c0001t0002g0042 others(6): Show |
10 | HG01496.hp2 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126+171_1126+176d others(8): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(1): Show |
G | 8 | a0001c0001t0003g0080 a0001c0001t0008g0043 a0001c0001t0008g0284 others(5): Show |
9 | HG01192.hp2 HG02647.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126+169_1126+176d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(3): Show |
G | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(3): Show |
7 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126+167_1126+176d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0250 a0001c0001t0003g0168 |
2 | HG01993.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1126+165_1126+176d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(7): Show |
G | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1126+163_1126+176d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(9): Show |
G | 4 | a0001c0001t0002g0007 a0001c0001t0010g0025 a0001c0001t0021g0217 others(1): Show |
6 | HG00099.hp1 HG02257.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126+161_1126+176d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(11): Show |
G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
10 | HG01069.hp2 HG02055.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126+159_1126+176d others(20): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0005g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1126+153_1126+176d others(26): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1126+149_1126+176d others(30): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(23): Show |
G | 1 | a0001c0001t0004g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1126+147_1126+176d others(32): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(25): Show |
G | 1 | a0001c0001t0002g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1126+145_1126+176d others(34): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291567 | GTATATAT others(27): Show |
G | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1126+143_1126+176d others(36): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291567 | |||||||
| chr12:75291579 | A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1126+164_1126+165i others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291579 | |||||||
| chr12:75291591 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1126+131_1126+152d others(24): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291591 | |||||||
| chr12:75291593 | ATATATAT others(13): Show |
A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
79 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1126+131_1126+150d others(22): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291593 | |||||||
| chr12:75291595 | ATATATAT others(11): Show |
A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0071 others(5): Show |
9 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126+131_1126+148d others(20): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291595 | |||||||
| chr12:75291598 | T | G | 3 | a0002c0002t0001g0006 a0002c0002t0001g0030 a0002c0002t0001g0199 |
4 | HG00408.hp2 HG02132.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126+146A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | |||||||
| chr12:75291598 | T | TATATATA others(1): Show |
2 | a0001c0001t0002g0035 a0001c0001t0002g0243 |
3 | HG02074.hp1 NA18951.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1126+145_1126+146i others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | |||||||
| chr12:75291598 | T | TATATATA others(3): Show |
1 | a0001c0001t0002g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1126+145_1126+146i others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291598 | |||||||
| chr12:75291686 | T | C | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1126+58A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 13/16 | chr12 | 75291686 | |||||||
| chr12:75291903 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1050-83A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75291903 | |||||||
| chr12:75292052 | T | C | 29 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0033 others(26): Show |
44 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1050-232A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292052 | |||||||
| chr12:75292221 | C | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(175): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1050-401G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292221 | |||||||
| chr12:75292223 | C | T | 3 | a0001c0001t0004g0138 a0001c0001t0004g0159 a0001c0001t0004g0160 |
3 | HG00280.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1050-403G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292223 | |||||||
| chr12:75292308 | C | T | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1050-488G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292308 | |||||||
| chr12:75292455 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1050-635C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292455 | |||||||
| chr12:75292489 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1050-669G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292489 | |||||||
| chr12:75292588 | TATATTAT others(6): Show |
T | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1049+648_1049+660d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292588 | |||||||
| chr12:75292614 | T | C | 4 | a0001c0001t0008g0043 a0001c0001t0008g0284 a0001c0001t0008g0285 others(1): Show |
5 | HG02647.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+635A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292614 | |||||||
| chr12:75292614 | T | TATCTATA others(18): Show |
1 | a0001c0001t0006g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1049+610_1049+634d others(27): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 12/16 | chr12 | 75292614 | |||||||
| chr12:75293405 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
230 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.931-38C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293405 | |||||||
| chr12:75293465 | G | A | 2 | a0001c0001t0013g0140 a0001c0001t0013g0146 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.931-98C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293465 | |||||||
| chr12:75293492 | T | C | 1 | a0001c0013t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.931-125A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293492 | |||||||
| chr12:75293542 | T | A | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.931-175A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293542 | |||||||
| chr12:75293743 | C | T | 1 | a0001c0001t0024g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.931-376G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293743 | |||||||
| chr12:75293873 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.931-506A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75293873 | |||||||
| chr12:75294134 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.931-767G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294134 | |||||||
| chr12:75294208 | C | T | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.931-841G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294208 | |||||||
| chr12:75294608 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.931-1241G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294608 | |||||||
| chr12:75294667 | G | T | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.931-1300C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294667 | |||||||
| chr12:75294707 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931-1340C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294707 | |||||||
| chr12:75294755 | ATG | A | 5 | a0002c0002t0001g0031 a0002c0002t0001g0193 a0002c0002t0001g0194 others(2): Show |
6 | HG02257.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.931-1390_931-1389d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294755 | |||||||
| chr12:75294868 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.931-1501G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294868 | |||||||
| chr12:75294899 | A | T | 1 | a0001c0001t0004g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.931-1532T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75294899 | |||||||
| chr12:75295318 | T | C | 4 | a0001c0001t0002g0035 a0001c0001t0002g0230 a0001c0001t0002g0242 others(1): Show |
5 | HG00597.hp1 HG02074.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-1951A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295318 | |||||||
| chr12:75295470 | C | T | 1 | a0001c0013t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.931-2103G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295470 | |||||||
| chr12:75295991 | T | C | 1 | a0001c0001t0004g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.931-2624A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75295991 | |||||||
| chr12:75296209 | T | TTA | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.930+2477_930+2478i others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296209 | |||||||
| chr12:75296273 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.930+2414A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296273 | |||||||
| chr12:75296453 | A | G | 4 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0001t0021g0217 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+2234T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296453 | |||||||
| chr12:75296867 | C | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.930+1820G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75296867 | |||||||
| chr12:75297007 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.930+1680A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297007 | |||||||
| chr12:75297178 | T | C | 3 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.930+1509A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297178 | |||||||
| chr12:75297443 | C | T | 1 | a0001c0001t0005g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.930+1244G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297443 | |||||||
| chr12:75297456 | T | C | 3 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 |
3 | HG02723.hp1 HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.930+1231A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297456 | |||||||
| chr12:75297719 | C | T | 1 | a0001c0001t0003g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.930+968G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297719 | |||||||
| chr12:75297795 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.930+892A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297795 | |||||||
| chr12:75297992 | T | G | 1 | a0001c0001t0003g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.930+695A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75297992 | |||||||
| chr12:75298018 | A | C | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.930+669T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298018 | |||||||
| chr12:75298101 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.930+586T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298101 | |||||||
| chr12:75298222 | T | G | 1 | a0001c0001t0014g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.930+465A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298222 | |||||||
| chr12:75298225 | C | T | 1 | a0001c0001t0004g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.930+462G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298225 | |||||||
| chr12:75298481 | A | C | 66 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(63): Show |
88 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.930+206T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298481 | |||||||
| chr12:75298618 | C | T | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.930+69G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 11/16 | chr12 | 75298618 | |||||||
| chr12:75298808 | A | G | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.837-28T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 10/16 | chr12 | 75298808 | |||||||
| chr12:75298827 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.836+44C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 10/16 | chr12 | 75298827 | |||||||
| chr12:75298975 | A | T | 120 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(117): Show |
155 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.741-9T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75298975 | |||||||
| chr12:75299085 | G | A | 1 | a0001c0001t0002g0261 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.741-119C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299085 | |||||||
| chr12:75299188 | T | G | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-222A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299188 | |||||||
| chr12:75299206 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.741-240G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299206 | |||||||
| chr12:75299271 | G | A | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-305C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299271 | |||||||
| chr12:75299349 | A | G | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.741-383T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299349 | |||||||
| chr12:75299520 | C | T | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+317G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299520 | |||||||
| chr12:75299692 | A | G | 1 | a0008c0015t0001g0171 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.740+145T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299692 | |||||||
| chr12:75299722 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.740+115C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299722 | |||||||
| chr12:75299740 | C | T | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+97G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299740 | |||||||
| chr12:75299751 | A | C | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.740+86T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 9/16 | chr12 | 75299751 | |||||||
| chr12:75299971 | G | A | 103 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(100): Show |
134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-60C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75299971 | |||||||
| chr12:75299981 | A | G | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.666-70T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75299981 | |||||||
| chr12:75300034 | T | TA | 6 | a0001c0001t0013g0140 a0001c0001t0013g0146 a0001c0003t0031g0292 others(3): Show |
6 | HG00609.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-124dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300034 | |||||||
| chr12:75300043 | A | C | 1 | a0001c0001t0003g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.666-132T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300043 | |||||||
| chr12:75300101 | G | T | 31 | a0001c0001t0002g0208 a0001c0001t0002g0219 a0001c0001t0002g0220 others(28): Show |
37 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-190C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300101 | |||||||
| chr12:75300226 | T | C | 31 | a0001c0001t0002g0208 a0001c0001t0002g0219 a0001c0001t0002g0220 others(28): Show |
37 | HG00280.hp1 HG01109.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.666-315A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300226 | |||||||
| chr12:75300276 | G | T | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-365C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300276 | |||||||
| chr12:75300282 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
111 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.666-371G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300282 | |||||||
| chr12:75300328 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-417C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300328 | |||||||
| chr12:75300339 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-428C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300339 | |||||||
| chr12:75300353 | G | A | 2 | a0001c0001t0014g0145 a0001c0003t0014g0059 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.666-442C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300353 | |||||||
| chr12:75300414 | G | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.666-503C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300414 | |||||||
| chr12:75300425 | G | A | 103 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(100): Show |
134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-514C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300425 | |||||||
| chr12:75300439 | T | C | 103 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(100): Show |
134 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.666-528A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300439 | |||||||
| chr12:75300543 | C | G | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-632G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300543 | |||||||
| chr12:75300555 | C | CA | 56 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(53): Show |
67 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.666-645dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | C | CAA | 13 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0106 others(10): Show |
13 | HG01243.hp2 HG01952.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.666-646_666-645dup others(2): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CA | C | 6 | a0001c0001t0001g0023 a0001c0001t0009g0103 a0001c0001t0009g0104 others(3): Show |
7 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-645delT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAA | C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
13 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.666-646_666-645del others(2): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAAA | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.666-647_666-645del others(3): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0235 a0001c0001t0002g0274 a0001c0001t0005g0245 |
3 | HG02129.hp1 NA18941.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.666-654_666-645del others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAAAAAAA others(4): Show |
C | 85 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(82): Show |
113 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.666-655_666-645del others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAAAAAAA others(5): Show |
C | 14 | a0001c0001t0004g0135 a0001c0001t0004g0136 a0001c0001t0004g0137 others(11): Show |
17 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-656_666-645del others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300555 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.666-657_666-645del others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300555 | |||||||
| chr12:75300759 | T | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(170): Show |
222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.666-848A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300759 | |||||||
| chr12:75300764 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666-853G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300764 | |||||||
| chr12:75300945 | T | C | 1 | a0001c0001t0002g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.666-1034A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300945 | |||||||
| chr12:75300971 | G | C | 72 | a0001c0001t0001g0234 a0001c0001t0002g0007 a0001c0001t0002g0013 others(69): Show |
97 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.666-1060C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75300971 | |||||||
| chr12:75301051 | C | A | 1 | a0001c0001t0021g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.666-1140G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301051 | |||||||
| chr12:75301100 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1189T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301100 | |||||||
| chr12:75301106 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1195T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301106 | |||||||
| chr12:75301234 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(170): Show |
222 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.666-1323T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301234 | |||||||
| chr12:75301326 | A | G | 1 | a0002c0002t0001g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.666-1415T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301326 | |||||||
| chr12:75301432 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-1521A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301432 | |||||||
| chr12:75301434 | G | T | 4 | a0001c0001t0004g0024 a0001c0001t0004g0166 a0001c0001t0004g0167 others(1): Show |
5 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-1523C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301434 | |||||||
| chr12:75301662 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.666-1751A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301662 | |||||||
| chr12:75301797 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(175): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.666-1886T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301797 | |||||||
| chr12:75301860 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.666-1949T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301860 | |||||||
| chr12:75301884 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.666-1973G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301884 | |||||||
| chr12:75301894 | A | G | 6 | a0001c0001t0010g0025 a0001c0001t0013g0140 a0001c0001t0013g0146 others(3): Show |
7 | HG01884.hp1 HG02056.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-1983T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75301894 | |||||||
| chr12:75302147 | T | A | 87 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(84): Show |
114 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.666-2236A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302147 | |||||||
| chr12:75302185 | G | A | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.666-2274C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302185 | |||||||
| chr12:75302298 | G | A | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-2387C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302298 | |||||||
| chr12:75302628 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(11): Show |
18 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+2129C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302628 | |||||||
| chr12:75302633 | G | A | 5 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(2): Show |
6 | HG01243.hp1 HG02004.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+2124C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302633 | |||||||
| chr12:75302650 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.665+2107C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302650 | |||||||
| chr12:75302945 | A | G | 1 | a0002c0002t0001g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.665+1812T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75302945 | |||||||
| chr12:75303021 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.665+1736T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303021 | |||||||
| chr12:75303112 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.665+1645G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303112 | |||||||
| chr12:75303176 | A | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1581T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303176 | |||||||
| chr12:75303275 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.665+1482G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303275 | |||||||
| chr12:75303487 | G | A | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.665+1270C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303487 | |||||||
| chr12:75303616 | G | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1141C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303616 | |||||||
| chr12:75303659 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.665+1098C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303659 | |||||||
| chr12:75303720 | G | A | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+1037C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303720 | |||||||
| chr12:75303798 | C | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+959G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303798 | |||||||
| chr12:75303859 | G | A | 3 | a0001c0001t0003g0014 a0001c0001t0003g0150 a0001c0001t0003g0151 |
5 | HG01496.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+898C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303859 | |||||||
| chr12:75303877 | A | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+880T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303877 | |||||||
| chr12:75303951 | T | A | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.665+806A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75303951 | |||||||
| chr12:75304017 | C | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.665+740G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304017 | |||||||
| chr12:75304139 | T | G | 1 | a0002c0002t0001g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.665+618A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304139 | |||||||
| chr12:75304148 | A | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+609T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304148 | |||||||
| chr12:75304177 | G | A | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+580C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304177 | |||||||
| chr12:75304353 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0007g0128 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+404A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304353 | |||||||
| chr12:75304427 | T | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+330A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304427 | |||||||
| chr12:75304448 | A | G | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.665+309T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304448 | |||||||
| chr12:75304473 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.665+284C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304473 | |||||||
| chr12:75304514 | G | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+243C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304514 | |||||||
| chr12:75304515 | T | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+242A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304515 | |||||||
| chr12:75304551 | T | A | 2 | a0001c0001t0001g0149 a0001c0001t0007g0128 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+206A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304551 | |||||||
| chr12:75304552 | C | A | 2 | a0001c0001t0001g0149 a0001c0001t0007g0128 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.665+205G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304552 | |||||||
| chr12:75304614 | A | C | 13 | a0002c0002t0001g0004 a0002c0002t0001g0026 a0002c0002t0001g0175 others(10): Show |
17 | HG00558.hp1 NA18942.hp1 NA18954.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+143T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304614 | |||||||
| chr12:75304747 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.665+10T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 8/16 | chr12 | 75304747 | |||||||
| chr12:75305029 | T | C | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-153A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305029 | |||||||
| chr12:75305079 | C | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-203G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305079 | |||||||
| chr12:75305196 | C | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.546-320G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305196 | |||||||
| chr12:75305292 | G | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.546-416C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305292 | |||||||
| chr12:75305582 | C | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-706G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305582 | |||||||
| chr12:75305600 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.546-724G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305600 | |||||||
| chr12:75305607 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.546-731G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305607 | |||||||
| chr12:75305647 | C | T | 25 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(22): Show |
29 | HG00280.hp1 HG01168.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.546-771G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305647 | |||||||
| chr12:75305706 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546-830G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305706 | |||||||
| chr12:75305901 | C | T | 2 | a0001c0003t0002g0018 a0001c0003t0014g0059 |
3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.546-1025G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305901 | |||||||
| chr12:75305953 | CA | C | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-1078delT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305953 | |||||||
| chr12:75305984 | G | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-1108C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75305984 | |||||||
| chr12:75306144 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.546-1268G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306144 | |||||||
| chr12:75306316 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0087 others(2): Show |
6 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-1440G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306316 | |||||||
| chr12:75306322 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.546-1446G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306322 | |||||||
| chr12:75306883 | C | T | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-2007G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306883 | |||||||
| chr12:75306911 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.546-2035A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306911 | |||||||
| chr12:75306925 | A | C | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2049T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306925 | |||||||
| chr12:75306948 | C | G | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2072G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75306948 | |||||||
| chr12:75307125 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.546-2249C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307125 | |||||||
| chr12:75307158 | G | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-2282C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307158 | |||||||
| chr12:75307691 | G | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.546-2815C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307691 | |||||||
| chr12:75307995 | A | C | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.546-3119T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75307995 | |||||||
| chr12:75308065 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.546-3189G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308065 | |||||||
| chr12:75308333 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0119 |
3 | HG01255.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.546-3457C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308333 | |||||||
| chr12:75308380 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.546-3504G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308380 | |||||||
| chr12:75308466 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.546-3590A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308466 | |||||||
| chr12:75308496 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546-3620C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308496 | |||||||
| chr12:75308677 | G | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3801C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308677 | |||||||
| chr12:75308687 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0026g0222 |
2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.546-3811A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308687 | |||||||
| chr12:75308723 | T | C | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG02523.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.546-3847A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308723 | |||||||
| chr12:75308803 | A | G | 1 | a0001c0003t0001g0143 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.546-3927T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308803 | |||||||
| chr12:75308818 | T | TA | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3943_546-3942i others(3): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308818 | |||||||
| chr12:75308819 | T | A | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-3943A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308819 | |||||||
| chr12:75308830 | A | G | 1 | a0001c0001t0007g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.546-3954T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308830 | |||||||
| chr12:75308890 | G | A | 3 | a0001c0001t0004g0024 a0001c0001t0004g0166 a0001c0001t0004g0167 |
4 | HG01109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+3958C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308890 | |||||||
| chr12:75308902 | C | CA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(199): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.545+3945dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308902 | |||||||
| chr12:75308902 | C | CAA | 16 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0083 others(13): Show |
18 | HG01175.hp2 HG01361.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.545+3944_545+3945d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308902 | |||||||
| chr12:75308925 | G | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(223): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.545+3923C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308925 | |||||||
| chr12:75308930 | A | T | 7 | a0001c0003t0001g0143 a0001c0003t0002g0018 a0001c0003t0014g0059 others(4): Show |
8 | HG01243.hp1 HG02004.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+3918T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75308930 | |||||||
| chr12:75309077 | A | T | 2 | a0001c0003t0002g0018 a0001c0003t0014g0059 |
3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.545+3771T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309077 | |||||||
| chr12:75309218 | C | T | 1 | a0002c0002t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.545+3630G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309218 | |||||||
| chr12:75309789 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.545+3059G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309789 | |||||||
| chr12:75309805 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+3043C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75309805 | |||||||
| chr12:75310190 | G | T | 1 | a0002c0002t0001g0175 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.545+2658C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310190 | |||||||
| chr12:75310266 | C | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.545+2582G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310266 | |||||||
| chr12:75310284 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.545+2564C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310284 | |||||||
| chr12:75310371 | T | A | 1 | a0001c0001t0001g0039 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.545+2477A>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310371 | |||||||
| chr12:75310472 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.545+2376C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310472 | |||||||
| chr12:75310742 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+2106C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310742 | |||||||
| chr12:75310769 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.545+2079C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310769 | |||||||
| chr12:75310787 | G | C | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+2061C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310787 | |||||||
| chr12:75310834 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0261 |
2 | NA18991.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.545+2014T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310834 | |||||||
| chr12:75310969 | A | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.545+1879T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310969 | |||||||
| chr12:75310991 | G | A | 64 | a0001c0001t0001g0156 a0001c0001t0007g0152 a0001c0001t0007g0154 others(61): Show |
81 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.545+1857C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75310991 | |||||||
| chr12:75311086 | T | C | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.545+1762A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311086 | |||||||
| chr12:75311149 | G | T | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0013 others(2): Show |
7 | HG01069.hp2 HG01243.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+1699C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311149 | |||||||
| chr12:75311158 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.545+1690G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311158 | |||||||
| chr12:75311366 | A | G | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1482T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311366 | |||||||
| chr12:75311429 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | NA18944.hp1 NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.545+1419C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311429 | |||||||
| chr12:75311685 | C | A | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.545+1163G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311685 | |||||||
| chr12:75311699 | GGAAAAAA others(3): Show |
G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG02040.hp1 NA18942.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+1139_545+1148d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(4): Show |
G | 22 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0065 others(19): Show |
23 | HG00544.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.545+1138_545+1148d others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(5): Show |
G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.545+1137_545+1148d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(6): Show |
G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0087 a0001c0001t0001g0089 others(4): Show |
7 | HG01081.hp2 HG01256.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1136_545+1148d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(7): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.545+1135_545+1148d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(17): Show |
G | 1 | a0001c0003t0032g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.545+1125_545+1148d others(26): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(18): Show |
G | 1 | a0001c0003t0031g0292 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.545+1124_545+1148d others(27): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311699 | GGAAAAAA others(19): Show |
G | 2 | a0001c0003t0002g0018 a0001c0003t0014g0059 |
3 | HG02622.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.545+1123_545+1148d others(28): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311699 | |||||||
| chr12:75311700 | G | A | 2 | a0001c0001t0002g0275 a0001c0001t0004g0223 |
2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.545+1148C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | |||||||
| chr12:75311700 | G | GA | 8 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0038 others(5): Show |
9 | HG00673.hp1 HG02015.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.545+1147dupT | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | |||||||
| chr12:75311700 | G | GAA | 7 | a0001c0001t0001g0039 a0001c0001t0002g0016 a0001c0001t0002g0017 others(4): Show |
8 | HG02523.hp1 HG02683.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+1146_545+1147d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | |||||||
| chr12:75311700 | GAAAAAAA others(5): Show |
G | 1 | a0002c0002t0001g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.545+1136_545+1147d others(14): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311700 | |||||||
| chr12:75311701 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0170 a0001c0001t0010g0025 |
4 | HG02257.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1136_545+1146d others(13): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311701 | |||||||
| chr12:75311701 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0002g0253 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.545+1124_545+1146d others(25): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311701 | |||||||
| chr12:75311702 | AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0003g0260 a0001c0001t0004g0024 a0001c0001t0004g0147 others(2): Show |
5 | HG01109.hp1 HG01255.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+1136_545+1145d others(12): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311702 | |||||||
| chr12:75311702 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.545+1124_545+1145d others(24): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311702 | |||||||
| chr12:75311703 | A | G | 1 | a0002c0002t0001g0032 | 2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.545+1145T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311703 | |||||||
| chr12:75311703 | AAAAAAAA others(2): Show |
A | 27 | a0001c0001t0001g0134 a0001c0001t0001g0163 a0001c0001t0001g0169 others(24): Show |
28 | HG00280.hp1 HG01168.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.545+1136_545+1144d others(11): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311703 | |||||||
| chr12:75311704 | AAAAAAAA others(1): Show |
A | 14 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0003g0014 others(11): Show |
16 | HG01243.hp2 HG01361.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.545+1136_545+1143d others(10): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311704 | |||||||
| chr12:75311705 | AAAAAAAC | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0141 a0001c0001t0002g0142 others(2): Show |
7 | HG01069.hp2 HG02004.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+1136_545+1142d others(9): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311705 | |||||||
| chr12:75311705 | AAAAAAAC others(12): Show |
A | 1 | a0001c0001t0003g0255 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.545+1124_545+1142d others(21): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311705 | |||||||
| chr12:75311707 | AAAAACAA others(10): Show |
A | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(2): Show |
5 | HG00609.hp2 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1124_545+1140d others(19): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311707 | |||||||
| chr12:75311708 | AAAACAAA others(9): Show |
A | 26 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0033 others(23): Show |
40 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.545+1124_545+1139d others(18): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311708 | |||||||
| chr12:75311709 | AAACAAAA others(8): Show |
A | 11 | a0001c0001t0001g0234 a0001c0001t0002g0015 a0001c0001t0002g0231 others(8): Show |
11 | HG01106.hp1 HG01175.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.545+1124_545+1138d others(17): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311709 | |||||||
| chr12:75311710 | AACAAAAA others(7): Show |
A | 48 | a0001c0001t0001g0156 a0001c0001t0007g0152 a0001c0001t0007g0155 others(45): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.545+1124_545+1137d others(16): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311710 | |||||||
| chr12:75311711 | AC | A | 4 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0002g0256 others(1): Show |
4 | HG01099.hp1 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1136delG | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311711 | |||||||
| chr12:75311711 | ACAAAAAA others(6): Show |
A | 15 | a0001c0001t0004g0136 a0001c0001t0007g0154 a0001c0001t0007g0158 others(12): Show |
15 | HG00544.hp2 HG00621.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+1124_545+1136d others(15): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311711 | |||||||
| chr12:75311712 | C | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.545+1136G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311712 | |||||||
| chr12:75311720 | A | C | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.545+1128T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311720 | |||||||
| chr12:75311724 | C | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(180): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.545+1124G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311724 | |||||||
| chr12:75311761 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.545+1087C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311761 | |||||||
| chr12:75311796 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.545+1052C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311796 | |||||||
| chr12:75311801 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.545+1047G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311801 | |||||||
| chr12:75311935 | G | C | 1 | a0001c0003t0002g0018 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.545+913C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311935 | |||||||
| chr12:75311951 | G | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.545+897C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75311951 | |||||||
| chr12:75312349 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.545+499G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75312349 | |||||||
| chr12:75312573 | AT | A | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+274delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 7/16 | chr12 | 75312573 | |||||||
| chr12:75312940 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.478-25A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75312940 | |||||||
| chr12:75313017 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.478-102C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313017 | |||||||
| chr12:75313026 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.478-111T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313026 | |||||||
| chr12:75313127 | G | C | 1 | a0001c0001t0002g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478-212C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313127 | |||||||
| chr12:75313154 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0003g0041 |
3 | HG01070.hp2 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.478-239T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313154 | |||||||
| chr12:75313201 | T | G | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.478-286A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313201 | |||||||
| chr12:75313429 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.478-514T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313429 | |||||||
| chr12:75313616 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.478-701T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313616 | |||||||
| chr12:75313697 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.478-782A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75313697 | |||||||
| chr12:75314139 | C | T | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1224G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314139 | |||||||
| chr12:75314192 | C | T | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1277G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314192 | |||||||
| chr12:75314303 | T | C | 3 | a0001c0001t0001g0116 a0006c0009t0001g0070 a0006c0016t0001g0123 |
3 | NA18747.hp1 NA19079.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.478-1388A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314303 | |||||||
| chr12:75314357 | T | C | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.478-1442A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314357 | |||||||
| chr12:75314626 | AT | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.477+1685delA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314626 | |||||||
| chr12:75314728 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.477+1584G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314728 | |||||||
| chr12:75314812 | T | C | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+1500A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75314812 | |||||||
| chr12:75315110 | A | G | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477+1202T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315110 | |||||||
| chr12:75315290 | G | T | 7 | a0001c0001t0004g0044 a0001c0001t0004g0129 a0001c0001t0004g0282 others(4): Show |
9 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.477+1022C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315290 | |||||||
| chr12:75315378 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477+934G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315378 | |||||||
| chr12:75315687 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.477+625G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315687 | |||||||
| chr12:75315700 | T | C | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+612A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315700 | |||||||
| chr12:75315907 | T | TTGCTTCA | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.477+404_477+405ins others(7): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315907 | |||||||
| chr12:75315988 | C | T | 1 | a0001c0001t0026g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477+324G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75315988 | |||||||
| chr12:75316104 | C | A | 4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+208G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75316104 | |||||||
| chr12:75316224 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.477+88G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 6/16 | chr12 | 75316224 | |||||||
| chr12:75316479 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18612.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.355-45T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316479 | |||||||
| chr12:75316582 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.355-148T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316582 | |||||||
| chr12:75316607 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.355-173G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316607 | |||||||
| chr12:75316865 | A | G | 1 | a0002c0002t0015g0046 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.355-431T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316865 | |||||||
| chr12:75316941 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.355-507G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75316941 | |||||||
| chr12:75317082 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0117 |
4 | HG02040.hp1 NA18944.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-648A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317082 | |||||||
| chr12:75317133 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.355-699A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317133 | |||||||
| chr12:75317219 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0127 |
4 | HG01261.hp1 HG01358.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-785C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317219 | |||||||
| chr12:75317370 | C | T | 6 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(3): Show |
7 | HG01243.hp1 HG02056.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-936G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317370 | |||||||
| chr12:75317650 | T | C | 2 | a0001c0003t0031g0292 a0001c0003t0032g0293 |
2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.355-1216A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317650 | |||||||
| chr12:75317774 | T | C | 1 | a0002c0004t0001g0202 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.355-1340A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317774 | |||||||
| chr12:75317794 | CAT | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
8 | HG00544.hp1 HG01255.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-1362_355-1361d others(4): Show |
CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75317794 | |||||||
| chr12:75318006 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.355-1572G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318006 | |||||||
| chr12:75318220 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.355-1786C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318220 | |||||||
| chr12:75318341 | C | T | 1 | a0002c0002t0008g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355-1907G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318341 | |||||||
| chr12:75318390 | C | T | 1 | a0001c0003t0031g0292 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.355-1956G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318390 | |||||||
| chr12:75318440 | C | T | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0138 others(2): Show |
7 | HG01168.hp2 HG01361.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-2006G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318440 | |||||||
| chr12:75318766 | A | AT | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.355-2333dupA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318766 | |||||||
| chr12:75318797 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.355-2363A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318797 | |||||||
| chr12:75318882 | A | G | 63 | a0001c0001t0001g0156 a0001c0001t0007g0152 a0001c0001t0007g0154 others(60): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.355-2448T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75318882 | |||||||
| chr12:75319293 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+2107C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319293 | |||||||
| chr12:75319310 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.354+2090C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319310 | |||||||
| chr12:75319466 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.354+1934G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319466 | |||||||
| chr12:75319611 | G | A | 4 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(1): Show |
5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+1789C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319611 | |||||||
| chr12:75319676 | G | C | 1 | a0001c0001t0003g0173 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.354+1724C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319676 | |||||||
| chr12:75319720 | C | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+1680G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319720 | |||||||
| chr12:75319881 | T | C | 1 | a0001c0001t0026g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.354+1519A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75319881 | |||||||
| chr12:75320339 | C | A | 1 | a0001c0001t0004g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+1061G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320339 | |||||||
| chr12:75320548 | C | A | 31 | a0001c0001t0001g0039 a0001c0001t0002g0016 a0001c0001t0002g0017 others(28): Show |
40 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.354+852G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320548 | |||||||
| chr12:75320640 | T | C | 6 | a0002c0002t0001g0032 a0002c0002t0001g0204 a0002c0002t0001g0206 others(3): Show |
7 | HG00544.hp2 HG00621.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+760A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320640 | |||||||
| chr12:75320771 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.354+629A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320771 | |||||||
| chr12:75320883 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.354+517A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320883 | |||||||
| chr12:75320916 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0004g0135 a0001c0001t0004g0279 |
3 | HG01884.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.354+484G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75320916 | |||||||
| chr12:75321119 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.354+281G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75321119 | |||||||
| chr12:75321235 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354+165G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 5/16 | chr12 | 75321235 | |||||||
| chr12:75321778 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.178-202G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75321778 | |||||||
| chr12:75322066 | C | A | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.178-490G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322066 | |||||||
| chr12:75322183 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178-607T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322183 | |||||||
| chr12:75322304 | A | T | 2 | a0001c0001t0003g0150 a0001c0001t0003g0151 |
2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.178-728T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322304 | |||||||
| chr12:75322354 | C | T | 4 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(1): Show |
5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-778G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322354 | |||||||
| chr12:75322358 | C | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-782G>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322358 | |||||||
| chr12:75322498 | G | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.177+679C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322498 | |||||||
| chr12:75322532 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0007g0128 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.177+645G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322532 | |||||||
| chr12:75322586 | T | C | 1 | a0001c0001t0005g0273 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.177+591A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322586 | |||||||
| chr12:75322681 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+496T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322681 | |||||||
| chr12:75322822 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.177+355G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322822 | |||||||
| chr12:75322864 | T | C | 1 | a0001c0001t0004g0223 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.177+313A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 4/16 | chr12 | 75322864 | |||||||
| chr12:75323223 | C | A | 1 | a0001c0001t0007g0211 | 1 | HG03540.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.132-1G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323223 | |||||||
| chr12:75323231 | C | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(16): Show |
24 | HG00438.hp2 HG00735.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.132-9G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323231 | |||||||
| chr12:75323326 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.132-104A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323326 | |||||||
| chr12:75323330 | G | A | 1 | a0002c0002t0001g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132-108C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323330 | |||||||
| chr12:75323401 | A | T | 1 | a0001c0003t0014g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.132-179T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323401 | |||||||
| chr12:75323527 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.132-305A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323527 | |||||||
| chr12:75323542 | G | A | 3 | a0002c0002t0001g0214 a0003c0006t0016g0295 a0003c0006t0016g0296 |
3 | HG01074.hp2 HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.132-320C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323542 | |||||||
| chr12:75323572 | T | C | 4 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(1): Show |
5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-350A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323572 | |||||||
| chr12:75323699 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.132-477G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323699 | |||||||
| chr12:75323943 | A | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.132-721T>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75323943 | |||||||
| chr12:75324074 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.132-852A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324074 | |||||||
| chr12:75324162 | C | T | 1 | a0002c0002t0001g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132-940G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324162 | |||||||
| chr12:75324173 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | NA18951.hp2 NA18954.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.132-951A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324173 | |||||||
| chr12:75324506 | A | G | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.131+733T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324506 | |||||||
| chr12:75324512 | C | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.131+727G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324512 | |||||||
| chr12:75324643 | G | T | 28 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
34 | HG01069.hp2 HG01168.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.131+596C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 3/16 | chr12 | 75324643 | |||||||
| chr12:75325308 | T | C | 1 | a0002c0002t0001g0215 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.82-20A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325308 | |||||||
| chr12:75325622 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.82-334A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325622 | |||||||
| chr12:75325808 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.82-520C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325808 | |||||||
| chr12:75325904 | A | G | 70 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0062 others(67): Show |
94 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.81+514T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75325904 | |||||||
| chr12:75326051 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0021g0217 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.81+367A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75326051 | |||||||
| chr12:75326401 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+17T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 2/16 | chr12 | 75326401 | |||||||
| chr12:75326870 | G | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-343C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75326870 | |||||||
| chr12:75326907 | A | G | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-29-380T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75326907 | |||||||
| chr12:75327005 | G | C | 1 | a0005c0005t0002g0040 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-29-478C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327005 | |||||||
| chr12:75327007 | C | A | 1 | a0005c0005t0002g0040 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-29-480G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327007 | |||||||
| chr12:75327108 | C | A | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-29-581G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327108 | |||||||
| chr12:75327212 | G | A | 1 | a0002c0002t0028g0218 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-29-685C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327212 | |||||||
| chr12:75327255 | G | T | 7 | a0001c0001t0004g0044 a0001c0001t0004g0129 a0001c0001t0004g0282 others(4): Show |
9 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-728C>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327255 | |||||||
| chr12:75327339 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.-29-812T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327339 | |||||||
| chr12:75327443 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-916T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327443 | |||||||
| chr12:75327478 | C | T | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-29-951G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327478 | |||||||
| chr12:75327479 | C | T | 1 | a0001c0001t0007g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29-952G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327479 | |||||||
| chr12:75327553 | T | C | 4 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(1): Show |
5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-1026A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327553 | |||||||
| chr12:75327567 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.-29-1040A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327567 | |||||||
| chr12:75327769 | T | C | 1 | a0001c0003t0032g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-29-1242A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327769 | |||||||
| chr12:75327885 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.-29-1358T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327885 | |||||||
| chr12:75327919 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29-1392T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327919 | |||||||
| chr12:75327926 | T | C | 2 | a0003c0006t0016g0295 a0003c0006t0016g0296 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-29-1399A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75327926 | |||||||
| chr12:75328017 | G | A | 67 | a0001c0001t0001g0039 a0001c0001t0001g0226 a0001c0001t0001g0227 others(64): Show |
91 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-29-1490C>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328017 | |||||||
| chr12:75328060 | A | C | 1 | a0001c0001t0027g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-29-1533T>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328060 | |||||||
| chr12:75328141 | C | A | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-29-1614G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328141 | |||||||
| chr12:75328219 | C | T | 4 | a0001c0003t0002g0018 a0001c0003t0014g0059 a0001c0003t0031g0292 others(1): Show |
5 | HG02056.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1648G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328219 | |||||||
| chr12:75328521 | G | C | 1 | a0001c0001t0001g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-30+1346C>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328521 | |||||||
| chr12:75328527 | C | A | 1 | a0001c0001t0002g0275 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-30+1340G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328527 | |||||||
| chr12:75328591 | C | A | 1 | a0001c0001t0003g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-30+1276G>T | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328591 | |||||||
| chr12:75328668 | A | G | 2 | a0001c0003t0031g0292 a0001c0003t0032g0293 |
2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-30+1199T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328668 | |||||||
| chr12:75328876 | A | G | 2 | a0001c0003t0031g0292 a0001c0003t0032g0293 |
2 | HG02056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-30+991T>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328876 | |||||||
| chr12:75328881 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0277 a0001c0001t0002g0278 |
4 | NA18968.hp1 NA18974.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+986A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328881 | |||||||
| chr12:75328968 | T | C | 1 | a0001c0001t0004g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30+899A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328968 | |||||||
| chr12:75328985 | T | G | 2 | a0004c0007t0001g0280 a0004c0007t0001g0281 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-30+882A>C | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75328985 | |||||||
| chr12:75329245 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-30+622G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329245 | |||||||
| chr12:75329427 | T | C | 6 | a0001c0001t0004g0044 a0001c0001t0004g0282 a0001c0001t0004g0283 others(3): Show |
8 | HG02055.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30+440A>G | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329427 | |||||||
| chr12:75329475 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(10): Show |
17 | HG00438.hp2 HG00735.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30+392G>A | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329475 | |||||||
| chr12:75329485 | A | AT | 289 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-30+381dupA | CAPS2 | ENSG00000180881.21 | transcript | ENST00000699294.1 | protein_coding | 1/16 | chr12 | 75329485 |