Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 845 |
| ensemblid | ENSG00000118729.13 |
| hgncid | 1513 |
| symbol | CASQ2 |
| name | calsequestrin 2 |
| refseq_nuc | NM_001232.4 |
| refseq_prot | NP_001223.2 |
| ensembl_nuc | ENST00000261448.6 |
| ensembl_prot | ENSP00000261448.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 115700021 |
| end | 115768714 |
| strand | - |
| ver | v1.2 |
| region | chr1:115700021-115768714 |
| region5000 | chr1:115695021-115773714 |
| regionname0 | CASQ2_chr1_115700021_115768714 |
| regionname5000 | CASQ2_chr1_115695021_115773714 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 399 | 216 | 49 | 48 | 86 | 6 | 26 | 67 | CASQ2_chr1_115695021_115773714 | CASQ2 | MKRTH others(394): Show |
chr1 | 115695021 | 115773714 |
| a0002 | 0/1 | 399 | 119 | 32 | 10 | 62 | 4 | 10 | 43 | CASQ2_chr1_115695021_115773714 | CASQ2 | MKRTH others(394): Show |
chr1 | 115695021 | 115773714 |
| a0003 | 0/0 | 399 | 21 | 1 | 4 | 16 | 0 | 0 | 16 | CASQ2_chr1_115695021_115773714 | CASQ2 | MKRTH others(394): Show |
chr1 | 115695021 | 115773714 |
| a0004 | 0/0 | 399 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | MKRTH others(394): Show |
chr1 | 115695021 | 115773714 |
| a0005 | 0/0 | 399 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | MKRTH others(394): Show |
chr1 | 115695021 | 115773714 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1197 | 107 | 23 | 23 | 41 | 4 | 16 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0001c0002 | 1/0 | 1197 | 97 | 21 | 20 | 44 | 2 | 9 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0001c0006 | 0/0 | 1197 | 6 | 0 | 5 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0001c0007 | 0/0 | 1197 | 5 | 5 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0001c0010 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0002c0003 | 0/0 | 1197 | 64 | 19 | 5 | 33 | 2 | 5 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0002c0004 | 0/1 | 1197 | 54 | 12 | 5 | 29 | 2 | 5 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0002c0013 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0003c0005 | 0/0 | 1197 | 20 | 1 | 4 | 15 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0003c0012 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0004c0008 | 0/0 | 1197 | 5 | 5 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0005c0009 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 | ||
| a0005c0011 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | ATGAA others(1192): Show |
chr1 | 115695021 | 115773714 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2590 | 71 | 7 | 10 | 39 | 4 | 11 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0004 | 0/0 | 2593 | 10 | 5 | 3 | 1 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0005 | 0/0 | 2592 | 16 | 2 | 10 | 1 | 0 | 3 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0008 | 0/0 | 2590 | 5 | 5 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0014 | 0/0 | 2592 | 2 | 2 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0015 | 0/0 | 2590 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0019 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0001t0021 | 0/0 | 2590 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0001 | 0/0 | 2593 | 24 | 10 | 12 | 1 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0003 | 0/0 | 2593 | 66 | 8 | 8 | 41 | 2 | 7 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0006 | 0/0 | 2593 | 2 | 0 | 0 | 2 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0012 | 1/0 | 2593 | 3 | 2 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0013 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0002t0022 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0001c0006t0003 | 0/0 | 2593 | 6 | 0 | 5 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0007t0009 | 0/0 | 2593 | 4 | 4 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0001c0007t0020 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0001c0010t0003 | 0/0 | 2593 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0003t0001 | 0/0 | 2593 | 42 | 10 | 3 | 24 | 1 | 4 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0003t0003 | 0/0 | 2593 | 6 | 0 | 1 | 3 | 1 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0003t0006 | 0/0 | 2593 | 6 | 0 | 0 | 6 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0003t0007 | 0/0 | 2593 | 6 | 6 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0003t0010 | 0/0 | 2593 | 4 | 3 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0002 | 0/1 | 2590 | 21 | 4 | 4 | 6 | 2 | 4 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0004 | 0/0 | 2593 | 24 | 0 | 1 | 23 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0005 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0011 | 0/0 | 2593 | 4 | 4 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0015 | 0/0 | 2590 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0016 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0017 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2587): Show |
chr1 | 115695021 | 115773714 |
| a0002c0004t0018 | 0/0 | 2590 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2585): Show |
chr1 | 115695021 | 115773714 |
| a0002c0013t0009 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0003c0005t0001 | 0/0 | 2593 | 20 | 1 | 4 | 15 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0003c0012t0004 | 0/0 | 2593 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0004c0008t0001 | 0/0 | 2593 | 4 | 4 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0004c0008t0003 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0005c0009t0001 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0005c0009t0013 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| a0005c0011t0001 | 0/0 | 2593 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | AGAGC others(2588): Show |
chr1 | 115695021 | 115773714 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0014g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0015g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0001t0021g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0012g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0002t0022g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0006t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0007t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0007t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0007t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0007t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0007t0020g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0001c0010t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0006g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0010g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0003t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0017g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0004t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0002c0013t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0003c0012t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0004c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0004c0008t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0004c0008t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0004c0008t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0004c0008t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0005c0009t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0005c0009t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| a0005c0011t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0002 | c0004 | t0002 | g0266 | EUR | FIN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0209 | EUR | FIN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0288 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00438 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0341 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00558 | hp1 | a0002 | c0003 | t0006 | g0345 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0042 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00597 | hp2 | a0002 | c0004 | t0004 | g0325 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00609 | hp2 | a0002 | c0004 | t0004 | g0333 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0260 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00642 | hp2 | a0002 | c0004 | t0004 | g0283 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0039 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0342 | EAS | CHS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00735 | hp1 | a0002 | c0004 | t0002 | g0337 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0226 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01071 | hp2 | a0002 | c0004 | t0002 | g0306 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01106 | hp2 | a0001 | c0006 | t0003 | g0182 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0254 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01175 | hp1 | a0002 | c0003 | t0010 | g0012 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0350 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0225 | AMR | PUR | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0204 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01258 | hp2 | a0001 | c0006 | t0003 | g0168 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01261 | hp1 | a0002 | c0004 | t0002 | g0272 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01261 | hp2 | a0003 | c0005 | t0001 | g0246 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0299 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0045 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0287 | EUR | IBS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | IBS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0050 | EUR | IBS | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01884 | hp1 | a0002 | c0003 | t0010 | g0009 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01884 | hp2 | a0002 | c0004 | t0011 | g0015 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01891 | hp2 | a0002 | c0003 | t0010 | g0013 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01934 | hp1 | a0002 | c0004 | t0002 | g0279 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01943 | hp1 | a0001 | c0006 | t0003 | g0169 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01943 | hp2 | a0003 | c0005 | t0001 | g0251 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0145 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01981 | hp2 | a0001 | c0006 | t0003 | g0177 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02015 | hp1 | a0002 | c0003 | t0006 | g0354 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0338 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0265 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02071 | hp1 | a0002 | c0004 | t0004 | g0278 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0223 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0141 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02132 | hp1 | a0002 | c0004 | t0004 | g0329 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0164 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0301 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02145 | hp1 | a0001 | c0007 | t0009 | g0163 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0002 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02148 | hp1 | a0003 | c0005 | t0001 | g0250 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0348 | EAS | CDX | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | CDX | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | CDX | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | CDX | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02257 | hp1 | a0002 | c0003 | t0007 | g0017 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02258 | hp1 | a0001 | c0007 | t0020 | g0028 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0144 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02280 | hp1 | a0002 | c0004 | t0015 | g0320 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0330 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02293 | hp2 | a0001 | c0006 | t0003 | g0183 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02300 | hp1 | a0003 | c0005 | t0001 | g0241 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0197 | AMR | PEL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0002 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0231 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02523 | hp1 | a0002 | c0004 | t0002 | g0346 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02572 | hp1 | a0005 | c0009 | t0001 | g0060 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0148 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0057 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02615 | hp2 | a0004 | c0008 | t0001 | g0273 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02622 | hp2 | a0002 | c0004 | t0018 | g0022 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02630 | hp2 | a0002 | c0003 | t0007 | g0020 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02647 | hp2 | a0004 | c0008 | t0001 | g0311 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02698 | hp2 | a0001 | c0002 | t0022 | g0178 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02717 | hp1 | a0004 | c0008 | t0001 | g0355 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0343 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02723 | hp2 | a0002 | c0004 | t0011 | g0019 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02735 | hp1 | a0002 | c0004 | t0002 | g0271 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0049 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0255 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0307 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0270 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02818 | hp2 | a0002 | c0003 | t0007 | g0023 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0055 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0220 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02895 | hp1 | a0002 | c0004 | t0017 | g0016 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0027 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02922 | hp2 | a0002 | c0003 | t0007 | g0021 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02965 | hp1 | a0001 | c0007 | t0009 | g0180 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0158 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0263 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02970 | hp2 | a0002 | c0004 | t0011 | g0014 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0222 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03017 | hp1 | a0002 | c0004 | t0002 | g0323 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0212 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0291 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03041 | hp2 | a0005 | c0009 | t0013 | g0035 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03130 | hp1 | a0002 | c0004 | t0002 | g0259 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03139 | hp1 | a0002 | c0004 | t0011 | g0025 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0018 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0264 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0214 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0304 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03225 | hp2 | a0004 | c0008 | t0001 | g0308 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03239 | hp1 | a0002 | c0004 | t0002 | g0285 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03239 | hp2 | a0002 | c0004 | t0002 | g0256 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0298 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03486 | hp2 | a0002 | c0003 | t0007 | g0024 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0218 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03540 | hp1 | a0002 | c0004 | t0016 | g0010 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0228 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0339 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0077 | SAS | PJL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03834 | hp1 | a0001 | c0001 | t0021 | g0126 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03834 | hp2 | a0002 | c0004 | t0005 | g0318 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0048 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0211 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0321 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0284 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0151 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04184 | hp2 | a0001 | c0006 | t0003 | g0184 | SAS | BEB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0351 | SAS | STU | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18522 | hp2 | a0002 | c0003 | t0010 | g0011 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18612 | hp2 | a0002 | c0003 | t0006 | g0353 | EAS | CHB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0322 | EAS | CHB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | CHB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18939 | hp1 | a0003 | c0005 | t0001 | g0239 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18939 | hp2 | a0003 | c0012 | t0004 | g0243 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0349 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18946 | hp2 | a0002 | c0004 | t0004 | g0331 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18948 | hp2 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18949 | hp1 | a0003 | c0005 | t0001 | g0244 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18952 | hp2 | a0003 | c0005 | t0001 | g0006 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18961 | hp1 | a0002 | c0004 | t0004 | g0007 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18966 | hp2 | a0002 | c0003 | t0003 | g0257 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18968 | hp1 | a0002 | c0004 | t0004 | g0276 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18970 | hp2 | a0003 | c0005 | t0001 | g0238 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18971 | hp1 | a0002 | c0004 | t0004 | g0261 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18971 | hp2 | a0001 | c0010 | t0003 | g0208 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18981 | hp2 | a0003 | c0005 | t0001 | g0240 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18983 | hp2 | a0002 | c0004 | t0004 | g0332 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18984 | hp1 | a0002 | c0004 | t0004 | g0007 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18984 | hp2 | a0002 | c0003 | t0006 | g0314 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18986 | hp1 | a0002 | c0003 | t0006 | g0315 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18986 | hp2 | a0003 | c0005 | t0001 | g0247 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18988 | hp1 | a0002 | c0003 | t0006 | g0328 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18988 | hp2 | a0003 | c0005 | t0001 | g0252 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0347 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18991 | hp2 | a0002 | c0004 | t0004 | g0274 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0334 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0340 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18998 | hp2 | a0002 | c0004 | t0004 | g0292 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18999 | hp1 | a0002 | c0004 | t0004 | g0296 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19001 | hp1 | a0003 | c0005 | t0001 | g0234 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0335 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19004 | hp2 | a0002 | c0004 | t0004 | g0344 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19005 | hp1 | a0002 | c0004 | t0004 | g0269 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0237 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19006 | hp2 | a0003 | c0005 | t0001 | g0242 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19007 | hp1 | a0002 | c0004 | t0002 | g0316 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19030 | hp2 | a0005 | c0011 | t0001 | g0140 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0305 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19043 | hp2 | a0004 | c0008 | t0003 | g0352 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19054 | hp1 | a0003 | c0005 | t0001 | g0236 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19056 | hp1 | a0002 | c0004 | t0004 | g0277 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19057 | hp1 | a0002 | c0004 | t0002 | g0319 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19064 | hp1 | a0003 | c0005 | t0001 | g0235 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19066 | hp1 | a0002 | c0004 | t0002 | g0281 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19067 | hp1 | a0003 | c0005 | t0001 | g0006 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19068 | hp1 | a0002 | c0004 | t0004 | g0293 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19070 | hp2 | a0002 | c0004 | t0004 | g0008 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19074 | hp1 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19074 | hp2 | a0002 | c0004 | t0004 | g0282 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0327 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19078 | hp1 | a0002 | c0004 | t0002 | g0324 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19078 | hp2 | a0003 | c0005 | t0001 | g0248 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19080 | hp1 | a0002 | c0004 | t0002 | g0302 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19081 | hp1 | a0002 | c0004 | t0004 | g0310 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19084 | hp2 | a0002 | c0004 | t0004 | g0294 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19086 | hp2 | a0002 | c0004 | t0004 | g0295 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19091 | hp2 | a0002 | c0004 | t0004 | g0008 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0030 | AFR | YRI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20129 | hp1 | a0001 | c0007 | t0009 | g0179 | AFR | ASW | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20129 | hp2 | a0002 | c0004 | t0002 | g0336 | AFR | ASW | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20805 | hp1 | a0002 | c0004 | t0002 | g0290 | EUR | TSI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0289 | EUR | TSI | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0213 | SAS | GIH | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | GIH | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0317 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0205 | AMR | CLM | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02109 | hp2 | a0001 | c0002 | t0012 | g0033 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02486 | hp1 | a0002 | c0013 | t0009 | g0297 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0221 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02559 | hp1 | a0002 | c0004 | t0002 | g0253 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0173 | AFR | ACB | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0300 | AFR | MSL | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG06807 | hp1 | a0001 | c0002 | t0013 | g0032 | AFR | USA | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | USA | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | USA | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA20300 | hp2 | a0003 | c0005 | t0001 | g0245 | AFR | USA | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| NA21309 | hp2 | a0001 | c0007 | t0009 | g0053 | AFR | LWK | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0002 | g0275 | REF | REF | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0012 | g0034 | REF | REF | CASQ2_chr1_115695021_115773714 | CASQ2 | chr1 | 115695021 | 115773714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115726998 | T | C | 2 | a0004 a0005 |
8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
missense_variant | MODERATE | c.731A>G | p.His244Arg | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/11 | 904/2593 | 731/1200 | 244/399 | chr1 | 115726998 | |||
| chr1:115726999 | G | A | 1 | a0005 | 2 | HG02572.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.730C>T | p.His244Tyr | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/11 | 903/2593 | 730/1200 | 244/399 | chr1 | 115726999 | |||
| chr1:115768316 | C | T | 1 | a0003 | 21 | HG01261.hp2 HG01943.hp2 HG02148.hp1 others(18): Show |
missense_variant | MODERATE | c.226G>A | p.Val76Met | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/11 | 399/2593 | 226/1200 | 76/399 | chr1 | 115768316 | |||
| chr1:115768346 | T | C | 3 | a0002 a0003 a0004 |
144 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
missense_variant | MODERATE | c.196A>G | p.Thr66Ala | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/11 | 369/2593 | 196/1200 | 66/399 | chr1 | 115768346 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115701247 | A | G | 1 | a0001c0006 | 6 | HG01106.hp2 HG01258.hp2 HG01943.hp1 others(3): Show |
synonymous_variant | LOW | c.1194T>C | p.Asp398Asp | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 1367/2593 | 1194/1200 | 398/399 | chr1 | 115701247 | |||
| chr1:115701256 | G | A | 3 | a0001c0001 a0002c0004 a0003c0012 |
161 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(158): Show |
synonymous_variant | LOW | c.1185C>T | p.Asp395Asp | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 1358/2593 | 1185/1200 | 395/399 | chr1 | 115701256 | |||
| chr1:115702930 | A | G | 2 | a0001c0007 a0002c0013 |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.1005T>C | p.Asn335Asn | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/11 | 1178/2593 | 1005/1200 | 335/399 | chr1 | 115702930 | |||
| chr1:115725517 | A | G | 1 | a0001c0010 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.774T>C | p.Phe258Phe | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/11 | 947/2593 | 774/1200 | 258/399 | chr1 | 115725517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115700116 | CAT | C | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0015 others(4): Show |
100 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1123_*1124delAT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 1123 | chr1 | 115700116 | ||||||
| chr1:115700178 | A | G | 2 | a0001c0001t0015 a0002c0004t0015 |
2 | HG02280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1063T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 1063 | chr1 | 115700178 | ||||||
| chr1:115700223 | AT | A | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(11): Show |
123 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1017delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 1017 | chr1 | 115700223 | ||||||
| chr1:115700609 | C | G | 30 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(27): Show |
269 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 632 | chr1 | 115700609 | ||||||
| chr1:115700759 | G | A | 27 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(24): Show |
263 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*482C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 482 | chr1 | 115700759 | ||||||
| chr1:115700783 | C | T | 1 | a0001c0001t0021 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*458G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 458 | chr1 | 115700783 | ||||||
| chr1:115701098 | C | T | 2 | a0001c0002t0006 a0002c0003t0006 |
8 | HG00438.hp1 HG00558.hp1 HG02015.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 143 | chr1 | 115701098 | ||||||
| chr1:115701103 | A | G | 5 | a0001c0001t0004 a0001c0001t0019 a0002c0004t0004 others(2): Show |
40 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*138T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 11/11 | 138 | chr1 | 115701103 | ||||||
| chr1:115768562 | C | T | 2 | a0002c0003t0010 a0002c0004t0016 |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/11 | 21 | chr1 | 115768562 | ||||||
| chr1:115768577 | T | C | 32 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(29): Show |
349 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(346): Show |
5_prime_UTR_variant | MODIFIER | c.-36A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/11 | 36 | chr1 | 115768577 | ||||||
| chr1:115768678 | A | G | 6 | a0002c0003t0007 a0002c0003t0010 a0002c0004t0011 others(3): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-137T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/11 | 137 | chr1 | 115768678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115701518 | C | A | 1 | a0001c0002t0003g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1015-92G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701518 | |||||||
| chr1:115701545 | C | T | 86 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(83): Show |
87 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1015-119G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701545 | |||||||
| chr1:115701574 | C | T | 1 | a0001c0002t0003g0040 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1015-148G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701574 | |||||||
| chr1:115701677 | C | A | 99 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(96): Show |
100 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(97): Show |
intron_variant | MODIFIER | c.1015-251G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701677 | |||||||
| chr1:115701904 | T | G | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1015-478A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701904 | |||||||
| chr1:115701929 | A | AT | 100 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(97): Show |
101 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.1015-504dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701929 | |||||||
| chr1:115701985 | T | C | 90 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(87): Show |
92 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1015-559A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701985 | |||||||
| chr1:115701986 | G | A | 1 | a0002c0003t0001g0309 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1015-560C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115701986 | |||||||
| chr1:115702372 | T | G | 1 | a0001c0001t0002g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1014+549A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702372 | |||||||
| chr1:115702386 | G | A | 4 | a0002c0003t0001g0260 a0002c0003t0001g0267 a0002c0003t0001g0268 others(1): Show |
4 | HG00621.hp2 NA18982.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+535C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702386 | |||||||
| chr1:115702529 | C | T | 148 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(145): Show |
154 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.1014+392G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702529 | |||||||
| chr1:115702620 | C | T | 241 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(238): Show |
247 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1014+301G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702620 | |||||||
| chr1:115702720 | C | T | 1 | a0001c0001t0005g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014+201G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702720 | |||||||
| chr1:115702741 | C | T | 7 | a0001c0002t0003g0057 a0002c0003t0007g0023 a0002c0003t0007g0024 others(4): Show |
7 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014+180G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702741 | |||||||
| chr1:115702760 | G | T | 52 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(49): Show |
54 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1014+161C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702760 | |||||||
| chr1:115702912 | G | A | 6 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+9C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 10/10 | chr1 | 115702912 | |||||||
| chr1:115703034 | G | C | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.940-39C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703034 | |||||||
| chr1:115703055 | C | A | 6 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-60G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703055 | |||||||
| chr1:115703139 | TG | T | 7 | a0001c0002t0006g0043 a0001c0002t0006g0229 a0002c0003t0006g0314 others(4): Show |
7 | HG00438.hp1 HG00558.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-145delC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703139 | |||||||
| chr1:115703188 | C | T | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.940-193G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703188 | |||||||
| chr1:115703278 | T | C | 148 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(145): Show |
152 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.940-283A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703278 | |||||||
| chr1:115703457 | G | A | 148 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(145): Show |
152 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.940-462C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703457 | |||||||
| chr1:115703501 | A | G | 148 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(145): Show |
152 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.940-506T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703501 | |||||||
| chr1:115703532 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.940-537G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703532 | |||||||
| chr1:115703627 | C | T | 9 | a0001c0002t0003g0038 a0001c0002t0003g0091 a0001c0002t0003g0199 others(6): Show |
9 | HG00597.hp1 HG02015.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.940-632G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703627 | |||||||
| chr1:115703629 | T | A | 153 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(150): Show |
158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.940-634A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703629 | |||||||
| chr1:115703650 | C | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0165 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.940-655G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703650 | |||||||
| chr1:115703683 | A | G | 1 | a0001c0001t0008g0029 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.940-688T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703683 | |||||||
| chr1:115703911 | CA | C | 128 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(125): Show |
133 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.940-917delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703911 | |||||||
| chr1:115703922 | A | C | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.940-927T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703922 | |||||||
| chr1:115703923 | A | C | 1 | a0001c0002t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.940-928T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703923 | |||||||
| chr1:115703923 | AC | A | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.940-929delG | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703923 | |||||||
| chr1:115703924 | C | A | 1 | a0001c0002t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.940-929G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115703924 | |||||||
| chr1:115704053 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.940-1058G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704053 | |||||||
| chr1:115704057 | G | A | 89 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(86): Show |
90 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.940-1062C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704057 | |||||||
| chr1:115704131 | C | T | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.939+1061G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704131 | |||||||
| chr1:115704170 | C | A | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.939+1022G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704170 | |||||||
| chr1:115704212 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.939+980T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704212 | |||||||
| chr1:115704229 | T | C | 5 | a0001c0002t0006g0043 a0001c0002t0006g0229 a0002c0003t0006g0314 others(2): Show |
5 | HG00438.hp1 HG00558.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+963A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704229 | |||||||
| chr1:115704261 | C | T | 1 | a0002c0004t0017g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.939+931G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704261 | |||||||
| chr1:115704429 | A | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(88): Show |
92 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(89): Show |
intron_variant | MODIFIER | c.939+763T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704429 | |||||||
| chr1:115704501 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.939+691C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704501 | |||||||
| chr1:115704643 | C | T | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.939+549G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704643 | |||||||
| chr1:115704696 | A | G | 1 | a0002c0004t0018g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+496T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704696 | |||||||
| chr1:115704702 | C | T | 1 | a0002c0003t0001g0335 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.939+490G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704702 | |||||||
| chr1:115704800 | T | A | 1 | a0001c0002t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+392A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704800 | |||||||
| chr1:115704845 | C | T | 245 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(242): Show |
251 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.939+347G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704845 | |||||||
| chr1:115704846 | G | A | 1 | a0001c0002t0003g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.939+346C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704846 | |||||||
| chr1:115704848 | T | C | 7 | a0001c0001t0005g0001 a0001c0001t0005g0142 a0001c0001t0005g0143 others(4): Show |
9 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.939+344A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704848 | |||||||
| chr1:115704914 | G | C | 154 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(151): Show |
159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.939+278C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704914 | |||||||
| chr1:115704924 | C | T | 6 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0002c0004t0002g0253 others(3): Show |
6 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+268G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704924 | |||||||
| chr1:115704936 | C | A | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.939+256G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704936 | |||||||
| chr1:115704936 | C | G | 154 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(151): Show |
159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.939+256G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115704936 | |||||||
| chr1:115705002 | C | T | 2 | a0002c0004t0002g0279 a0002c0004t0002g0285 |
2 | HG01934.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.939+190G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115705002 | |||||||
| chr1:115705060 | C | A | 6 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+132G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115705060 | |||||||
| chr1:115705077 | G | A | 1 | a0002c0003t0001g0326 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.939+115C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115705077 | |||||||
| chr1:115705107 | T | C | 1 | a0001c0006t0003g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.939+85A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115705107 | |||||||
| chr1:115705169 | G | A | 153 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(150): Show |
158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.939+23C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 9/10 | chr1 | 115705169 | |||||||
| chr1:115705456 | G | C | 1 | a0001c0002t0001g0156 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.839-164C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705456 | |||||||
| chr1:115705545 | C | T | 3 | a0001c0001t0005g0162 a0001c0001t0005g0165 a0002c0004t0016g0010 |
3 | HG01891.hp1 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.839-253G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705545 | |||||||
| chr1:115705595 | C | T | 1 | a0002c0003t0001g0267 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.839-303G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705595 | |||||||
| chr1:115705632 | A | G | 1 | a0002c0004t0002g0302 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.839-340T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705632 | |||||||
| chr1:115705648 | G | A | 1 | a0001c0002t0003g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.839-356C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705648 | |||||||
| chr1:115705930 | G | C | 1 | a0001c0002t0013g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.839-638C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705930 | |||||||
| chr1:115705969 | C | T | 153 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(150): Show |
158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.839-677G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115705969 | |||||||
| chr1:115706084 | A | G | 2 | a0001c0002t0003g0160 a0001c0002t0003g0161 |
2 | NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.839-792T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706084 | |||||||
| chr1:115706131 | T | C | 153 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(150): Show |
158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.839-839A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706131 | |||||||
| chr1:115706175 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0005g0151 |
2 | HG01978.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.839-883G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706175 | |||||||
| chr1:115706176 | G | A | 1 | a0002c0003t0001g0322 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.839-884C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706176 | |||||||
| chr1:115706195 | CGT | C | 3 | a0002c0003t0001g0263 a0002c0003t0001g0264 a0002c0003t0001g0330 |
3 | HG02280.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.839-905_839-904del others(2): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706195 | |||||||
| chr1:115706482 | A | C | 155 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0002g0233 others(152): Show |
160 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.839-1190T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706482 | |||||||
| chr1:115706520 | A | T | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.839-1228T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706520 | |||||||
| chr1:115706595 | A | G | 1 | a0001c0002t0003g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.839-1303T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706595 | |||||||
| chr1:115706602 | G | T | 1 | a0002c0003t0001g0339 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.839-1310C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706602 | |||||||
| chr1:115706637 | T | C | 3 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 |
3 | HG02257.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.839-1345A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706637 | |||||||
| chr1:115706741 | G | T | 5 | a0001c0002t0003g0201 a0001c0002t0003g0207 a0001c0002t0003g0224 others(2): Show |
5 | HG00597.hp1 HG02015.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1449C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706741 | |||||||
| chr1:115706766 | TC | T | 7 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0008g0026 others(4): Show |
7 | HG01934.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.839-1475delG | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115706766 | |||||||
| chr1:115707036 | C | CT | 170 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(167): Show |
173 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.839-1745dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707036 | |||||||
| chr1:115707084 | A | G | 1 | a0002c0004t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.839-1792T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707084 | |||||||
| chr1:115707093 | A | T | 155 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0002g0233 others(152): Show |
160 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.839-1801T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707093 | |||||||
| chr1:115707120 | G | C | 151 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(148): Show |
156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.839-1828C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707120 | |||||||
| chr1:115707222 | G | T | 2 | a0001c0001t0002g0233 a0001c0001t0008g0031 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.839-1930C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707222 | |||||||
| chr1:115707381 | C | G | 258 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(255): Show |
264 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(261): Show |
intron_variant | MODIFIER | c.839-2089G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707381 | |||||||
| chr1:115707431 | C | G | 4 | a0001c0002t0003g0141 a0001c0002t0003g0170 a0001c0002t0003g0181 others(1): Show |
4 | HG02071.hp2 HG02129.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.839-2139G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707431 | |||||||
| chr1:115707438 | C | T | 14 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0008g0026 others(11): Show |
14 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.839-2146G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707438 | |||||||
| chr1:115707439 | G | A | 6 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-2147C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707439 | |||||||
| chr1:115707557 | C | T | 152 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(149): Show |
157 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.839-2265G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707557 | |||||||
| chr1:115707623 | G | A | 4 | a0001c0002t0003g0005 a0001c0002t0003g0087 a0001c0002t0003g0196 others(1): Show |
5 | NA18943.hp2 NA18950.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-2331C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707623 | |||||||
| chr1:115707650 | T | A | 1 | a0001c0001t0002g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.839-2358A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707650 | |||||||
| chr1:115707689 | G | A | 7 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0008g0026 others(4): Show |
7 | HG01934.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.839-2397C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707689 | |||||||
| chr1:115707967 | C | G | 5 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-2675G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707967 | |||||||
| chr1:115707991 | C | T | 65 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(62): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.839-2699G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115707991 | |||||||
| chr1:115708048 | G | A | 1 | a0001c0002t0003g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.839-2756C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708048 | |||||||
| chr1:115708051 | A | C | 1 | a0001c0002t0003g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.839-2759T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708051 | |||||||
| chr1:115708078 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.839-2786G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708078 | |||||||
| chr1:115708187 | T | A | 1 | a0001c0002t0003g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.839-2895A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708187 | |||||||
| chr1:115708207 | C | A | 42 | a0001c0001t0004g0059 a0001c0001t0004g0062 a0001c0001t0004g0063 others(39): Show |
44 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.839-2915G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708207 | |||||||
| chr1:115708304 | G | A | 42 | a0001c0001t0004g0059 a0001c0001t0004g0062 a0001c0001t0004g0063 others(39): Show |
44 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.839-3012C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708304 | |||||||
| chr1:115708402 | A | G | 152 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(149): Show |
157 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.839-3110T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708402 | |||||||
| chr1:115708423 | G | A | 3 | a0002c0003t0001g0300 a0002c0003t0001g0304 a0002c0003t0001g0343 |
3 | HG02717.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.839-3131C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708423 | |||||||
| chr1:115708451 | A | C | 258 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(255): Show |
264 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(261): Show |
intron_variant | MODIFIER | c.839-3159T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708451 | |||||||
| chr1:115708529 | G | C | 93 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(90): Show |
94 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-3237C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708529 | |||||||
| chr1:115708531 | G | A | 150 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(147): Show |
155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.839-3239C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708531 | |||||||
| chr1:115708675 | A | G | 93 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(90): Show |
94 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.839-3383T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708675 | |||||||
| chr1:115708904 | G | A | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0217 |
3 | HG02258.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.839-3612C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708904 | |||||||
| chr1:115708930 | T | C | 1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.839-3638A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115708930 | |||||||
| chr1:115709192 | AT | A | 244 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(241): Show |
250 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.839-3901delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709192 | |||||||
| chr1:115709203 | A | G | 6 | a0001c0007t0009g0053 a0001c0007t0009g0163 a0001c0007t0009g0179 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-3911T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709203 | |||||||
| chr1:115709238 | C | T | 140 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(137): Show |
145 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.839-3946G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709238 | |||||||
| chr1:115709258 | T | G | 93 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0008g0026 others(90): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.839-3966A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709258 | |||||||
| chr1:115709305 | C | A | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(89): Show |
93 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(90): Show |
intron_variant | MODIFIER | c.839-4013G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709305 | |||||||
| chr1:115709444 | G | A | 1 | a0003c0005t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.839-4152C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709444 | |||||||
| chr1:115709458 | A | G | 152 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0004g0059 others(149): Show |
157 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.839-4166T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709458 | |||||||
| chr1:115709465 | A | G | 1 | a0001c0001t0005g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.839-4173T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709465 | |||||||
| chr1:115709486 | A | C | 43 | a0001c0001t0004g0059 a0001c0001t0004g0062 a0001c0001t0004g0063 others(40): Show |
45 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.839-4194T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709486 | |||||||
| chr1:115709510 | A | T | 2 | a0002c0003t0001g0305 a0002c0003t0001g0307 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.839-4218T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709510 | |||||||
| chr1:115709628 | A | T | 1 | a0001c0002t0003g0197 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.839-4336T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709628 | |||||||
| chr1:115709691 | A | T | 88 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(85): Show |
90 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.839-4399T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709691 | |||||||
| chr1:115709703 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.839-4411C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709703 | |||||||
| chr1:115709822 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.839-4530A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115709822 | |||||||
| chr1:115710007 | A | AT | 7 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0002t0003g0057 others(4): Show |
7 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-4716dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710007 | |||||||
| chr1:115710036 | G | A | 7 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0002t0003g0057 others(4): Show |
7 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-4744C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710036 | |||||||
| chr1:115710180 | T | A | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-4888A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710180 | |||||||
| chr1:115710224 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.839-4932T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710224 | |||||||
| chr1:115710252 | A | T | 1 | a0002c0003t0007g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.839-4960T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710252 | |||||||
| chr1:115710315 | G | C | 1 | a0001c0002t0003g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.839-5023C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710315 | |||||||
| chr1:115710454 | T | C | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.839-5162A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710454 | |||||||
| chr1:115710515 | G | A | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-5223C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710515 | |||||||
| chr1:115710535 | G | A | 6 | a0001c0001t0002g0004 a0001c0001t0002g0092 a0001c0001t0002g0093 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-5243C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710535 | |||||||
| chr1:115710653 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.839-5361C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710653 | |||||||
| chr1:115710721 | C | A | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.839-5429G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710721 | |||||||
| chr1:115710788 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.839-5496G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710788 | |||||||
| chr1:115710864 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.839-5572C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710864 | |||||||
| chr1:115710974 | C | T | 1 | a0002c0003t0001g0288 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.839-5682G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115710974 | |||||||
| chr1:115711020 | G | A | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.839-5728C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711020 | |||||||
| chr1:115711047 | G | C | 103 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(100): Show |
104 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.839-5755C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711047 | |||||||
| chr1:115711127 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.839-5835C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711127 | |||||||
| chr1:115711140 | C | T | 1 | a0001c0002t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.839-5848G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711140 | |||||||
| chr1:115711325 | C | T | 2 | a0001c0002t0003g0170 a0001c0002t0003g0185 |
2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.839-6033G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711325 | |||||||
| chr1:115711364 | T | G | 1 | a0001c0001t0005g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.839-6072A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711364 | |||||||
| chr1:115711441 | G | A | 1 | a0002c0004t0017g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.839-6149C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711441 | |||||||
| chr1:115711591 | A | AG | 7 | a0001c0001t0002g0071 a0001c0001t0002g0119 a0001c0001t0014g0002 others(4): Show |
8 | HG01978.hp2 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+6248dupC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711591 | |||||||
| chr1:115711592 | G | GGT | 182 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(179): Show |
185 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.838+6247_838+6248i others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711592 | |||||||
| chr1:115711592 | G | GGTT | 47 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0065 others(44): Show |
49 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.838+6247_838+6248i others(5): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711592 | |||||||
| chr1:115711592 | G | GGTTT | 4 | a0002c0004t0004g0269 a0002c0004t0004g0274 a0002c0004t0004g0295 others(1): Show |
4 | HG02622.hp2 NA18991.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+6247_838+6248i others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711592 | |||||||
| chr1:115711593 | A | T | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.838+6247T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711593 | |||||||
| chr1:115711593 | AT | A | 12 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0036 others(9): Show |
12 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.838+6246delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711593 | |||||||
| chr1:115711624 | G | A | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.838+6216C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711624 | |||||||
| chr1:115711683 | C | T | 5 | a0001c0002t0003g0160 a0001c0002t0003g0161 a0001c0002t0003g0186 others(2): Show |
5 | NA18949.hp2 NA18951.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+6157G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711683 | |||||||
| chr1:115711811 | T | C | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.838+6029A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711811 | |||||||
| chr1:115711932 | G | T | 239 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(236): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.838+5908C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711932 | |||||||
| chr1:115711992 | C | A | 2 | a0001c0002t0003g0160 a0001c0002t0003g0161 |
2 | NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.838+5848G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115711992 | |||||||
| chr1:115712077 | A | G | 226 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(223): Show |
232 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.838+5763T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712077 | |||||||
| chr1:115712120 | C | T | 226 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(223): Show |
232 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.838+5720G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712120 | |||||||
| chr1:115712125 | T | C | 12 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0036 others(9): Show |
12 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.838+5715A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712125 | |||||||
| chr1:115712155 | G | A | 1 | a0003c0005t0001g0239 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.838+5685C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712155 | |||||||
| chr1:115712430 | C | T | 12 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0036 others(9): Show |
12 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.838+5410G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712430 | |||||||
| chr1:115712508 | C | T | 246 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(243): Show |
252 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.838+5332G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712508 | |||||||
| chr1:115712569 | G | A | 1 | a0001c0001t0005g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.838+5271C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712569 | |||||||
| chr1:115712630 | A | G | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+5210T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712630 | |||||||
| chr1:115712672 | C | T | 9 | a0002c0003t0001g0305 a0002c0003t0001g0307 a0004c0008t0001g0273 others(6): Show |
9 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.838+5168G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712672 | |||||||
| chr1:115712691 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.838+5149T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712691 | |||||||
| chr1:115712788 | G | A | 19 | a0003c0005t0001g0006 a0003c0005t0001g0234 a0003c0005t0001g0235 others(16): Show |
20 | HG01261.hp2 HG01943.hp2 HG02148.hp1 others(17): Show |
intron_variant | MODIFIER | c.838+5052C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712788 | |||||||
| chr1:115712830 | T | A | 1 | a0002c0004t0011g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.838+5010A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712830 | |||||||
| chr1:115712850 | C | T | 226 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(223): Show |
232 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.838+4990G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712850 | |||||||
| chr1:115712853 | C | CA | 12 | a0001c0001t0002g0052 a0001c0001t0008g0029 a0001c0001t0008g0031 others(9): Show |
12 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.838+4986dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712853 | |||||||
| chr1:115712853 | C | CAA | 8 | a0001c0001t0002g0233 a0001c0002t0012g0030 a0001c0002t0012g0033 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+4985_838+4986d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712853 | |||||||
| chr1:115712853 | CA | C | 7 | a0001c0001t0002g0061 a0001c0001t0004g0059 a0001c0002t0003g0057 others(4): Show |
7 | HG01934.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.838+4986delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712853 | |||||||
| chr1:115712867 | AAG | A | 22 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0065 others(19): Show |
22 | HG00323.hp1 HG00673.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+4971_838+4972d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712867 | |||||||
| chr1:115712868 | AG | A | 196 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(193): Show |
202 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.838+4971delC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712868 | |||||||
| chr1:115712869 | G | A | 14 | a0001c0001t0002g0104 a0001c0001t0002g0233 a0001c0001t0008g0029 others(11): Show |
14 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.838+4971C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712869 | |||||||
| chr1:115712972 | G | A | 2 | a0002c0003t0001g0305 a0002c0003t0001g0307 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.838+4868C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115712972 | |||||||
| chr1:115713201 | T | C | 1 | a0002c0003t0007g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.838+4639A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713201 | |||||||
| chr1:115713383 | A | G | 246 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(243): Show |
252 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.838+4457T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713383 | |||||||
| chr1:115713387 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0117 |
2 | NA18979.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.838+4453C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713387 | |||||||
| chr1:115713735 | C | T | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.838+4105G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713735 | |||||||
| chr1:115713806 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.838+4034C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713806 | |||||||
| chr1:115713864 | G | A | 3 | a0002c0003t0007g0020 a0002c0004t0011g0015 a0002c0004t0011g0025 |
3 | HG01884.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.838+3976C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713864 | |||||||
| chr1:115713874 | T | C | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+3966A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713874 | |||||||
| chr1:115713916 | C | T | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.838+3924G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713916 | |||||||
| chr1:115713927 | G | A | 6 | a0002c0004t0002g0256 a0002c0004t0002g0266 a0002c0004t0002g0270 others(3): Show |
6 | HG00323.hp1 HG01071.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+3913C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115713927 | |||||||
| chr1:115714224 | T | G | 89 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(86): Show |
91 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.838+3616A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714224 | |||||||
| chr1:115714251 | A | G | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.838+3589T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714251 | |||||||
| chr1:115714531 | T | C | 240 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(237): Show |
246 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.838+3309A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714531 | |||||||
| chr1:115714564 | T | A | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.838+3276A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714564 | |||||||
| chr1:115714682 | T | C | 226 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(223): Show |
232 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.838+3158A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714682 | |||||||
| chr1:115714988 | A | G | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.838+2852T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115714988 | |||||||
| chr1:115715008 | T | G | 2 | a0005c0009t0001g0060 a0005c0009t0013g0035 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.838+2832A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715008 | |||||||
| chr1:115715222 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.838+2618A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715222 | |||||||
| chr1:115715270 | C | T | 230 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(227): Show |
236 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.838+2570G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715270 | |||||||
| chr1:115715280 | G | A | 1 | a0003c0005t0001g0247 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.838+2560C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715280 | |||||||
| chr1:115715321 | G | A | 1 | a0001c0002t0003g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.838+2519C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715321 | |||||||
| chr1:115715328 | C | T | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+2512G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715328 | |||||||
| chr1:115715380 | G | A | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.838+2460C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715380 | |||||||
| chr1:115715383 | C | T | 3 | a0002c0004t0004g0007 a0002c0004t0004g0274 a0002c0004t0004g0292 |
4 | NA18961.hp1 NA18984.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+2457G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715383 | |||||||
| chr1:115715801 | T | C | 1 | a0002c0004t0017g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.838+2039A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715801 | |||||||
| chr1:115715889 | G | A | 1 | a0002c0004t0002g0346 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.838+1951C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715889 | |||||||
| chr1:115715935 | C | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.838+1905G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115715935 | |||||||
| chr1:115716006 | G | A | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.838+1834C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716006 | |||||||
| chr1:115716025 | A | C | 100 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(97): Show |
101 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.838+1815T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716025 | |||||||
| chr1:115716297 | G | T | 3 | a0001c0001t0002g0094 a0001c0001t0002g0110 a0001c0001t0002g0123 |
3 | HG02129.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.838+1543C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716297 | |||||||
| chr1:115716441 | T | C | 245 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(242): Show |
251 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.838+1399A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716441 | |||||||
| chr1:115716708 | A | G | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+1132T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716708 | |||||||
| chr1:115716718 | G | A | 239 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(236): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.838+1122C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716718 | |||||||
| chr1:115716758 | C | T | 8 | a0001c0002t0003g0091 a0001c0002t0003g0199 a0001c0002t0003g0201 others(5): Show |
8 | HG00597.hp1 HG02015.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+1082G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716758 | |||||||
| chr1:115716800 | T | C | 3 | a0002c0003t0007g0020 a0002c0004t0011g0015 a0002c0004t0011g0025 |
3 | HG01884.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.838+1040A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716800 | |||||||
| chr1:115716807 | C | A | 83 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(80): Show |
84 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.838+1033G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716807 | |||||||
| chr1:115716851 | T | C | 14 | a0001c0001t0002g0052 a0001c0001t0002g0233 a0001c0001t0008g0029 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.838+989A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716851 | |||||||
| chr1:115716978 | G | A | 232 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(229): Show |
238 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.838+862C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115716978 | |||||||
| chr1:115717042 | A | C | 3 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG00741.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+798T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717042 | |||||||
| chr1:115717092 | G | A | 239 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(236): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.838+748C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717092 | |||||||
| chr1:115717153 | A | G | 1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.838+687T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717153 | |||||||
| chr1:115717262 | T | G | 1 | a0001c0010t0003g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.838+578A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717262 | |||||||
| chr1:115717439 | C | T | 1 | a0001c0001t0005g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.838+401G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717439 | |||||||
| chr1:115717445 | C | G | 239 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(236): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.838+395G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717445 | |||||||
| chr1:115717573 | CACTG | C | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+263_838+266del others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717573 | |||||||
| chr1:115717613 | A | G | 1 | a0002c0004t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.838+227T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717613 | |||||||
| chr1:115717651 | C | T | 1 | a0002c0004t0016g0010 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.838+189G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717651 | |||||||
| chr1:115717669 | G | A | 1 | a0001c0002t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.838+171C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717669 | |||||||
| chr1:115717839 | C | T | 1 | a0002c0003t0006g0315 | 1 | NA18986.hp1 | splice_donor_variant&intron_variant | HIGH | c.838+1G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 8/10 | chr1 | 115717839 | |||||||
| chr1:115717911 | A | T | 245 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(242): Show |
251 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.784-17T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115717911 | |||||||
| chr1:115717923 | C | T | 99 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(96): Show |
100 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(97): Show |
intron_variant | MODIFIER | c.784-29G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115717923 | |||||||
| chr1:115717946 | G | A | 1 | a0002c0003t0006g0328 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.784-52C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115717946 | |||||||
| chr1:115717949 | T | C | 4 | a0001c0001t0005g0162 a0001c0001t0014g0002 a0002c0004t0016g0010 others(1): Show |
5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-55A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115717949 | |||||||
| chr1:115717983 | G | A | 239 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(236): Show |
245 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.784-89C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115717983 | |||||||
| chr1:115718386 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0008g0031 |
2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.784-492C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115718386 | |||||||
| chr1:115718554 | G | T | 227 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(224): Show |
232 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.784-660C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115718554 | |||||||
| chr1:115718647 | G | T | 1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-753C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115718647 | |||||||
| chr1:115718793 | C | G | 3 | a0001c0001t0002g0061 a0001c0002t0003g0057 a0002c0004t0002g0259 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.784-899G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115718793 | |||||||
| chr1:115719158 | T | C | 1 | a0001c0001t0004g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.784-1264A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115719158 | |||||||
| chr1:115719275 | T | TC | 247 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(244): Show |
253 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.784-1382dupG | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115719275 | |||||||
| chr1:115719277 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.784-1383C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115719277 | |||||||
| chr1:115719358 | C | T | 1 | a0001c0002t0003g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.784-1464G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115719358 | |||||||
| chr1:115720225 | T | C | 11 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0036 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.784-2331A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720225 | |||||||
| chr1:115720248 | C | T | 1 | a0002c0003t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.784-2354G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720248 | |||||||
| chr1:115720276 | C | T | 14 | a0001c0001t0002g0052 a0001c0001t0002g0233 a0001c0001t0008g0029 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.784-2382G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720276 | |||||||
| chr1:115720295 | T | G | 191 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(188): Show |
194 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.784-2401A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720295 | |||||||
| chr1:115720306 | T | A | 7 | a0001c0001t0005g0165 a0001c0002t0003g0214 a0001c0002t0003g0220 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-2412A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720306 | |||||||
| chr1:115720409 | G | A | 1 | a0002c0003t0001g0309 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.784-2515C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720409 | |||||||
| chr1:115720549 | C | A | 30 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(27): Show |
32 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.784-2655G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720549 | |||||||
| chr1:115720680 | C | T | 1 | a0002c0004t0017g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-2786G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720680 | |||||||
| chr1:115720693 | C | A | 3 | a0001c0001t0002g0061 a0001c0002t0003g0057 a0002c0004t0002g0259 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.784-2799G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720693 | |||||||
| chr1:115720709 | C | T | 1 | a0001c0002t0003g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.784-2815G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720709 | |||||||
| chr1:115720780 | C | T | 7 | a0001c0001t0005g0165 a0001c0002t0003g0214 a0001c0002t0003g0220 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-2886G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720780 | |||||||
| chr1:115720838 | T | C | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.784-2944A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720838 | |||||||
| chr1:115720870 | T | C | 1 | a0001c0002t0003g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.784-2976A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720870 | |||||||
| chr1:115720872 | G | A | 1 | a0002c0004t0011g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.784-2978C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115720872 | |||||||
| chr1:115721029 | G | A | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-3135C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721029 | |||||||
| chr1:115721272 | C | G | 97 | a0001c0001t0002g0061 a0001c0002t0001g0003 a0001c0002t0001g0046 others(94): Show |
99 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.784-3378G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721272 | |||||||
| chr1:115721303 | C | T | 238 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(235): Show |
244 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.784-3409G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721303 | |||||||
| chr1:115721489 | C | T | 1 | a0002c0003t0001g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.784-3595G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721489 | |||||||
| chr1:115721845 | A | G | 1 | a0002c0003t0001g0349 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.783+3663T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721845 | |||||||
| chr1:115721850 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.783+3658G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115721850 | |||||||
| chr1:115722133 | C | A | 97 | a0001c0001t0002g0061 a0001c0002t0001g0003 a0001c0002t0001g0046 others(94): Show |
99 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.783+3375G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722133 | |||||||
| chr1:115722133 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.783+3375G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722133 | |||||||
| chr1:115722253 | C | G | 1 | a0002c0003t0006g0314 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.783+3255G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722253 | |||||||
| chr1:115722502 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.783+3006T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722502 | |||||||
| chr1:115722806 | G | T | 1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783+2702C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722806 | |||||||
| chr1:115722907 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.783+2601C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115722907 | |||||||
| chr1:115723055 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.783+2453T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723055 | |||||||
| chr1:115723055 | A | T | 1 | a0002c0004t0017g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.783+2453T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723055 | |||||||
| chr1:115723092 | C | G | 1 | a0001c0007t0009g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783+2416G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723092 | |||||||
| chr1:115723144 | T | G | 13 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0031 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+2364A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723144 | |||||||
| chr1:115723167 | T | C | 14 | a0001c0001t0002g0052 a0001c0001t0002g0233 a0001c0001t0008g0029 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.783+2341A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723167 | |||||||
| chr1:115723267 | T | TATC | 32 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(29): Show |
34 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.783+2238_783+2240d others(5): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723267 | |||||||
| chr1:115723270 | CT | C | 6 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0003t0010g0009 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+2237delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723270 | |||||||
| chr1:115723274 | C | CATCTATC others(1): Show |
102 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(99): Show |
104 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.783+2226_783+2233d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723274 | |||||||
| chr1:115723274 | C | CT | 38 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(35): Show |
40 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.783+2233_783+2234i others(3): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723274 | |||||||
| chr1:115723274 | C | CTATCATC others(1): Show |
18 | a0001c0002t0001g0175 a0002c0003t0001g0260 a0002c0003t0001g0262 others(15): Show |
18 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.783+2233_783+2234i others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723274 | |||||||
| chr1:115723274 | C | CTATCATC others(5): Show |
79 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0002t0001g0003 others(76): Show |
81 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.783+2233_783+2234i others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723274 | |||||||
| chr1:115723274 | C | CTATCTAT others(5): Show |
1 | a0002c0003t0001g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.783+2233_783+2234i others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723274 | |||||||
| chr1:115723283 | A | ATCTATCT others(19): Show |
1 | a0001c0007t0009g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783+2224_783+2225i others(28): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723283 | |||||||
| chr1:115723289 | C | A | 1 | a0001c0007t0009g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783+2219G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723289 | |||||||
| chr1:115723293 | A | ATATCTAT others(9): Show |
1 | a0002c0003t0001g0312 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.783+2199_783+2214d others(18): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723293 | |||||||
| chr1:115723293 | A | ATATCTAT others(1): Show |
8 | a0001c0001t0008g0029 a0001c0001t0008g0036 a0001c0002t0012g0030 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+2214_783+2215i others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723293 | |||||||
| chr1:115723293 | A | ATATCTAT others(5): Show |
1 | a0001c0002t0012g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+2214_783+2215i others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723293 | |||||||
| chr1:115723305 | T | C | 10 | a0001c0001t0008g0029 a0001c0001t0008g0036 a0001c0002t0012g0030 others(7): Show |
10 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.783+2203A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATC | 54 | a0001c0001t0002g0052 a0001c0001t0002g0111 a0001c0001t0002g0113 others(51): Show |
56 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.783+2199_783+2202d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATCTAT others(1): Show |
47 | a0001c0001t0002g0051 a0001c0001t0002g0054 a0001c0001t0002g0068 others(44): Show |
47 | HG00323.hp1 HG01192.hp1 HG01981.hp1 others(44): Show |
intron_variant | MODIFIER | c.783+2195_783+2202d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATCTAT others(5): Show |
76 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(73): Show |
78 | HG00438.hp2 HG00597.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.783+2191_783+2202d others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATCTAT others(9): Show |
46 | a0001c0001t0002g0004 a0001c0001t0002g0082 a0001c0001t0002g0083 others(43): Show |
47 | HG00558.hp1 HG00609.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.783+2187_783+2202d others(18): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATCTAT others(13): Show |
23 | a0001c0001t0002g0061 a0001c0001t0002g0090 a0001c0001t0005g0162 others(20): Show |
24 | HG00423.hp2 HG00438.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.783+2183_783+2202d others(22): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723305 | T | TTATCTAT others(17): Show |
2 | a0001c0002t0003g0057 a0002c0003t0006g0354 |
2 | HG02015.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.783+2179_783+2202d others(26): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723305 | |||||||
| chr1:115723471 | A | T | 2 | a0001c0002t0003g0091 a0001c0002t0003g0199 |
2 | NA18980.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.783+2037T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723471 | |||||||
| chr1:115723516 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.783+1992A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723516 | |||||||
| chr1:115723561 | A | G | 14 | a0001c0001t0002g0052 a0001c0001t0002g0233 a0001c0001t0008g0029 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.783+1947T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723561 | |||||||
| chr1:115723598 | T | C | 1 | a0002c0003t0001g0341 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.783+1910A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115723598 | |||||||
| chr1:115724115 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.783+1393G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724115 | |||||||
| chr1:115724138 | A | G | 5 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0002g0116 others(2): Show |
5 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+1370T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724138 | |||||||
| chr1:115724281 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.783+1227C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724281 | |||||||
| chr1:115724297 | T | G | 1 | a0001c0002t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.783+1211A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724297 | |||||||
| chr1:115724316 | T | C | 1 | a0002c0003t0001g0347 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.783+1192A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724316 | |||||||
| chr1:115724451 | C | T | 13 | a0001c0001t0004g0059 a0001c0001t0004g0062 a0001c0001t0004g0063 others(10): Show |
13 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+1057G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724451 | |||||||
| chr1:115724536 | A | G | 1 | a0001c0001t0005g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.783+972T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724536 | |||||||
| chr1:115724622 | T | A | 1 | a0002c0003t0010g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.783+886A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724622 | |||||||
| chr1:115724623 | A | G | 1 | a0002c0003t0010g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.783+885T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724623 | |||||||
| chr1:115724627 | A | T | 37 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(34): Show |
39 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.783+881T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724627 | |||||||
| chr1:115724685 | C | T | 1 | a0002c0004t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.783+823G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724685 | |||||||
| chr1:115724771 | T | A | 6 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+737A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724771 | |||||||
| chr1:115724791 | A | G | 1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.783+717T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724791 | |||||||
| chr1:115724984 | A | T | 31 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(28): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.783+524T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724984 | |||||||
| chr1:115724996 | C | A | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.783+512G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115724996 | |||||||
| chr1:115725065 | T | C | 1 | a0001c0002t0003g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.783+443A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115725065 | |||||||
| chr1:115725155 | C | T | 15 | a0001c0001t0002g0052 a0001c0001t0002g0233 a0001c0001t0008g0026 others(12): Show |
15 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.783+353G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115725155 | |||||||
| chr1:115725228 | G | A | 6 | a0004c0008t0001g0273 a0004c0008t0001g0308 a0004c0008t0001g0311 others(3): Show |
6 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+280C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115725228 | |||||||
| chr1:115725398 | C | T | 1 | a0002c0003t0007g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.783+110G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115725398 | |||||||
| chr1:115725456 | T | C | 8 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0079 others(5): Show |
8 | NA18965.hp1 NA18995.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.783+52A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 7/10 | chr1 | 115725456 | |||||||
| chr1:115725557 | G | GA | 31 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0217 others(28): Show |
32 | HG00621.hp1 HG01261.hp2 HG01884.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.738-5dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725557 | |||||||
| chr1:115725557 | GA | G | 13 | a0001c0001t0002g0121 a0001c0001t0008g0026 a0001c0002t0001g0047 others(10): Show |
13 | HG01175.hp1 HG01891.hp2 HG01952.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.738-5delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725557 | |||||||
| chr1:115725557 | GAA | G | 192 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(189): Show |
196 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
splice_region_variant&intron_variant | LOW | c.738-6_738-5delTT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725557 | |||||||
| chr1:115725557 | GAAA | G | 18 | a0001c0001t0002g0068 a0001c0001t0002g0105 a0001c0001t0002g0233 others(15): Show |
19 | HG01981.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.738-7_738-5delTTT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725557 | |||||||
| chr1:115725662 | C | T | 224 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(221): Show |
230 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.738-109G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725662 | |||||||
| chr1:115725674 | G | A | 6 | a0001c0001t0005g0165 a0001c0002t0003g0214 a0001c0002t0003g0220 others(3): Show |
6 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-121C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725674 | |||||||
| chr1:115725945 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.738-392C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725945 | |||||||
| chr1:115725953 | T | C | 1 | a0001c0002t0003g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.738-400A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115725953 | |||||||
| chr1:115726078 | A | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(222): Show |
231 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.738-525T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726078 | |||||||
| chr1:115726150 | G | A | 1 | a0002c0004t0004g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.738-597C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726150 | |||||||
| chr1:115726230 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.738-677T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726230 | |||||||
| chr1:115726291 | G | A | 13 | a0001c0001t0002g0233 a0001c0001t0008g0029 a0001c0001t0008g0031 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.737+701C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726291 | |||||||
| chr1:115726406 | T | C | 219 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(216): Show |
224 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.737+586A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726406 | |||||||
| chr1:115726423 | C | T | 4 | a0001c0002t0003g0005 a0001c0002t0003g0087 a0001c0002t0003g0196 others(1): Show |
5 | NA18943.hp2 NA18950.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.737+569G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726423 | |||||||
| chr1:115726542 | G | T | 2 | a0001c0002t0003g0225 a0001c0002t0003g0228 |
2 | HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.737+450C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726542 | |||||||
| chr1:115726710 | C | A | 259 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(256): Show |
265 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(262): Show |
intron_variant | MODIFIER | c.737+282G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 6/10 | chr1 | 115726710 | |||||||
| chr1:115727406 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.607-284A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115727406 | |||||||
| chr1:115727410 | A | G | 1 | a0002c0004t0002g0302 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.607-288T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115727410 | |||||||
| chr1:115727554 | G | A | 1 | a0002c0003t0001g0286 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.607-432C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115727554 | |||||||
| chr1:115727613 | T | G | 85 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(82): Show |
86 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.607-491A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115727613 | |||||||
| chr1:115727876 | T | C | 30 | a0001c0001t0004g0072 a0001c0001t0004g0159 a0001c0001t0004g0192 others(27): Show |
32 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.607-754A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115727876 | |||||||
| chr1:115728157 | G | A | 1 | a0002c0004t0002g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.607-1035C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728157 | |||||||
| chr1:115728256 | T | C | 1 | a0001c0002t0001g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.607-1134A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728256 | |||||||
| chr1:115728426 | T | C | 246 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(243): Show |
252 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.607-1304A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728426 | |||||||
| chr1:115728446 | T | C | 30 | a0001c0001t0004g0192 a0001c0001t0004g0206 a0001c0001t0004g0215 others(27): Show |
33 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.607-1324A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728446 | |||||||
| chr1:115728450 | T | C | 1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.607-1328A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728450 | |||||||
| chr1:115728704 | C | A | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-1582G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728704 | |||||||
| chr1:115728851 | C | T | 1 | a0002c0003t0001g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.607-1729G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115728851 | |||||||
| chr1:115729008 | T | C | 1 | a0002c0004t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.607-1886A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729008 | |||||||
| chr1:115729035 | C | CT | 46 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0061 others(43): Show |
48 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.607-1914dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729035 | |||||||
| chr1:115729035 | C | CTT | 6 | a0001c0001t0002g0123 a0001c0001t0002g0174 a0001c0001t0005g0077 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-1915_607-1914d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729035 | |||||||
| chr1:115729035 | CT | C | 50 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0065 others(47): Show |
52 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.607-1914delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729035 | |||||||
| chr1:115729344 | C | T | 3 | a0002c0003t0001g0300 a0002c0003t0001g0304 a0002c0003t0001g0343 |
3 | HG02717.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.607-2222G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729344 | |||||||
| chr1:115729354 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.607-2232G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729354 | |||||||
| chr1:115729383 | G | A | 2 | a0001c0001t0004g0215 a0001c0001t0004g0216 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.607-2261C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729383 | |||||||
| chr1:115729675 | A | G | 1 | a0002c0003t0006g0328 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.607-2553T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729675 | |||||||
| chr1:115729699 | C | G | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.607-2577G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729699 | |||||||
| chr1:115729761 | G | A | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-2639C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729761 | |||||||
| chr1:115729862 | T | C | 102 | a0001c0001t0002g0061 a0001c0001t0002g0153 a0001c0001t0004g0217 others(99): Show |
104 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.607-2740A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729862 | |||||||
| chr1:115729938 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.607-2816G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729938 | |||||||
| chr1:115729939 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.607-2817C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115729939 | |||||||
| chr1:115730008 | C | T | 2 | a0001c0001t0004g0159 a0001c0001t0019g0027 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607-2886G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730008 | |||||||
| chr1:115730096 | A | G | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.606+2805T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730096 | |||||||
| chr1:115730167 | C | G | 102 | a0001c0001t0002g0061 a0001c0001t0002g0153 a0001c0001t0004g0217 others(99): Show |
104 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.606+2734G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730167 | |||||||
| chr1:115730238 | G | T | 1 | a0001c0002t0001g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.606+2663C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730238 | |||||||
| chr1:115730258 | T | C | 1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.606+2643A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730258 | |||||||
| chr1:115730380 | T | C | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.606+2521A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730380 | |||||||
| chr1:115730666 | C | G | 2 | a0002c0003t0003g0254 a0002c0003t0003g0255 |
2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.606+2235G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730666 | |||||||
| chr1:115730867 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+2034T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730867 | |||||||
| chr1:115730919 | C | G | 2 | a0002c0003t0001g0291 a0002c0003t0001g0298 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.606+1982G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115730919 | |||||||
| chr1:115731082 | C | T | 8 | a0001c0001t0008g0026 a0002c0003t0007g0023 a0002c0003t0007g0024 others(5): Show |
8 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.606+1819G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731082 | |||||||
| chr1:115731090 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+1811T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731090 | |||||||
| chr1:115731167 | A | G | 247 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(244): Show |
253 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.606+1734T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731167 | |||||||
| chr1:115731177 | A | T | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+1724T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731177 | |||||||
| chr1:115731289 | G | A | 9 | a0001c0001t0004g0159 a0001c0001t0019g0027 a0002c0003t0007g0023 others(6): Show |
9 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1612C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731289 | |||||||
| chr1:115731359 | A | C | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+1542T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731359 | |||||||
| chr1:115731391 | T | A | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+1510A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731391 | |||||||
| chr1:115731498 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.606+1403A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731498 | |||||||
| chr1:115731564 | G | A | 2 | a0001c0001t0004g0159 a0001c0001t0019g0027 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.606+1337C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731564 | |||||||
| chr1:115731711 | C | T | 82 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(79): Show |
83 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.606+1190G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731711 | |||||||
| chr1:115731780 | T | C | 1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.606+1121A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115731780 | |||||||
| chr1:115732064 | G | A | 1 | a0001c0001t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.606+837C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732064 | |||||||
| chr1:115732107 | G | A | 6 | a0001c0001t0005g0165 a0001c0002t0003g0214 a0001c0002t0003g0220 others(3): Show |
6 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+794C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732107 | |||||||
| chr1:115732163 | C | T | 5 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0099 others(2): Show |
5 | NA18948.hp1 NA18968.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.606+738G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732163 | |||||||
| chr1:115732311 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+590C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732311 | |||||||
| chr1:115732457 | C | G | 1 | a0001c0002t0012g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.606+444G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732457 | |||||||
| chr1:115732472 | C | T | 1 | a0002c0004t0011g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.606+429G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732472 | |||||||
| chr1:115732531 | G | A | 98 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(95): Show |
100 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.606+370C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732531 | |||||||
| chr1:115732879 | T | C | 1 | a0003c0005t0001g0249 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.606+22A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 5/10 | chr1 | 115732879 | |||||||
| chr1:115733154 | T | C | 2 | a0001c0001t0004g0159 a0001c0001t0019g0027 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.533-180A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733154 | |||||||
| chr1:115733230 | G | A | 1 | a0002c0003t0001g0313 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.533-256C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733230 | |||||||
| chr1:115733245 | G | A | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.533-271C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733245 | |||||||
| chr1:115733332 | T | A | 4 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 others(1): Show |
4 | HG02257.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-358A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733332 | |||||||
| chr1:115733379 | A | C | 1 | a0002c0013t0009g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.533-405T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733379 | |||||||
| chr1:115733410 | A | G | 81 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(78): Show |
82 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.533-436T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733410 | |||||||
| chr1:115733602 | C | T | 7 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0002g0107 others(4): Show |
8 | HG02145.hp2 HG02451.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.533-628G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733602 | |||||||
| chr1:115733842 | A | G | 1 | a0002c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533-868T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115733842 | |||||||
| chr1:115734043 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.533-1069G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734043 | |||||||
| chr1:115734135 | C | T | 1 | a0002c0003t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.533-1161G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734135 | |||||||
| chr1:115734349 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.533-1375T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734349 | |||||||
| chr1:115734724 | ACTTAT | A | 9 | a0001c0001t0004g0159 a0001c0001t0019g0027 a0002c0003t0007g0023 others(6): Show |
9 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.533-1755_533-1751d others(7): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734724 | |||||||
| chr1:115734743 | C | G | 1 | a0002c0004t0002g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.533-1769G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734743 | |||||||
| chr1:115734910 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.533-1936G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734910 | |||||||
| chr1:115734957 | G | A | 1 | a0001c0001t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.533-1983C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734957 | |||||||
| chr1:115734968 | G | T | 75 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(72): Show |
76 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.533-1994C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115734968 | |||||||
| chr1:115735033 | C | T | 3 | a0001c0002t0003g0164 a0001c0002t0003g0171 a0001c0002t0003g0210 |
3 | HG02132.hp2 NA18940.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.533-2059G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735033 | |||||||
| chr1:115735138 | A | G | 2 | a0001c0001t0004g0217 a0002c0004t0002g0259 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.533-2164T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735138 | |||||||
| chr1:115735261 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.533-2287A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735261 | |||||||
| chr1:115735344 | C | A | 75 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(72): Show |
76 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.533-2370G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735344 | |||||||
| chr1:115735378 | A | G | 43 | a0001c0001t0004g0192 a0001c0001t0004g0206 a0001c0001t0004g0215 others(40): Show |
46 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.533-2404T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735378 | |||||||
| chr1:115735614 | C | G | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.532+2610G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735614 | |||||||
| chr1:115735882 | C | A | 182 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(179): Show |
185 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.532+2342G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735882 | |||||||
| chr1:115735899 | C | T | 10 | a0001c0002t0001g0067 a0001c0002t0001g0132 a0001c0002t0001g0133 others(7): Show |
10 | HG01433.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.532+2325G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115735899 | |||||||
| chr1:115736164 | GA | G | 9 | a0001c0001t0002g0068 a0001c0001t0014g0002 a0001c0002t0003g0158 others(6): Show |
10 | HG01981.hp1 HG02071.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+2059delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736164 | |||||||
| chr1:115736204 | C | A | 1 | a0001c0002t0003g0225 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+2020G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736204 | |||||||
| chr1:115736251 | A | T | 52 | a0001c0001t0004g0159 a0001c0001t0004g0192 a0001c0001t0004g0206 others(49): Show |
55 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.532+1973T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736251 | |||||||
| chr1:115736330 | C | G | 1 | a0003c0005t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.532+1894G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736330 | |||||||
| chr1:115736498 | G | A | 2 | a0001c0001t0002g0108 a0001c0002t0001g0157 |
2 | HG02083.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.532+1726C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736498 | |||||||
| chr1:115736659 | G | A | 3 | a0001c0002t0003g0211 a0001c0002t0003g0212 a0001c0002t0003g0213 |
3 | HG03017.hp2 HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.532+1565C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736659 | |||||||
| chr1:115736691 | T | A | 3 | a0001c0001t0014g0002 a0002c0003t0006g0328 a0002c0013t0009g0297 |
4 | HG02145.hp2 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+1533A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736691 | |||||||
| chr1:115736785 | C | A | 98 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(95): Show |
100 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.532+1439G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736785 | |||||||
| chr1:115736795 | T | G | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+1429A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736795 | |||||||
| chr1:115736881 | A | G | 1 | a0002c0003t0001g0322 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.532+1343T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736881 | |||||||
| chr1:115736964 | C | T | 1 | a0001c0002t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.532+1260G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115736964 | |||||||
| chr1:115737187 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0233 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.532+1037C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737187 | |||||||
| chr1:115737523 | G | A | 98 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(95): Show |
100 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.532+701C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737523 | |||||||
| chr1:115737664 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.532+560G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737664 | |||||||
| chr1:115737771 | G | A | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.532+453C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737771 | |||||||
| chr1:115737927 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.532+297C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737927 | |||||||
| chr1:115737966 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.532+258A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115737966 | |||||||
| chr1:115738011 | C | A | 5 | a0002c0004t0004g0282 a0002c0004t0004g0293 a0002c0004t0004g0331 others(2): Show |
5 | NA18946.hp2 NA18983.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+213G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 4/10 | chr1 | 115738011 | |||||||
| chr1:115738613 | G | A | 1 | a0002c0004t0002g0337 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.421-278C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738613 | |||||||
| chr1:115738705 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.421-370A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738705 | |||||||
| chr1:115738745 | T | C | 199 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(196): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.421-410A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738745 | |||||||
| chr1:115738798 | T | C | 199 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(196): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.421-463A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738798 | |||||||
| chr1:115738856 | C | T | 199 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(196): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.421-521G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738856 | |||||||
| chr1:115738899 | T | A | 199 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(196): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.421-564A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738899 | |||||||
| chr1:115738913 | A | G | 63 | a0001c0001t0004g0192 a0001c0001t0004g0206 a0001c0001t0004g0215 others(60): Show |
64 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.421-578T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115738913 | |||||||
| chr1:115739028 | C | A | 4 | a0001c0002t0001g0152 a0001c0002t0001g0154 a0001c0002t0001g0155 others(1): Show |
4 | HG00639.hp2 HG01081.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-693G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739028 | |||||||
| chr1:115739056 | CT | C | 6 | a0001c0002t0001g0078 a0002c0003t0001g0298 a0002c0003t0001g0303 others(3): Show |
6 | HG00323.hp1 HG01175.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-722delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739056 | |||||||
| chr1:115739061 | T | TA | 81 | a0001c0001t0002g0174 a0001c0001t0004g0192 a0001c0001t0004g0206 others(78): Show |
81 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.421-727_421-726ins others(1): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739061 | |||||||
| chr1:115739061 | T | TAA | 3 | a0002c0004t0002g0253 a0002c0004t0002g0279 a0002c0004t0002g0285 |
3 | HG01934.hp1 HG02559.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.421-727_421-726ins others(2): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739061 | |||||||
| chr1:115739062 | T | A | 191 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(188): Show |
196 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.421-727A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739062 | |||||||
| chr1:115739063 | T | A | 206 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0159 others(203): Show |
211 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.421-728A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739063 | |||||||
| chr1:115739063 | TA | T | 109 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(106): Show |
110 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(107): Show |
intron_variant | MODIFIER | c.421-729delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739063 | |||||||
| chr1:115739064 | A | T | 1 | a0002c0004t0004g0008 | 2 | NA19070.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.421-729T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739064 | |||||||
| chr1:115739124 | C | CTTTTTTT others(11): Show |
7 | a0001c0001t0002g0081 a0001c0002t0001g0166 a0001c0002t0003g0186 others(4): Show |
7 | HG01074.hp1 HG03017.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-790_421-789ins others(18): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739124 | |||||||
| chr1:115739124 | C | CTTTTTTT others(12): Show |
158 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0002g0083 others(155): Show |
163 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.421-790_421-789ins others(19): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739124 | |||||||
| chr1:115739124 | C | CTTTTTTT others(13): Show |
42 | a0001c0001t0002g0174 a0001c0001t0005g0142 a0001c0001t0005g0144 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.421-790_421-789ins others(20): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739124 | |||||||
| chr1:115739124 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0001g0155 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.421-790_421-789ins others(21): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739124 | |||||||
| chr1:115739130 | G | T | 208 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(205): Show |
213 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.421-795C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739130 | |||||||
| chr1:115739138 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.421-803C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739138 | |||||||
| chr1:115739197 | C | T | 91 | a0001c0001t0002g0153 a0001c0001t0004g0217 a0001c0001t0005g0001 others(88): Show |
94 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.421-862G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739197 | |||||||
| chr1:115739228 | T | C | 2 | a0001c0002t0003g0038 a0001c0002t0003g0041 |
2 | NA18955.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.421-893A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739228 | |||||||
| chr1:115739283 | A | G | 274 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(271): Show |
280 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.421-948T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739283 | |||||||
| chr1:115739283 | A | T | 1 | a0002c0004t0004g0269 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.421-948T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739283 | |||||||
| chr1:115739284 | T | G | 264 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(261): Show |
268 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.421-949A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739284 | |||||||
| chr1:115739288 | TG | T | 14 | a0001c0001t0004g0216 a0001c0002t0006g0229 a0002c0003t0001g0265 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.421-954delC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739288 | |||||||
| chr1:115739289 | G | T | 259 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(256): Show |
265 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.421-954C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739289 | |||||||
| chr1:115739291 | A | T | 273 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(270): Show |
279 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.421-956T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739291 | |||||||
| chr1:115739292 | T | G | 1 | a0002c0004t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.421-957A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739292 | |||||||
| chr1:115739305 | T | C | 1 | a0001c0002t0003g0218 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.421-970A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739305 | |||||||
| chr1:115739307 | G | A | 1 | a0002c0003t0001g0287 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.421-972C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739307 | |||||||
| chr1:115739308 | G | A | 5 | a0001c0002t0001g0175 a0002c0003t0001g0284 a0002c0003t0001g0299 others(2): Show |
5 | HG01175.hp2 HG01192.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-973C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739308 | |||||||
| chr1:115739319 | A | G | 1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.421-984T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739319 | |||||||
| chr1:115739357 | A | C | 200 | a0001c0001t0002g0100 a0001c0001t0002g0122 a0001c0001t0002g0130 others(197): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.421-1022T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739357 | |||||||
| chr1:115739395 | A | G | 17 | a0001c0001t0004g0217 a0001c0001t0005g0165 a0001c0002t0003g0160 others(14): Show |
18 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(15): Show |
intron_variant | MODIFIER | c.421-1060T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739395 | |||||||
| chr1:115739596 | T | C | 1 | a0001c0002t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.420+1132A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739596 | |||||||
| chr1:115739601 | G | A | 194 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(191): Show |
198 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.420+1127C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739601 | |||||||
| chr1:115739733 | A | G | 2 | a0002c0004t0002g0279 a0002c0004t0002g0285 |
2 | HG01934.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.420+995T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739733 | |||||||
| chr1:115739795 | T | A | 1 | a0001c0002t0003g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.420+933A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739795 | |||||||
| chr1:115739796 | T | A | 1 | a0001c0002t0003g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.420+932A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739796 | |||||||
| chr1:115739797 | A | G | 1 | a0001c0002t0003g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.420+931T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739797 | |||||||
| chr1:115739816 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.420+912A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739816 | |||||||
| chr1:115739969 | C | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.420+759G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739969 | |||||||
| chr1:115739970 | G | A | 5 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0002g0116 others(2): Show |
5 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+758C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115739970 | |||||||
| chr1:115740096 | C | T | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+632G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740096 | |||||||
| chr1:115740175 | C | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.420+553G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740175 | |||||||
| chr1:115740306 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.420+422A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740306 | |||||||
| chr1:115740502 | A | T | 1 | a0001c0002t0003g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.420+226T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740502 | |||||||
| chr1:115740508 | A | G | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+220T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740508 | |||||||
| chr1:115740722 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
splice_region_variant&intron_variant | LOW | c.420+6T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 3/10 | chr1 | 115740722 | |||||||
| chr1:115740846 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.320-18C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115740846 | |||||||
| chr1:115740905 | G | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-77C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115740905 | |||||||
| chr1:115741004 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-176T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741004 | |||||||
| chr1:115741078 | A | G | 198 | a0001c0001t0002g0105 a0001c0001t0002g0153 a0001c0001t0002g0174 others(195): Show |
203 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.320-250T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741078 | |||||||
| chr1:115741096 | C | A | 1 | a0001c0006t0003g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.320-268G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741096 | |||||||
| chr1:115741106 | G | A | 2 | a0002c0004t0017g0016 a0005c0011t0001g0140 |
2 | HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.320-278C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741106 | |||||||
| chr1:115741126 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-298A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741126 | |||||||
| chr1:115741186 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-358G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741186 | |||||||
| chr1:115741191 | A | C | 2 | a0001c0001t0004g0159 a0001c0001t0019g0027 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.320-363T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741191 | |||||||
| chr1:115741228 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-400T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741228 | |||||||
| chr1:115741300 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-472A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741300 | |||||||
| chr1:115741407 | A | G | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.320-579T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741407 | |||||||
| chr1:115741514 | A | C | 198 | a0001c0001t0002g0105 a0001c0001t0002g0153 a0001c0001t0002g0174 others(195): Show |
203 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.320-686T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741514 | |||||||
| chr1:115741560 | A | T | 196 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(193): Show |
201 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.320-732T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741560 | |||||||
| chr1:115741613 | A | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-785T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741613 | |||||||
| chr1:115741700 | G | A | 223 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(220): Show |
230 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.320-872C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741700 | |||||||
| chr1:115741829 | C | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1001G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741829 | |||||||
| chr1:115741866 | G | A | 345 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(342): Show |
354 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(351): Show |
intron_variant | MODIFIER | c.320-1038C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741866 | |||||||
| chr1:115741926 | G | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1098C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741926 | |||||||
| chr1:115741936 | A | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1108T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741936 | |||||||
| chr1:115741954 | G | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1126C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741954 | |||||||
| chr1:115741981 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.320-1153C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741981 | |||||||
| chr1:115741985 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1157T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741985 | |||||||
| chr1:115741990 | C | T | 1 | a0001c0007t0009g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.320-1162G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115741990 | |||||||
| chr1:115742032 | T | C | 3 | a0001c0002t0003g0204 a0001c0002t0003g0225 a0001c0002t0003g0228 |
3 | HG01192.hp2 HG01257.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.320-1204A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742032 | |||||||
| chr1:115742132 | C | A | 1 | a0002c0003t0001g0341 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.320-1304G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742132 | |||||||
| chr1:115742259 | G | A | 2 | a0005c0009t0001g0060 a0005c0009t0013g0035 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.320-1431C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742259 | |||||||
| chr1:115742267 | G | A | 3 | a0001c0001t0014g0002 a0002c0004t0017g0016 a0005c0011t0001g0140 |
4 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-1439C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742267 | |||||||
| chr1:115742275 | C | A | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.320-1447G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742275 | |||||||
| chr1:115742293 | A | G | 1 | a0001c0007t0020g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.320-1465T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742293 | |||||||
| chr1:115742299 | A | G | 77 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(74): Show |
78 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.320-1471T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742299 | |||||||
| chr1:115742323 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1495G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742323 | |||||||
| chr1:115742324 | C | T | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-1496G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742324 | |||||||
| chr1:115742337 | G | C | 1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.320-1509C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742337 | |||||||
| chr1:115742376 | G | A | 308 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(305): Show |
314 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.320-1548C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742376 | |||||||
| chr1:115742402 | G | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1574C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742402 | |||||||
| chr1:115742483 | C | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1655G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742483 | |||||||
| chr1:115742515 | G | A | 308 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(305): Show |
314 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.320-1687C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742515 | |||||||
| chr1:115742526 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1698T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742526 | |||||||
| chr1:115742568 | G | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1740C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742568 | |||||||
| chr1:115742726 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.320-1898T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742726 | |||||||
| chr1:115742756 | G | A | 2 | a0001c0001t0004g0159 a0001c0001t0019g0027 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.320-1928C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742756 | |||||||
| chr1:115742768 | C | CTGTT | 47 | a0001c0002t0001g0003 a0001c0002t0001g0047 a0001c0002t0003g0039 others(44): Show |
49 | HG00609.hp2 HG00673.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.320-1944_320-1941d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742768 | |||||||
| chr1:115742768 | CTGTT | C | 9 | a0001c0001t0005g0077 a0001c0001t0005g0151 a0001c0001t0005g0162 others(6): Show |
10 | HG00438.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.320-1944_320-1941d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742768 | |||||||
| chr1:115742768 | CTGTTTGT others(1): Show |
C | 94 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(91): Show |
95 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(92): Show |
intron_variant | MODIFIER | c.320-1948_320-1941d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742768 | |||||||
| chr1:115742768 | CTGTTTGT others(5): Show |
C | 25 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(22): Show |
25 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.320-1952_320-1941d others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742768 | |||||||
| chr1:115742828 | T | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+2000A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742828 | |||||||
| chr1:115742913 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1915G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742913 | |||||||
| chr1:115742949 | G | A | 1 | a0002c0003t0001g0327 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.319+1879C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115742949 | |||||||
| chr1:115743030 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1798G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743030 | |||||||
| chr1:115743067 | G | A | 7 | a0001c0001t0004g0159 a0001c0001t0019g0027 a0002c0003t0010g0009 others(4): Show |
7 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+1761C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743067 | |||||||
| chr1:115743099 | G | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1729C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743099 | |||||||
| chr1:115743143 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.319+1685T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743143 | |||||||
| chr1:115743168 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.319+1660T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743168 | |||||||
| chr1:115743193 | T | TTTTG | 7 | a0001c0001t0002g0070 a0001c0001t0002g0082 a0001c0001t0002g0083 others(4): Show |
7 | NA18943.hp1 NA18951.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1631_319+1634d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743193 | |||||||
| chr1:115743193 | TTTTGTTT others(5): Show |
T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1623_319+1634d others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743193 | |||||||
| chr1:115743197 | G | A | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+1631C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743197 | |||||||
| chr1:115743197 | G | GTTTA | 34 | a0001c0001t0002g0061 a0001c0001t0008g0026 a0001c0001t0008g0031 others(31): Show |
35 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.319+1627_319+1630d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743197 | |||||||
| chr1:115743197 | G | GTTTATTT others(1): Show |
7 | a0001c0002t0001g0056 a0002c0003t0007g0023 a0002c0003t0007g0024 others(4): Show |
7 | HG02818.hp2 HG03195.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+1623_319+1630d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743197 | |||||||
| chr1:115743197 | GTTTA | G | 5 | a0001c0001t0002g0127 a0001c0001t0002g0130 a0001c0001t0004g0062 others(2): Show |
5 | HG02258.hp2 HG02523.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+1627_319+1630d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743197 | |||||||
| chr1:115743197 | GTTTATTT others(5): Show |
G | 6 | a0001c0001t0008g0037 a0002c0003t0010g0009 a0002c0003t0010g0011 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+1619_319+1630d others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743197 | |||||||
| chr1:115743201 | A | G | 68 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(65): Show |
69 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.319+1627T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743201 | |||||||
| chr1:115743205 | A | G | 2 | a0001c0001t0002g0127 a0001c0001t0002g0130 |
2 | HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.319+1623T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743205 | |||||||
| chr1:115743232 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1596A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743232 | |||||||
| chr1:115743285 | T | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1543A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743285 | |||||||
| chr1:115743319 | C | T | 3 | a0001c0001t0014g0002 a0002c0004t0017g0016 a0005c0011t0001g0140 |
4 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1509G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743319 | |||||||
| chr1:115743352 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1476A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743352 | |||||||
| chr1:115743394 | C | T | 7 | a0001c0001t0004g0159 a0001c0001t0019g0027 a0002c0003t0010g0009 others(4): Show |
7 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+1434G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743394 | |||||||
| chr1:115743544 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1284T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743544 | |||||||
| chr1:115743665 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1163T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743665 | |||||||
| chr1:115743689 | C | CT | 26 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(23): Show |
26 | HG01884.hp2 HG02109.hp1 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.319+1138dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743689 | |||||||
| chr1:115743689 | CTT | C | 196 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(193): Show |
201 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.319+1137_319+1138d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743689 | |||||||
| chr1:115743703 | T | C | 1 | a0005c0011t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319+1125A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743703 | |||||||
| chr1:115743766 | A | AT | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+1061dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743766 | |||||||
| chr1:115743941 | A | T | 200 | a0001c0001t0002g0061 a0001c0001t0002g0153 a0001c0001t0002g0174 others(197): Show |
205 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.319+887T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743941 | |||||||
| chr1:115743982 | C | CA | 109 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(106): Show |
111 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(108): Show |
intron_variant | MODIFIER | c.319+845dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743982 | |||||||
| chr1:115743982 | C | CAA | 7 | a0001c0001t0002g0233 a0002c0013t0009g0297 a0004c0008t0001g0273 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+844_319+845dup others(2): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743982 | |||||||
| chr1:115743982 | CAA | C | 196 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(193): Show |
201 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.319+844_319+845del others(2): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743982 | |||||||
| chr1:115743996 | G | A | 103 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(100): Show |
104 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(101): Show |
intron_variant | MODIFIER | c.319+832C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115743996 | |||||||
| chr1:115744005 | G | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+823C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744005 | |||||||
| chr1:115744012 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+816G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744012 | |||||||
| chr1:115744036 | C | T | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+792G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744036 | |||||||
| chr1:115744141 | C | CA | 13 | a0001c0001t0002g0052 a0001c0001t0004g0159 a0001c0001t0019g0027 others(10): Show |
13 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.319+686dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744141 | |||||||
| chr1:115744141 | CAAA | C | 194 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(191): Show |
199 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.319+684_319+686del others(3): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744141 | |||||||
| chr1:115744197 | C | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+631G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744197 | |||||||
| chr1:115744197 | C | T | 2 | a0001c0002t0001g0132 a0001c0002t0001g0135 |
2 | HG01433.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.319+631G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744197 | |||||||
| chr1:115744338 | G | C | 68 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(65): Show |
69 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.319+490C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744338 | |||||||
| chr1:115744362 | A | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+466T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744362 | |||||||
| chr1:115744434 | C | T | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+394G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744434 | |||||||
| chr1:115744444 | C | T | 1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.319+384G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744444 | |||||||
| chr1:115744492 | A | G | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.319+336T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744492 | |||||||
| chr1:115744615 | C | G | 2 | a0001c0002t0001g0155 a0001c0002t0001g0156 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.319+213G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744615 | |||||||
| chr1:115744684 | C | T | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+144G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744684 | |||||||
| chr1:115744736 | C | A | 3 | a0001c0002t0003g0164 a0001c0002t0003g0171 a0001c0002t0003g0210 |
3 | HG02132.hp2 NA18940.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.319+92G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 2/10 | chr1 | 115744736 | |||||||
| chr1:115744992 | A | G | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235-80T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115744992 | |||||||
| chr1:115745013 | A | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-101T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745013 | |||||||
| chr1:115745030 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-118C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745030 | |||||||
| chr1:115745061 | T | C | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-149A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745061 | |||||||
| chr1:115745213 | G | A | 5 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0002g0116 others(2): Show |
5 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-301C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745213 | |||||||
| chr1:115745354 | A | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-442T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745354 | |||||||
| chr1:115745361 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.235-449C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745361 | |||||||
| chr1:115745361 | G | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-449C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745361 | |||||||
| chr1:115745376 | TC | T | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-465delG | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745376 | |||||||
| chr1:115745406 | G | T | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-494C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745406 | |||||||
| chr1:115745439 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-527A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745439 | |||||||
| chr1:115745484 | C | T | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-572G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745484 | |||||||
| chr1:115745509 | G | C | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-597C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745509 | |||||||
| chr1:115745536 | A | T | 3 | a0001c0002t0003g0164 a0001c0002t0003g0171 a0001c0002t0003g0210 |
3 | HG02132.hp2 NA18940.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.235-624T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745536 | |||||||
| chr1:115745540 | C | T | 3 | a0001c0002t0003g0164 a0001c0002t0003g0171 a0001c0002t0003g0210 |
3 | HG02132.hp2 NA18940.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.235-628G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745540 | |||||||
| chr1:115745574 | T | C | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-662A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745574 | |||||||
| chr1:115745603 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-691A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745603 | |||||||
| chr1:115745632 | C | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-720G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745632 | |||||||
| chr1:115745746 | CT | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-835delA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115745746 | |||||||
| chr1:115746056 | T | A | 7 | a0001c0002t0006g0043 a0001c0002t0006g0229 a0002c0003t0006g0314 others(4): Show |
7 | HG00438.hp1 HG00558.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-1144A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746056 | |||||||
| chr1:115746113 | T | C | 111 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(108): Show |
112 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(109): Show |
intron_variant | MODIFIER | c.235-1201A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746113 | |||||||
| chr1:115746114 | G | A | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-1202C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746114 | |||||||
| chr1:115746153 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-1241C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746153 | |||||||
| chr1:115746158 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.235-1246C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746158 | |||||||
| chr1:115746161 | G | GT | 189 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(186): Show |
192 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.235-1250dupA | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746161 | |||||||
| chr1:115746161 | G | GTT | 8 | a0001c0001t0005g0001 a0001c0001t0005g0142 a0001c0001t0005g0143 others(5): Show |
10 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.235-1251_235-1250d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746161 | |||||||
| chr1:115746204 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-1292A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746204 | |||||||
| chr1:115746297 | A | G | 1 | a0002c0003t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.235-1385T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746297 | |||||||
| chr1:115746377 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.235-1465A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746377 | |||||||
| chr1:115746433 | C | T | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-1521G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746433 | |||||||
| chr1:115746460 | T | C | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-1548A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746460 | |||||||
| chr1:115746543 | A | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-1631T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746543 | |||||||
| chr1:115746606 | C | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-1694G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746606 | |||||||
| chr1:115746634 | T | C | 1 | a0003c0005t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.235-1722A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746634 | |||||||
| chr1:115746758 | T | C | 7 | a0001c0001t0004g0159 a0001c0001t0019g0027 a0002c0003t0010g0009 others(4): Show |
7 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1846A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746758 | |||||||
| chr1:115746850 | A | G | 1 | a0001c0001t0014g0002 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.235-1938T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115746850 | |||||||
| chr1:115747086 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-2174A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747086 | |||||||
| chr1:115747107 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-2195A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747107 | |||||||
| chr1:115747165 | G | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-2253C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747165 | |||||||
| chr1:115747203 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-2291A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747203 | |||||||
| chr1:115747255 | T | C | 1 | a0002c0004t0002g0281 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.235-2343A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747255 | |||||||
| chr1:115747351 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235-2439G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747351 | |||||||
| chr1:115747427 | C | T | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-2515G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747427 | |||||||
| chr1:115747459 | G | C | 1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.235-2547C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747459 | |||||||
| chr1:115747659 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-2747A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747659 | |||||||
| chr1:115747683 | G | C | 1 | a0001c0007t0009g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.235-2771C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747683 | |||||||
| chr1:115747736 | A | T | 111 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(108): Show |
112 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(109): Show |
intron_variant | MODIFIER | c.235-2824T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747736 | |||||||
| chr1:115747825 | C | A | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-2913G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747825 | |||||||
| chr1:115747843 | GGTTTTTG others(4): Show |
G | 111 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(108): Show |
112 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(109): Show |
intron_variant | MODIFIER | c.235-2942_235-2932d others(13): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747843 | |||||||
| chr1:115747943 | C | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3031G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115747943 | |||||||
| chr1:115748049 | A | G | 197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-3137T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748049 | |||||||
| chr1:115748095 | T | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3183A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748095 | |||||||
| chr1:115748106 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3194C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748106 | |||||||
| chr1:115748336 | C | T | 1 | a0002c0003t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.235-3424G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748336 | |||||||
| chr1:115748404 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3492C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748404 | |||||||
| chr1:115748438 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.235-3526G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748438 | |||||||
| chr1:115748445 | G | A | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3533C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748445 | |||||||
| chr1:115748473 | A | G | 315 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(312): Show |
321 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(318): Show |
intron_variant | MODIFIER | c.235-3561T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748473 | |||||||
| chr1:115748539 | C | CTCTTATT | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3634_235-3628d others(9): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748539 | |||||||
| chr1:115748580 | A | G | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-3668T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748580 | |||||||
| chr1:115748763 | T | C | 1 | a0002c0003t0006g0314 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.235-3851A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748763 | |||||||
| chr1:115748818 | T | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-3906A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748818 | |||||||
| chr1:115748900 | A | G | 1 | a0001c0002t0003g0171 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.235-3988T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748900 | |||||||
| chr1:115748954 | T | C | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4042A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748954 | |||||||
| chr1:115748988 | C | T | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-4076G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115748988 | |||||||
| chr1:115749043 | A | C | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4131T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749043 | |||||||
| chr1:115749059 | A | C | 1 | a0002c0003t0001g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235-4147T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749059 | |||||||
| chr1:115749108 | C | T | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-4196G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749108 | |||||||
| chr1:115749153 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.235-4241A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749153 | |||||||
| chr1:115749255 | C | T | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4343G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749255 | |||||||
| chr1:115749264 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4352T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749264 | |||||||
| chr1:115749379 | G | T | 1 | a0001c0002t0003g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.235-4467C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749379 | |||||||
| chr1:115749391 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.235-4479G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749391 | |||||||
| chr1:115749402 | G | A | 2 | a0002c0003t0001g0288 a0002c0003t0001g0322 |
2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.235-4490C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749402 | |||||||
| chr1:115749412 | T | C | 1 | a0001c0002t0003g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235-4500A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749412 | |||||||
| chr1:115749415 | C | T | 199 | a0001c0001t0002g0065 a0001c0001t0002g0153 a0001c0001t0002g0174 others(196): Show |
204 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.235-4503G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749415 | |||||||
| chr1:115749451 | C | T | 1 | a0001c0002t0003g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.235-4539G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749451 | |||||||
| chr1:115749464 | T | C | 1 | a0002c0003t0003g0255 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.235-4552A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749464 | |||||||
| chr1:115749470 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4558T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749470 | |||||||
| chr1:115749555 | C | G | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-4643G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749555 | |||||||
| chr1:115749734 | G | A | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4822C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749734 | |||||||
| chr1:115749748 | T | C | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4836A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749748 | |||||||
| chr1:115749766 | C | T | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4854G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749766 | |||||||
| chr1:115749781 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4869T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749781 | |||||||
| chr1:115749827 | A | G | 198 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0159 others(195): Show |
203 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.235-4915T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749827 | |||||||
| chr1:115749848 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-4936T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749848 | |||||||
| chr1:115749966 | T | C | 77 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(74): Show |
78 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.235-5054A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115749966 | |||||||
| chr1:115750261 | T | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-5349A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750261 | |||||||
| chr1:115750287 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-5375T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750287 | |||||||
| chr1:115750291 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.235-5379T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750291 | |||||||
| chr1:115750340 | T | C | 2 | a0002c0003t0010g0012 a0002c0003t0010g0013 |
2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.235-5428A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750340 | |||||||
| chr1:115750375 | G | T | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235-5463C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750375 | |||||||
| chr1:115750490 | A | C | 198 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0159 others(195): Show |
203 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.235-5578T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750490 | |||||||
| chr1:115750497 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-5585C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750497 | |||||||
| chr1:115750677 | T | C | 7 | a0001c0001t0005g0001 a0001c0001t0005g0143 a0001c0001t0005g0144 others(4): Show |
9 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.235-5765A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750677 | |||||||
| chr1:115750712 | T | G | 2 | a0002c0004t0004g0008 a0002c0004t0004g0329 |
3 | HG02132.hp1 NA19070.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.235-5800A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750712 | |||||||
| chr1:115750896 | C | CTGTAGGT others(19): Show |
197 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(194): Show |
202 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-5985_235-5984i others(28): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750896 | |||||||
| chr1:115750988 | G | T | 1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-6076C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115750988 | |||||||
| chr1:115751025 | A | C | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-6113T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751025 | |||||||
| chr1:115751248 | G | C | 1 | a0002c0003t0003g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.235-6336C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751248 | |||||||
| chr1:115751276 | A | G | 95 | a0001c0001t0004g0159 a0001c0001t0004g0217 a0001c0002t0001g0003 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-6364T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751276 | |||||||
| chr1:115751342 | T | C | 94 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(91): Show |
96 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-6430A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751342 | |||||||
| chr1:115751370 | A | T | 1 | a0002c0003t0001g0339 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.235-6458T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751370 | |||||||
| chr1:115751392 | G | A | 3 | a0001c0001t0019g0027 a0005c0009t0001g0060 a0005c0009t0013g0035 |
3 | HG02572.hp1 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.235-6480C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751392 | |||||||
| chr1:115751396 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-6484C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751396 | |||||||
| chr1:115751428 | G | T | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-6516C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751428 | |||||||
| chr1:115751433 | G | GC | 209 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(206): Show |
213 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.235-6522dupG | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751433 | |||||||
| chr1:115751447 | A | T | 209 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(206): Show |
213 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.235-6535T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751447 | |||||||
| chr1:115751469 | T | C | 209 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(206): Show |
213 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.235-6557A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751469 | |||||||
| chr1:115751493 | A | C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0112 a0001c0001t0002g0117 |
3 | NA18979.hp1 NA18982.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.235-6581T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751493 | |||||||
| chr1:115751504 | T | TA | 199 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0054 others(196): Show |
202 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.235-6593dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751504 | |||||||
| chr1:115751504 | TA | T | 3 | a0001c0001t0014g0002 a0002c0004t0017g0016 a0005c0011t0001g0140 |
4 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-6593delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751504 | |||||||
| chr1:115751588 | C | T | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235-6676G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751588 | |||||||
| chr1:115751593 | G | A | 315 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(312): Show |
321 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(318): Show |
intron_variant | MODIFIER | c.235-6681C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751593 | |||||||
| chr1:115751601 | G | T | 1 | a0001c0002t0003g0223 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.235-6689C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751601 | |||||||
| chr1:115751668 | T | C | 1 | a0001c0002t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.235-6756A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751668 | |||||||
| chr1:115751671 | TA | T | 7 | a0001c0001t0008g0026 a0002c0003t0001g0349 a0002c0003t0010g0009 others(4): Show |
7 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-6760delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751671 | |||||||
| chr1:115751671 | TAAAA | T | 209 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(206): Show |
213 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.235-6763_235-6760d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115751671 | |||||||
| chr1:115752065 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.235-7153T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752065 | |||||||
| chr1:115752069 | C | A | 103 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0004g0192 others(100): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-7157G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752069 | |||||||
| chr1:115752212 | A | G | 26 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(23): Show |
26 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.235-7300T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752212 | |||||||
| chr1:115752379 | A | C | 1 | a0002c0004t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235-7467T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752379 | |||||||
| chr1:115752386 | G | A | 313 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(310): Show |
319 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.235-7474C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752386 | |||||||
| chr1:115752392 | C | A | 6 | a0001c0002t0003g0038 a0001c0002t0003g0039 a0001c0002t0003g0040 others(3): Show |
6 | HG00558.hp2 HG00673.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-7480G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752392 | |||||||
| chr1:115752440 | G | A | 313 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(310): Show |
319 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.235-7528C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752440 | |||||||
| chr1:115752512 | AG | A | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-7601delC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752512 | |||||||
| chr1:115752655 | T | A | 1 | a0002c0004t0002g0323 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.235-7743A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752655 | |||||||
| chr1:115752898 | A | C | 95 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-7986T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752898 | |||||||
| chr1:115752983 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.235-8071C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115752983 | |||||||
| chr1:115753044 | T | A | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-8132A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753044 | |||||||
| chr1:115753053 | A | G | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-8141T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753053 | |||||||
| chr1:115753163 | G | A | 1 | a0002c0003t0003g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.235-8251C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753163 | |||||||
| chr1:115753387 | C | A | 3 | a0001c0001t0008g0029 a0001c0001t0008g0036 a0001c0007t0020g0028 |
3 | HG02257.hp2 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235-8475G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753387 | |||||||
| chr1:115753447 | T | A | 1 | a0001c0002t0003g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.235-8535A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753447 | |||||||
| chr1:115753504 | C | CA | 308 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(305): Show |
314 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(311): Show |
intron_variant | MODIFIER | c.235-8593dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753504 | |||||||
| chr1:115753600 | G | A | 3 | a0001c0001t0014g0002 a0002c0004t0017g0016 a0005c0011t0001g0140 |
4 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-8688C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753600 | |||||||
| chr1:115753643 | A | T | 1 | a0002c0004t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.235-8731T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753643 | |||||||
| chr1:115753731 | T | C | 350 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(347): Show |
359 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(356): Show |
intron_variant | MODIFIER | c.235-8819A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753731 | |||||||
| chr1:115753741 | A | G | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-8829T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753741 | |||||||
| chr1:115753817 | G | A | 1 | a0001c0002t0003g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.235-8905C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753817 | |||||||
| chr1:115753889 | T | A | 95 | a0001c0001t0004g0217 a0001c0002t0001g0003 a0001c0002t0001g0046 others(92): Show |
97 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.235-8977A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753889 | |||||||
| chr1:115753892 | G | GA | 33 | a0001c0001t0002g0052 a0001c0001t0002g0054 a0001c0001t0002g0061 others(30): Show |
33 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.235-8981dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753892 | |||||||
| chr1:115753913 | C | G | 303 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(300): Show |
311 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.235-9001G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753913 | |||||||
| chr1:115753951 | C | A | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235-9039G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115753951 | |||||||
| chr1:115754010 | A | G | 103 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(100): Show |
106 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.235-9098T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754010 | |||||||
| chr1:115754032 | C | T | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-9120G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754032 | |||||||
| chr1:115754051 | C | G | 6 | a0002c0013t0009g0297 a0004c0008t0001g0273 a0004c0008t0001g0308 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-9139G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754051 | |||||||
| chr1:115754110 | C | G | 1 | a0001c0006t0003g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.235-9198G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754110 | |||||||
| chr1:115754144 | C | A | 1 | a0002c0003t0001g0339 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.235-9232G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754144 | |||||||
| chr1:115754156 | A | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(75): Show |
79 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(76): Show |
intron_variant | MODIFIER | c.235-9244T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754156 | |||||||
| chr1:115754228 | C | A | 31 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(28): Show |
31 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.235-9316G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754228 | |||||||
| chr1:115754257 | C | T | 1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.235-9345G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754257 | |||||||
| chr1:115754334 | T | C | 1 | a0001c0001t0002g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.235-9422A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754334 | |||||||
| chr1:115754353 | G | A | 1 | a0002c0003t0003g0258 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.235-9441C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754353 | |||||||
| chr1:115754413 | A | G | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9501T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754413 | |||||||
| chr1:115754445 | T | A | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9533A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754445 | |||||||
| chr1:115754564 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.235-9652A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754564 | |||||||
| chr1:115754591 | G | A | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9679C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754591 | |||||||
| chr1:115754592 | C | G | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9680G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754592 | |||||||
| chr1:115754671 | T | C | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9759A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754671 | |||||||
| chr1:115754677 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.235-9765G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754677 | |||||||
| chr1:115754772 | C | T | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-9860G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115754772 | |||||||
| chr1:115755137 | C | A | 102 | a0001c0001t0002g0153 a0001c0001t0002g0174 a0001c0001t0002g0195 others(99): Show |
105 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.235-10225G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755137 | |||||||
| chr1:115755154 | T | C | 1 | a0002c0004t0004g0296 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.235-10242A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755154 | |||||||
| chr1:115755334 | TAGTCCCT others(6): Show |
T | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-10435_235-1042 others(17): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755334 | |||||||
| chr1:115755382 | A | G | 1 | a0003c0005t0001g0249 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.235-10470T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755382 | |||||||
| chr1:115755443 | C | A | 104 | a0001c0001t0002g0233 a0001c0001t0004g0217 a0001c0001t0019g0027 others(101): Show |
106 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.235-10531G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755443 | |||||||
| chr1:115755466 | A | G | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-10554T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755466 | |||||||
| chr1:115755516 | C | T | 6 | a0001c0001t0002g0112 a0002c0003t0007g0020 a0002c0003t0007g0023 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-10604G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755516 | |||||||
| chr1:115755529 | G | A | 2 | a0001c0002t0003g0173 a0001c0002t0003g0226 |
2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.235-10617C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755529 | |||||||
| chr1:115755728 | C | G | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-10816G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755728 | |||||||
| chr1:115755836 | C | T | 1 | a0001c0007t0009g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.235-10924G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755836 | |||||||
| chr1:115755856 | G | A | 2 | a0002c0003t0007g0017 a0002c0003t0007g0021 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.235-10944C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755856 | |||||||
| chr1:115755953 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(73): Show |
77 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.235-11041C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755953 | |||||||
| chr1:115755978 | A | ACTT | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-11069_235-1106 others(7): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115755978 | |||||||
| chr1:115756092 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.235-11180G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756092 | |||||||
| chr1:115756102 | T | C | 1 | a0001c0001t0021g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.235-11190A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756102 | |||||||
| chr1:115756218 | C | T | 2 | a0001c0001t0008g0029 a0001c0001t0008g0036 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.235-11306G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756218 | |||||||
| chr1:115756219 | G | A | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-11307C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756219 | |||||||
| chr1:115756233 | A | G | 350 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(347): Show |
359 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(356): Show |
intron_variant | MODIFIER | c.235-11321T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756233 | |||||||
| chr1:115756233 | A | T | 1 | a0002c0004t0015g0320 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-11321T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756233 | |||||||
| chr1:115756418 | A | G | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-11506T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756418 | |||||||
| chr1:115756435 | A | C | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-11523T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756435 | |||||||
| chr1:115756440 | T | C | 1 | a0002c0004t0004g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.235-11528A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756440 | |||||||
| chr1:115756636 | G | T | 28 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(25): Show |
28 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.234+11672C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756636 | |||||||
| chr1:115756663 | G | A | 1 | a0002c0003t0006g0328 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.234+11645C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756663 | |||||||
| chr1:115756681 | G | A | 27 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(24): Show |
27 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.234+11627C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756681 | |||||||
| chr1:115756768 | G | A | 1 | a0001c0002t0003g0218 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.234+11540C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756768 | |||||||
| chr1:115756820 | G | A | 11 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(8): Show |
11 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+11488C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756820 | |||||||
| chr1:115756960 | A | G | 23 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(20): Show |
23 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.234+11348T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756960 | |||||||
| chr1:115756968 | A | T | 26 | a0001c0001t0005g0162 a0001c0007t0009g0163 a0002c0004t0002g0316 others(23): Show |
28 | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.234+11340T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115756968 | |||||||
| chr1:115757048 | C | T | 22 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(19): Show |
24 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.234+11260G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757048 | |||||||
| chr1:115757124 | A | G | 6 | a0002c0004t0004g0282 a0002c0004t0004g0293 a0002c0004t0004g0325 others(3): Show |
6 | HG00597.hp2 NA18946.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+11184T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757124 | |||||||
| chr1:115757211 | G | GCATTTCT others(3): Show |
1 | a0002c0003t0001g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.234+11087_234+1109 others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757211 | |||||||
| chr1:115757225 | T | A | 1 | a0002c0003t0006g0345 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234+11083A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757225 | |||||||
| chr1:115757347 | A | G | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+10961T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757347 | |||||||
| chr1:115757516 | A | G | 76 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(73): Show |
77 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.234+10792T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757516 | |||||||
| chr1:115757527 | G | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+10781C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757527 | |||||||
| chr1:115757596 | T | C | 2 | a0001c0001t0019g0027 a0005c0009t0013g0035 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.234+10712A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757596 | |||||||
| chr1:115757604 | C | T | 2 | a0002c0003t0003g0254 a0002c0003t0003g0255 |
2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.234+10704G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757604 | |||||||
| chr1:115757708 | C | A | 5 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0002g0116 others(2): Show |
5 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+10600G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757708 | |||||||
| chr1:115757796 | T | C | 1 | a0001c0007t0020g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234+10512A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757796 | |||||||
| chr1:115757804 | A | C | 2 | a0001c0001t0019g0027 a0005c0009t0013g0035 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.234+10504T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757804 | |||||||
| chr1:115757817 | C | T | 2 | a0001c0001t0002g0061 a0001c0002t0003g0057 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.234+10491G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757817 | |||||||
| chr1:115757834 | C | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+10474G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757834 | |||||||
| chr1:115757981 | G | A | 81 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(78): Show |
82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.234+10327C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115757981 | |||||||
| chr1:115758115 | T | C | 83 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(80): Show |
84 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.234+10193A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758115 | |||||||
| chr1:115758398 | T | C | 128 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(125): Show |
132 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.234+9910A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758398 | |||||||
| chr1:115758513 | G | A | 2 | a0001c0001t0005g0162 a0001c0007t0009g0163 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.234+9795C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758513 | |||||||
| chr1:115758627 | G | A | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+9681C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758627 | |||||||
| chr1:115758850 | C | T | 1 | a0002c0003t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.234+9458G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758850 | |||||||
| chr1:115758936 | C | A | 323 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(320): Show |
329 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(326): Show |
intron_variant | MODIFIER | c.234+9372G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758936 | |||||||
| chr1:115758944 | G | A | 83 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(80): Show |
84 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.234+9364C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115758944 | |||||||
| chr1:115759042 | C | T | 1 | a0001c0002t0003g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.234+9266G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759042 | |||||||
| chr1:115759049 | T | G | 129 | a0001c0001t0002g0233 a0001c0002t0001g0003 a0001c0002t0001g0046 others(126): Show |
133 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.234+9259A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759049 | |||||||
| chr1:115759052 | C | T | 2 | a0001c0001t0005g0162 a0001c0007t0009g0163 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.234+9256G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759052 | |||||||
| chr1:115759069 | T | C | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+9239A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759069 | |||||||
| chr1:115759079 | A | T | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+9229T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759079 | |||||||
| chr1:115759252 | A | G | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+9056T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759252 | |||||||
| chr1:115759278 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.234+9030C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759278 | |||||||
| chr1:115759283 | G | A | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+9025C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759283 | |||||||
| chr1:115759565 | C | T | 12 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+8743G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759565 | |||||||
| chr1:115759864 | G | A | 1 | a0003c0005t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234+8444C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759864 | |||||||
| chr1:115759971 | C | T | 81 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(78): Show |
82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.234+8337G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115759971 | |||||||
| chr1:115760080 | C | A | 79 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(76): Show |
80 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.234+8228G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760080 | |||||||
| chr1:115760302 | C | T | 180 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(177): Show |
182 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.234+8006G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760302 | |||||||
| chr1:115760307 | C | G | 3 | a0001c0002t0003g0170 a0001c0002t0003g0181 a0001c0002t0003g0185 |
3 | HG02071.hp2 HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.234+8001G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760307 | |||||||
| chr1:115760460 | T | C | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(89): Show |
93 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(90): Show |
intron_variant | MODIFIER | c.234+7848A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760460 | |||||||
| chr1:115760685 | T | A | 2 | a0002c0003t0010g0009 a0002c0003t0010g0011 |
2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+7623A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760685 | |||||||
| chr1:115760736 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.234+7572G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760736 | |||||||
| chr1:115760783 | G | A | 5 | a0002c0003t0010g0009 a0002c0003t0010g0011 a0002c0003t0010g0012 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+7525C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115760783 | |||||||
| chr1:115761159 | C | T | 8 | a0001c0001t0005g0165 a0001c0002t0003g0214 a0001c0002t0003g0220 others(5): Show |
8 | HG02451.hp2 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+7149G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761159 | |||||||
| chr1:115761183 | G | C | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+7125C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761183 | |||||||
| chr1:115761321 | C | T | 1 | a0003c0005t0001g0242 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234+6987G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761321 | |||||||
| chr1:115761353 | C | A | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+6955G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761353 | |||||||
| chr1:115761354 | C | A | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+6954G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761354 | |||||||
| chr1:115761369 | C | G | 1 | a0001c0002t0001g0003 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.234+6939G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761369 | |||||||
| chr1:115761402 | A | AAAGAAGA others(242): Show |
1 | a0003c0005t0001g0248 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.234+6905_234+6906i others(251): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAG | 16 | a0001c0002t0001g0152 a0001c0002t0001g0167 a0001c0002t0003g0038 others(13): Show |
16 | HG01070.hp1 HG01081.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+6905_234+6906i others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(229): Show |
1 | a0002c0003t0001g0309 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.234+6905_234+6906i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(241): Show |
1 | a0002c0004t0004g0292 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.234+6905_234+6906i others(250): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(226): Show |
1 | a0002c0004t0004g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.234+6905_234+6906i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(226): Show |
1 | a0002c0004t0004g0276 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.234+6905_234+6906i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(223): Show |
1 | a0003c0005t0001g0241 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.234+6905_234+6906i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(232): Show |
1 | a0001c0002t0001g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.234+6905_234+6906i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AAGAAGAA others(202): Show |
1 | a0002c0004t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.234+6905_234+6906i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | AG | 12 | a0001c0001t0004g0216 a0001c0002t0003g0198 a0001c0002t0003g0200 others(9): Show |
12 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.234+6905_234+6906i others(3): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761402 | A | G | 3 | a0001c0001t0019g0027 a0001c0002t0003g0048 a0005c0009t0013g0035 |
3 | HG02922.hp1 HG03041.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.234+6906T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761402 | |||||||
| chr1:115761404 | A | G | 1 | a0002c0003t0001g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234+6904T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761404 | |||||||
| chr1:115761405 | G | C | 77 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(74): Show |
78 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.234+6903C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761405 | |||||||
| chr1:115761426 | G | GAAGGGCA others(26): Show |
1 | a0002c0003t0007g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6881_234+6882i others(35): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761426 | |||||||
| chr1:115761427 | A | C | 1 | a0002c0004t0011g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.234+6881T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761427 | |||||||
| chr1:115761429 | G | GGGCAA | 3 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 |
3 | HG01884.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6878_234+6879i others(7): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761429 | |||||||
| chr1:115761429 | G | GGGCAACA others(4): Show |
1 | a0002c0004t0011g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234+6878_234+6879i others(13): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761429 | |||||||
| chr1:115761429 | G | GGGCAACA others(23): Show |
5 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+6878_234+6879i others(32): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761429 | |||||||
| chr1:115761430 | A | C | 3 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 |
3 | HG01884.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6878T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761430 | |||||||
| chr1:115761432 | G | T | 2 | a0002c0004t0011g0014 a0002c0004t0017g0016 |
2 | HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234+6876C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761432 | |||||||
| chr1:115761435 | G | A | 1 | a0002c0004t0011g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234+6873C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761435 | |||||||
| chr1:115761435 | G | T | 3 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 |
3 | HG01884.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6873C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761435 | |||||||
| chr1:115761438 | G | A | 3 | a0002c0004t0011g0014 a0002c0004t0011g0025 a0002c0004t0017g0016 |
3 | HG02895.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.234+6870C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761438 | |||||||
| chr1:115761438 | GA | G | 35 | a0001c0001t0002g0004 a0001c0001t0002g0054 a0001c0001t0002g0065 others(32): Show |
36 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.234+6869delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761438 | |||||||
| chr1:115761439 | A | AAG | 159 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0061 others(156): Show |
160 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.234+6868_234+6869i others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAG | 3 | a0001c0001t0004g0062 a0001c0002t0001g0058 a0001c0002t0003g0042 |
3 | HG00558.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(7): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(248): Show |
1 | a0002c0004t0004g0274 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(257): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(238): Show |
1 | a0002c0004t0002g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(247): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0002c0003t0001g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(184): Show |
1 | a0003c0005t0001g0240 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(193): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(245): Show |
1 | a0001c0001t0008g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(254): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0002c0004t0004g0332 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(241): Show |
1 | a0002c0004t0004g0007 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(250): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(227): Show |
1 | a0002c0004t0004g0293 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(236): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(221): Show |
1 | a0002c0003t0001g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(231): Show |
1 | a0003c0005t0001g0242 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(240): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0003t0001g0287 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0004t0002g0323 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(220): Show |
1 | a0003c0005t0001g0236 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0002c0003t0001g0312 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(227): Show |
1 | a0002c0003t0001g0334 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(236): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(178): Show |
1 | a0002c0003t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(187): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(187): Show |
1 | a0002c0004t0015g0320 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(196): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(220): Show |
1 | a0004c0008t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(224): Show |
1 | a0001c0001t0008g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(233): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(236): Show |
1 | a0004c0008t0001g0273 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0002c0004t0004g0331 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0002c0004t0004g0007 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(191): Show |
1 | a0002c0003t0006g0328 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(192): Show |
1 | a0002c0003t0003g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(201): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(198): Show |
1 | a0002c0003t0001g0280 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(207): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(241): Show |
1 | a0003c0005t0001g0249 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(250): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(190): Show |
1 | a0003c0005t0001g0238 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(199): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(202): Show |
2 | a0002c0003t0001g0286 a0002c0004t0005g0318 |
2 | HG00609.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0002c0003t0003g0338 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0003t0001g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(211): Show |
1 | a0002c0004t0004g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(229): Show |
1 | a0003c0012t0004g0243 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(225): Show |
1 | a0002c0004t0004g0344 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(234): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(208): Show |
1 | a0002c0003t0001g0265 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(230): Show |
1 | a0002c0003t0001g0341 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(239): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(205): Show |
1 | a0002c0003t0003g0255 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0001c0001t0014g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(224): Show |
1 | a0002c0003t0001g0313 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(233): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0003c0005t0001g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(236): Show |
1 | a0003c0005t0001g0006 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(184): Show |
3 | a0002c0003t0001g0327 a0002c0003t0001g0349 a0003c0005t0001g0235 |
3 | NA18946.hp1 NA19064.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(193): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0003t0001g0326 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(195): Show |
1 | a0002c0004t0002g0281 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(204): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0001c0007t0020g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0002c0003t0001g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(205): Show |
1 | a0002c0004t0002g0302 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(229): Show |
1 | a0002c0004t0004g0333 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0002c0003t0001g0339 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0003t0003g0254 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0004c0008t0001g0311 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0001t0014g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(239): Show |
1 | a0002c0004t0004g0310 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(248): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(207): Show |
1 | a0001c0002t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(216): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(222): Show |
1 | a0002c0003t0001g0350 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(231): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
3 | a0002c0003t0001g0291 a0003c0005t0001g0006 a0003c0005t0001g0252 |
3 | HG03041.hp1 NA18952.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(187): Show |
1 | a0002c0003t0001g0351 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(196): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(193): Show |
1 | a0002c0003t0006g0354 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(202): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(187): Show |
2 | a0002c0003t0006g0353 a0003c0005t0001g0239 |
2 | NA18612.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(196): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(190): Show |
1 | a0003c0005t0001g0237 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(199): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0004t0002g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0002c0003t0003g0258 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0002c0004t0002g0337 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(215): Show |
1 | a0003c0005t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(230): Show |
1 | a0002c0004t0002g0272 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(239): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(236): Show |
1 | a0001c0001t0008g0029 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(220): Show |
1 | a0001c0001t0008g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(233): Show |
1 | a0002c0003t0003g0257 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(242): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(228): Show |
1 | a0002c0004t0004g0295 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(237): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0002c0004t0004g0296 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(190): Show |
1 | a0002c0004t0004g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(199): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0002c0004t0004g0008 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(191): Show |
1 | a0002c0004t0004g0278 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(202): Show |
1 | a0002c0003t0001g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(208): Show |
1 | a0002c0003t0001g0301 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(242): Show |
1 | a0002c0003t0001g0342 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(251): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(208): Show |
1 | a0002c0003t0001g0263 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(206): Show |
1 | a0001c0001t0004g0216 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(205): Show |
1 | a0002c0003t0001g0348 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0002c0004t0002g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(190): Show |
1 | a0002c0003t0001g0321 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(199): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
2 | a0002c0004t0004g0325 a0003c0005t0001g0247 |
2 | HG00597.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(220): Show |
1 | a0002c0004t0002g0316 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0002c0004t0004g0261 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0002c0004t0004g0008 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0004t0002g0306 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(196): Show |
1 | a0002c0003t0001g0322 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(205): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0003t0001g0288 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(208): Show |
1 | a0002c0003t0001g0299 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(163): Show |
1 | a0002c0004t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(172): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(236): Show |
1 | a0001c0001t0008g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(192): Show |
1 | a0002c0004t0002g0324 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(201): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(193): Show |
1 | a0002c0003t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(202): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(184): Show |
1 | a0001c0002t0006g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(193): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0004t0002g0346 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0003c0005t0001g0251 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(191): Show |
1 | a0002c0004t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(208): Show |
1 | a0002c0003t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0003c0005t0001g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(230): Show |
1 | a0002c0004t0004g0294 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(239): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0004t0002g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0002c0003t0001g0335 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(196): Show |
1 | a0002c0003t0006g0345 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(205): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(181): Show |
1 | a0002c0004t0002g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(190): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0002c0003t0001g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(195): Show |
1 | a0001c0002t0003g0160 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(204): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(198): Show |
1 | a0001c0002t0003g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(207): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0001c0002t0001g0003 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(239): Show |
1 | a0001c0002t0001g0003 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(248): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(196): Show |
1 | a0002c0004t0002g0336 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(205): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0004t0002g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(214): Show |
1 | a0002c0004t0004g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(217): Show |
1 | a0002c0003t0006g0315 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(166): Show |
1 | a0002c0003t0001g0347 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(175): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(228): Show |
1 | a0001c0002t0012g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(237): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(190): Show |
1 | a0002c0003t0006g0314 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(199): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0001g0047 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(202): Show |
1 | a0003c0005t0001g0250 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(221): Show |
1 | a0001c0002t0012g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0001c0002t0013g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0003g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(220): Show |
1 | a0001c0001t0002g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(199): Show |
1 | a0001c0001t0002g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(227): Show |
1 | a0002c0013t0009g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(236): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(193): Show |
1 | a0001c0001t0004g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(202): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(250): Show |
1 | a0001c0002t0001g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(259): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(253): Show |
1 | a0001c0001t0005g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(262): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(223): Show |
2 | a0001c0002t0001g0155 a0001c0002t0001g0156 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0001t0004g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(211): Show |
1 | a0001c0002t0001g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
1 | a0001c0001t0005g0001 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(221): Show |
1 | a0001c0001t0005g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0001c0001t0005g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0001t0005g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(232): Show |
2 | a0001c0001t0005g0144 a0001c0001t0005g0145 |
2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(235): Show |
1 | a0001c0001t0005g0001 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(241): Show |
1 | a0001c0001t0005g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(250): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0001t0005g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(189): Show |
1 | a0001c0002t0003g0210 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(198): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(192): Show |
1 | a0001c0002t0003g0171 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(201): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0003g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(211): Show |
1 | a0001c0002t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAAGAA others(186): Show |
1 | a0001c0002t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.234+6868_234+6869i others(195): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | AAGAGGAA others(150): Show |
1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+6868_234+6869i others(159): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761439 | A | ACTCAGTC others(11): Show |
3 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 |
3 | HG01884.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6868_234+6869i others(20): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761439 | |||||||
| chr1:115761440 | A | AGAAGAAG others(234): Show |
1 | a0004c0008t0001g0308 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234+6867_234+6868i others(243): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761440 | |||||||
| chr1:115761440 | A | AGAAGAAG others(223): Show |
1 | a0004c0008t0003g0352 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234+6867_234+6868i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761440 | |||||||
| chr1:115761440 | A | AGAAGAAG others(241): Show |
1 | a0001c0001t0005g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.234+6867_234+6868i others(250): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761440 | |||||||
| chr1:115761441 | A | G | 2 | a0001c0001t0005g0162 a0002c0004t0015g0320 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.234+6867T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761441 | |||||||
| chr1:115761442 | G | A | 2 | a0002c0004t0011g0014 a0002c0004t0017g0016 |
2 | HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234+6866C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761442 | |||||||
| chr1:115761443 | A | G | 2 | a0001c0001t0005g0001 a0002c0003t0001g0307 |
4 | HG00642.hp1 HG01074.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+6865T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761443 | |||||||
| chr1:115761444 | A | G | 1 | a0001c0007t0009g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.234+6864T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761444 | |||||||
| chr1:115761446 | A | G | 5 | a0001c0001t0004g0159 a0001c0001t0005g0144 a0001c0001t0005g0145 others(2): Show |
5 | HG01952.hp1 HG02148.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+6862T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761446 | |||||||
| chr1:115761449 | A | G | 8 | a0001c0001t0005g0143 a0001c0002t0001g0155 a0001c0002t0001g0156 others(5): Show |
8 | HG00673.hp2 HG01071.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+6859T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761449 | |||||||
| chr1:115761452 | A | AGGAAGAA others(218): Show |
1 | a0002c0004t0002g0319 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.234+6855_234+6856i others(227): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761452 | |||||||
| chr1:115761452 | A | G | 7 | a0001c0001t0002g0069 a0001c0001t0004g0072 a0001c0001t0005g0142 others(4): Show |
7 | HG00438.hp2 HG01361.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+6856T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761452 | |||||||
| chr1:115761455 | A | AAGAAGAA others(214): Show |
1 | a0001c0002t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.234+6852_234+6853i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761455 | |||||||
| chr1:115761455 | A | G | 4 | a0001c0001t0002g0153 a0001c0002t0001g0152 a0001c0002t0001g0154 others(1): Show |
4 | HG00639.hp2 HG01081.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+6853T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761455 | |||||||
| chr1:115761458 | A | AAAAAGAA others(134): Show |
1 | a0002c0003t0007g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(143): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(232): Show |
1 | a0001c0002t0001g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(235): Show |
1 | a0001c0002t0003g0228 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(229): Show |
1 | a0001c0010t0003g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(229): Show |
1 | a0001c0002t0003g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(211): Show |
1 | a0001c0002t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(209): Show |
1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(223): Show |
1 | a0001c0002t0003g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(236): Show |
1 | a0001c0002t0003g0230 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(232): Show |
1 | a0001c0002t0001g0135 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(241): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(188): Show |
1 | a0005c0011t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(197): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(223): Show |
1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(220): Show |
1 | a0001c0002t0003g0207 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(217): Show |
1 | a0001c0002t0003g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(199): Show |
1 | a0001c0002t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(155): Show |
1 | a0001c0001t0004g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(164): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(131): Show |
1 | a0002c0003t0001g0260 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(140): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(211): Show |
2 | a0001c0002t0003g0005 a0001c0002t0003g0196 |
3 | NA18943.hp2 NA18950.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(205): Show |
2 | a0001c0002t0003g0050 a0001c0002t0003g0191 |
2 | HG00639.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(211): Show |
1 | a0001c0001t0004g0206 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(202): Show |
1 | a0001c0002t0003g0189 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(214): Show |
1 | a0001c0002t0003g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(219): Show |
1 | a0001c0002t0003g0087 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(228): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(212): Show |
1 | a0001c0001t0002g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(221): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(218): Show |
1 | a0001c0001t0002g0118 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(227): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(206): Show |
1 | a0001c0001t0002g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(206): Show |
1 | a0001c0001t0002g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(207): Show |
1 | a0001c0001t0002g0088 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(216): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(202): Show |
1 | a0001c0001t0004g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(203): Show |
1 | a0001c0002t0003g0048 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(212): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(224): Show |
1 | a0001c0001t0002g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(233): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(209): Show |
1 | a0001c0002t0003g0091 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(215): Show |
2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(216): Show |
1 | a0001c0001t0002g0081 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(225): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(216): Show |
1 | a0001c0001t0002g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(225): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(208): Show |
1 | a0001c0001t0002g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(209): Show |
1 | a0001c0001t0002g0086 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(215): Show |
1 | a0001c0001t0002g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(210): Show |
1 | a0001c0001t0002g0083 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(219): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(209): Show |
1 | a0001c0001t0002g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(208): Show |
1 | a0001c0001t0002g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAA others(170): Show |
1 | a0001c0007t0009g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(179): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGAG others(206): Show |
1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(200): Show |
1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(209): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(207): Show |
1 | a0001c0001t0021g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(216): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(194): Show |
1 | a0001c0001t0002g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(203): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(219): Show |
1 | a0001c0001t0002g0068 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(228): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(188): Show |
1 | a0001c0001t0002g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(197): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(195): Show |
1 | a0001c0001t0002g0127 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(204): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAAGGG others(182): Show |
1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(191): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAGGAA others(210): Show |
1 | a0001c0001t0002g0128 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(219): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAGGAA others(191): Show |
1 | a0001c0001t0002g0101 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.234+6849_234+6850i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAGGAA others(203): Show |
3 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0109 |
3 | HG01106.hp1 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(212): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGAGGAA others(197): Show |
1 | a0001c0001t0002g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(206): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGGGGAA others(205): Show |
1 | a0001c0001t0002g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGGGGAA others(191): Show |
2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | NA18948.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AAGGGGAA others(185): Show |
1 | a0001c0001t0002g0095 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(194): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AGGAAGGG others(206): Show |
1 | a0001c0001t0002g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AGGAAGGG others(200): Show |
1 | a0001c0001t0002g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.234+6849_234+6850i others(209): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | AGGAGGAA others(203): Show |
1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.234+6849_234+6850i others(212): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761458 | A | G | 12 | a0001c0001t0002g0069 a0001c0001t0004g0072 a0001c0001t0004g0216 others(9): Show |
12 | HG01109.hp1 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+6850T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761458 | |||||||
| chr1:115761459 | A | AGAAGAAG others(152): Show |
1 | a0002c0003t0001g0268 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.234+6848_234+6849i others(161): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761459 | |||||||
| chr1:115761459 | A | AGAAGAGG others(152): Show |
1 | a0002c0003t0001g0303 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.234+6848_234+6849i others(161): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761459 | |||||||
| chr1:115761461 | A | AAGAGGAG others(220): Show |
1 | a0001c0002t0006g0229 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.234+6846_234+6847i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761461 | |||||||
| chr1:115761462 | A | AGAAGAAG others(152): Show |
1 | a0001c0001t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234+6845_234+6846i others(161): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761462 | |||||||
| chr1:115761462 | A | AGAAGAAG others(149): Show |
1 | a0002c0003t0001g0267 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.234+6845_234+6846i others(158): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761462 | |||||||
| chr1:115761462 | A | AGAAGAAG others(152): Show |
1 | a0005c0009t0013g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.234+6845_234+6846i others(161): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761462 | |||||||
| chr1:115761462 | A | G | 1 | a0001c0001t0004g0217 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.234+6846T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761462 | |||||||
| chr1:115761464 | G | A | 205 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0054 others(202): Show |
207 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.234+6844C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GAAGAGGA others(227): Show |
1 | a0002c0004t0004g0269 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(236): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGAAGGGG others(196): Show |
1 | a0001c0001t0002g0103 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(205): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(223): Show |
1 | a0001c0001t0002g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.234+6843_234+6844i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(197): Show |
1 | a0001c0001t0002g0102 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.234+6843_234+6844i others(206): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(209): Show |
1 | a0001c0001t0002g0108 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(210): Show |
1 | a0001c0001t0002g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(219): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(203): Show |
1 | a0001c0001t0002g0114 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(212): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(206): Show |
1 | a0002c0003t0001g0343 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.234+6843_234+6844i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761464 | G | GGGAAGGG others(164): Show |
1 | a0001c0001t0005g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+6843_234+6844i others(173): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761464 | |||||||
| chr1:115761465 | A | AGGGCAAC others(191): Show |
1 | a0002c0003t0010g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.234+6842_234+6843i others(200): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761465 | |||||||
| chr1:115761465 | A | G | 2 | a0001c0001t0004g0217 a0001c0002t0003g0042 |
2 | HG00558.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.234+6843T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761465 | |||||||
| chr1:115761466 | G | GAAGAAGA others(195): Show |
1 | a0003c0005t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.234+6841_234+6842i others(204): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761466 | |||||||
| chr1:115761467 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0001g0133 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGAAGAA others(221): Show |
1 | a0001c0001t0002g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.234+6840_234+6841i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGAAGAA others(223): Show |
1 | a0001c0002t0001g0137 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGG | 4 | a0001c0001t0002g0109 a0001c0002t0003g0045 a0001c0002t0003g0160 others(1): Show |
4 | HG01361.hp2 HG01978.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+6840_234+6841i others(5): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(233): Show |
1 | a0001c0001t0002g0107 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.234+6840_234+6841i others(242): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(215): Show |
2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | NA18995.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.234+6840_234+6841i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(223): Show |
1 | a0001c0001t0002g0051 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(209): Show |
1 | a0001c0001t0002g0115 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(222): Show |
1 | a0001c0001t0002g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(231): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(209): Show |
3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG01515.hp2 HG01517.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.234+6840_234+6841i others(218): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AAGGGGAA others(197): Show |
1 | a0001c0001t0002g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.234+6840_234+6841i others(206): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AGGAGGAA others(211): Show |
2 | a0001c0002t0003g0201 a0001c0002t0003g0202 |
2 | HG00597.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.234+6840_234+6841i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AGGAGGAA others(211): Show |
1 | a0001c0002t0003g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.234+6840_234+6841i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | AGGAGGAA others(202): Show |
3 | a0001c0002t0003g0220 a0001c0002t0003g0221 a0001c0002t0003g0222 |
3 | HG02486.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.234+6840_234+6841i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761467 | A | G | 7 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0105 others(4): Show |
7 | HG01891.hp1 HG02523.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+6841T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761467 | |||||||
| chr1:115761469 | G | A | 5 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+6839C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761469 | |||||||
| chr1:115761470 | A | AAGGGCAA others(197): Show |
1 | a0002c0003t0010g0012 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.234+6837_234+6838i others(206): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761470 | |||||||
| chr1:115761470 | A | G | 65 | a0001c0001t0002g0004 a0001c0001t0002g0068 a0001c0001t0002g0069 others(62): Show |
67 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.234+6838T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761470 | |||||||
| chr1:115761471 | A | G | 6 | a0001c0001t0004g0215 a0001c0002t0001g0167 a0001c0002t0003g0186 others(3): Show |
6 | HG01070.hp1 HG01109.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+6837T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761471 | |||||||
| chr1:115761472 | G | A | 4 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+6836C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761472 | |||||||
| chr1:115761473 | A | AAGAAGAA others(235): Show |
1 | a0001c0002t0003g0211 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(244): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAA others(238): Show |
1 | a0001c0002t0003g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(247): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAA others(230): Show |
1 | a0001c0002t0003g0176 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(239): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAA others(220): Show |
1 | a0001c0002t0003g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAG others(219): Show |
1 | a0001c0002t0003g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(228): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAG others(223): Show |
2 | a0001c0002t0003g0198 a0001c0002t0003g0232 |
2 | NA18966.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.234+6834_234+6835i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAG others(217): Show |
1 | a0001c0002t0003g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAAGAG others(228): Show |
1 | a0001c0002t0003g0225 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(237): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(223): Show |
1 | a0001c0002t0003g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(232): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(220): Show |
1 | a0001c0002t0003g0199 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(217): Show |
1 | a0001c0002t0003g0223 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(208): Show |
1 | a0001c0002t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(214): Show |
1 | a0001c0002t0003g0197 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGAGGAG others(221): Show |
1 | a0001c0002t0003g0203 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGGGGAA others(215): Show |
1 | a0001c0001t0002g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGGGGAA others(215): Show |
1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGGGGAA others(215): Show |
1 | a0001c0001t0002g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGGGGAA others(212): Show |
1 | a0001c0001t0002g0073 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(221): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AAGGGGAA others(198): Show |
1 | a0001c0001t0005g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(207): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAAGAA others(211): Show |
1 | a0001c0002t0003g0044 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAAGAA others(213): Show |
1 | a0001c0002t0003g0040 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(222): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAAGGG others(206): Show |
1 | a0001c0001t0002g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAGGAA others(220): Show |
1 | a0001c0002t0003g0213 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.234+6834_234+6835i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAGGAA others(217): Show |
1 | a0001c0002t0003g0200 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAGGAA others(214): Show |
1 | a0001c0002t0003g0224 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.234+6834_234+6835i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAGGAA others(205): Show |
2 | a0001c0002t0001g0166 a0001c0006t0003g0184 |
2 | HG01074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.234+6834_234+6835i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | AGGAGGAA others(208): Show |
3 | a0001c0001t0005g0165 a0001c0002t0003g0231 a0001c0007t0009g0180 |
3 | HG02451.hp2 HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.234+6834_234+6835i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761473 | A | G | 25 | a0001c0001t0002g0051 a0001c0001t0002g0074 a0001c0001t0002g0075 others(22): Show |
25 | HG00597.hp1 HG01361.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.234+6835T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761473 | |||||||
| chr1:115761474 | A | G | 7 | a0001c0001t0004g0215 a0001c0002t0001g0167 a0001c0002t0003g0186 others(4): Show |
7 | HG00621.hp2 HG01070.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+6834T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761474 | |||||||
| chr1:115761476 | A | AAGAAGAA others(229): Show |
1 | a0001c0001t0002g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0003g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGAAGAA others(226): Show |
1 | a0001c0002t0003g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(235): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGAAGAG others(217): Show |
1 | a0001c0002t0003g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGAGGAG others(217): Show |
1 | a0001c0002t0003g0219 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(226): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGCAA others(203): Show |
1 | a0002c0003t0010g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(212): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGCAA others(204): Show |
1 | a0002c0003t0010g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(213): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGCAA others(206): Show |
1 | a0002c0004t0016g0010 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGGAA others(215): Show |
1 | a0001c0002t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGGAA others(221): Show |
1 | a0001c0001t0002g0089 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(230): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGGAA others(215): Show |
1 | a0002c0003t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(224): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AAGGGGAA others(229): Show |
1 | a0001c0002t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.234+6831_234+6832i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AGGAAGGG others(206): Show |
1 | a0001c0007t0009g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(215): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AGGAGGAA others(211): Show |
1 | a0001c0002t0022g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AGGAGGAA others(211): Show |
1 | a0001c0002t0003g0218 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | AGGAGGAA others(214): Show |
1 | a0001c0002t0003g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.234+6831_234+6832i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761476 | A | G | 50 | a0001c0001t0002g0004 a0001c0001t0002g0068 a0001c0001t0002g0069 others(47): Show |
52 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.234+6832T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761476 | |||||||
| chr1:115761477 | A | G | 1 | a0001c0001t0005g0150 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.234+6831T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761477 | |||||||
| chr1:115761479 | A | AAGAGGAG others(220): Show |
2 | a0001c0002t0003g0170 a0001c0002t0003g0185 |
2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.234+6828_234+6829i others(229): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | AGGAGGAA others(229): Show |
1 | a0001c0002t0003g0188 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.234+6828_234+6829i others(238): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | AGGAGGAA others(214): Show |
1 | a0001c0006t0003g0168 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.234+6828_234+6829i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | AGGAGGAA others(211): Show |
2 | a0001c0006t0003g0182 a0001c0006t0003g0183 |
2 | HG01106.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.234+6828_234+6829i others(220): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | AGGAGGAA others(214): Show |
1 | a0001c0007t0009g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234+6828_234+6829i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | AGGAGGAA others(212): Show |
1 | a0001c0002t0003g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.234+6828_234+6829i others(221): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761479 | A | G | 10 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 others(7): Show |
10 | HG01074.hp1 HG02965.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+6829T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761479 | |||||||
| chr1:115761481 | G | A | 2 | a0002c0004t0011g0014 a0002c0004t0017g0016 |
2 | HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234+6827C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761481 | |||||||
| chr1:115761482 | A | AAGAAGAA others(194): Show |
1 | a0001c0002t0001g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.234+6825_234+6826i others(203): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761482 | A | AAGAAGAA others(185): Show |
1 | a0005c0009t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.234+6825_234+6826i others(194): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761482 | A | AAGAGGAA others(161): Show |
1 | a0001c0001t0002g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.234+6825_234+6826i others(170): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761482 | A | AAGGGGAA others(161): Show |
5 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0021 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+6825_234+6826i others(170): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761482 | A | AGGAGGAA others(214): Show |
1 | a0001c0006t0003g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.234+6825_234+6826i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761482 | A | G | 16 | a0001c0001t0002g0069 a0001c0001t0002g0071 a0001c0001t0002g0125 others(13): Show |
16 | HG01175.hp1 HG01255.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+6826T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761482 | |||||||
| chr1:115761486 | A | T | 1 | a0003c0005t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.234+6822T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761486 | |||||||
| chr1:115761488 | G | A | 317 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(314): Show |
325 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.234+6820C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(236): Show |
1 | a0002c0003t0001g0340 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.234+6819_234+6820i others(245): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(244): Show |
1 | a0001c0002t0001g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.234+6819_234+6820i others(253): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(164): Show |
1 | a0001c0001t0002g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.234+6819_234+6820i others(173): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(173): Show |
1 | a0001c0001t0002g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.234+6819_234+6820i others(182): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(173): Show |
2 | a0001c0001t0004g0062 a0001c0001t0015g0055 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.234+6819_234+6820i others(182): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(199): Show |
1 | a0001c0002t0003g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.234+6819_234+6820i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(199): Show |
1 | a0001c0001t0004g0217 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.234+6819_234+6820i others(208): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(202): Show |
1 | a0001c0002t0003g0042 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.234+6819_234+6820i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(161): Show |
1 | a0001c0001t0004g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.234+6819_234+6820i others(170): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761488 | G | GGGAAGGG others(143): Show |
4 | a0002c0003t0007g0023 a0002c0003t0007g0024 a0002c0004t0011g0015 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+6819_234+6820i others(152): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761488 | |||||||
| chr1:115761494 | A | G | 6 | a0001c0007t0009g0053 a0002c0003t0010g0009 a0002c0003t0010g0011 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+6814T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761494 | |||||||
| chr1:115761497 | G | A | 290 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(287): Show |
298 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.234+6811C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GAGAAGAA others(2): Show |
2 | a0001c0001t0008g0026 a0001c0001t0014g0002 |
3 | HG02055.hp1 HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.234+6802_234+6810d others(11): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GAGAAGAA others(5): Show |
1 | a0001c0001t0019g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234+6799_234+6810d others(14): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GAGAAGAA others(17): Show |
1 | a0005c0009t0013g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.234+6787_234+6810d others(26): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GAGAAGAA others(200): Show |
1 | a0001c0002t0003g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(209): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(179): Show |
1 | a0001c0002t0001g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(188): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(182): Show |
1 | a0001c0001t0002g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(191): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(183): Show |
1 | a0001c0001t0002g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(192): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(214): Show |
1 | a0001c0002t0003g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.234+6810_234+6811i others(223): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(208): Show |
1 | a0001c0002t0003g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(217): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(205): Show |
1 | a0001c0006t0003g0169 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(202): Show |
1 | a0001c0002t0001g0167 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.234+6810_234+6811i others(211): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(205): Show |
1 | a0001c0002t0003g0214 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.234+6810_234+6811i others(214): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(200): Show |
1 | a0001c0001t0004g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.234+6810_234+6811i others(209): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761497 | G | GGGAAGGG others(164): Show |
2 | a0002c0004t0011g0014 a0002c0004t0017g0016 |
2 | HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234+6810_234+6811i others(173): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761497 | |||||||
| chr1:115761500 | A | G | 6 | a0001c0007t0009g0053 a0002c0003t0010g0009 a0002c0003t0010g0011 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+6808T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761500 | |||||||
| chr1:115761516 | A | G | 6 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 others(3): Show |
6 | HG01433.hp2 HG02895.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+6792T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761516 | |||||||
| chr1:115761519 | A | G | 6 | a0001c0002t0003g0038 a0001c0002t0003g0039 a0001c0002t0003g0040 others(3): Show |
6 | HG00558.hp2 HG00673.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+6789T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761519 | |||||||
| chr1:115761526 | GAA | G | 8 | a0001c0002t0001g0047 a0002c0003t0003g0257 a0002c0003t0003g0258 others(5): Show |
8 | HG01261.hp2 HG01952.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+6780_234+6781d others(4): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761526 | |||||||
| chr1:115761528 | A | AG | 50 | a0001c0002t0001g0003 a0001c0002t0001g0175 a0002c0003t0001g0260 others(47): Show |
53 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.234+6779dupC | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAG | 15 | a0001c0002t0001g0046 a0002c0003t0001g0265 a0002c0003t0001g0299 others(12): Show |
15 | HG00741.hp2 HG01361.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG | 9 | a0002c0003t0001g0262 a0002c0003t0001g0291 a0002c0003t0001g0298 others(6): Show |
9 | HG01109.hp1 HG02015.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(9): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(3): Show |
8 | a0002c0003t0001g0263 a0002c0003t0001g0264 a0002c0003t0001g0334 others(5): Show |
8 | HG00609.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(12): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(9): Show |
1 | a0002c0003t0003g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.234+6779_234+6780i others(18): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(12): Show |
1 | a0002c0004t0002g0259 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.234+6779_234+6780i others(21): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(15): Show |
5 | a0002c0003t0001g0287 a0002c0003t0006g0345 a0002c0004t0002g0279 others(2): Show |
5 | HG00558.hp1 HG01515.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(24): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(18): Show |
17 | a0002c0003t0001g0280 a0002c0003t0001g0286 a0002c0003t0001g0288 others(14): Show |
17 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(27): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761528 | A | AGAAGAAG others(21): Show |
15 | a0001c0002t0006g0043 a0002c0003t0001g0284 a0002c0003t0001g0321 others(12): Show |
15 | HG00438.hp1 HG00597.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+6779_234+6780i others(30): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761528 | |||||||
| chr1:115761530 | A | AAGAAGAA others(3): Show |
1 | a0001c0002t0003g0210 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.234+6777_234+6778i others(12): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761530 | |||||||
| chr1:115761531 | G | A | 1 | a0001c0002t0003g0210 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.234+6777C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761531 | |||||||
| chr1:115761533 | T | C | 7 | a0001c0002t0006g0043 a0002c0003t0006g0314 a0002c0003t0006g0315 others(4): Show |
7 | HG00438.hp1 HG00558.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+6775A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761533 | |||||||
| chr1:115761653 | C | T | 2 | a0001c0001t0002g0052 a0001c0007t0009g0053 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.234+6655G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761653 | |||||||
| chr1:115761680 | G | T | 129 | a0001c0001t0002g0233 a0001c0002t0001g0003 a0001c0002t0001g0046 others(126): Show |
133 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.234+6628C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761680 | |||||||
| chr1:115761684 | G | C | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+6624C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761684 | |||||||
| chr1:115761750 | A | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | NA18951.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.234+6558T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761750 | |||||||
| chr1:115761756 | A | G | 1 | a0001c0007t0020g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234+6552T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761756 | |||||||
| chr1:115761835 | TA | T | 12 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+6472delT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761835 | |||||||
| chr1:115761876 | C | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+6432G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115761876 | |||||||
| chr1:115762199 | A | C | 321 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(318): Show |
327 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(324): Show |
intron_variant | MODIFIER | c.234+6109T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762199 | |||||||
| chr1:115762285 | T | C | 10 | a0001c0002t0001g0067 a0001c0002t0001g0132 a0001c0002t0001g0133 others(7): Show |
10 | HG01433.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+6023A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762285 | |||||||
| chr1:115762325 | T | G | 84 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(81): Show |
85 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.234+5983A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762325 | |||||||
| chr1:115762703 | C | T | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+5605G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762703 | |||||||
| chr1:115762850 | G | T | 175 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(172): Show |
177 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.234+5458C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762850 | |||||||
| chr1:115762869 | A | G | 2 | a0001c0001t0019g0027 a0005c0009t0013g0035 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.234+5439T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762869 | |||||||
| chr1:115762968 | C | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+5340G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115762968 | |||||||
| chr1:115763057 | G | T | 175 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(172): Show |
177 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.234+5251C>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763057 | |||||||
| chr1:115763108 | G | A | 1 | a0002c0003t0001g0347 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.234+5200C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763108 | |||||||
| chr1:115763248 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+5060A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763248 | |||||||
| chr1:115763269 | G | A | 1 | a0001c0002t0003g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234+5039C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763269 | |||||||
| chr1:115763445 | A | G | 1 | a0002c0004t0004g0274 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.234+4863T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763445 | |||||||
| chr1:115763488 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.234+4820A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763488 | |||||||
| chr1:115763706 | A | G | 346 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(343): Show |
355 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.234+4602T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763706 | |||||||
| chr1:115763856 | T | G | 2 | a0001c0001t0005g0162 a0001c0007t0009g0163 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.234+4452A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763856 | |||||||
| chr1:115763869 | C | T | 1 | a0001c0001t0015g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.234+4439G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763869 | |||||||
| chr1:115763959 | G | A | 175 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(172): Show |
177 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.234+4349C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115763959 | |||||||
| chr1:115764127 | G | C | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+4181C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764127 | |||||||
| chr1:115764194 | A | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+4114T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764194 | |||||||
| chr1:115764304 | T | C | 3 | a0001c0002t0003g0211 a0001c0002t0003g0212 a0001c0002t0003g0213 |
3 | HG03017.hp2 HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.234+4004A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764304 | |||||||
| chr1:115764408 | T | A | 1 | a0001c0002t0003g0176 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.234+3900A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764408 | |||||||
| chr1:115764409 | A | T | 1 | a0001c0002t0003g0176 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.234+3899T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764409 | |||||||
| chr1:115764538 | C | T | 2 | a0001c0001t0005g0162 a0001c0007t0009g0163 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.234+3770G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764538 | |||||||
| chr1:115764777 | A | G | 176 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(173): Show |
178 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.234+3531T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764777 | |||||||
| chr1:115764781 | T | G | 2 | a0001c0001t0005g0162 a0001c0007t0009g0163 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.234+3527A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764781 | |||||||
| chr1:115764862 | G | A | 1 | a0002c0003t0001g0348 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.234+3446C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115764862 | |||||||
| chr1:115765079 | A | C | 92 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(89): Show |
93 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(90): Show |
intron_variant | MODIFIER | c.234+3229T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765079 | |||||||
| chr1:115765225 | G | A | 81 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(78): Show |
82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.234+3083C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765225 | |||||||
| chr1:115765527 | G | C | 345 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(342): Show |
354 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(351): Show |
intron_variant | MODIFIER | c.234+2781C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765527 | |||||||
| chr1:115765601 | A | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+2707T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765601 | |||||||
| chr1:115765636 | C | T | 321 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(318): Show |
327 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(324): Show |
intron_variant | MODIFIER | c.234+2672G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765636 | |||||||
| chr1:115765890 | C | T | 128 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(125): Show |
132 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.234+2418G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765890 | |||||||
| chr1:115765956 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+2352G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765956 | |||||||
| chr1:115765986 | C | T | 18 | a0001c0001t0002g0052 a0002c0003t0007g0017 a0002c0003t0007g0018 others(15): Show |
18 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.234+2322G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115765986 | |||||||
| chr1:115766013 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.234+2295C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766013 | |||||||
| chr1:115766108 | G | A | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+2200C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766108 | |||||||
| chr1:115766319 | C | T | 14 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0064 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+1989G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766319 | |||||||
| chr1:115766326 | C | A | 1 | a0002c0003t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.234+1982G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766326 | |||||||
| chr1:115766353 | A | C | 321 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(318): Show |
327 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(324): Show |
intron_variant | MODIFIER | c.234+1955T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766353 | |||||||
| chr1:115766369 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+1939T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766369 | |||||||
| chr1:115766392 | A | G | 2 | a0001c0001t0019g0027 a0005c0009t0013g0035 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.234+1916T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766392 | |||||||
| chr1:115766405 | G | A | 77 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(74): Show |
78 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.234+1903C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766405 | |||||||
| chr1:115766460 | G | A | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+1848C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766460 | |||||||
| chr1:115766469 | C | A | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+1839G>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766469 | |||||||
| chr1:115766562 | G | A | 127 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(124): Show |
131 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.234+1746C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766562 | |||||||
| chr1:115766579 | C | T | 83 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0004g0192 others(80): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.234+1729G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766579 | |||||||
| chr1:115766655 | T | C | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+1653A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766655 | |||||||
| chr1:115766724 | C | G | 77 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0052 others(74): Show |
78 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.234+1584G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766724 | |||||||
| chr1:115766739 | C | G | 1 | a0002c0004t0005g0318 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.234+1569G>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766739 | |||||||
| chr1:115766817 | T | G | 127 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(124): Show |
131 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.234+1491A>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766817 | |||||||
| chr1:115766865 | T | TGATA | 72 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0004g0159 others(69): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.234+1439_234+1442d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | T | TGATAGAT others(1): Show |
10 | a0001c0001t0002g0233 a0001c0002t0003g0050 a0001c0002t0003g0231 others(7): Show |
11 | HG01175.hp2 HG01517.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+1435_234+1442d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | TGATA | T | 56 | a0001c0001t0002g0174 a0001c0001t0004g0059 a0001c0001t0005g0001 others(53): Show |
58 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.234+1439_234+1442d others(6): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | TGATAGAT others(1): Show |
T | 10 | a0001c0001t0002g0054 a0001c0001t0005g0165 a0001c0001t0008g0026 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+1435_234+1442d others(10): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | TGATAGAT others(9): Show |
T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0052 a0001c0001t0002g0125 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+1427_234+1442d others(18): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | TGATAGAT others(13): Show |
T | 58 | a0001c0001t0002g0051 a0001c0001t0002g0069 a0001c0001t0002g0070 others(55): Show |
58 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.234+1423_234+1442d others(22): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766865 | TGATAGAT others(17): Show |
T | 1 | a0001c0001t0002g0068 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.234+1419_234+1442d others(26): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766865 | |||||||
| chr1:115766945 | T | TA | 75 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(72): Show |
76 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.234+1362_234+1363i others(3): Show |
CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766945 | |||||||
| chr1:115766946 | T | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0051 a0001c0001t0002g0068 others(73): Show |
77 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.234+1362A>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766946 | |||||||
| chr1:115766946 | T | TA | 15 | a0001c0001t0002g0052 a0001c0001t0002g0054 a0001c0001t0002g0061 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.234+1361dupT | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766946 | |||||||
| chr1:115766947 | A | T | 19 | a0001c0001t0005g0162 a0001c0007t0009g0163 a0002c0003t0007g0017 others(16): Show |
19 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.234+1361T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115766947 | |||||||
| chr1:115767079 | A | C | 1 | a0001c0001t0002g0051 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.234+1229T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767079 | |||||||
| chr1:115767178 | G | A | 127 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(124): Show |
131 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.234+1130C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767178 | |||||||
| chr1:115767244 | T | C | 128 | a0001c0001t0002g0233 a0001c0002t0001g0003 a0001c0002t0001g0046 others(125): Show |
132 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.234+1064A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767244 | |||||||
| chr1:115767452 | A | G | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+856T>C | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767452 | |||||||
| chr1:115767534 | G | A | 20 | a0001c0001t0002g0153 a0001c0001t0004g0159 a0001c0001t0005g0001 others(17): Show |
22 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.234+774C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767534 | |||||||
| chr1:115767562 | A | C | 2 | a0001c0002t0003g0160 a0001c0002t0003g0161 |
2 | NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.234+746T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767562 | |||||||
| chr1:115767568 | A | C | 128 | a0001c0001t0002g0233 a0001c0002t0001g0003 a0001c0002t0001g0046 others(125): Show |
132 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.234+740T>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767568 | |||||||
| chr1:115767677 | T | C | 86 | a0001c0001t0002g0174 a0001c0001t0002g0195 a0001c0001t0002g0233 others(83): Show |
87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.234+631A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767677 | |||||||
| chr1:115767679 | C | T | 3 | a0001c0002t0003g0048 a0001c0002t0003g0049 a0001c0002t0003g0050 |
3 | HG01517.hp2 HG02735.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.234+629G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767679 | |||||||
| chr1:115767764 | T | C | 145 | a0001c0001t0002g0233 a0001c0002t0001g0003 a0001c0002t0001g0046 others(142): Show |
149 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.234+544A>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767764 | |||||||
| chr1:115767809 | C | T | 127 | a0001c0002t0001g0003 a0001c0002t0001g0046 a0001c0002t0001g0047 others(124): Show |
131 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.234+499G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767809 | |||||||
| chr1:115767868 | C | T | 1 | a0001c0002t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.234+440G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115767868 | |||||||
| chr1:115768061 | A | T | 7 | a0001c0002t0003g0038 a0001c0002t0003g0039 a0001c0002t0003g0040 others(4): Show |
7 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+247T>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115768061 | |||||||
| chr1:115768092 | G | A | 1 | a0002c0003t0006g0354 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.234+216C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115768092 | |||||||
| chr1:115768197 | G | C | 141 | a0002c0003t0001g0260 a0002c0003t0001g0262 a0002c0003t0001g0263 others(138): Show |
144 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.234+111C>G | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115768197 | |||||||
| chr1:115768251 | G | A | 1 | a0004c0008t0001g0355 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.234+57C>T | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115768251 | |||||||
| chr1:115768279 | C | T | 17 | a0002c0003t0007g0017 a0002c0003t0007g0018 a0002c0003t0007g0020 others(14): Show |
17 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+29G>A | CASQ2 | ENSG00000118729.13 | transcript | ENST00000261448.6 | protein_coding | 1/10 | chr1 | 115768279 |