Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11131 |
| ensemblid | ENSG00000137225.13 |
| hgncid | 1478 |
| symbol | CAPN11 |
| name | calpain 11 |
| refseq_nuc | NM_007058.4 |
| refseq_prot | NP_008989.2 |
| ensembl_nuc | ENST00000398776.2 |
| ensembl_prot | ENSP00000381758.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 44158820 |
| end | 44184401 |
| strand | + |
| ver | v1.2 |
| region | chr6:44158820-44184401 |
| region5000 | chr6:44153820-44189401 |
| regionname0 | CAPN11_chr6_44158820_44184401 |
| regionname5000 | CAPN11_chr6_44153820_44189401 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 739 | 459 | 100 | 78 | 215 | 18 | 46 | 168 | CAPN11_chr6_44153820_44189401 | CAPN11 | MLYSP others(734): Show |
chr6 | 44153820 | 44189401 |
| a0002 | 0/0 | 13 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | MLYSP others(8): Show |
chr6 | 44153820 | 44189401 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2217 | 458 | 100 | 78 | 214 | 18 | 46 | CAPN11_chr6_44153820_44189401 | CAPN11 | ATGCT others(2212): Show |
chr6 | 44153820 | 44189401 | ||
| a0001c0002 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | ATGCT others(2212): Show |
chr6 | 44153820 | 44189401 | ||
| a0002c0003 | 0/0 | 40 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | ATGCT others(35): Show |
chr6 | 44153820 | 44189401 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2718 | 320 | 37 | 43 | 193 | 11 | 34 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0002 | 0/0 | 2718 | 101 | 50 | 24 | 18 | 3 | 6 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0003 | 0/0 | 2718 | 15 | 7 | 4 | 0 | 3 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0004 | 0/0 | 2718 | 8 | 5 | 2 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0005 | 0/0 | 2718 | 6 | 0 | 1 | 0 | 1 | 4 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0006 | 0/0 | 2718 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0007 | 0/0 | 2718 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0008 | 0/0 | 2718 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0001t0009 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0001c0002t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(2713): Show |
chr6 | 44153820 | 44189401 |
| a0002c0003t0001 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | AACTG others(536): Show |
chr6 | 44153820 | 44189401 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 69 | 1 | 10 | 45 | 5 | 7 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0002 | 0/0 | 51 | 9 | 14 | 26 | 0 | 2 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0003 | 0/0 | 47 | 3 | 7 | 28 | 2 | 7 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0004 | 0/0 | 50 | 1 | 4 | 36 | 1 | 8 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0005 | 0/0 | 32 | 5 | 1 | 20 | 1 | 5 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0008 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 0 | 1 | 0 | 2 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0001 | 0/0 | 17 | 6 | 5 | 4 | 0 | 2 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0002 | 0/0 | 19 | 6 | 7 | 4 | 2 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0003 | 0/0 | 8 | 2 | 4 | 0 | 0 | 2 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0005 | 0/0 | 14 | 4 | 6 | 3 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0002 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0003 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0004g0001 | 0/0 | 5 | 3 | 1 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | GBR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | FIN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | CHB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19076 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | GIH | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | USA | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0036 | REF | REF | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CAPN11_chr6_44153820_44189401 | CAPN11 | chr6 | 44153820 | 44189401 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44162359 | TTGAATAA others(21444): Show |
T | 1 | a0002 | 1 | NA18747.hp2 | exon_loss_variant | HIGH | c.16+3496_2193+47del | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/23 | chr6 | 44162359 | |||||||
| chr6:44166785 | G | A | 1 | a0001 | 2 | HG01361.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.44G>A | p.Ser15Asn | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/23 | 73/2718 | 44/2220 | 15/739 | chr6 | 44166785 | |||
| chr6:44166803 | A | C | 1 | a0001 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.62A>C | p.Glu21Ala | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/23 | 91/2718 | 62/2220 | 21/739 | chr6 | 44166803 | |||
| chr6:44166814 | C | T | 1 | a0001 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.73C>T | p.Arg25Trp | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/23 | 102/2718 | 73/2220 | 25/739 | chr6 | 44166814 | |||
| chr6:44169328 | C | T | 1 | a0001 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.136C>T | p.Arg46Trp | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 3/23 | 165/2718 | 136/2220 | 46/739 | chr6 | 44169328 | |||
| chr6:44169963 | C | T | 1 | a0001 | 4 | HG02280.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
stop_gained | HIGH | c.397C>T | p.Gln133* | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/23 | 426/2718 | 397/2220 | 133/739 | chr6 | 44169963 | |||
| chr6:44172317 | T | TGGCTGCC | 1 | a0001 | 21 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(18): Show |
frameshift_variant | HIGH | c.426_432dupGGCTGCC | p.Ile145fs | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/23 | 462/2718 | 433/2220 | 145/739 | INFO_REALIGN_3_PRIME | chr6 | 44172317 | ||
| chr6:44172367 | G | A | 1 | a0001 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.475G>A | p.Val159Met | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/23 | 504/2718 | 475/2220 | 159/739 | chr6 | 44172367 | |||
| chr6:44173351 | G | A | 1 | a0001 | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
missense_variant | MODERATE | c.796G>A | p.Val266Met | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/23 | 825/2718 | 796/2220 | 266/739 | chr6 | 44173351 | |||
| chr6:44176996 | C | T | 1 | a0001 | 1 | HG02723.hp1 | missense_variant&splice_region_variant | MODERATE | c.1235C>T | p.Pro412Leu | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/23 | 1264/2718 | 1235/2220 | 412/739 | chr6 | 44176996 | |||
| chr6:44177326 | T | C | 1 | a0001 | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
missense_variant | MODERATE | c.1322T>C | p.Val441Ala | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/23 | 1351/2718 | 1322/2220 | 441/739 | chr6 | 44177326 | |||
| chr6:44180040 | G | A | 1 | a0001 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1517G>A | p.Arg506Gln | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 14/23 | 1546/2718 | 1517/2220 | 506/739 | chr6 | 44180040 | |||
| chr6:44180081 | A | G | 1 | a0001 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1558A>G | p.Ile520Val | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 14/23 | 1587/2718 | 1558/2220 | 520/739 | chr6 | 44180081 | |||
| chr6:44180084 | A | G | 1 | a0001 | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
missense_variant | MODERATE | c.1561A>G | p.Ile521Val | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 14/23 | 1590/2718 | 1561/2220 | 521/739 | chr6 | 44180084 | |||
| chr6:44181190 | G | GCTTCCCT others(65): Show |
1 | a0001 | 1 | NA18979.hp2 | disruptive_inframe_insertion | MODERATE | c.1870-61_1880dupCTT others(69): Show |
p.Ser627_Gly628insPh others(70): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/23 | 1910/2718 | 1881/2220 | 627/739 | INFO_REALIGN_3_PRIME | chr6 | 44181190 | ||
| chr6:44183753 | G | A | 1 | a0001 | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
missense_variant | MODERATE | c.2183G>A | p.Ser728Asn | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 22/23 | 2212/2718 | 2183/2220 | 728/739 | chr6 | 44183753 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44158854 | G | A | 1 | a0001c0002 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.6G>A | p.Leu2Leu | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/23 | 35/2718 | 6/2220 | 2/739 | chr6 | 44158854 | |||
| chr6:44169926 | A | G | 1 | a0001c0001 | 6 | HG00438.hp1 HG00558.hp1 HG02056.hp2 others(3): Show |
synonymous_variant | LOW | c.360A>G | p.Leu120Leu | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/23 | 389/2718 | 360/2220 | 120/739 | chr6 | 44169926 | |||
| chr6:44172345 | C | T | 1 | a0001c0001 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.453C>T | p.Cys151Cys | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/23 | 482/2718 | 453/2220 | 151/739 | chr6 | 44172345 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44183956 | C | T | 1 | a0001c0001t0009 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 24 | chr6 | 44183956 | ||||||
| chr6:44184028 | G | A | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 |
118 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*96G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 96 | chr6 | 44184028 | ||||||
| chr6:44184067 | G | C | 2 | a0001c0001t0003 a0001c0001t0008 |
17 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 135 | chr6 | 44184067 | ||||||
| chr6:44184097 | T | C | 1 | a0001c0001t0007 | 2 | HG01168.hp2 HG01928.hp1 |
3_prime_UTR_variant | MODIFIER | c.*165T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 165 | chr6 | 44184097 | ||||||
| chr6:44184106 | C | T | 1 | a0001c0001t0004 | 8 | HG01106.hp1 HG01243.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 174 | chr6 | 44184106 | ||||||
| chr6:44184152 | C | A | 1 | a0001c0001t0006 | 3 | HG00423.hp1 NA18943.hp2 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*220C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 220 | chr6 | 44184152 | ||||||
| chr6:44184331 | C | T | 1 | a0001c0001t0005 | 6 | HG00140.hp2 HG01167.hp2 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*399C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 23/23 | 399 | chr6 | 44184331 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:44158956 | GTGCCCCT others(36): Show |
G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(23): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.16+139_16+181delCC others(41): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44158956 | ||||||
| chr6:44159067 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16+203C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159067 | |||||||
| chr6:44159070 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(11): Show |
24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.16+206C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159070 | |||||||
| chr6:44159128 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0002g0012 |
6 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+264G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159128 | |||||||
| chr6:44159131 | C | CAGG | 24 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(21): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.16+269_16+271dupGG others(1): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44159131 | ||||||
| chr6:44159166 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0002g0013 |
5 | HG02155.hp1 NA18939.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+302T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159166 | |||||||
| chr6:44159395 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.16+531G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159395 | |||||||
| chr6:44159585 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.16+721G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159585 | |||||||
| chr6:44159705 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.16+841A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159705 | |||||||
| chr6:44159781 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+917C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159781 | |||||||
| chr6:44159908 | G | T | 1 | a0001c0001t0001g0024 | 2 | NA19007.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.16+1044G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159908 | |||||||
| chr6:44159985 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(13): Show |
77 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.16+1121T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44159985 | |||||||
| chr6:44160018 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.16+1154C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160018 | |||||||
| chr6:44160042 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.16+1178G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160042 | |||||||
| chr6:44160082 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(12): Show |
76 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.16+1218C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160082 | |||||||
| chr6:44160083 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16+1219G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160083 | |||||||
| chr6:44160089 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.16+1225G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160089 | |||||||
| chr6:44160097 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
69 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.16+1233G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160097 | |||||||
| chr6:44160112 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0006 |
10 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+1248G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160112 | |||||||
| chr6:44160144 | A | T | 1 | a0001c0001t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.16+1280A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160144 | |||||||
| chr6:44160356 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.16+1492G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160356 | |||||||
| chr6:44160384 | G | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0043 others(5): Show |
11 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+1520G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160384 | |||||||
| chr6:44160431 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16+1567C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160431 | |||||||
| chr6:44160477 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0002g0007 others(2): Show |
12 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.16+1613C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160477 | |||||||
| chr6:44160510 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.16+1646G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160510 | |||||||
| chr6:44160595 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0002g0018 |
3 | HG00099.hp2 HG00280.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.16+1731C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160595 | |||||||
| chr6:44160612 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0002g0015 a0001c0001t0002g0020 |
8 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.16+1748G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160612 | |||||||
| chr6:44160616 | C | CA | 3 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0002g0015 |
7 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+1760dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44160616 | ||||||
| chr6:44160625 | C | A | 1 | a0001c0001t0006g0035 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.16+1761C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160625 | |||||||
| chr6:44160627 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.16+1763T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160627 | |||||||
| chr6:44160764 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16+1900G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160764 | |||||||
| chr6:44160805 | C | T | 1 | a0001c0001t0001g0022 | 2 | NA18946.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.16+1941C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160805 | |||||||
| chr6:44160881 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.16+2017A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44160881 | |||||||
| chr6:44161021 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0002g0014 |
4 | NA18942.hp1 NA18946.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2157G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161021 | |||||||
| chr6:44161177 | G | GT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(15): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.16+2327dupT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44161177 | ||||||
| chr6:44161177 | GT | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(32): Show |
152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.16+2327delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44161177 | ||||||
| chr6:44161177 | GTT | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+2326_16+2327del others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44161177 | ||||||
| chr6:44161200 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.16+2336T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161200 | |||||||
| chr6:44161247 | TGGAGTGC others(1077): Show |
T | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+2385_16+3468del | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44161247 | ||||||
| chr6:44161267 | T | C | 1 | a0001c0001t0006g0035 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.16+2403T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161267 | |||||||
| chr6:44161269 | G | T | 1 | a0001c0001t0006g0035 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.16+2405G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161269 | |||||||
| chr6:44161316 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.16+2452C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161316 | |||||||
| chr6:44161337 | C | A | 1 | a0001c0001t0001g0013 | 2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.16+2473C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161337 | |||||||
| chr6:44161366 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.16+2502A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161366 | |||||||
| chr6:44161476 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0043 others(9): Show |
61 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.16+2612A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161476 | |||||||
| chr6:44161504 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.16+2640G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161504 | |||||||
| chr6:44161513 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.16+2649C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161513 | |||||||
| chr6:44161609 | C | T | 1 | a0001c0001t0001g0004 | 2 | NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.16+2745C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161609 | |||||||
| chr6:44161747 | T | G | 3 | a0001c0001t0002g0002 a0001c0001t0003g0001 a0001c0001t0005g0009 |
3 | HG00738.hp1 HG01070.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.16+2883T>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161747 | |||||||
| chr6:44161851 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.16+2987T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161851 | |||||||
| chr6:44161867 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.16+3003G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161867 | |||||||
| chr6:44161870 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.16+3006C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161870 | |||||||
| chr6:44161925 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
4 | NA18956.hp2 NA18974.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+3061G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44161925 | |||||||
| chr6:44162157 | G | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.16+3293G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162157 | |||||||
| chr6:44162163 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.16+3299G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162163 | |||||||
| chr6:44162181 | C | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+3317C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162181 | |||||||
| chr6:44162207 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0020 |
9 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.16+3343C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162207 | |||||||
| chr6:44162282 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16+3418C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162282 | |||||||
| chr6:44162338 | G | T | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+3474G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162338 | |||||||
| chr6:44162341 | G | A | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+3477G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162341 | |||||||
| chr6:44162346 | C | A | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+3482C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162346 | |||||||
| chr6:44162348 | T | C | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+3484T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162348 | |||||||
| chr6:44162357 | C | A | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+3493C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162357 | |||||||
| chr6:44162368 | G | GAC | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
39 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.16+3545_16+3546dup others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | G | GACAC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
15 | HG01169.hp2 HG01884.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+3543_16+3546dup others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | G | GACACAC | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(2): Show |
6 | HG01243.hp1 HG01346.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+3541_16+3546dup others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | G | GACACACA others(3): Show |
1 | a0001c0001t0002g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.16+3537_16+3546dup others(10): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GAC | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(40): Show |
164 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.16+3545_16+3546del others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GACAC | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
49 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.16+3543_16+3546del others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GACACAC | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
16 | HG00323.hp1 HG02071.hp2 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.16+3541_16+3546del others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GACACACA others(1): Show |
G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(5): Show |
15 | HG00621.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.16+3539_16+3546del others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GACACACA others(7): Show |
G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
5 | HG01884.hp1 HG01952.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3533_16+3546del others(14): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162368 | GACACACA others(9): Show |
G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(10): Show |
50 | HG00544.hp1 HG00733.hp2 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.16+3531_16+3546del others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44162368 | ||||||
| chr6:44162426 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.16+3562G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162426 | |||||||
| chr6:44162529 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.16+3665G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162529 | |||||||
| chr6:44162530 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.16+3666A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162530 | |||||||
| chr6:44162545 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
27 | HG00558.hp2 HG00741.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.16+3681G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162545 | |||||||
| chr6:44162593 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16+3729C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162593 | |||||||
| chr6:44162647 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.16+3783G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162647 | |||||||
| chr6:44162650 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.16+3786A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162650 | |||||||
| chr6:44162779 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16+3915T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162779 | |||||||
| chr6:44162938 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0014 |
4 | NA18962.hp1 NA18998.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-3820G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44162938 | |||||||
| chr6:44163041 | G | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(1): Show |
9 | HG01255.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-3717G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163041 | |||||||
| chr6:44163133 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.17-3625A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163133 | |||||||
| chr6:44163134 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.17-3624A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163134 | |||||||
| chr6:44163173 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.17-3585G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163173 | |||||||
| chr6:44163174 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.17-3584G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163174 | |||||||
| chr6:44163451 | A | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(13): Show |
44 | HG00544.hp1 HG02071.hp1 HG02135.hp1 others(41): Show |
intron_variant | MODIFIER | c.17-3307A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163451 | |||||||
| chr6:44163459 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.17-3299G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163459 | |||||||
| chr6:44163733 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.17-3025C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163733 | |||||||
| chr6:44163981 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.17-2777G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44163981 | |||||||
| chr6:44164043 | C | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.17-2715C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164043 | |||||||
| chr6:44164051 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.17-2707C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164051 | |||||||
| chr6:44164060 | G | C | 1 | a0001c0001t0002g0015 | 4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-2698G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164060 | |||||||
| chr6:44164396 | AGGCATCT others(13): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17-2361_17-2342del others(20): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164396 | |||||||
| chr6:44164591 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.17-2167G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164591 | |||||||
| chr6:44164665 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.17-2093G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164665 | |||||||
| chr6:44164832 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.17-1926A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164832 | |||||||
| chr6:44164841 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 |
4 | HG00673.hp1 HG02027.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-1917G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164841 | |||||||
| chr6:44164877 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0048 |
3 | HG02559.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.17-1881A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44164877 | |||||||
| chr6:44164880 | T | TTTTA | 6 | a0001c0001t0001g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(3): Show |
8 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-1858_17-1855dup others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 44164880 | ||||||
| chr6:44165045 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.17-1713C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165045 | |||||||
| chr6:44165143 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(7): Show |
11 | HG01243.hp1 HG01346.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.17-1615C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165143 | |||||||
| chr6:44165282 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.17-1476T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165282 | |||||||
| chr6:44165355 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.17-1403A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165355 | |||||||
| chr6:44165484 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.17-1274A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165484 | |||||||
| chr6:44165573 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0002g0002 a0001c0001t0002g0007 others(2): Show |
8 | HG02809.hp2 HG02886.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-1185G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165573 | |||||||
| chr6:44165676 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.17-1082A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165676 | |||||||
| chr6:44165716 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0004g0001 |
2 | HG02300.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.17-1042C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165716 | |||||||
| chr6:44165841 | G | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.17-917G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165841 | |||||||
| chr6:44165912 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.17-846G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165912 | |||||||
| chr6:44165961 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17-797C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44165961 | |||||||
| chr6:44166058 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
37 | HG00544.hp1 HG02071.hp1 HG02135.hp1 others(34): Show |
intron_variant | MODIFIER | c.17-700G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44166058 | |||||||
| chr6:44166330 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.17-428G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44166330 | |||||||
| chr6:44166342 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.17-416G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44166342 | |||||||
| chr6:44166542 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.17-216C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 1/22 | chr6 | 44166542 | |||||||
| chr6:44166844 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.88+15C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44166844 | |||||||
| chr6:44166873 | TTCC | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.88+52_88+54delCCT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44166873 | ||||||
| chr6:44166899 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+70C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44166899 | |||||||
| chr6:44166937 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.88+108G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44166937 | |||||||
| chr6:44166983 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0005g0003 |
2 | HG00140.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.88+154G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44166983 | |||||||
| chr6:44167045 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.88+216G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167045 | |||||||
| chr6:44167082 | G | T | 1 | a0001c0001t0001g0005 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.88+253G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167082 | |||||||
| chr6:44167091 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
36 | HG02071.hp1 HG02135.hp1 HG02602.hp1 others(33): Show |
intron_variant | MODIFIER | c.88+262C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167091 | |||||||
| chr6:44167092 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
36 | HG02071.hp1 HG02135.hp1 HG02602.hp1 others(33): Show |
intron_variant | MODIFIER | c.88+263C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167092 | |||||||
| chr6:44167116 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
35 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+287C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167116 | |||||||
| chr6:44167127 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.88+298T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167127 | |||||||
| chr6:44167135 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.88+306G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167135 | |||||||
| chr6:44167137 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.88+308T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167137 | |||||||
| chr6:44167262 | G | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.88+433G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167262 | |||||||
| chr6:44167297 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.88+468G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167297 | |||||||
| chr6:44167358 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(45): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.88+529T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167358 | |||||||
| chr6:44167385 | C | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+556C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167385 | |||||||
| chr6:44167413 | A | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.88+584A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167413 | |||||||
| chr6:44167497 | C | CA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(27): Show |
86 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.88+692dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167497 | ||||||
| chr6:44167497 | C | CAA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(12): Show |
30 | HG01106.hp1 HG01884.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.88+691_88+692dupAA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167497 | ||||||
| chr6:44167497 | CA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
41 | HG01070.hp2 HG01515.hp2 HG02071.hp1 others(38): Show |
intron_variant | MODIFIER | c.88+692delA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167497 | ||||||
| chr6:44167497 | CAA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0050 others(2): Show |
11 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+691_88+692delAA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167497 | ||||||
| chr6:44167520 | AATAG | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(4): Show |
15 | HG02135.hp1 NA18945.hp2 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.88+692_88+695delAT others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167520 | |||||||
| chr6:44167525 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(4): Show |
15 | HG02135.hp1 NA18945.hp2 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.88+696C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167525 | |||||||
| chr6:44167555 | T | TA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(14): Show |
28 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+738dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167555 | ||||||
| chr6:44167555 | T | TAA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
37 | HG02071.hp1 HG02135.hp1 HG02145.hp1 others(34): Show |
intron_variant | MODIFIER | c.88+737_88+738dupAA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167555 | ||||||
| chr6:44167555 | TA | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.88+738delA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167555 | ||||||
| chr6:44167555 | TAA | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+737_88+738delAA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167555 | ||||||
| chr6:44167614 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.88+785A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167614 | |||||||
| chr6:44167657 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+828C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167657 | |||||||
| chr6:44167681 | T | C | 1 | a0001c0001t0003g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+852T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167681 | |||||||
| chr6:44167798 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.88+969C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167798 | |||||||
| chr6:44167915 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.88+1086T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167915 | |||||||
| chr6:44167916 | G | GA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(45): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.88+1097dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167916 | ||||||
| chr6:44167916 | G | GAA | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(42): Show |
114 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.88+1096_88+1097dup others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44167916 | ||||||
| chr6:44167958 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+1129T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44167958 | |||||||
| chr6:44168020 | T | TA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
36 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.88+1200dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44168020 | ||||||
| chr6:44168049 | CAG | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0048 |
3 | HG02559.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.88+1223_88+1224del others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44168049 | ||||||
| chr6:44168076 | T | G | 1 | a0001c0001t0001g0004 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.89-1205T>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168076 | |||||||
| chr6:44168151 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.89-1130C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168151 | |||||||
| chr6:44168415 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.89-866G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168415 | |||||||
| chr6:44168691 | C | T | 1 | a0001c0001t0004g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.89-590C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168691 | |||||||
| chr6:44168706 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.89-575G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168706 | |||||||
| chr6:44168774 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0048 |
3 | HG02559.hp2 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.89-507C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168774 | |||||||
| chr6:44168827 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(16): Show |
45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.89-454G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168827 | |||||||
| chr6:44168893 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(17): Show |
48 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-388T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168893 | |||||||
| chr6:44168930 | A | AT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.89-342dupT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 44168930 | ||||||
| chr6:44168943 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0005 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.89-338G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44168943 | |||||||
| chr6:44169093 | G | C | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.89-188G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44169093 | |||||||
| chr6:44169162 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(64): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.89-119A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44169162 | |||||||
| chr6:44169174 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.89-107T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44169174 | |||||||
| chr6:44169252 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.89-29C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 2/22 | chr6 | 44169252 | |||||||
| chr6:44169805 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.340-101C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 3/22 | chr6 | 44169805 | |||||||
| chr6:44170096 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.409+121C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170096 | |||||||
| chr6:44170200 | C | A | 1 | a0001c0001t0001g0003 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.409+225C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170200 | |||||||
| chr6:44170257 | TA | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0002g0001 others(2): Show |
6 | HG01069.hp2 HG02523.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.409+292delA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 44170257 | ||||||
| chr6:44170285 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.409+310C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170285 | |||||||
| chr6:44170296 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.409+321G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170296 | |||||||
| chr6:44170390 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(5): Show |
12 | HG00408.hp2 HG00609.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.409+415C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170390 | |||||||
| chr6:44170461 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0002g0013 |
2 | HG02132.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.409+486T>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170461 | |||||||
| chr6:44170525 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.409+550G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170525 | |||||||
| chr6:44170552 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.409+577C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170552 | |||||||
| chr6:44170576 | G | T | 1 | a0001c0001t0002g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.409+601G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170576 | |||||||
| chr6:44170606 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.409+631G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170606 | |||||||
| chr6:44170685 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
35 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.409+710G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170685 | |||||||
| chr6:44170702 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.409+727T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170702 | |||||||
| chr6:44170754 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(9): Show |
13 | HG01243.hp1 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.409+779T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170754 | |||||||
| chr6:44170761 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.409+786C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170761 | |||||||
| chr6:44170768 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.409+793T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170768 | |||||||
| chr6:44170847 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.409+872T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170847 | |||||||
| chr6:44170870 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.409+895G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170870 | |||||||
| chr6:44170987 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(43): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.409+1012G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44170987 | |||||||
| chr6:44171014 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.409+1039A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171014 | |||||||
| chr6:44171031 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.409+1056C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171031 | |||||||
| chr6:44171118 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.409+1143C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171118 | |||||||
| chr6:44171183 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0024 |
5 | NA18940.hp2 NA18994.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.410-1119C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171183 | |||||||
| chr6:44171210 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.410-1092A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171210 | |||||||
| chr6:44171232 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.410-1070C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171232 | |||||||
| chr6:44171336 | G | T | 1 | a0001c0001t0001g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.410-966G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171336 | |||||||
| chr6:44171337 | C | A | 1 | a0001c0001t0001g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.410-965C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171337 | |||||||
| chr6:44171400 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-902C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171400 | |||||||
| chr6:44171420 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(20): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.410-882C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171420 | |||||||
| chr6:44171465 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.410-837C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171465 | |||||||
| chr6:44171524 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.410-778G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171524 | |||||||
| chr6:44171546 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.410-756G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171546 | |||||||
| chr6:44171586 | G | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.410-716G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171586 | |||||||
| chr6:44171597 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410-705G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171597 | |||||||
| chr6:44171685 | T | TA | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.410-608dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 44171685 | ||||||
| chr6:44171754 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.410-548G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171754 | |||||||
| chr6:44171927 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0051 |
3 | HG02486.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.410-375G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171927 | |||||||
| chr6:44171930 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.410-372G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171930 | |||||||
| chr6:44171984 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410-318C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171984 | |||||||
| chr6:44171985 | G | C | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410-317G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44171985 | |||||||
| chr6:44172026 | A | C | 1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.410-276A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44172026 | |||||||
| chr6:44172132 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(10): Show |
21 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.410-170C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44172132 | |||||||
| chr6:44172181 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.410-121C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 4/22 | chr6 | 44172181 | |||||||
| chr6:44172437 | G | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
15 | HG01243.hp1 HG01243.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.528+17G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172437 | |||||||
| chr6:44172538 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.528+118A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172538 | |||||||
| chr6:44172583 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.528+163C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172583 | |||||||
| chr6:44172621 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.528+201A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172621 | |||||||
| chr6:44172659 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(15): Show |
50 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.528+239C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172659 | |||||||
| chr6:44172675 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.528+255G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172675 | |||||||
| chr6:44172786 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.529-154C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172786 | |||||||
| chr6:44172840 | A | C | 1 | a0001c0001t0001g0004 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.529-100A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 5/22 | chr6 | 44172840 | |||||||
| chr6:44173081 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
splice_region_variant&intron_variant | LOW | c.662+8C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 6/22 | chr6 | 44173081 | |||||||
| chr6:44173541 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.831+155G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173541 | |||||||
| chr6:44173552 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 |
4 | HG00099.hp2 HG00323.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+166C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173552 | |||||||
| chr6:44173570 | G | GT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.831+193dupT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44173570 | ||||||
| chr6:44173578 | TTG | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
69 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.831+194_831+195del others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44173578 | ||||||
| chr6:44173579 | TG | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
175 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.831+194delG | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173579 | |||||||
| chr6:44173580 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(6): Show |
18 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+194G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173580 | |||||||
| chr6:44173583 | T | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.831+197T>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173583 | |||||||
| chr6:44173584 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.831+198G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173584 | |||||||
| chr6:44173728 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.831+342G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173728 | |||||||
| chr6:44173729 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.831+343T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173729 | |||||||
| chr6:44173738 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.831+352C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173738 | |||||||
| chr6:44173869 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.831+483C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173869 | |||||||
| chr6:44173948 | C | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(16): Show |
48 | HG01243.hp1 HG01346.hp2 HG01934.hp2 others(45): Show |
intron_variant | MODIFIER | c.831+562C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173948 | |||||||
| chr6:44173980 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.831+594C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173980 | |||||||
| chr6:44173981 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.831+595T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173981 | |||||||
| chr6:44173995 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.831+609G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44173995 | |||||||
| chr6:44174000 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.831+614A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44174000 | |||||||
| chr6:44174438 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(18): Show |
53 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.831+1052G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44174438 | |||||||
| chr6:44174515 | C | CA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
7 | HG01433.hp2 HG01884.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+1147dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174515 | ||||||
| chr6:44174515 | CA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.831+1147delA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174515 | ||||||
| chr6:44174515 | CAA | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(9): Show |
14 | HG01106.hp1 HG01257.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+1146_831+1147d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174515 | ||||||
| chr6:44174599 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.831+1213G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44174599 | |||||||
| chr6:44174616 | C | CT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
19 | HG00673.hp1 HG01175.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.831+1251dupT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174616 | ||||||
| chr6:44174616 | CT | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(61): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.831+1251delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174616 | ||||||
| chr6:44174616 | CTT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(15): Show |
45 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.831+1250_831+1251d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44174616 | ||||||
| chr6:44174779 | A | C | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.832-1289A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44174779 | |||||||
| chr6:44174826 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-1242G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44174826 | |||||||
| chr6:44175032 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.832-1036G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175032 | |||||||
| chr6:44175071 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.832-997C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175071 | |||||||
| chr6:44175073 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
67 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.832-995T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175073 | |||||||
| chr6:44175207 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.832-861C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175207 | |||||||
| chr6:44175402 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.832-666T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175402 | |||||||
| chr6:44175429 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0008 |
3 | NA18948.hp2 NA19001.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.832-639G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175429 | |||||||
| chr6:44175467 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.832-601G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175467 | |||||||
| chr6:44175503 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.832-565C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175503 | |||||||
| chr6:44175571 | T | C | 1 | a0001c0001t0001g0005 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.832-497T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175571 | |||||||
| chr6:44175624 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.832-444G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175624 | |||||||
| chr6:44175638 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.832-430G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175638 | |||||||
| chr6:44175704 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-364G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175704 | |||||||
| chr6:44175795 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.832-273A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175795 | |||||||
| chr6:44175797 | T | TAAC | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.832-269_832-268ins others(3): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 44175797 | ||||||
| chr6:44175810 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.832-258G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175810 | |||||||
| chr6:44175976 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.832-92C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44175976 | |||||||
| chr6:44176065 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.832-3T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 7/22 | chr6 | 44176065 | |||||||
| chr6:44176169 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(9): Show |
13 | HG01243.hp1 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+18C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 8/22 | chr6 | 44176169 | |||||||
| chr6:44176170 | G | A | 1 | a0001c0001t0003g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.915+19G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 8/22 | chr6 | 44176170 | |||||||
| chr6:44176193 | A | AGGAGGAG others(15): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.915+43_916-38dupGG others(20): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr6 | 44176193 | ||||||
| chr6:44176355 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(16): Show |
38 | HG01069.hp2 HG01106.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1001+17C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 9/22 | chr6 | 44176355 | |||||||
| chr6:44176458 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0005 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1001+120A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 9/22 | chr6 | 44176458 | |||||||
| chr6:44176491 | A | C | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1002-90A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 9/22 | chr6 | 44176491 | |||||||
| chr6:44176563 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0005 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1002-18C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 9/22 | chr6 | 44176563 | |||||||
| chr6:44176764 | G | T | 1 | a0001c0001t0001g0002 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1077-74G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 10/22 | chr6 | 44176764 | |||||||
| chr6:44176799 | A | C | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077-39A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 10/22 | chr6 | 44176799 | |||||||
| chr6:44177006 | A | AG | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(13): Show |
59 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1237+12dupG | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr6 | 44177006 | ||||||
| chr6:44177026 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1237+28T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177026 | |||||||
| chr6:44177061 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
262 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(259): Show |
intron_variant | MODIFIER | c.1237+63C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177061 | |||||||
| chr6:44177106 | G | T | 1 | a0001c0001t0001g0004 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1237+108G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177106 | |||||||
| chr6:44177124 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(25): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1238-118T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177124 | |||||||
| chr6:44177211 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1238-31G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177211 | |||||||
| chr6:44177220 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0020 |
6 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-22C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 11/22 | chr6 | 44177220 | |||||||
| chr6:44177441 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1416+21G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177441 | |||||||
| chr6:44177444 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1416+24C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177444 | |||||||
| chr6:44177475 | C | CCTTT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(15): Show |
39 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1416+72_1416+75dup others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44177475 | ||||||
| chr6:44177475 | C | CCTTTCTT others(1): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
52 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1416+68_1416+75dup others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44177475 | ||||||
| chr6:44177475 | C | CCTTTCTT others(5): Show |
1 | a0001c0001t0001g0024 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1416+64_1416+75dup others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44177475 | ||||||
| chr6:44177496 | T | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(18): Show |
57 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1416+76T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177496 | |||||||
| chr6:44177569 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(27): Show |
102 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1416+149C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177569 | |||||||
| chr6:44177573 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1416+153A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177573 | |||||||
| chr6:44177586 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1416+166C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177586 | |||||||
| chr6:44177632 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1416+212G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177632 | |||||||
| chr6:44177647 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1416+227C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177647 | |||||||
| chr6:44177739 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0018 |
3 | HG00280.hp1 HG02015.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1416+319G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177739 | |||||||
| chr6:44177762 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
4 | NA18612.hp2 NA18978.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+342C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177762 | |||||||
| chr6:44177808 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1416+388C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177808 | |||||||
| chr6:44177918 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1416+498C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177918 | |||||||
| chr6:44177945 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1416+525C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177945 | |||||||
| chr6:44177993 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1416+573G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44177993 | |||||||
| chr6:44178023 | A | T | 6 | a0001c0001t0001g0005 a0001c0001t0002g0002 a0001c0001t0002g0004 others(3): Show |
9 | HG00609.hp2 HG02040.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1416+603A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178023 | |||||||
| chr6:44178032 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0025 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1416+612C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178032 | |||||||
| chr6:44178094 | C | G | 1 | a0001c0001t0002g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1416+674C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178094 | |||||||
| chr6:44178110 | C | T | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1416+690C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178110 | |||||||
| chr6:44178162 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 |
4 | HG00099.hp2 HG00323.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+742G>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178162 | |||||||
| chr6:44178170 | GAATACTA others(6): Show |
G | 1 | a0001c0001t0002g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1416+754_1416+766d others(15): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44178170 | ||||||
| chr6:44178201 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
5 | HG02280.hp2 HG02559.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416+781G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178201 | |||||||
| chr6:44178322 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1416+902G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178322 | |||||||
| chr6:44178649 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1417-970A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178649 | |||||||
| chr6:44178676 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
19 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1417-943G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178676 | |||||||
| chr6:44178703 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1417-916A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178703 | |||||||
| chr6:44178748 | AT | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
93 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1417-869delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44178748 | ||||||
| chr6:44178749 | T | TA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
64 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(3): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
20 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAA | 5 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0048 others(2): Show |
6 | HG02486.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(5): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAAA | 3 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0002g0021 |
3 | HG03041.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1417-870_1417-869i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAAAA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0041 others(15): Show |
28 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(7): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAAAAA | 5 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(2): Show |
5 | HG01069.hp2 HG01175.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAAAAAA | 10 | a0001c0001t0001g0002 a0001c0001t0002g0001 a0001c0001t0002g0002 others(7): Show |
18 | HG00280.hp1 HG02109.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(9): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | T | TAAAAAAA others(1): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
12 | HG00609.hp2 HG02040.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1417-870_1417-869i others(10): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178749 | TTA | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0022 |
3 | HG01515.hp2 HG01516.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1417-869_1417-868d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178749 | |||||||
| chr6:44178750 | T | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1417-869T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178750 | |||||||
| chr6:44178750 | T | TA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
7 | HG01175.hp2 HG03491.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-846dupA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44178750 | ||||||
| chr6:44178750 | TA | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(9): Show |
33 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1417-846delA | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44178750 | ||||||
| chr6:44178780 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1417-839G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178780 | |||||||
| chr6:44178844 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
19 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1417-775G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178844 | |||||||
| chr6:44178877 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0019 |
3 | HG02886.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1417-742C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44178877 | |||||||
| chr6:44179144 | A | C | 1 | a0001c0001t0001g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1417-475A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179144 | |||||||
| chr6:44179216 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1417-403C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179216 | |||||||
| chr6:44179235 | T | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
19 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1417-384T>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179235 | |||||||
| chr6:44179274 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(1): Show |
6 | HG00438.hp1 HG00558.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-345C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179274 | |||||||
| chr6:44179302 | A | AT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1417-301dupT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44179302 | ||||||
| chr6:44179302 | AT | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(11): Show |
24 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.1417-301delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr6 | 44179302 | ||||||
| chr6:44179368 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1417-251G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179368 | |||||||
| chr6:44179600 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
84 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1417-19C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179600 | |||||||
| chr6:44179618 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02280.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1417-1G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 12/22 | chr6 | 44179618 | |||||||
| chr6:44180220 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1640+57A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 14/22 | chr6 | 44180220 | |||||||
| chr6:44180668 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.1746+6C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 16/22 | chr6 | 44180668 | |||||||
| chr6:44180831 | C | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(9): Show |
39 | HG00741.hp1 HG01070.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1804+26C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 17/22 | chr6 | 44180831 | |||||||
| chr6:44181161 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1870-91G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 18/22 | chr6 | 44181161 | |||||||
| chr6:44181180 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1870-72A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 18/22 | chr6 | 44181180 | |||||||
| chr6:44181211 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1870-41C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 18/22 | chr6 | 44181211 | |||||||
| chr6:44181347 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1938+27C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181347 | |||||||
| chr6:44181376 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1938+56A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181376 | |||||||
| chr6:44181416 | C | CCACACAC others(22): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(2): Show |
7 | HG00323.hp2 HG01261.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+109_1938+110i others(31): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181416 | ||||||
| chr6:44181416 | CCA | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1938+112_1938+113d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181416 | ||||||
| chr6:44181416 | CCACA | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
74 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1938+110_1938+113d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181416 | ||||||
| chr6:44181418 | A | ACACACAC others(22): Show |
17 | a0001c0001t0001g0011 a0001c0001t0002g0002 a0001c0001t0002g0003 others(14): Show |
29 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1938+111_1938+112i others(31): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181418 | ||||||
| chr6:44181427 | C | CACCCAAC others(120): Show |
1 | a0001c0001t0002g0014 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1938+109_1938+110i others(129): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181427 | ||||||
| chr6:44181427 | C | CACCCAAC others(243): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
7 | HG01069.hp1 HG01070.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+109_1938+110i others(252): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181427 | ||||||
| chr6:44181427 | C | CACCCAAC others(108): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
5 | NA18612.hp2 NA18952.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+109_1938+110i others(117): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181427 | ||||||
| chr6:44181427 | C | CACCCAAC others(241): Show |
22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
59 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1938+109_1938+110i others(250): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181427 | ||||||
| chr6:44181427 | C | CACCCAAC others(239): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0007 |
2 | HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1938+109_1938+110i others(248): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181427 | ||||||
| chr6:44181427 | C | CCCAACCA others(239): Show |
3 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0032 |
5 | HG01106.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+107_1938+108i others(248): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181427 | |||||||
| chr6:44181431 | C | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
79 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1938+111C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181431 | |||||||
| chr6:44181434 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1938+114C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181434 | |||||||
| chr6:44181437 | A | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
4 | HG02451.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+117A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181437 | |||||||
| chr6:44181438 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
4 | HG02451.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+118C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181438 | |||||||
| chr6:44181441 | C | CACCACAC others(344): Show |
1 | a0001c0001t0001g0001 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1938+144_1938+145i others(353): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181441 | C | CACCACAC others(342): Show |
1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1938+144_1938+145i others(351): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181441 | C | CATACAGA others(123): Show |
1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1938+122_1938+123i others(132): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181441 | C | CATACAGA others(127): Show |
1 | a0001c0001t0002g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1938+122_1938+123i others(136): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181441 | C | CATACAGA others(168): Show |
1 | a0001c0001t0002g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+122_1938+123i others(177): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181441 | C | CATACAGA others(125): Show |
1 | a0001c0001t0002g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1938+122_1938+123i others(134): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181441 | ||||||
| chr6:44181448 | CT | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
3 | HG02451.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1938+129delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181448 | |||||||
| chr6:44181449 | T | A | 1 | a0001c0001t0002g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+129T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181449 | |||||||
| chr6:44181449 | T | TCA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
43 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1938+147_1938+148d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | T | TCACA | 7 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0019 others(4): Show |
9 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938+145_1938+148d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | T | TCACACAC others(28): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(13): Show |
44 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1938+144_1938+145i others(37): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | T | TCACACAC others(30): Show |
1 | a0001c0001t0001g0001 | 2 | NA19007.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1938+144_1938+145i others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | T | TCACACAC others(26): Show |
1 | a0001c0001t0001g0002 | 6 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+140_1938+141i others(35): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | T | TCTCA | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(2): Show |
7 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+130_1938+131i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | TCA | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
164 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1938+147_1938+148d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | TCACACA | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 |
3 | HG02965.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+143_1938+148d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181449 | TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
12 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1938+141_1938+148d others(10): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181449 | ||||||
| chr6:44181451 | A | ACACACAC others(342): Show |
1 | a0001c0001t0001g0002 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1938+144_1938+145i others(351): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181451 | ||||||
| chr6:44181451 | A | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(1): Show |
5 | HG01243.hp1 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+131A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181451 | |||||||
| chr6:44181453 | A | ACACACAC others(126): Show |
1 | a0001c0001t0002g0001 | 4 | HG01361.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+148_1938+149i others(135): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181453 | ||||||
| chr6:44181453 | A | ACACACAC others(124): Show |
9 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(6): Show |
15 | HG00741.hp1 HG01070.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1938+148_1938+149i others(133): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181453 | ||||||
| chr6:44181453 | A | ACACACAC others(120): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0002 |
3 | HG01257.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1938+148_1938+149i others(129): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181453 | ||||||
| chr6:44181455 | A | ACACACAC others(69): Show |
1 | a0001c0001t0002g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+148_1938+149i others(78): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181455 | ||||||
| chr6:44181455 | A | ACACACAC others(71): Show |
1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1938+148_1938+149i others(80): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181455 | ||||||
| chr6:44181455 | A | ACACACAC others(122): Show |
1 | a0001c0001t0002g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1938+148_1938+149i others(131): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181455 | ||||||
| chr6:44181455 | A | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
3 | HG02451.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1938+135A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181455 | |||||||
| chr6:44181457 | A | ACACACAC others(233): Show |
2 | a0001c0001t0002g0006 a0001c0001t0002g0019 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1938+148_1938+149i others(242): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181457 | ||||||
| chr6:44181457 | A | ACACACAC others(235): Show |
1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1938+148_1938+149i others(244): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181457 | ||||||
| chr6:44181459 | A | ACACACAC others(233): Show |
1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1938+148_1938+149i others(242): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181459 | ||||||
| chr6:44181461 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(2): Show |
7 | HG00323.hp2 HG01261.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+141A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181461 | |||||||
| chr6:44181462 | C | CACACCCA others(329): Show |
1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1938+146_1938+147i others(338): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181462 | ||||||
| chr6:44181462 | C | CACACCCA others(286): Show |
1 | a0001c0001t0001g0004 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1938+146_1938+147i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181462 | ||||||
| chr6:44181462 | C | CACTCACA others(218): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
6 | HG00544.hp1 HG03704.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+144_1938+145i others(227): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181462 | ||||||
| chr6:44181462 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1938+142C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181462 | |||||||
| chr6:44181463 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0002g0020 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+143A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181463 | |||||||
| chr6:44181464 | CACACTCA others(3): Show |
C | 2 | a0001c0001t0001g0039 a0001c0001t0002g0020 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+148_1938+157d others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181464 | ||||||
| chr6:44181467 | ACT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(4): Show |
9 | HG00323.hp2 HG01261.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+149_1938+150d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181467 | ||||||
| chr6:44181473 | A | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(4): Show |
9 | HG00323.hp2 HG01261.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+153A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181473 | |||||||
| chr6:44181474 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(4): Show |
9 | HG00323.hp2 HG01261.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+154T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181474 | |||||||
| chr6:44181474 | T | TACACAAC others(179): Show |
1 | a0001c0001t0001g0005 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1938+157_1938+158i others(188): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181474 | ||||||
| chr6:44181474 | T | TACACAAC others(177): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
17 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1938+157_1938+158i others(186): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181474 | ||||||
| chr6:44181474 | T | TACACAAC others(175): Show |
1 | a0001c0001t0001g0002 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1938+157_1938+158i others(184): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181474 | ||||||
| chr6:44181474 | T | TACACAAC others(177): Show |
1 | a0001c0001t0001g0001 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1938+157_1938+158i others(186): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181474 | ||||||
| chr6:44181474 | T | TACACAAC others(175): Show |
2 | a0001c0001t0001g0045 a0001c0001t0008g0009 |
2 | HG00733.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1938+157_1938+158i others(184): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181474 | ||||||
| chr6:44181478 | G | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
23 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1938+158G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181478 | |||||||
| chr6:44181490 | CCA | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(20): Show |
52 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1938+188_1938+189d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181490 | ||||||
| chr6:44181490 | CCACA | C | 4 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0017 others(1): Show |
5 | HG02622.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+186_1938+189d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181490 | ||||||
| chr6:44181492 | A | ACACT | 3 | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0002g0019 |
4 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+175_1938+176i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181492 | ||||||
| chr6:44181494 | A | ACT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
14 | HG00544.hp1 HG01257.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1938+175_1938+176i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181494 | ||||||
| chr6:44181495 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 |
3 | HG02965.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+175C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181495 | |||||||
| chr6:44181496 | A | ACACATAC others(122): Show |
3 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 |
6 | HG02280.hp2 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1938+180_1938+181i others(131): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181496 | ||||||
| chr6:44181496 | A | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
34 | HG00741.hp1 HG01070.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1938+176A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181496 | |||||||
| chr6:44181498 | A | ACACACAC others(112): Show |
1 | a0001c0001t0001g0003 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1938+185_1938+186i others(121): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181498 | ||||||
| chr6:44181498 | A | ACATACAC others(120): Show |
2 | a0001c0001t0002g0005 a0001c0001t0002g0011 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1938+180_1938+181i others(129): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181498 | ||||||
| chr6:44181503 | C | CACACTCA others(142): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
32 | HG00140.hp2 HG01167.hp2 HG01975.hp2 others(29): Show |
intron_variant | MODIFIER | c.1938+187_1938+188i others(151): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181503 | ||||||
| chr6:44181503 | C | CACACTCA others(140): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 |
10 | HG00544.hp2 HG00558.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1938+187_1938+188i others(149): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181503 | ||||||
| chr6:44181503 | C | CACACTCA others(142): Show |
1 | a0001c0001t0001g0001 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1938+187_1938+188i others(151): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181503 | ||||||
| chr6:44181503 | C | CTCACATA others(138): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0050 |
3 | NA18955.hp2 NA19012.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1938+183_1938+184i others(147): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181503 | |||||||
| chr6:44181503 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1938+183C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181503 | |||||||
| chr6:44181508 | A | T | 1 | a0001c0001t0001g0004 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1938+188A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181508 | |||||||
| chr6:44181537 | T | TCA | 9 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(6): Show |
16 | HG00741.hp1 HG01255.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1938+231_1938+232d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181537 | ||||||
| chr6:44181537 | T | TCACA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(8): Show |
21 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1938+229_1938+232d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181537 | ||||||
| chr6:44181537 | T | TCACACAC others(54): Show |
1 | a0001c0001t0002g0005 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1938+229_1938+230i others(63): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181537 | ||||||
| chr6:44181537 | TCA | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
92 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1938+231_1938+232d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181537 | ||||||
| chr6:44181544 | CACACACA others(30): Show |
C | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1938+231_1938+267d others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181544 | ||||||
| chr6:44181546 | C | CACAT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
40 | HG00323.hp2 HG00609.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1938+229_1938+230i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181546 | ||||||
| chr6:44181546 | C | CAT | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
5 | NA18612.hp2 NA18952.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+227_1938+228i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181546 | ||||||
| chr6:44181546 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1938+226C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181546 | |||||||
| chr6:44181574 | C | CCA | 3 | a0001c0001t0001g0011 a0001c0001t0002g0018 a0001c0001t0002g0020 |
4 | HG00280.hp1 HG01891.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+259_1938+260d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
20 | HG01069.hp2 HG01106.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1938+257_1938+260d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACAC others(128): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
4 | NA18612.hp2 NA18978.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+260_1938+261i others(137): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
128 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1938+259_1938+260i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(1): Show |
45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1938+259_1938+260i others(10): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(3): Show |
6 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(3): Show |
12 | HG00733.hp2 HG01358.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1938+259_1938+260i others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(5): Show |
3 | a0001c0001t0001g0004 a0001c0001t0002g0001 a0001c0001t0002g0006 |
4 | HG01257.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+259_1938+260i others(14): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(126): Show |
1 | a0001c0001t0001g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1938+259_1938+260i others(135): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(42): Show |
1 | a0001c0001t0002g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1938+259_1938+260i others(51): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(48): Show |
1 | a0001c0001t0001g0004 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1938+259_1938+260i others(57): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(122): Show |
1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(131): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(122): Show |
1 | a0001c0001t0001g0002 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(131): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(124): Show |
1 | a0001c0001t0001g0002 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1938+259_1938+260i others(133): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(126): Show |
22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
132 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1938+259_1938+260i others(135): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(171): Show |
1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1938+259_1938+260i others(180): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(124): Show |
1 | a0001c0001t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1938+259_1938+260i others(133): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(87): Show |
1 | a0001c0001t0001g0003 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(96): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(169): Show |
1 | a0001c0001t0002g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(178): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(44): Show |
1 | a0001c0001t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(53): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CCACACTC others(207): Show |
1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1938+259_1938+260i others(216): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181574 | ||||||
| chr6:44181574 | C | CTCACA | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
6 | HG00544.hp1 HG03704.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+254_1938+255i others(7): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181574 | |||||||
| chr6:44181581 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1938+261T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181581 | |||||||
| chr6:44181581 | T | CACACACT others(120): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(1): Show |
5 | HG01433.hp2 HG03942.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+260_1938+261i others(129): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181581 | |||||||
| chr6:44181588 | T | A | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1938+268T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181588 | |||||||
| chr6:44181590 | A | G | 1 | a0001c0001t0004g0001 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1938+270A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181590 | |||||||
| chr6:44181607 | C | CACTCACA others(30): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
37 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1938+289_1938+290i others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181607 | ||||||
| chr6:44181609 | C | CT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(3): Show |
7 | NA18955.hp2 NA18998.hp1 NA19007.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+289_1938+290i others(3): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181609 | |||||||
| chr6:44181609 | CCACACT | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
5 | HG03704.hp1 NA18941.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+295_1938+300d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181609 | ||||||
| chr6:44181614 | CT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
37 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1938+295delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181614 | |||||||
| chr6:44181615 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(3): Show |
7 | NA18955.hp2 NA18998.hp1 NA19007.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+295T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181615 | |||||||
| chr6:44181615 | T | TCA | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
37 | HG01123.hp2 HG01243.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1938+306_1938+307d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181615 | ||||||
| chr6:44181615 | T | TCACACAC others(30): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
18 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1938+307_1938+308i others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181615 | ||||||
| chr6:44181615 | TCA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0002g0006 others(2): Show |
6 | HG02258.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+306_1938+307d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181615 | ||||||
| chr6:44181617 | A | ACACACAC others(28): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
4 | HG00738.hp2 HG01255.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+307_1938+308i others(37): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(790): Show |
1 | a0001c0001t0002g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1938+307_1938+308i others(799): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(680): Show |
1 | a0001c0001t0003g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(689): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(637): Show |
1 | a0001c0001t0003g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(646): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(2123): Show |
1 | a0001c0001t0003g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(2132): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(641): Show |
1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(650): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(637): Show |
1 | a0001c0001t0003g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(646): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(2286): Show |
1 | a0001c0001t0003g0004 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(2295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(641): Show |
1 | a0001c0001t0002g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(650): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(637): Show |
1 | a0001c0001t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(646): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(2333): Show |
1 | a0001c0001t0002g0003 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1938+307_1938+308i others(2342): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(2280): Show |
1 | a0001c0001t0003g0003 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1938+307_1938+308i others(2289): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(680): Show |
1 | a0001c0001t0003g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1938+307_1938+308i others(689): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181617 | A | ACACACAC others(26): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(3): Show |
7 | NA18955.hp2 NA18998.hp1 NA19007.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+307_1938+308i others(35): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181617 | ||||||
| chr6:44181621 | A | ACACATAC others(118): Show |
1 | a0001c0001t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1938+305_1938+306i others(127): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181621 | ||||||
| chr6:44181622 | CACACAT | C | 2 | a0001c0001t0001g0006 a0001c0001t0002g0020 |
4 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+308_1938+313d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181622 | ||||||
| chr6:44181624 | CACAT | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(34): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1938+308_1938+311d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181624 | ||||||
| chr6:44181626 | CAT | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 |
3 | NA18972.hp2 NA19012.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1938+308_1938+309d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181626 | ||||||
| chr6:44181628 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
82 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1938+308T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181628 | |||||||
| chr6:44181632 | CACTCACA others(34): Show |
C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0012 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+353_1938+393d others(43): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181632 | ||||||
| chr6:44181648 | CAACCA | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 |
3 | NA18990.hp2 NA19006.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1938+329_1938+333d others(7): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181648 | |||||||
| chr6:44181658 | ACACT | A | 2 | a0001c0001t0002g0020 a0001c0001t0003g0017 |
3 | HG01891.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1938+342_1938+345d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181658 | ||||||
| chr6:44181660 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0009 |
2 | HG01433.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1938+340A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181660 | |||||||
| chr6:44181660 | ACT | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(8): Show |
17 | HG01123.hp2 HG02055.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1938+342_1938+343d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181660 | ||||||
| chr6:44181662 | T | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(6): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1938+342T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181662 | |||||||
| chr6:44181662 | T | TCA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(29): Show |
108 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1938+351_1938+352d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181662 | ||||||
| chr6:44181662 | T | TCACA | 9 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(6): Show |
21 | HG00609.hp2 HG00733.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1938+349_1938+352d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181662 | ||||||
| chr6:44181664 | ACACACAC others(153): Show |
A | 1 | a0001c0001t0001g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1938+353_1938+512d others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181664 | ||||||
| chr6:44181666 | ACACACAT others(30): Show |
A | 1 | a0001c0001t0001g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1938+353_1938+389d others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181666 | ||||||
| chr6:44181669 | C | CACACACA others(120): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1938+352_1938+353i others(129): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181669 | ||||||
| chr6:44181669 | C | CACACAT | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1938+352_1938+353i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181669 | ||||||
| chr6:44181669 | C | CACACATA others(214): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG04199.hp2 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1938+352_1938+353i others(223): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181669 | ||||||
| chr6:44181669 | C | CAT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
20 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1938+350_1938+351i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181669 | ||||||
| chr6:44181669 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(4): Show |
9 | HG01106.hp2 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938+349C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181669 | |||||||
| chr6:44181673 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1938+353T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181673 | |||||||
| chr6:44181673 | T | TACAC | 18 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(15): Show |
25 | HG00099.hp1 HG00323.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1938+355_1938+356i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181673 | ||||||
| chr6:44181676 | T | A | 3 | a0001c0001t0001g0039 a0001c0001t0002g0003 a0001c0001t0002g0020 |
3 | HG03209.hp2 HG03540.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1938+356T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181676 | |||||||
| chr6:44181678 | A | T | 1 | a0001c0001t0002g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1938+358A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181678 | |||||||
| chr6:44181680 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0002g0020 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+360A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181680 | |||||||
| chr6:44181681 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0002g0020 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+361T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181681 | |||||||
| chr6:44181702 | CT | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
3 | HG02451.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1938+383delT | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181702 | |||||||
| chr6:44181703 | TCA | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(1): Show |
4 | HG02135.hp1 HG02165.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+397_1938+398d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181703 | ||||||
| chr6:44181705 | A | T | 1 | a0001c0001t0002g0005 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1938+385A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181705 | |||||||
| chr6:44181708 | C | CAT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(25): Show |
96 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1938+389_1938+390i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181708 | ||||||
| chr6:44181708 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1938+388C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181708 | |||||||
| chr6:44181710 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1938+390C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181710 | |||||||
| chr6:44181712 | C | CACACACA others(152): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0003 |
2 | HG01070.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1938+398_1938+399i others(161): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACACAT | 10 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0005 others(7): Show |
15 | HG02055.hp1 HG02622.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1938+397_1938+398i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACACATA others(905): Show |
1 | a0001c0001t0003g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1938+397_1938+398i others(914): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACACATA others(895): Show |
1 | a0001c0001t0001g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1938+397_1938+398i others(904): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACACTCA others(154): Show |
2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
5 | HG02280.hp2 HG02559.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+396_1938+397i others(163): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACAT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1938+395_1938+396i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CACTCACA others(673): Show |
1 | a0001c0001t0001g0005 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1938+394_1938+395i others(682): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | CAT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0003g0002 |
3 | HG02896.hp2 HG04184.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1938+393_1938+394i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181712 | ||||||
| chr6:44181712 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
22 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.1938+392C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181712 | |||||||
| chr6:44181715 | A | ACATACAC others(87): Show |
1 | a0001c0001t0003g0003 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1938+397_1938+398i others(96): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181715 | ||||||
| chr6:44181715 | A | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
100 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1938+395A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181715 | |||||||
| chr6:44181717 | A | T | 1 | a0001c0001t0002g0005 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1938+397A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181717 | |||||||
| chr6:44181719 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(34): Show |
119 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1938+399T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181719 | |||||||
| chr6:44181720 | C | CACAT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1938+403_1938+404i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(677): Show |
1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(686): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(1056): Show |
1 | a0001c0001t0001g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(1065): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(683): Show |
1 | a0001c0001t0001g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(692): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(673): Show |
1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(682): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(677): Show |
1 | a0001c0001t0002g0015 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1938+403_1938+404i others(686): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(681): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0015 |
2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1938+403_1938+404i others(690): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(157): Show |
1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(166): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(679): Show |
1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(688): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(155): Show |
2 | a0001c0001t0001g0006 a0001c0001t0002g0003 |
3 | HG01884.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1938+403_1938+404i others(164): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(1003): Show |
1 | a0001c0001t0001g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(1012): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(1089): Show |
1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(1098): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(1083): Show |
1 | a0001c0001t0001g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(1092): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(1081): Show |
1 | a0001c0001t0001g0003 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1938+403_1938+404i others(1090): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(156): Show |
10 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(7): Show |
20 | HG01109.hp1 HG01168.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.1938+403_1938+404i others(165): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(154): Show |
1 | a0001c0001t0002g0005 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(163): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(156): Show |
1 | a0001c0001t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(165): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(154): Show |
1 | a0001c0001t0002g0001 | 2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1938+403_1938+404i others(163): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(114): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1938+403_1938+404i others(123): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CACATACA others(38): Show |
1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1938+403_1938+404i others(47): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181720 | ||||||
| chr6:44181720 | C | CTCACATA others(71): Show |
1 | a0001c0001t0002g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+400_1938+401i others(80): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181720 | |||||||
| chr6:44181720 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(33): Show |
113 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1938+400C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181720 | |||||||
| chr6:44181722 | C | T | 1 | a0001c0001t0002g0005 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1938+402C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181722 | |||||||
| chr6:44181724 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0002g0001 a0001c0001t0003g0003 |
3 | HG03130.hp1 HG03540.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1938+404G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181724 | |||||||
| chr6:44181727 | A | AGACACAA others(328): Show |
1 | a0001c0001t0002g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1938+407_1938+408i others(337): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181727 | |||||||
| chr6:44181738 | ACACT | A | 3 | a0001c0001t0002g0005 a0001c0001t0003g0001 a0001c0001t0003g0026 |
4 | HG02622.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+422_1938+425d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181738 | ||||||
| chr6:44181740 | ACT | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0012 others(3): Show |
9 | HG02809.hp2 HG02886.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+422_1938+423d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181740 | ||||||
| chr6:44181741 | C | CACACATA others(26): Show |
1 | a0001c0001t0001g0003 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1938+421_1938+422i others(35): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181741 | |||||||
| chr6:44181742 | T | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0020 |
4 | HG01891.hp1 HG02055.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+422T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181742 | |||||||
| chr6:44181742 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1938+422T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181742 | |||||||
| chr6:44181742 | T | TCA | 2 | a0001c0001t0001g0006 a0001c0001t0001g0051 |
3 | HG02486.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1938+433_1938+434d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181742 | ||||||
| chr6:44181742 | TCA | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1938+433_1938+434d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181742 | ||||||
| chr6:44181742 | TCACACA | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
18 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1938+429_1938+434d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181742 | ||||||
| chr6:44181742 | TCACACAC others(77): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0002g0020 |
3 | HG03209.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+435_1938+518d others(86): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181742 | ||||||
| chr6:44181744 | A | ACACACAC others(30): Show |
1 | a0001c0001t0001g0003 | 2 | NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1938+434_1938+435i others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181744 | ||||||
| chr6:44181748 | A | ACACACAC others(71): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
40 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1938+434_1938+435i others(80): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181748 | ||||||
| chr6:44181748 | A | ACACACAC others(69): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
25 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1938+434_1938+435i others(78): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181748 | ||||||
| chr6:44181748 | A | ACACACAC others(67): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0028 |
2 | HG00621.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1938+434_1938+435i others(76): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181748 | ||||||
| chr6:44181748 | A | ACACACAC others(187): Show |
1 | a0001c0001t0001g0005 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1938+434_1938+435i others(196): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181748 | ||||||
| chr6:44181748 | A | ATACACAC others(395): Show |
1 | a0001c0001t0002g0001 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1938+428_1938+429i others(404): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181748 | |||||||
| chr6:44181748 | A | ATACACAC others(112): Show |
1 | a0001c0001t0001g0002 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1938+428_1938+429i others(121): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181748 | |||||||
| chr6:44181748 | A | ATACACAC others(110): Show |
1 | a0001c0001t0001g0004 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1938+428_1938+429i others(119): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181748 | |||||||
| chr6:44181748 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1938+428A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181748 | |||||||
| chr6:44181753 | CAT | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0023 others(4): Show |
10 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1938+435_1938+436d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181753 | ||||||
| chr6:44181755 | T | C | 18 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(15): Show |
47 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.1938+435T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181755 | |||||||
| chr6:44181783 | C | CCA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
5 | HG01175.hp1 NA18972.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+474_1938+475d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181783 | ||||||
| chr6:44181783 | C | CCACACAC others(124): Show |
1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1938+473_1938+474i others(133): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181783 | ||||||
| chr6:44181783 | C | CCACACAC others(77): Show |
1 | a0001c0001t0001g0023 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1938+473_1938+474i others(86): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181783 | ||||||
| chr6:44181783 | C | CCACACT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1938+468_1938+469i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181783 | ||||||
| chr6:44181783 | CCA | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0051 |
4 | HG02486.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+474_1938+475d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181783 | ||||||
| chr6:44181785 | A | ACACACAC others(178): Show |
1 | a0001c0001t0002g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1938+475_1938+476i others(187): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | A | ACACACAC others(289): Show |
1 | a0001c0001t0003g0003 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1938+475_1938+476i others(298): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | A | ACACT | 7 | a0001c0001t0001g0003 a0001c0001t0002g0019 a0001c0001t0002g0025 others(4): Show |
9 | HG00099.hp1 HG00323.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+468_1938+469i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | A | ACACTCAC others(328): Show |
2 | a0001c0001t0002g0005 a0001c0001t0002g0014 |
2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1938+468_1938+469i others(337): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | A | ACACTCAC others(452): Show |
3 | a0001c0001t0001g0005 a0001c0001t0002g0002 a0001c0001t0002g0004 |
7 | HG00609.hp2 HG02155.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+468_1938+469i others(461): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | A | ACACTCAC others(450): Show |
2 | a0001c0001t0002g0005 a0001c0001t0002g0013 |
2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1938+468_1938+469i others(459): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181785 | ACACACAC others(69): Show |
A | 1 | a0001c0001t0002g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1938+476_1938+551d others(78): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181785 | ||||||
| chr6:44181787 | A | ACT | 5 | a0001c0001t0001g0005 a0001c0001t0002g0002 a0001c0001t0002g0005 others(2): Show |
8 | HG01943.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+468_1938+469i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181787 | ||||||
| chr6:44181787 | A | ACTCACAC others(203): Show |
1 | a0001c0001t0001g0005 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1938+468_1938+469i others(212): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181787 | ||||||
| chr6:44181787 | A | ACTCACAC others(444): Show |
5 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(2): Show |
8 | HG00733.hp2 HG01358.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+468_1938+469i others(453): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181787 | ||||||
| chr6:44181787 | ACACACAC others(67): Show |
A | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1938+476_1938+549d others(76): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181787 | ||||||
| chr6:44181788 | CACACACA others(28): Show |
C | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1938+469_1938+503d others(37): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181788 | |||||||
| chr6:44181789 | A | ACACACAC others(116): Show |
3 | a0001c0001t0002g0003 a0001c0001t0003g0001 a0001c0001t0003g0003 |
3 | HG00738.hp1 HG01081.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1938+475_1938+476i others(125): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181789 | ||||||
| chr6:44181789 | A | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(9): Show |
14 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1938+469A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181789 | |||||||
| chr6:44181794 | CAT | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 |
4 | HG01070.hp1 HG02683.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+476_1938+477d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181794 | ||||||
| chr6:44181796 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
76 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1938+476T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181796 | |||||||
| chr6:44181796 | TAC | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
18 | HG01069.hp2 HG02015.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1938+481_1938+482d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181796 | ||||||
| chr6:44181798 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1938+478C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181798 | |||||||
| chr6:44181824 | C | CCA | 4 | a0001c0001t0001g0002 a0001c0001t0002g0012 a0001c0001t0002g0015 others(1): Show |
8 | HG00280.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+518_1938+519d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(5): Show |
17 | HG01069.hp2 HG02015.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1938+516_1938+519d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(133): Show |
1 | a0001c0001t0002g0002 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1938+519_1938+520i others(142): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(131): Show |
11 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(8): Show |
14 | HG01168.hp2 HG01255.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1938+519_1938+520i others(140): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(133): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0002 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1938+519_1938+520i others(142): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(127): Show |
1 | a0001c0001t0002g0002 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1938+519_1938+520i others(136): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(129): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 |
8 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+519_1938+520i others(138): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(131): Show |
1 | a0001c0001t0002g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1938+519_1938+520i others(140): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(127): Show |
1 | a0001c0001t0002g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1938+519_1938+520i others(136): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(129): Show |
1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1938+519_1938+520i others(138): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(131): Show |
1 | a0001c0001t0002g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1938+519_1938+520i others(140): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(129): Show |
1 | a0001c0001t0002g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+519_1938+520i others(138): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(125): Show |
1 | a0001c0001t0002g0005 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1938+519_1938+520i others(134): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(129): Show |
1 | a0001c0001t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1938+519_1938+520i others(138): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(534): Show |
1 | a0001c0001t0003g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1938+519_1938+520i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACAC others(524): Show |
1 | a0001c0001t0001g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1938+519_1938+520i others(533): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACT | 2 | a0001c0001t0001g0002 a0001c0001t0002g0003 |
3 | HG01168.hp1 HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1938+509_1938+510i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(3): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
86 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1938+509_1938+510i others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(745): Show |
1 | a0001c0001t0003g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(754): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(790): Show |
1 | a0001c0001t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(799): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1569): Show |
1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(1578): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1408): Show |
1 | a0001c0001t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(1417): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1406): Show |
1 | a0001c0001t0002g0002 | 2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1938+509_1938+510i others(1415): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(516): Show |
1 | a0001c0001t0003g0001 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(525): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1436): Show |
1 | a0001c0001t0003g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(1445): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(344): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0019 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1938+509_1938+510i others(353): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(342): Show |
1 | a0001c0001t0002g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(351): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(340): Show |
1 | a0001c0001t0002g0021 | 3 | HG03041.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+509_1938+510i others(349): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1434): Show |
1 | a0001c0001t0003g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(1443): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(342): Show |
1 | a0001c0001t0002g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(351): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(514): Show |
1 | a0001c0001t0003g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(523): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(50): Show |
1 | a0001c0001t0001g0003 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(59): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(142): Show |
1 | a0001c0001t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(151): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(788): Show |
1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(797): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(790): Show |
1 | a0001c0001t0003g0009 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(799): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(794): Show |
1 | a0001c0001t0003g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(803): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(788): Show |
1 | a0001c0001t0003g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(797): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(792): Show |
1 | a0001c0001t0002g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(801): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(95): Show |
1 | a0001c0001t0001g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(104): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(91): Show |
1 | a0001c0001t0002g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(100): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(89): Show |
1 | a0001c0001t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(98): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(1195): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0051 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1938+509_1938+510i others(1204): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(44): Show |
1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1938+509_1938+510i others(53): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | CCACACTC others(269): Show |
1 | a0001c0001t0001g0004 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1938+509_1938+510i others(278): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1938+504C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181824 | |||||||
| chr6:44181824 | CCA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(1): Show |
4 | HG00609.hp1 HG02004.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+518_1938+519d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181824 | CCACA | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0002g0006 others(2): Show |
7 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+516_1938+519d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181824 | ||||||
| chr6:44181826 | A | ACACTCTC others(115): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(1): Show |
5 | HG02083.hp2 HG02148.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+509_1938+510i others(124): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181826 | ||||||
| chr6:44181830 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0012 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+510A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181830 | |||||||
| chr6:44181833 | C | CACACAT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
74 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1938+518_1938+519i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181833 | ||||||
| chr6:44181833 | C | CACAT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(9): Show |
24 | HG00609.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1938+516_1938+517i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181833 | ||||||
| chr6:44181833 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1938+513C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181833 | |||||||
| chr6:44181837 | CACTCACA others(30): Show |
C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0012 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+520_1938+556d others(39): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181837 | ||||||
| chr6:44181840 | T | A | 1 | a0001c0001t0002g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1938+520T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181840 | |||||||
| chr6:44181851 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1938+531C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181851 | |||||||
| chr6:44181861 | C | CCA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0002g0014 |
4 | NA18942.hp1 NA19030.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+552_1938+553d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181861 | ||||||
| chr6:44181861 | C | CCACA | 7 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(4): Show |
19 | HG00609.hp2 HG00733.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1938+550_1938+553d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181861 | ||||||
| chr6:44181861 | C | CCACACA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0002g0012 others(1): Show |
7 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+548_1938+553d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181861 | ||||||
| chr6:44181861 | C | CCACACT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(20): Show |
72 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1938+546_1938+547i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181861 | ||||||
| chr6:44181863 | A | ACACACAC others(85): Show |
1 | a0001c0001t0001g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1938+553_1938+554i others(94): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181863 | ||||||
| chr6:44181863 | A | ACACACAC others(378): Show |
1 | a0001c0001t0001g0005 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1938+553_1938+554i others(387): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181863 | ||||||
| chr6:44181863 | A | ACACACAC others(841): Show |
1 | a0001c0001t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1938+553_1938+554i others(850): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181863 | ||||||
| chr6:44181863 | A | ACACT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
20 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1938+546_1938+547i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181863 | ||||||
| chr6:44181863 | A | ACACTCAC others(116): Show |
1 | a0001c0001t0003g0004 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1938+546_1938+547i others(125): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181863 | ||||||
| chr6:44181867 | A | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(29): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1938+547A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181867 | |||||||
| chr6:44181874 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1938+554T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181874 | |||||||
| chr6:44181878 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1938+558C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181878 | |||||||
| chr6:44181881 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1938+561T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181881 | |||||||
| chr6:44181906 | A | ACACACAC others(2108): Show |
1 | a0001c0001t0001g0002 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1938+587_1938+588i others(2117): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181906 | ||||||
| chr6:44181906 | A | ACACACAC others(243): Show |
1 | a0001c0001t0002g0001 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1938+587_1938+588i others(252): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181906 | ||||||
| chr6:44181908 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0001 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1938+588T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181908 | |||||||
| chr6:44181908 | T | TCA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0002g0020 |
5 | HG01891.hp1 HG02965.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+597_1938+598d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(659): Show |
1 | a0001c0001t0002g0006 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1938+598_1938+599i others(668): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(657): Show |
1 | a0001c0001t0001g0005 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(666): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(653): Show |
1 | a0001c0001t0002g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(662): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(657): Show |
1 | a0001c0001t0001g0001 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(666): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1846): Show |
1 | a0001c0001t0002g0002 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1855): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1844): Show |
1 | a0001c0001t0002g0005 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1853): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(688): Show |
1 | a0001c0001t0002g0013 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(697): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1739): Show |
1 | a0001c0001t0002g0001 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1748): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1737): Show |
1 | a0001c0001t0002g0038 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1746): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1739): Show |
1 | a0001c0001t0002g0013 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1748): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(2369): Show |
1 | a0001c0001t0002g0004 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(2378): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(653): Show |
1 | a0001c0001t0002g0003 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1938+598_1938+599i others(662): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1048): Show |
1 | a0001c0001t0002g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(1057): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1400): Show |
1 | a0001c0001t0002g0002 | 2 | NA18971.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1938+645_1938+646i others(1409): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(687): Show |
1 | a0001c0001t0002g0004 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1938+645_1938+646i others(696): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(730): Show |
3 | a0001c0001t0001g0005 a0001c0001t0002g0005 a0001c0001t0002g0013 |
4 | HG00609.hp2 HG02040.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+645_1938+646i others(739): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(728): Show |
1 | a0001c0001t0002g0002 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1938+645_1938+646i others(737): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1388): Show |
1 | a0001c0001t0002g0014 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1938+645_1938+646i others(1397): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1394): Show |
1 | a0001c0001t0002g0001 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1403): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1394): Show |
1 | a0001c0001t0001g0005 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1403): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1392): Show |
4 | a0001c0001t0001g0005 a0001c0001t0002g0002 a0001c0001t0002g0005 others(1): Show |
5 | HG01975.hp1 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+643_1938+644i others(1401): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181908 | T | TCACACAC others(1386): Show |
1 | a0001c0001t0002g0005 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1395): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181908 | ||||||
| chr6:44181912 | A | ACACACAC others(71): Show |
1 | a0001c0001t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1938+598_1938+599i others(80): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181912 | ||||||
| chr6:44181912 | A | ACACACAC others(73): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 |
4 | HG01884.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+598_1938+599i others(82): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181912 | ||||||
| chr6:44181912 | A | ACACACAT others(446): Show |
1 | a0001c0001t0002g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1938+645_1938+646i others(455): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181912 | ||||||
| chr6:44181912 | A | ACACACAT others(493): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0015 |
4 | HG02145.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+645_1938+646i others(502): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181912 | ||||||
| chr6:44181915 | CACAT | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
3 | HG03225.hp1 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1938+599_1938+602d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181915 | ||||||
| chr6:44181917 | CAT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
6 | HG02559.hp2 HG02965.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+599_1938+600d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181917 | ||||||
| chr6:44181919 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0033 others(8): Show |
18 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1938+599T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181919 | |||||||
| chr6:44181925 | C | CATACAGA others(562): Show |
1 | a0001c0001t0001g0002 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1938+605_1938+606i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181925 | |||||||
| chr6:44181925 | C | CTCACATA others(564): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
4 | NA18945.hp1 NA19000.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+645_1938+646i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0013 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1938+645_1938+646i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(560): Show |
1 | a0001c0001t0001g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1938+645_1938+646i others(569): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(558): Show |
1 | a0001c0001t0001g0008 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1938+645_1938+646i others(567): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(568): Show |
1 | a0001c0001t0001g0004 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(577): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(566): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
81 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(575): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(564): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
7 | HG00423.hp2 HG02015.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(566): Show |
1 | a0001c0001t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(575): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(564): Show |
1 | a0001c0001t0001g0005 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0001 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(519): Show |
1 | a0001c0001t0001g0001 | 7 | NA18951.hp1 NA18952.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(528): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(564): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
20 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0003 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(560): Show |
1 | a0001c0001t0001g0005 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(569): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(482): Show |
1 | a0001c0001t0001g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(491): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(562): Show |
1 | a0001c0001t0001g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(390): Show |
1 | a0001c0001t0001g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(399): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(476): Show |
1 | a0001c0001t0001g0002 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(485): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(564): Show |
1 | a0001c0001t0001g0003 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1938+690_1938+691i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181925 | C | CTCACATA others(478): Show |
1 | a0001c0001t0002g0005 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1938+686_1938+687i others(487): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181925 | ||||||
| chr6:44181926 | T | TCACATAC others(151): Show |
1 | a0001c0001t0002g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(160): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(333): Show |
1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(342): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(1351): Show |
1 | a0001c0001t0002g0002 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1360): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(288): Show |
1 | a0001c0001t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(297): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(333): Show |
1 | a0001c0001t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(342): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(333): Show |
8 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(5): Show |
13 | HG00741.hp1 HG01168.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1938+627_1938+628i others(342): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(329): Show |
1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(338): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(331): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(1): Show |
12 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1938+627_1938+628i others(340): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(331): Show |
1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(340): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(327): Show |
1 | a0001c0001t0002g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1938+627_1938+628i others(336): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(329): Show |
1 | a0001c0001t0002g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(338): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181926 | T | TCACATAC others(378): Show |
1 | a0001c0001t0002g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1938+627_1938+628i others(387): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181926 | ||||||
| chr6:44181933 | C | CAGACACA others(564): Show |
1 | a0001c0001t0001g0004 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181933 | ||||||
| chr6:44181937 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1938+617C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181937 | |||||||
| chr6:44181947 | CCACACT | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02965.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1938+633_1938+638d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181947 | ||||||
| chr6:44181948 | C | G | 1 | a0001c0001t0002g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1938+628C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181948 | |||||||
| chr6:44181953 | T | TCACACAC others(36): Show |
1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1938+645_1938+646i others(45): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(331): Show |
6 | a0001c0001t0001g0011 a0001c0001t0002g0002 a0001c0001t0002g0012 others(3): Show |
7 | HG00099.hp1 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+643_1938+644i others(340): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(329): Show |
1 | a0001c0001t0003g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(338): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(331): Show |
1 | a0001c0001t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(340): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(1431): Show |
1 | a0001c0001t0002g0021 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+643_1938+644i others(1440): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(1429): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0019 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1938+643_1938+644i others(1438): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(1431): Show |
1 | a0001c0001t0002g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1440): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(1425): Show |
1 | a0001c0001t0002g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1434): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(1425): Show |
1 | a0001c0001t0002g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(1434): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | T | TCACACAC others(329): Show |
1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1938+643_1938+644i others(338): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | TCA | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(7): Show |
13 | HG01168.hp1 HG01169.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1938+644_1938+645d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181953 | TCACACAC others(120): Show |
T | 2 | a0001c0001t0001g0039 a0001c0001t0002g0020 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1938+640_1938+766d others(2): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181953 | ||||||
| chr6:44181955 | A | ACACACAC others(36): Show |
1 | a0001c0001t0002g0002 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1938+645_1938+646i others(45): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181955 | ||||||
| chr6:44181955 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0005 |
2 | HG00140.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1938+635A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181955 | |||||||
| chr6:44181959 | A | ACACACAC others(497): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0041 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1938+645_1938+646i others(506): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181959 | ||||||
| chr6:44181959 | A | ACACATAC others(620): Show |
1 | a0001c0001t0003g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1938+643_1938+644i others(629): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181959 | ||||||
| chr6:44181959 | A | ACACATAC others(671): Show |
3 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0026 |
3 | HG02622.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1938+643_1938+644i others(680): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181959 | ||||||
| chr6:44181960 | C | T | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1938+640C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181960 | |||||||
| chr6:44181962 | CACAT | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(3): Show |
9 | HG00621.hp1 HG00735.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938+646_1938+649d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181962 | ||||||
| chr6:44181964 | CAT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(18): Show |
65 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1938+646_1938+647d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181964 | ||||||
| chr6:44181966 | T | C | 5 | a0001c0001t0002g0015 a0001c0001t0003g0001 a0001c0001t0003g0002 others(2): Show |
5 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+646T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181966 | |||||||
| chr6:44181966 | T | TACACACT others(32): Show |
1 | a0001c0001t0002g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1938+679_1938+680i others(41): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181966 | ||||||
| chr6:44181966 | T | TACACACT others(165): Show |
1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1938+726_1938+727i others(174): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181966 | ||||||
| chr6:44181973 | T | TCACATAC others(562): Show |
1 | a0001c0001t0002g0001 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181973 | ||||||
| chr6:44181976 | C | A | 1 | a0001c0001t0002g0002 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1938+656C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44181976 | |||||||
| chr6:44181980 | C | CAGACACA others(354): Show |
1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1938+679_1938+680i others(363): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181980 | ||||||
| chr6:44181980 | C | CAGACACA others(352): Show |
1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1938+679_1938+680i others(361): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181980 | ||||||
| chr6:44181980 | C | CAGACACA others(352): Show |
1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1938+679_1938+680i others(361): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181980 | ||||||
| chr6:44181994 | CCACACTC others(3): Show |
C | 1 | a0001c0001t0002g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1938+680_1938+689d others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181994 | ||||||
| chr6:44181998 | A | ACACACAC others(61): Show |
1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1938+679_1938+680i others(70): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44181998 | ||||||
| chr6:44182000 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0002g0018 |
7 | HG00280.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+680T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182000 | |||||||
| chr6:44182000 | TCA | T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+691_1938+692d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182000 | ||||||
| chr6:44182002 | A | ACACACAC others(524): Show |
1 | a0001c0001t0001g0002 | 5 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+689_1938+690i others(533): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182002 | ||||||
| chr6:44182006 | A | ACACTCAC others(145): Show |
1 | a0001c0001t0002g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1938+689_1938+690i others(154): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182006 | ||||||
| chr6:44182011 | CAT | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(1): Show |
4 | HG02559.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+693_1938+694d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182011 | ||||||
| chr6:44182013 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0002g0005 a0001c0001t0002g0019 others(2): Show |
6 | HG02615.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+693T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182013 | |||||||
| chr6:44182013 | T | TACACACT others(562): Show |
1 | a0001c0001t0001g0001 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(571): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182013 | ||||||
| chr6:44182035 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1938+715A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182035 | |||||||
| chr6:44182038 | ACACCACA others(70): Show |
A | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1938+722_1938+798d others(79): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182038 | ||||||
| chr6:44182041 | C | CCA | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
16 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(13): Show |
intron_variant | MODIFIER | c.1938+732_1938+733d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
78 | HG00280.hp2 HG00423.hp1 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.1938+730_1938+733d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACA | 16 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(13): Show |
52 | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1938+728_1938+733d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACAC others(566): Show |
1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(575): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACTC others(5): Show |
1 | a0001c0001t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1938+726_1938+727i others(14): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACTC others(7): Show |
1 | a0001c0001t0002g0013 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1938+726_1938+727i others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACTC others(2758): Show |
1 | a0001c0001t0003g0003 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1938+726_1938+727i others(2767): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACTC others(1408): Show |
1 | a0001c0001t0002g0004 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1938+726_1938+727i others(1417): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | C | CCACACTC others(847): Show |
1 | a0001c0001t0002g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1938+726_1938+727i others(856): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | CCACACAC others(24): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1938+734_1938+764d others(33): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182041 | CCACACAC others(26): Show |
C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG02559.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+738_1938+770d others(35): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182041 | ||||||
| chr6:44182042 | C | CACACTCA others(11): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(13): Show |
45 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1938+726_1938+727i others(20): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182042 | ||||||
| chr6:44182042 | C | CACACTCA others(54): Show |
1 | a0001c0001t0001g0001 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1938+726_1938+727i others(63): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182042 | ||||||
| chr6:44182042 | C | CACACTCA others(9): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0051 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1938+726_1938+727i others(18): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182042 | ||||||
| chr6:44182042 | C | CACACTCA others(7): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
23 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1938+726_1938+727i others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182042 | ||||||
| chr6:44182043 | A | ACACACAC others(564): Show |
1 | a0001c0001t0001g0002 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(573): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182043 | ||||||
| chr6:44182044 | C | CACACACA others(3): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0015 |
5 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+728_1938+737d others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182044 | ||||||
| chr6:44182044 | C | CACTCACA others(214): Show |
1 | a0001c0001t0002g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1938+726_1938+727i others(223): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182044 | ||||||
| chr6:44182045 | A | ACT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
7 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+726_1938+727i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182045 | ||||||
| chr6:44182049 | A | ACACACAC others(9): Show |
1 | a0001c0001t0002g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(18): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(14): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(484): Show |
1 | a0001c0001t0002g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(493): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(482): Show |
1 | a0001c0001t0002g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(491): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(486): Show |
1 | a0001c0001t0002g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(495): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(480): Show |
1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(489): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(726): Show |
1 | a0001c0001t0003g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(735): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(724): Show |
1 | a0001c0001t0003g0004 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(733): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(720): Show |
1 | a0001c0001t0002g0003 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(729): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(511): Show |
1 | a0001c0001t0002g0002 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(520): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(507): Show |
5 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0021 others(2): Show |
7 | HG01934.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+733_1938+734i others(516): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(505): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0012 |
3 | HG02055.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1938+733_1938+734i others(514): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(503): Show |
1 | a0001c0001t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(512): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(507): Show |
1 | a0001c0001t0003g0002 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(516): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(501): Show |
1 | a0001c0001t0001g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(510): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(1761): Show |
1 | a0001c0001t0003g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(1770): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(1761): Show |
1 | a0001c0001t0003g0001 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(1770): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(3): Show |
1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1938+733_1938+734i others(12): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(382): Show |
1 | a0001c0001t0002g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(391): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0003 | 4 | NA18970.hp1 NA19060.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+733_1938+734i others(18): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(720): Show |
1 | a0001c0001t0003g0003 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(729): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(505): Show |
1 | a0001c0001t0002g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(514): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAC others(480): Show |
1 | a0001c0001t0001g0005 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1938+733_1938+734i others(489): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAT others(7): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
5 | NA18972.hp2 NA19012.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+733_1938+734i others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACACAT others(1023): Show |
1 | a0001c0001t0002g0002 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(1032): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(5): Show |
1 | a0001c0001t0001g0002 | 5 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(14): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(160): Show |
1 | a0001c0001t0003g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(169): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(163): Show |
3 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0026 |
3 | HG02622.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1938+737_1938+738i others(172): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(896): Show |
1 | a0001c0001t0002g0003 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(905): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(50): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1938+737_1938+738i others(59): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(177): Show |
1 | a0001c0001t0001g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(186): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(224): Show |
1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(233): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(128): Show |
1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1938+737_1938+738i others(137): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(963): Show |
1 | a0001c0001t0002g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(972): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(961): Show |
1 | a0001c0001t0002g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+737_1938+738i others(970): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | ACACATAC others(959): Show |
1 | a0001c0001t0002g0006 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1938+737_1938+738i others(968): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182049 | ||||||
| chr6:44182049 | A | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
75 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1938+729A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182049 | |||||||
| chr6:44182053 | A | ACTCACAT others(169): Show |
1 | a0001c0001t0001g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1938+733_1938+734i others(178): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182053 | |||||||
| chr6:44182054 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
9 | HG00408.hp1 HG02015.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938+734T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182054 | |||||||
| chr6:44182058 | G | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
8 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+738G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182058 | |||||||
| chr6:44182064 | A | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
7 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+744A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182064 | |||||||
| chr6:44182065 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
7 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+745C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182065 | |||||||
| chr6:44182068 | C | CATACACA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
7 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+749_1938+750i others(9): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182068 | ||||||
| chr6:44182069 | AC | A | 10 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(7): Show |
29 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1938+751delC | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182069 | ||||||
| chr6:44182070 | CCA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1938+765_1938+766d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182070 | ||||||
| chr6:44182074 | A | AC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(3): Show |
7 | HG02015.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+755dupC | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACACACAC others(661): Show |
1 | a0001c0001t0002g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1938+765_1938+766i others(670): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACACACAT others(79): Show |
1 | a0001c0001t0002g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1938+760_1938+761i others(88): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
13 | HG00280.hp1 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1938+755_1938+756i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACTCACAC others(292): Show |
1 | a0001c0001t0001g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1938+755_1938+756i others(301): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACTCACAC others(296): Show |
1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1938+755_1938+756i others(305): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACTCACAC others(294): Show |
1 | a0001c0001t0001g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1938+755_1938+756i others(303): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACTCACAC others(1280): Show |
1 | a0001c0001t0002g0005 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1938+755_1938+756i others(1289): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | ACTCACAC others(163): Show |
1 | a0001c0001t0001g0049 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1938+755_1938+756i others(172): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182074 | ||||||
| chr6:44182074 | A | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0044 |
2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1938+754A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182074 | |||||||
| chr6:44182076 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1938+756A>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182076 | |||||||
| chr6:44182076 | A | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
55 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1938+756A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182076 | |||||||
| chr6:44182078 | A | ACACACAT others(534): Show |
1 | a0001c0001t0002g0005 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1938+764_1938+765i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182078 | ||||||
| chr6:44182078 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1938+758A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182078 | |||||||
| chr6:44182080 | A | ATACACAC others(428): Show |
1 | a0001c0001t0002g0005 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1938+760_1938+761i others(437): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182080 | |||||||
| chr6:44182080 | A | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG02559.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1938+760A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182080 | |||||||
| chr6:44182087 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(18): Show |
35 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1938+767T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182087 | |||||||
| chr6:44182087 | T | TACACACT others(438): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 |
6 | HG01255.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(447): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182087 | T | TACACACT others(534): Show |
1 | a0001c0001t0002g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182087 | T | TACACACT others(534): Show |
1 | a0001c0001t0002g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182087 | T | TACACACT others(536): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(1): Show |
7 | HG00733.hp2 HG01358.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(545): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182087 | T | TACACACT others(534): Show |
2 | a0001c0001t0001g0005 a0001c0001t0002g0005 |
2 | HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1938+800_1938+801i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182087 | T | TACACACT others(534): Show |
1 | a0001c0001t0001g0005 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(543): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182087 | ||||||
| chr6:44182115 | CCA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(1): Show |
4 | HG00597.hp2 HG02080.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+810_1939-810d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182115 | ||||||
| chr6:44182115 | CCACA | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(5): Show |
8 | HG02647.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1938+808_1939-810d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182115 | ||||||
| chr6:44182117 | A | ACACTCAC others(493): Show |
1 | a0001c0001t0002g0013 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(502): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(493): Show |
5 | a0001c0001t0001g0005 a0001c0001t0002g0002 a0001c0001t0002g0004 others(2): Show |
8 | HG00609.hp2 HG02155.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(502): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(487): Show |
1 | a0001c0001t0002g0001 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(496): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(499): Show |
1 | a0001c0001t0002g0014 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(508): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(491): Show |
1 | a0001c0001t0002g0005 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(500): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(493): Show |
2 | a0001c0001t0002g0005 a0001c0001t0003g0003 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1938+800_1938+801i others(502): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(118): Show |
1 | a0001c0001t0002g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(127): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182117 | A | ACACTCAC others(487): Show |
1 | a0001c0001t0002g0038 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(496): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182117 | ||||||
| chr6:44182119 | A | ACT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(45): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(477): Show |
1 | a0001c0001t0002g0001 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1938+800_1938+801i others(486): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(475): Show |
1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(484): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(479): Show |
1 | a0001c0001t0002g0002 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(488): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(479): Show |
5 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0046 others(2): Show |
9 | HG01109.hp1 HG01168.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(488): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(477): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 |
4 | HG01257.hp1 HG01258.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(486): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(477): Show |
1 | a0001c0001t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(486): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(79): Show |
1 | a0001c0001t0001g0002 | 5 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1938+800_1938+801i others(88): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(339): Show |
1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(348): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(475): Show |
1 | a0001c0001t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1938+800_1938+801i others(484): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | ACTCACAC others(475): Show |
1 | a0001c0001t0002g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1938+800_1938+801i others(484): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182119 | ||||||
| chr6:44182119 | A | T | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1938+799A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182119 | |||||||
| chr6:44182121 | A | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
78 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1938+801A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182121 | |||||||
| chr6:44182123 | A | T | 9 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(6): Show |
15 | HG00609.hp2 HG02040.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1938+803A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182123 | |||||||
| chr6:44182125 | A | ACACACAC others(393): Show |
1 | a0001c0001t0002g0001 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1939-810_1939-809i others(402): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182125 | ||||||
| chr6:44182125 | A | T | 11 | a0001c0001t0001g0002 a0001c0001t0002g0001 a0001c0001t0002g0002 others(8): Show |
21 | HG01070.hp1 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1938+805A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182125 | |||||||
| chr6:44182127 | A | ACACACTC others(471): Show |
1 | a0001c0001t0002g0005 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1939-810_1939-809i others(480): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182127 | ||||||
| chr6:44182128 | CACAT | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0006 |
4 | HG02630.hp2 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-809_1939-806d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182128 | ||||||
| chr6:44182132 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0002g0001 others(27): Show |
86 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1939-809T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182132 | |||||||
| chr6:44182132 | T | TACAGACA others(546): Show |
1 | a0001c0001t0002g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1939-806_1939-805i others(555): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182132 | ||||||
| chr6:44182144 | TAC | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0051 |
3 | HG00738.hp2 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1939-795_1939-794d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182144 | ||||||
| chr6:44182166 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1939-775T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182166 | |||||||
| chr6:44182166 | T | TCA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.1939-766_1939-765d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(833): Show |
1 | a0001c0001t0002g0002 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1939-765_1939-764i others(842): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(452): Show |
1 | a0001c0001t0002g0013 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1939-765_1939-764i others(461): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(190): Show |
1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1939-765_1939-764i others(199): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(122): Show |
1 | a0001c0001t0002g0018 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1939-765_1939-764i others(131): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(390): Show |
1 | a0001c0001t0001g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1939-765_1939-764i others(399): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182166 | T | TCACACAC others(261): Show |
1 | a0001c0001t0001g0012 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1939-684_1939-683i others(270): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182166 | ||||||
| chr6:44182173 | CACAT | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0005 others(1): Show |
7 | HG00741.hp1 HG01255.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1939-764_1939-761d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182173 | ||||||
| chr6:44182177 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0002g0001 |
5 | HG01175.hp2 HG01361.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939-764T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182177 | |||||||
| chr6:44182207 | A | ACACACAC others(22): Show |
1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1939-731_1939-730i others(31): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182207 | ||||||
| chr6:44182207 | ACACTCAC others(71): Show |
A | 1 | a0001c0001t0002g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1939-730_1939-653d others(80): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182207 | ||||||
| chr6:44182209 | A | ACACACAC others(61): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(1): Show |
6 | NA18972.hp2 NA18980.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939-731_1939-730i others(70): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182209 | ||||||
| chr6:44182211 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(3): Show |
8 | HG02895.hp2 NA18956.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.1939-730T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182211 | |||||||
| chr6:44182215 | A | ACACACAT others(947): Show |
1 | a0001c0001t0002g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1939-720_1939-719i others(956): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182215 | ||||||
| chr6:44182217 | A | ACACACAC others(75): Show |
1 | a0001c0001t0002g0001 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1939-718_1939-717i others(84): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182217 | ||||||
| chr6:44182220 | CACAT | C | 10 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(7): Show |
27 | HG01070.hp1 HG01109.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1939-717_1939-714d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182220 | ||||||
| chr6:44182224 | T | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0042 |
3 | HG01361.hp2 HG03225.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1939-717T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182224 | |||||||
| chr6:44182224 | T | TACACACT others(171): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0002g0015 |
4 | HG01884.hp2 HG02109.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-669_1939-668i others(180): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182224 | ||||||
| chr6:44182224 | T | TACACACT others(36): Show |
1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1939-684_1939-683i others(45): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182224 | ||||||
| chr6:44182252 | C | CCA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1939-674_1939-673d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(7): Show |
12 | HG00280.hp1 HG02015.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1939-676_1939-673d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0002g0001 others(1): Show |
7 | HG01069.hp2 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939-678_1939-673d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACAC others(175): Show |
1 | a0001c0001t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1939-669_1939-668i others(184): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACAC others(177): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0015 |
4 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-669_1939-668i others(186): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACAC others(179): Show |
1 | a0001c0001t0001g0003 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1939-669_1939-668i others(188): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACAC others(175): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(2): Show |
6 | HG01243.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939-675_1939-674i others(184): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACTC others(38): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0005 others(1): Show |
7 | HG00741.hp1 HG01255.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1939-684_1939-683i others(47): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182252 | C | CCACACTC others(40): Show |
1 | a0001c0001t0001g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1939-684_1939-683i others(49): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182252 | ||||||
| chr6:44182257 | C | CTCACACA others(7): Show |
2 | a0001c0001t0001g0002 a0001c0001t0002g0001 |
6 | HG02109.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939-684_1939-683i others(16): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182257 | |||||||
| chr6:44182264 | A | ACACACAC others(40): Show |
1 | a0001c0001t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1939-673_1939-672i others(49): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182264 | ||||||
| chr6:44182264 | A | ACACACAC others(288): Show |
1 | a0001c0001t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1939-673_1939-672i others(297): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182264 | ||||||
| chr6:44182264 | A | ACACACAC others(284): Show |
1 | a0001c0001t0001g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1939-673_1939-672i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182264 | ||||||
| chr6:44182264 | A | ACACACAG others(36): Show |
1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1939-673_1939-672i others(45): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182264 | ||||||
| chr6:44182264 | A | ACACACAG others(284): Show |
1 | a0001c0001t0001g0009 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1939-673_1939-672i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182264 | ||||||
| chr6:44182264 | A | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0001 |
6 | HG02109.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939-677A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182264 | |||||||
| chr6:44182269 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
36 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1939-672T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182269 | |||||||
| chr6:44182275 | C | CACAACCA others(284): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
4 | NA18942.hp2 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-651_1939-650i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182275 | ||||||
| chr6:44182275 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(2): Show |
5 | HG00738.hp2 HG01074.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-666C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182275 | |||||||
| chr6:44182285 | C | CCA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
90 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1939-630_1939-629d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(13): Show |
40 | HG00423.hp2 HG00438.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1939-632_1939-629d others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACA | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
7 | HG01243.hp1 HG01928.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939-634_1939-629d others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACAC others(204): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
3 | NA18972.hp2 NA18980.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1939-640_1939-639i others(213): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACAC others(278): Show |
1 | a0001c0001t0001g0005 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1939-640_1939-639i others(287): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACAC others(202): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1939-640_1939-639i others(211): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(286): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
11 | HG00140.hp2 HG02300.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1939-651_1939-650i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(284): Show |
1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1939-651_1939-650i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(286): Show |
1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1939-651_1939-650i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(292): Show |
1 | a0001c0001t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1939-651_1939-650i others(301): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(288): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(2): Show |
10 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1939-651_1939-650i others(297): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(286): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0045 others(1): Show |
6 | HG00733.hp1 HG01106.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939-651_1939-650i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(284): Show |
1 | a0001c0001t0001g0002 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1939-651_1939-650i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(319): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
20 | HG00544.hp2 HG00558.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.1939-651_1939-650i others(328): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(317): Show |
1 | a0001c0001t0001g0005 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1939-651_1939-650i others(326): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(317): Show |
1 | a0001c0001t0001g0001 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1939-651_1939-650i others(326): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | C | CCACACTC others(317): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
3 | HG02083.hp1 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1939-651_1939-650i others(326): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182285 | CCA | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1939-630_1939-629d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182285 | ||||||
| chr6:44182287 | A | ACACTCAC others(284): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG00735.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1939-651_1939-650i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182287 | ||||||
| chr6:44182291 | A | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0005g0001 others(2): Show |
5 | HG00544.hp1 HG01167.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-650A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182291 | |||||||
| chr6:44182297 | A | ACACACAC others(61): Show |
1 | a0001c0001t0002g0001 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1939-632_1939-631i others(70): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182297 | ||||||
| chr6:44182297 | A | ACACACAC others(24): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
13 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1939-635_1939-634i others(33): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182297 | ||||||
| chr6:44182305 | A | ACACTCAC others(18): Show |
1 | a0001c0001t0002g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1939-633_1939-632i others(27): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182305 | ||||||
| chr6:44182306 | C | CACACAT | 2 | a0001c0001t0002g0002 a0001c0001t0002g0013 |
4 | HG01109.hp1 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939-630_1939-629i others(8): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182306 | ||||||
| chr6:44182306 | C | CACAT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0039 others(10): Show |
19 | HG00609.hp2 HG01070.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1939-632_1939-631i others(6): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182306 | ||||||
| chr6:44182306 | C | CAT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0027 others(24): Show |
70 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.1939-634_1939-633i others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182306 | ||||||
| chr6:44182306 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1939-635C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182306 | |||||||
| chr6:44182308 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0002g0006 others(2): Show |
6 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939-633C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182308 | |||||||
| chr6:44182310 | C | CAGACACA others(63): Show |
1 | a0001c0001t0001g0002 | 5 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939-630_1939-629i others(72): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182310 | ||||||
| chr6:44182310 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
14 | HG00280.hp1 HG01069.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1939-631C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182310 | |||||||
| chr6:44182311 | ACT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(3): Show |
7 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939-628_1939-627d others(4): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182311 | ||||||
| chr6:44182313 | T | A | 1 | a0001c0001t0002g0001 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1939-628T>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182313 | |||||||
| chr6:44182317 | A | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0002g0006 others(2): Show |
6 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939-624A>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182317 | |||||||
| chr6:44182318 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0002g0006 others(2): Show |
6 | HG01891.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939-623T>C | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182318 | |||||||
| chr6:44182324 | C | CACAACCA others(286): Show |
3 | a0001c0001t0001g0010 a0001c0001t0005g0001 a0001c0001t0005g0009 |
3 | HG00544.hp1 HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1939-595_1939-594i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182324 | ||||||
| chr6:44182324 | C | CACAACCA others(284): Show |
1 | a0001c0001t0005g0004 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1939-595_1939-594i others(293): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182324 | ||||||
| chr6:44182324 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
74 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1939-617C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182324 | |||||||
| chr6:44182328 | A | ACCACACC others(286): Show |
1 | a0001c0001t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1939-595_1939-594i others(295): Show |
CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 44182328 | ||||||
| chr6:44182445 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0002g0001 others(27): Show |
94 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1939-496A>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182445 | |||||||
| chr6:44182472 | G | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(28): Show |
96 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1939-469G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182472 | |||||||
| chr6:44182547 | G | A | 1 | a0001c0001t0002g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1939-394G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182547 | |||||||
| chr6:44182548 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
104 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1939-393G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182548 | |||||||
| chr6:44182674 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1939-267C>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182674 | |||||||
| chr6:44182749 | G | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1939-192G>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 19/22 | chr6 | 44182749 | |||||||
| chr6:44183609 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2135-96C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 21/22 | chr6 | 44183609 | |||||||
| chr6:44183653 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
2 | NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2135-52G>A | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 21/22 | chr6 | 44183653 | |||||||
| chr6:44183686 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0012 |
3 | HG02055.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2135-19C>T | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 21/22 | chr6 | 44183686 | |||||||
| chr6:44183811 | C | G | 1 | a0002c0003t0001g0031 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2193+48C>G | CAPN11 | ENSG00000137225.13 | transcript | ENST00000398776.2 | protein_coding | 22/22 | chr6 | 44183811 |