| geneid | 92291 |
|---|---|
| ensemblid | ENSG00000162949.16 |
| hgncid | 16663 |
| symbol | CAPN13 |
| name | calpain 13 |
| refseq_nuc | NM_144575.3 |
| refseq_prot | NP_653176.2 |
| ensembl_nuc | ENST00000295055.12 |
| ensembl_prot | ENSP00000295055.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 30722771 |
| end | 30807446 |
| strand | - |
| ver | v1.2 |
| region | chr2:30722771-30807446 |
| region5000 | chr2:30717771-30812446 |
| regionname0 | CAPN13_chr2_30722771_30807446 |
| regionname5000 | CAPN13_chr2_30717771_30812446 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 669 | 260 | 83 | 42 | 98 | 11 | 25 | 74 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002 | 1/0 | 669 | 60 | 4 | 13 | 31 | 1 | 10 | 23 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003 | 0/0 | 669 | 31 | 0 | 4 | 23 | 1 | 3 | 19 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0004 | 0/0 | 669 | 11 | 0 | 1 | 10 | 0 | 0 | 8 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0005 | 0/0 | 669 | 8 | 0 | 4 | 0 | 3 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0006 | 0/0 | 669 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0007 | 0/0 | 669 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0008 | 0/0 | 669 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0009 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0010 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0011 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0012 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0013 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0014 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0015 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0016 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2010 | 163 | 69 | 17 | 50 | 7 | 19 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0002 | 0/0 | 2010 | 94 | 12 | 25 | 47 | 4 | 6 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0003 | 1/0 | 2010 | 60 | 4 | 13 | 31 | 1 | 10 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0004 | 0/0 | 2010 | 30 | 0 | 4 | 22 | 1 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0005 | 0/0 | 2010 | 11 | 0 | 1 | 10 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0006 | 0/0 | 2010 | 8 | 0 | 4 | 0 | 3 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0007 | 0/0 | 2010 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0008 | 0/0 | 2010 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0009 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0010 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0011 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0012 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0013 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0014 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0015 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0016 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0017 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0018 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0019 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0020 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| c0021 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 674 | 155 | 34 | 33 | 63 | 6 | 18 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0002 | 0/1 | 674 | 143 | 39 | 22 | 66 | 5 | 10 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0003 | 0/0 | 674 | 27 | 7 | 2 | 16 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0004 | 0/0 | 674 | 24 | 1 | 8 | 6 | 1 | 8 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0005 | 0/0 | 674 | 23 | 6 | 1 | 11 | 2 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0006 | 0/0 | 674 | 5 | 1 | 0 | 4 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0007 | 0/0 | 674 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0008 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0009 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0010 | 0/0 | 674 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0011 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| t0012 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0328 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0358 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2010 | 163 | 69 | 17 | 50 | 7 | 19 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002 | 0/0 | 2010 | 94 | 12 | 25 | 47 | 4 | 6 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0013 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0020 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0021 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002c0003 | 1/0 | 2010 | 60 | 4 | 13 | 31 | 1 | 10 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003c0004 | 0/0 | 2010 | 30 | 0 | 4 | 22 | 1 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003c0010 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0004c0005 | 0/0 | 2010 | 11 | 0 | 1 | 10 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0005c0006 | 0/0 | 2010 | 8 | 0 | 4 | 0 | 3 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0006c0007 | 0/0 | 2010 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0007c0008 | 0/0 | 2010 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0008c0009 | 0/0 | 2010 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0009c0014 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0010c0015 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0011c0016 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0012c0011 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0013c0012 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0014c0018 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0015c0017 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0016c0019 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2683 | 65 | 26 | 6 | 23 | 1 | 9 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0002 | 0/1 | 2683 | 51 | 28 | 5 | 9 | 3 | 5 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0003 | 0/0 | 2683 | 24 | 7 | 2 | 13 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0004 | 0/0 | 2683 | 9 | 1 | 4 | 0 | 0 | 4 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0005 | 0/0 | 2683 | 7 | 3 | 0 | 2 | 1 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0006 | 0/0 | 2683 | 4 | 1 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0007 | 0/0 | 2683 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0001t0008 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0001 | 0/0 | 2683 | 29 | 1 | 10 | 14 | 2 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0002 | 0/0 | 2683 | 46 | 7 | 12 | 23 | 2 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0003 | 0/0 | 2683 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0004 | 0/0 | 2683 | 3 | 0 | 2 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0005 | 0/0 | 2683 | 10 | 3 | 1 | 5 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0006 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0010 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0002t0012 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0013t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0020t0004 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0001c0021t0001 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002c0003t0001 | 1/0 | 2683 | 46 | 3 | 12 | 24 | 0 | 6 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002c0003t0002 | 0/0 | 2683 | 4 | 1 | 0 | 2 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002c0003t0004 | 0/0 | 2683 | 9 | 0 | 1 | 4 | 1 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0002c0003t0011 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003c0004t0002 | 0/0 | 2683 | 26 | 0 | 4 | 20 | 0 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003c0004t0005 | 0/0 | 2683 | 4 | 0 | 0 | 2 | 1 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0003c0010t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0004c0005t0001 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0004c0005t0002 | 0/0 | 2683 | 9 | 0 | 0 | 9 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0004c0005t0009 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0005c0006t0001 | 0/0 | 2683 | 7 | 0 | 3 | 0 | 3 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0005c0006t0004 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0006c0007t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0006c0007t0005 | 0/0 | 2683 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0007c0008t0001 | 0/0 | 2683 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0008c0009t0004 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0009c0014t0002 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0010c0015t0001 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0011c0016t0001 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0012c0011t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0013c0012t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0014c0018t0001 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0015c0017t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| a0016c0019t0001 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | copy fasta | chr2 | 30717771 | 30812446 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0358 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0010g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0013t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0020t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0021t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0328 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0011g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0010t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0006c0007t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0006c0007t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0006c0007t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0007c0008t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0007c0008t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0008c0009t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0009c0014t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0010c0015t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0011c0016t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0012c0011t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0013c0012t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0014c0018t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0015c0017t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0016c0019t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0198 | EUR | GBR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | GBR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0211 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00280 | hp2 | a0005 | c0006 | t0001 | g0092 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00323 | hp1 | a0003 | c0004 | t0005 | g0117 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0317 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00597 | hp1 | a0004 | c0005 | t0002 | g0351 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00621 | hp1 | a0004 | c0005 | t0002 | g0040 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00621 | hp2 | a0003 | c0004 | t0002 | g0056 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0372 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00735 | hp1 | a0002 | c0003 | t0004 | g0285 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00735 | hp2 | a0005 | c0006 | t0004 | g0151 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0377 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00741 | hp2 | a0009 | c0014 | t0002 | g0055 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0312 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0349 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0333 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0202 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01168 | hp2 | a0003 | c0004 | t0002 | g0018 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01169 | hp1 | a0003 | c0004 | t0002 | g0016 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0352 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0319 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01256 | hp2 | a0003 | c0004 | t0002 | g0135 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01258 | hp1 | a0003 | c0004 | t0002 | g0083 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01261 | hp1 | a0014 | c0018 | t0001 | g0326 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0348 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0193 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0366 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0194 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01361 | hp2 | a0005 | c0006 | t0001 | g0212 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01433 | hp2 | a0004 | c0005 | t0001 | g0080 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0344 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0093 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01516 | hp2 | a0005 | c0006 | t0001 | g0085 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0350 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0186 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0113 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0313 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0336 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0155 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0363 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0324 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0316 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0354 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0362 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0076 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02015 | hp2 | a0003 | c0004 | t0002 | g0182 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02027 | hp1 | a0003 | c0010 | t0002 | g0057 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02027 | hp2 | a0002 | c0003 | t0004 | g0172 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0308 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0356 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02129 | hp2 | a0015 | c0017 | t0002 | g0012 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02132 | hp2 | a0001 | c0002 | t0006 | g0163 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02135 | hp1 | a0003 | c0004 | t0005 | g0353 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0360 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02148 | hp1 | a0005 | c0006 | t0001 | g0332 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0217 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0359 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02155 | hp2 | a0010 | c0015 | t0001 | g0081 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02258 | hp1 | a0001 | c0013 | t0002 | g0075 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0378 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0318 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0218 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02622 | hp1 | a0001 | c0002 | t0012 | g0239 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02647 | hp2 | a0007 | c0008 | t0001 | g0276 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02698 | hp1 | a0008 | c0009 | t0004 | g0220 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02735 | hp1 | a0003 | c0004 | t0002 | g0052 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0210 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02738 | hp2 | a0005 | c0006 | t0001 | g0266 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02809 | hp1 | a0002 | c0003 | t0002 | g0214 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0371 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0361 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02895 | hp1 | a0013 | c0012 | t0002 | g0268 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0380 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0346 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03130 | hp1 | a0007 | c0008 | t0001 | g0281 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0343 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0379 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03491 | hp1 | a0002 | c0003 | t0004 | g0154 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0022 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0338 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03710 | hp1 | a0001 | c0002 | t0010 | g0364 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0367 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0084 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0166 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0375 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0200 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0370 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04199 | hp1 | a0002 | c0003 | t0004 | g0189 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04199 | hp2 | a0002 | c0003 | t0004 | g0307 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04204 | hp1 | a0003 | c0004 | t0005 | g0031 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0325 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0124 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | CHB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | CHB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18939 | hp1 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0337 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18942 | hp2 | a0001 | c0020 | t0004 | g0051 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0264 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18947 | hp2 | a0003 | c0004 | t0002 | g0251 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18949 | hp1 | a0004 | c0005 | t0002 | g0204 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18951 | hp2 | a0003 | c0004 | t0002 | g0168 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18952 | hp1 | a0003 | c0004 | t0002 | g0256 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18953 | hp1 | a0004 | c0005 | t0002 | g0034 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18954 | hp1 | a0001 | c0002 | t0005 | g0050 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18956 | hp2 | a0006 | c0007 | t0005 | g0263 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18961 | hp1 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18962 | hp2 | a0004 | c0005 | t0009 | g0209 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0347 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18964 | hp2 | a0003 | c0004 | t0002 | g0292 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18965 | hp1 | a0003 | c0004 | t0002 | g0167 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18966 | hp2 | a0002 | c0003 | t0004 | g0107 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18971 | hp1 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18973 | hp2 | a0002 | c0003 | t0002 | g0030 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18974 | hp1 | a0004 | c0005 | t0002 | g0226 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18975 | hp1 | a0002 | c0003 | t0011 | g0335 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0203 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18982 | hp2 | a0003 | c0004 | t0002 | g0205 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18986 | hp1 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18988 | hp2 | a0001 | c0002 | t0005 | g0026 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18990 | hp2 | a0006 | c0007 | t0005 | g0262 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18991 | hp1 | a0004 | c0005 | t0002 | g0259 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0323 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18995 | hp2 | a0004 | c0005 | t0002 | g0250 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18997 | hp2 | a0004 | c0005 | t0002 | g0105 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18999 | hp2 | a0001 | c0002 | t0005 | g0340 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19000 | hp2 | a0011 | c0016 | t0001 | g0369 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0334 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19009 | hp2 | a0002 | c0003 | t0004 | g0150 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0329 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19010 | hp2 | a0003 | c0004 | t0002 | g0097 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19011 | hp2 | a0003 | c0004 | t0002 | g0261 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19057 | hp2 | a0002 | c0003 | t0004 | g0025 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19058 | hp1 | a0003 | c0004 | t0002 | g0255 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19060 | hp2 | a0003 | c0004 | t0002 | g0219 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19065 | hp1 | a0003 | c0004 | t0002 | g0132 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19067 | hp1 | a0003 | c0004 | t0002 | g0178 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19070 | hp1 | a0003 | c0004 | t0002 | g0072 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19078 | hp1 | a0003 | c0004 | t0005 | g0374 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19081 | hp1 | a0003 | c0004 | t0002 | g0013 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19084 | hp2 | a0004 | c0005 | t0002 | g0257 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19089 | hp1 | a0006 | c0007 | t0002 | g0322 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19090 | hp1 | a0003 | c0004 | t0002 | g0314 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19091 | hp2 | a0003 | c0004 | t0002 | g0206 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20129 | hp1 | a0016 | c0019 | t0001 | g0138 | AFR | ASW | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0278 | AFR | ASW | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0091 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0006 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20805 | hp1 | a0005 | c0006 | t0001 | g0265 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20905 | hp1 | a0003 | c0004 | t0002 | g0077 | SAS | GIH | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20905 | hp2 | a0002 | c0003 | t0002 | g0339 | SAS | GIH | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0164 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01123 | hp2 | a0005 | c0006 | t0001 | g0109 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0123 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03471 | hp1 | a0012 | c0011 | t0002 | g0131 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG06807 | hp1 | a0001 | c0021 | t0001 | g0277 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0358 | REF | REF | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0328 | REF | REF | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30734460
|
A | G | 4 | a0003a0006a0009others(1): Show | 36 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
missense_variant | MODERATE | c.1787T>C | p.Ile596Thr | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/23 | 1964/2683 | 1787/2010 | 596/669 | chr2 | 30734460 | ||
| chr2:30741926
|
G | C | 1 | a0007 | 2 | HG02647.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1518C>G | p.Phe506Leu | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/23 | 1695/2683 | 1518/2010 | 506/669 | chr2 | 30741926 | ||
| chr2:30743428
|
G | A | 1 | a0012 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1400C>T | p.Ala467Val | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/23 | 1577/2683 | 1400/2010 | 467/669 | chr2 | 30743428 | ||
| chr2:30743440
|
C | T | 1 | a0010 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1388G>A | p.Arg463Gln | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/23 | 1565/2683 | 1388/2010 | 463/669 | chr2 | 30743440 | ||
| chr2:30743505
|
G | C | 1 | a0013 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1323C>G | p.Phe441Leu | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/23 | 1500/2683 | 1323/2010 | 441/669 | chr2 | 30743505 | ||
| chr2:30751242
|
C | T | 1 | a0015 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1097G>A | p.Arg366Gln | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/23 | 1274/2683 | 1097/2010 | 366/669 | chr2 | 30751242 | ||
| chr2:30753095
|
G | T | 2 | a0005a0009 | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
missense_variant | MODERATE | c.1045C>A | p.Gln349Lys | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/23 | 1222/2683 | 1045/2010 | 349/669 | chr2 | 30753095 | ||
| chr2:30758074
|
C | T | 9 | a0001a0003a0004others(6): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
missense_variant | MODERATE | c.838G>A | p.Ala280Thr | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/23 | 1015/2683 | 838/2010 | 280/669 | chr2 | 30758074 | ||
| chr2:30763111
|
G | A | 4 | a0004a0006a0014others(1): Show | 16 | HG00597.hp1 HG00621.hp1 HG01261.hp1 others(13): Show |
missense_variant | MODERATE | c.745C>T | p.His249Tyr | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/23 | 922/2683 | 745/2010 | 249/669 | chr2 | 30763111 | ||
| chr2:30763140
|
T | C | 1 | a0016 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.716A>G | p.Gln239Arg | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/23 | 893/2683 | 716/2010 | 239/669 | chr2 | 30763140 | ||
| chr2:30775937
|
C | T | 1 | a0008 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.380G>A | p.Arg127His | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/23 | 557/2683 | 380/2010 | 127/669 | chr2 | 30775937 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30753192
|
C | T | 8 | a0001c0002a0001c0013a0003c0004others(5): Show | 142 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(139): Show |
synonymous_variant | LOW | c.948G>A | p.Ser316Ser | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/23 | 1125/2683 | 948/2010 | 316/669 | chr2 | 30753192 | ||
| chr2:30754337
|
A | G | 1 | a0003c0010 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.894T>C | p.Asp298Asp | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/23 | 1071/2683 | 894/2010 | 298/669 | chr2 | 30754337 | ||
| chr2:30754346
|
T | C | 2 | a0001c0013a0016c0019 | 2 | HG02258.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.885A>G | p.Glu295Glu | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/23 | 1062/2683 | 885/2010 | 295/669 | chr2 | 30754346 | ||
| chr2:30764231
|
G | A | 1 | a0001c0020 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.600C>T | p.Ile200Ile | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/23 | 777/2683 | 600/2010 | 200/669 | chr2 | 30764231 | ||
| chr2:30777571
|
G | A | 1 | a0001c0021 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.267C>T | p.Gly89Gly | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/23 | 444/2683 | 267/2010 | 89/669 | chr2 | 30777571 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30722795
|
T | C | 5 | a0001c0001t0003a0001c0001t0006a0001c0002t0003others(2): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*472A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7965 | chr2 | 30722795 | |||||
| chr2:30722799
|
A | G | 1 | a0002c0003t0011 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7961 | chr2 | 30722799 | |||||
| chr2:30722803
|
A | C | 1 | a0004c0005t0009 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7957 | chr2 | 30722803 | |||||
| chr2:30722815
|
A | C | 1 | a0001c0002t0010 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7945 | chr2 | 30722815 | |||||
| chr2:30722975
|
T | C | 1 | a0001c0002t0012 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7785 | chr2 | 30722975 | |||||
| chr2:30723030
|
A | G | 17 | a0001c0001t0002a0001c0001t0005a0001c0002t0002others(14): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*237T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7730 | chr2 | 30723030 | |||||
| chr2:30723102
|
G | A | 5 | a0001c0001t0003a0001c0001t0006a0001c0002t0003others(2): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7658 | chr2 | 30723102 | |||||
| chr2:30723128
|
G | T | 1 | a0001c0001t0008 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7632 | chr2 | 30723128 | |||||
| chr2:30723134
|
T | C | 5 | a0001c0001t0003a0001c0001t0006a0001c0002t0003others(2): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*133A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7626 | chr2 | 30723134 | |||||
| chr2:30723174
|
T | C | 1 | a0001c0001t0007 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 23/23 | 7586 | chr2 | 30723174 | |||||
| chr2:30787346
|
C | T | 12 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(9): Show | 52 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/23 | 21 | chr2 | 30787346 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30723360
|
A | C | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-124T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723360 | ||||||
| chr2:30723482
|
C | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-246G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723482 | ||||||
| chr2:30723588
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-352T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723588 | ||||||
| chr2:30723751
|
A | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-515T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723751 | ||||||
| chr2:30723771
|
C | T | 1 | a0004c0005t0009g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*31-535G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723771 | ||||||
| chr2:30723851
|
AT | A | 34 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.*31-616delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723851 | ||||||
| chr2:30723870
|
C | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-634G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723870 | ||||||
| chr2:30723881
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-645T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723881 | ||||||
| chr2:30723887
|
G | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-651C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723887 | ||||||
| chr2:30723903
|
G | A | 1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*31-667C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723903 | ||||||
| chr2:30723949
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.*31-713A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30723949 | ||||||
| chr2:30724012
|
G | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-776C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724012 | ||||||
| chr2:30724055
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-819T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724055 | ||||||
| chr2:30724090
|
C | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-854G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724090 | ||||||
| chr2:30724154
|
A | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-918T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724154 | ||||||
| chr2:30724257
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.*31-1021T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724257 | ||||||
| chr2:30724270
|
T | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1034A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724270 | ||||||
| chr2:30724368
|
T | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1132A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724368 | ||||||
| chr2:30724423
|
G | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1187C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724423 | ||||||
| chr2:30724426
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1190T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724426 | ||||||
| chr2:30724444
|
G | A | 1 | a0001c0002t0010g0364 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*31-1208C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724444 | ||||||
| chr2:30724528
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0004g0041 | 2 | HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*31-1292G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724528 | ||||||
| chr2:30724588
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1352T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724588 | ||||||
| chr2:30724778
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0021t0001g0277 | 3 | HG03225.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.*31-1542T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724778 | ||||||
| chr2:30724805
|
C | A | 40 | a0001c0001t0002g0023a0001c0001t0002g0053a0001c0001t0002g0062others(37): Show | 40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.*31-1569G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724805 | ||||||
| chr2:30724806
|
G | C | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1570C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724806 | ||||||
| chr2:30724852
|
A | AATGAG | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.*31-1621_*31-1617d others(7): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724852 | ||||||
| chr2:30724917
|
G | T | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1681C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724917 | ||||||
| chr2:30724919
|
C | CA | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1684_*31-1683i others(3): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724919 | ||||||
| chr2:30724969
|
A | C | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1733T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724969 | ||||||
| chr2:30724970
|
T | A | 1 | a0001c0002t0002g0258 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.*31-1734A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30724970 | ||||||
| chr2:30725012
|
C | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1776G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725012 | ||||||
| chr2:30725108
|
A | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0271others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.*31-1872T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725108 | ||||||
| chr2:30725119
|
A | AAAT | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1884_*31-1883i others(5): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725119 | ||||||
| chr2:30725120
|
G | C | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1884C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725120 | ||||||
| chr2:30725121
|
G | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1885C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725121 | ||||||
| chr2:30725133
|
C | T | 1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*31-1897G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725133 | ||||||
| chr2:30725211
|
T | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-1975A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725211 | ||||||
| chr2:30725250
|
AAACATAT others(3): Show |
A | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-2024_*31-2015d others(12): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725250 | ||||||
| chr2:30725298
|
A | G | 199 | a0001c0001t0002g0023a0001c0001t0002g0044a0001c0001t0002g0047others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.*31-2062T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725298 | ||||||
| chr2:30725303
|
G | T | 9 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0002g0079others(6): Show | 9 | HG02257.hp2 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*31-2067C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725303 | ||||||
| chr2:30725400
|
G | A | 1 | a0001c0002t0002g0324 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.*31-2164C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725400 | ||||||
| chr2:30725434
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0002t0001g0106others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.*31-2198C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725434 | ||||||
| chr2:30725454
|
AC | A | 10 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0134others(7): Show | 10 | HG01496.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.*31-2219delG | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725454 | ||||||
| chr2:30725617
|
T | C | 213 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.*31-2381A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725617 | ||||||
| chr2:30725695
|
G | A | 1 | a0001c0002t0004g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.*31-2459C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725695 | ||||||
| chr2:30725797
|
C | G | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*31-2561G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725797 | ||||||
| chr2:30725885
|
A | C | 166 | a0001c0001t0002g0023a0001c0001t0002g0044a0001c0001t0002g0047others(163): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.*31-2649T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30725885 | ||||||
| chr2:30726012
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.*31-2776T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726012 | ||||||
| chr2:30726013
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0224a0001c0001t0004g0064 | 3 | HG01109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*31-2777C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726013 | ||||||
| chr2:30726059
|
A | G | 36 | a0001c0001t0002g0216a0001c0001t0002g0370a0003c0004t0002g0013others(33): Show | 36 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.*31-2823T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726059 | ||||||
| chr2:30726112
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*31-2876G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726112 | ||||||
| chr2:30726218
|
C | G | 199 | a0001c0001t0002g0023a0001c0001t0002g0044a0001c0001t0002g0047others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.*31-2982G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726218 | ||||||
| chr2:30726349
|
A | T | 200 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0044others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.*31-3113T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726349 | ||||||
| chr2:30726357
|
A | G | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.*31-3121T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726357 | ||||||
| chr2:30726385
|
A | G | 201 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0044others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.*31-3149T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726385 | ||||||
| chr2:30726507
|
GAACT | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0110 | 4 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.*31-3275_*31-3272d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726507 | ||||||
| chr2:30726531
|
G | T | 200 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0044others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.*31-3295C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726531 | ||||||
| chr2:30726535
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0271others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.*31-3299G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726535 | ||||||
| chr2:30726575
|
A | G | 1 | a0002c0003t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*31-3339T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726575 | ||||||
| chr2:30726660
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0365 | 3 | HG02280.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.*31-3424G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726660 | ||||||
| chr2:30726678
|
T | G | 1 | a0001c0001t0002g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*31-3442A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726678 | ||||||
| chr2:30726726
|
T | C | 215 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.*31-3490A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726726 | ||||||
| chr2:30726768
|
T | C | 215 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.*31-3532A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726768 | ||||||
| chr2:30726801
|
G | C | 207 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.*31-3565C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726801 | ||||||
| chr2:30726840
|
A | C | 3 | a0002c0003t0001g0323a0002c0003t0001g0337a0002c0003t0011g0335 | 3 | NA18942.hp1 NA18975.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.*31-3604T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726840 | ||||||
| chr2:30726841
|
A | G | 206 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.*31-3605T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726841 | ||||||
| chr2:30726863
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*31-3627T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726863 | ||||||
| chr2:30726864
|
A | G | 167 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0044others(164): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.*31-3628T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726864 | ||||||
| chr2:30726875
|
C | A | 4 | a0001c0001t0003g0125a0001c0001t0003g0244a0001c0001t0003g0298others(1): Show | 4 | HG00558.hp2 HG02040.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.*31-3639G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726875 | ||||||
| chr2:30726922
|
C | T | 173 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(170): Show | 173 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.*31-3686G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726922 | ||||||
| chr2:30727043
|
T | C | 216 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.*30+3687A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727043 | ||||||
| chr2:30727050
|
T | C | 1 | a0003c0004t0002g0013 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.*30+3680A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727050 | ||||||
| chr2:30727138
|
A | G | 13 | a0001c0001t0002g0104a0001c0001t0002g0126a0001c0001t0002g0176others(10): Show | 13 | HG01433.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.*30+3592T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727138 | ||||||
| chr2:30727236
|
A | G | 1 | a0001c0002t0002g0336 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*30+3494T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727236 | ||||||
| chr2:30727426
|
C | T | 9 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0002g0079others(6): Show | 9 | HG02257.hp2 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.*30+3304G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727426 | ||||||
| chr2:30727549
|
A | C | 1 | a0001c0001t0005g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*30+3181T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727549 | ||||||
| chr2:30727581
|
T | A | 1 | a0001c0001t0003g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*30+3149A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727581 | ||||||
| chr2:30727697
|
C | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.*30+3033G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727697 | ||||||
| chr2:30727708
|
A | G | 8 | a0002c0003t0001g0019a0002c0003t0001g0123a0002c0003t0001g0164others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.*30+3022T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727708 | ||||||
| chr2:30727812
|
C | G | 1 | a0001c0002t0002g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.*30+2918G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727812 | ||||||
| chr2:30727879
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.*30+2851A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727879 | ||||||
| chr2:30727901
|
C | T | 5 | a0001c0001t0002g0126a0001c0001t0002g0229a0001c0001t0002g0233others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.*30+2829G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727901 | ||||||
| chr2:30727989
|
C | T | 1 | a0002c0003t0002g0020 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.*30+2741G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30727989 | ||||||
| chr2:30728163
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.*30+2567A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728163 | ||||||
| chr2:30728319
|
T | C | 114 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0061others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.*30+2411A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728319 | ||||||
| chr2:30728414
|
AATAATAT others(8): Show |
A | 1 | a0002c0003t0001g0378 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*30+2301_*30+2315d others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728414 | ||||||
| chr2:30728528
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*30+2202C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728528 | ||||||
| chr2:30728620
|
T | C | 202 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0044others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.*30+2110A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728620 | ||||||
| chr2:30728700
|
T | C | 15 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0238others(12): Show | 15 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.*30+2030A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728700 | ||||||
| chr2:30728748
|
A | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0271others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.*30+1982T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728748 | ||||||
| chr2:30728761
|
A | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.*30+1969T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728761 | ||||||
| chr2:30728768
|
G | A | 1 | a0002c0003t0001g0264 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.*30+1962C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728768 | ||||||
| chr2:30728808
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.*30+1922T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728808 | ||||||
| chr2:30728860
|
C | T | 1 | a0006c0007t0002g0322 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.*30+1870G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30728860 | ||||||
| chr2:30729044
|
T | G | 9 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0279others(6): Show | 9 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.*30+1686A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729044 | ||||||
| chr2:30729050
|
T | G | 1 | a0003c0004t0005g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*30+1680A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729050 | ||||||
| chr2:30729053
|
A | G | 170 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(167): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.*30+1677T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729053 | ||||||
| chr2:30729066
|
G | C | 163 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0047others(160): Show | 163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.*30+1664C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729066 | ||||||
| chr2:30729118
|
T | C | 219 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.*30+1612A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729118 | ||||||
| chr2:30729281
|
C | A | 1 | a0001c0002t0005g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*30+1449G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729281 | ||||||
| chr2:30729281
|
C | T | 2 | a0003c0004t0002g0251a0003c0004t0002g0314 | 2 | NA18947.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.*30+1449G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729281 | ||||||
| chr2:30729330
|
C | A | 4 | a0001c0001t0003g0103a0001c0001t0003g0108a0001c0001t0003g0180others(1): Show | 4 | NA18960.hp1 NA18988.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.*30+1400G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729330 | ||||||
| chr2:30729411
|
C | T | 3 | a0001c0001t0003g0043a0001c0001t0003g0096a0001c0001t0006g0359 | 3 | HG02155.hp1 NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.*30+1319G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729411 | ||||||
| chr2:30729624
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.*30+1106A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729624 | ||||||
| chr2:30729688
|
G | A | 24 | a0001c0001t0002g0023a0001c0001t0002g0053a0001c0001t0002g0062others(21): Show | 24 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.*30+1042C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729688 | ||||||
| chr2:30729768
|
G | C | 1 | a0002c0003t0004g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.*30+962C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729768 | ||||||
| chr2:30730100
|
A | G | 2 | a0001c0002t0005g0340a0001c0002t0005g0347 | 2 | NA18963.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.*30+630T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730100 | ||||||
| chr2:30730121
|
C | T | 115 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0061others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.*30+609G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730121 | ||||||
| chr2:30730349
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*30+381C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730349 | ||||||
| chr2:30730402
|
A | T | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.*30+328T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730402 | ||||||
| chr2:30730427
|
C | T | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.*30+303G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730427 | ||||||
| chr2:30730434
|
G | T | 112 | a0001c0001t0002g0047a0001c0001t0002g0061a0001c0001t0002g0183others(109): Show | 112 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.*30+296C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730434 | ||||||
| chr2:30730493
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0274 | 3 | HG02559.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*30+237A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730493 | ||||||
| chr2:30730602
|
T | A | 1 | a0003c0010t0002g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*30+128A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30730602 | ||||||
| chr2:30730896
|
C | T | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1984-110G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30730896 | ||||||
| chr2:30730930
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1984-144C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30730930 | ||||||
| chr2:30730956
|
T | G | 2 | a0001c0001t0003g0345a0001c0001t0003g0380 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1984-170A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30730956 | ||||||
| chr2:30731026
|
G | A | 1 | a0004c0005t0002g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1984-240C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30731026 | ||||||
| chr2:30731150
|
A | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0274 | 3 | HG02559.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1983+194T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30731150 | ||||||
| chr2:30731218
|
G | T | 1 | a0001c0002t0010g0364 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1983+126C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30731218 | ||||||
| chr2:30731232
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1983+112G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30731232 | ||||||
| chr2:30731323
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1983+21C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 21/22 | chr2 | 30731323 | ||||||
| chr2:30731451
|
C | A | 2 | a0001c0001t0003g0345a0001c0001t0003g0380 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1928-52G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731451 | ||||||
| chr2:30731532
|
T | C | 1 | a0001c0002t0002g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1928-133A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731532 | ||||||
| chr2:30731575
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0271 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1928-176C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731575 | ||||||
| chr2:30731755
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1928-356G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731755 | ||||||
| chr2:30731930
|
T | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1927+508A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731930 | ||||||
| chr2:30731932
|
G | A | 2 | a0005c0006t0001g0085a0005c0006t0001g0332 | 2 | HG01516.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1927+506C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731932 | ||||||
| chr2:30731950
|
G | A | 1 | a0002c0003t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1927+488C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30731950 | ||||||
| chr2:30732100
|
G | T | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1927+338C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732100 | ||||||
| chr2:30732170
|
G | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0365 | 3 | HG02280.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1927+268C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732170 | ||||||
| chr2:30732220
|
G | A | 49 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0279others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1927+218C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732220 | ||||||
| chr2:30732252
|
G | T | 76 | a0001c0001t0001g0173a0001c0001t0002g0047a0001c0001t0002g0061others(73): Show | 76 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1927+186C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732252 | ||||||
| chr2:30732256
|
G | C | 44 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0002g0023others(41): Show | 44 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1927+182C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732256 | ||||||
| chr2:30732288
|
A | G | 212 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1927+150T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732288 | ||||||
| chr2:30732310
|
A | G | 156 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0002g0023others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1927+128T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732310 | ||||||
| chr2:30732359
|
G | C | 1 | a0008c0009t0004g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1927+79C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732359 | ||||||
| chr2:30732597
|
G | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0127others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799-31C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30732597 | ||||||
| chr2:30732659
|
G | A | 2 | a0001c0002t0002g0316a0003c0004t0005g0353 | 2 | HG01975.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1799-93C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30732659 | ||||||
| chr2:30732662
|
C | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1799-96G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30732662 | ||||||
| chr2:30732833
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0110 | 4 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1799-267G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30732833 | ||||||
| chr2:30733201
|
C | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1799-635G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733201 | ||||||
| chr2:30733224
|
A | G | 78 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0061others(75): Show | 78 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1799-658T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733224 | ||||||
| chr2:30733308
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1799-742G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733308 | ||||||
| chr2:30733334
|
T | TCTCCTGC others(7): Show |
288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1799-769_1799-768i others(16): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733334 | ||||||
| chr2:30733372
|
A | G | 36 | a0001c0001t0002g0370a0003c0004t0002g0013a0003c0004t0002g0016others(33): Show | 36 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1799-806T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733372 | ||||||
| chr2:30733478
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1799-912G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733478 | ||||||
| chr2:30733550
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1798+899G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733550 | ||||||
| chr2:30733648
|
T | A | 1 | a0003c0004t0002g0205 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1798+801A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733648 | ||||||
| chr2:30733689
|
C | T | 1 | a0001c0002t0002g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1798+760G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733689 | ||||||
| chr2:30733724
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1798+725C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733724 | ||||||
| chr2:30733855
|
G | T | 32 | a0001c0001t0002g0216a0001c0001t0003g0009a0001c0001t0003g0036others(29): Show | 32 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.1798+594C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733855 | ||||||
| chr2:30733925
|
C | T | 36 | a0001c0001t0001g0271a0003c0004t0002g0013a0003c0004t0002g0016others(33): Show | 36 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1798+524G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30733925 | ||||||
| chr2:30734094
|
G | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0365 | 3 | HG02280.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1798+355C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30734094 | ||||||
| chr2:30734103
|
C | T | 14 | a0001c0001t0001g0284a0001c0002t0001g0003a0001c0002t0001g0014others(11): Show | 15 | HG00280.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1798+346G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30734103 | ||||||
| chr2:30734202
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1798+247G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30734202 | ||||||
| chr2:30734324
|
C | T | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1798+125G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 19/22 | chr2 | 30734324 | ||||||
| chr2:30734650
|
G | A | 3 | a0001c0001t0002g0115a0001c0001t0002g0222a0001c0001t0002g0235 | 3 | HG03516.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1723-126C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30734650 | ||||||
| chr2:30734814
|
A | G | 46 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(43): Show | 46 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1723-290T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30734814 | ||||||
| chr2:30734883
|
A | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0253 | 2 | NA18993.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1723-359T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30734883 | ||||||
| chr2:30735096
|
A | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0271others(2): Show | 5 | HG02965.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-572T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735096 | ||||||
| chr2:30735106
|
A | C | 50 | a0001c0001t0001g0279a0001c0001t0002g0068a0001c0001t0002g0071others(47): Show | 50 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1723-582T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735106 | ||||||
| chr2:30735125
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1723-601G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735125 | ||||||
| chr2:30735271
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1723-747C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735271 | ||||||
| chr2:30735388
|
C | T | 1 | a0002c0003t0001g0348 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1723-864G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735388 | ||||||
| chr2:30735444
|
C | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1723-920G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735444 | ||||||
| chr2:30735524
|
T | C | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1722+979A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735524 | ||||||
| chr2:30735600
|
C | G | 52 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0002g0079others(49): Show | 52 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1722+903G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735600 | ||||||
| chr2:30735602
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1722+901G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735602 | ||||||
| chr2:30735610
|
C | G | 6 | a0001c0002t0002g0120a0001c0002t0002g0201a0001c0002t0002g0287others(3): Show | 6 | HG02071.hp2 NA18612.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1722+893G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735610 | ||||||
| chr2:30735619
|
T | C | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1722+884A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735619 | ||||||
| chr2:30735633
|
G | A | 14 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0002g0079others(11): Show | 14 | HG01496.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1722+870C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735633 | ||||||
| chr2:30735687
|
G | A | 4 | a0001c0001t0002g0133a0001c0001t0002g0230a0001c0001t0002g0231others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1722+816C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735687 | ||||||
| chr2:30735689
|
G | A | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1722+814C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735689 | ||||||
| chr2:30735832
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1722+671T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735832 | ||||||
| chr2:30735902
|
G | T | 1 | a0001c0002t0002g0174 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1722+601C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30735902 | ||||||
| chr2:30736072
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1722+431C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736072 | ||||||
| chr2:30736234
|
C | G | 182 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0191others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1722+269G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736234 | ||||||
| chr2:30736280
|
C | G | 1 | a0001c0002t0006g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1722+223G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736280 | ||||||
| chr2:30736366
|
T | C | 5 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0316others(2): Show | 5 | HG01346.hp1 HG01358.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1722+137A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736366 | ||||||
| chr2:30736390
|
G | A | 1 | a0001c0002t0005g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1722+113C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736390 | ||||||
| chr2:30736396
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(231): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1722+107C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736396 | ||||||
| chr2:30736500
|
T | C | 6 | a0001c0001t0001g0199a0001c0001t0001g0327a0001c0001t0002g0370others(3): Show | 6 | HG00741.hp1 HG01258.hp2 HG02602.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1722+3A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 18/22 | chr2 | 30736500 | ||||||
| chr2:30736651
|
G | C | 1 | a0001c0002t0005g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1654-80C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30736651 | ||||||
| chr2:30736690
|
C | T | 1 | a0001c0002t0003g0033 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1654-119G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30736690 | ||||||
| chr2:30736696
|
G | T | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1654-125C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30736696 | ||||||
| chr2:30736961
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(188): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1654-390G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30736961 | ||||||
| chr2:30737016
|
G | A | 41 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(38): Show | 41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1654-445C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737016 | ||||||
| chr2:30737077
|
G | A | 1 | a0001c0001t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1654-506C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737077 | ||||||
| chr2:30737251
|
A | G | 1 | a0001c0002t0005g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1654-680T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737251 | ||||||
| chr2:30737268
|
A | G | 1 | a0002c0003t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1654-697T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737268 | ||||||
| chr2:30737318
|
A | G | 2 | a0001c0001t0003g0043a0001c0001t0006g0359 | 2 | HG02155.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1654-747T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737318 | ||||||
| chr2:30737331
|
C | T | 10 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0002g0079others(7): Show | 10 | HG01496.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1654-760G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737331 | ||||||
| chr2:30737356
|
G | A | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1654-785C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737356 | ||||||
| chr2:30737379
|
G | A | 43 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(40): Show | 43 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1654-808C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737379 | ||||||
| chr2:30737429
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0365others(2): Show | 5 | HG02280.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1653+806C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737429 | ||||||
| chr2:30737565
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1653+670A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737565 | ||||||
| chr2:30737633
|
T | C | 42 | a0001c0001t0001g0191a0001c0001t0002g0023a0001c0001t0002g0053others(39): Show | 42 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1653+602A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737633 | ||||||
| chr2:30737729
|
G | A | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1653+506C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737729 | ||||||
| chr2:30737777
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1653+458C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737777 | ||||||
| chr2:30737805
|
C | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1653+430G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737805 | ||||||
| chr2:30737966
|
G | GAC | 41 | a0001c0001t0001g0140a0001c0001t0001g0191a0001c0001t0001g0195others(38): Show | 41 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1653+267_1653+268d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
G | GACAC | 21 | a0001c0001t0001g0146a0001c0001t0001g0279a0001c0001t0002g0104others(18): Show | 21 | HG01071.hp1 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1653+265_1653+268d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
GAC | G | 102 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0070others(99): Show | 104 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1653+267_1653+268d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
GACAC | G | 11 | a0001c0001t0001g0049a0001c0001t0001g0327a0001c0001t0002g0121others(8): Show | 11 | HG00423.hp1 HG01069.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1653+265_1653+268d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
GACACAC | G | 96 | a0001c0001t0001g0284a0001c0001t0002g0047a0001c0001t0002g0061others(93): Show | 97 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1653+263_1653+268d others(8): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
GACACACA others(3): Show |
G | 3 | a0001c0001t0003g0244a0001c0001t0003g0298a0001c0001t0003g0321 | 3 | HG00558.hp2 HG02523.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1653+259_1653+268d others(12): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30737966
|
GACACACA others(5): Show |
G | 1 | a0001c0002t0002g0112 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1653+257_1653+268d others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737966 | ||||||
| chr2:30738156
|
C | G | 38 | a0001c0001t0001g0280a0001c0001t0002g0370a0003c0004t0002g0013others(35): Show | 38 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1653+79G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30738156 | ||||||
| chr2:30738527
|
G | A | 42 | a0001c0001t0001g0279a0001c0001t0002g0023a0001c0001t0002g0053others(39): Show | 42 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1537-70C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738527 | ||||||
| chr2:30738534
|
AG | A | 17 | a0001c0001t0001g0271a0001c0001t0001g0284a0001c0001t0002g0275others(14): Show | 18 | HG00280.hp2 HG00735.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1537-78delC | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738534 | ||||||
| chr2:30738586
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0002g0185a0001c0001t0002g0222others(5): Show | 8 | HG01496.hp2 HG02895.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1537-129C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738586 | ||||||
| chr2:30738628
|
T | C | 1 | a0003c0004t0002g0013 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1537-171A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738628 | ||||||
| chr2:30738648
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1537-191G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738648 | ||||||
| chr2:30738711
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1537-254T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738711 | ||||||
| chr2:30738780
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(184): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1537-323G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738780 | ||||||
| chr2:30738866
|
ATGTGTGT others(16): Show |
A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1537-432_1537-410d others(25): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738866 | ||||||
| chr2:30738876
|
GT | G | 61 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0001g0279others(58): Show | 62 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1537-420delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738876 | ||||||
| chr2:30738877
|
T | TG | 4 | a0001c0001t0001g0238a0001c0001t0001g0267a0001c0001t0001g0280others(1): Show | 4 | HG02280.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537-421_1537-420i others(3): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738877 | ||||||
| chr2:30738948
|
A | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1537-491T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738948 | ||||||
| chr2:30739131
|
C | A | 54 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0001g0284others(51): Show | 55 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1537-674G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739131 | ||||||
| chr2:30739285
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG00738.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1537-828C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739285 | ||||||
| chr2:30739322
|
G | C | 2 | a0001c0001t0001g0327a0001c0001t0004g0377 | 2 | HG00741.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1537-865C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739322 | ||||||
| chr2:30739400
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1537-943G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739400 | ||||||
| chr2:30739444
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1537-987A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739444 | ||||||
| chr2:30739522
|
G | C | 4 | a0003c0004t0002g0205a0003c0004t0002g0292a0003c0004t0005g0374others(1): Show | 4 | NA18964.hp2 NA18982.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-1065C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739522 | ||||||
| chr2:30739567
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1537-1110T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739567 | ||||||
| chr2:30739694
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1537-1237C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739694 | ||||||
| chr2:30739700
|
T | C | 19 | a0001c0002t0001g0017a0001c0002t0001g0253a0001c0002t0002g0021others(16): Show | 19 | HG00597.hp1 HG00621.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.1537-1243A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739700 | ||||||
| chr2:30739748
|
C | T | 1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1537-1291G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739748 | ||||||
| chr2:30739779
|
G | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1537-1322C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739779 | ||||||
| chr2:30739809
|
T | G | 12 | a0001c0013t0002g0075a0005c0006t0001g0085a0005c0006t0001g0092others(9): Show | 12 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537-1352A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739809 | ||||||
| chr2:30739928
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1537-1471C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30739928 | ||||||
| chr2:30740068
|
A | G | 31 | a0001c0001t0002g0370a0001c0002t0002g0008a0001c0002t0002g0207others(28): Show | 31 | HG00323.hp1 HG00621.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.1537-1611T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740068 | ||||||
| chr2:30740082
|
G | GT | 6 | a0002c0003t0001g0203a0002c0003t0001g0348a0002c0003t0001g0360others(3): Show | 6 | HG01261.hp2 HG01952.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-1626dupA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740082 | ||||||
| chr2:30740082
|
GT | G | 114 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0054others(111): Show | 114 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1537-1626delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740082 | ||||||
| chr2:30740082
|
GTT | G | 9 | a0001c0001t0001g0279a0001c0001t0003g0043a0001c0002t0002g0111others(6): Show | 9 | HG00642.hp1 HG01346.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537-1627_1537-162 others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740082 | ||||||
| chr2:30740082
|
GTTT | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(189): Show | 195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1537-1628_1537-162 others(7): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740082 | ||||||
| chr2:30740091
|
T | TTG | 9 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(6): Show | 9 | HG00735.hp2 HG01123.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-1635_1537-163 others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740091 | ||||||
| chr2:30740092
|
T | TG | 7 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0212others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1537-1636_1537-163 others(5): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740092 | ||||||
| chr2:30740093
|
T | G | 12 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0002g0115others(9): Show | 12 | HG00099.hp2 HG00639.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537-1636A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740093 | ||||||
| chr2:30740094
|
T | G | 80 | a0001c0001t0001g0054a0001c0001t0001g0090a0001c0001t0001g0094others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1537-1637A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740094 | ||||||
| chr2:30740095
|
T | G | 7 | a0001c0001t0003g0043a0001c0002t0002g0149a0001c0002t0002g0174others(4): Show | 7 | HG01346.hp2 HG01891.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-1638A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740095 | ||||||
| chr2:30740096
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(189): Show | 195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1537-1639A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740096 | ||||||
| chr2:30740097
|
T | G | 2 | a0001c0002t0005g0026a0003c0004t0002g0182 | 2 | HG02015.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1537-1640A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740097 | ||||||
| chr2:30740099
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1537-1642A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740099 | ||||||
| chr2:30740100
|
T | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-1643A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740100 | ||||||
| chr2:30740106
|
T | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(90): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1537-1649A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740106 | ||||||
| chr2:30740170
|
C | T | 1 | a0001c0002t0001g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1537-1713G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740170 | ||||||
| chr2:30740186
|
G | C | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1536+1722C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740186 | ||||||
| chr2:30740239
|
C | T | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1536+1669G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740239 | ||||||
| chr2:30740309
|
G | A | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1536+1599C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740309 | ||||||
| chr2:30740314
|
C | T | 2 | a0005c0006t0001g0109a0005c0006t0004g0151 | 2 | HG00735.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1536+1594G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740314 | ||||||
| chr2:30740315
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1536+1593C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740315 | ||||||
| chr2:30740335
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(89): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1536+1573G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740335 | ||||||
| chr2:30740498
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(94): Show | 99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1536+1410T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740498 | ||||||
| chr2:30740798
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1536+1110G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740798 | ||||||
| chr2:30740906
|
C | T | 1 | a0002c0003t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1536+1002G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740906 | ||||||
| chr2:30740971
|
G | A | 1 | a0003c0004t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1536+937C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740971 | ||||||
| chr2:30741042
|
G | A | 2 | a0002c0003t0001g0200a0008c0009t0004g0220 | 2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1536+866C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741042 | ||||||
| chr2:30741078
|
T | G | 1 | a0002c0003t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1536+830A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741078 | ||||||
| chr2:30741238
|
A | C | 1 | a0001c0013t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1536+670T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741238 | ||||||
| chr2:30741261
|
A | G | 2 | a0001c0002t0002g0069a0001c0002t0002g0371 | 2 | HG02004.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1536+647T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741261 | ||||||
| chr2:30741540
|
G | A | 1 | a0001c0002t0001g0305 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1536+368C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741540 | ||||||
| chr2:30741574
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0229 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1536+334C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741574 | ||||||
| chr2:30741598
|
G | A | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1536+310C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741598 | ||||||
| chr2:30741666
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1536+242G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741666 | ||||||
| chr2:30741766
|
G | A | 32 | a0001c0002t0002g0008a0001c0002t0002g0207a0001c0002t0002g0258others(29): Show | 32 | HG00323.hp1 HG00621.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.1536+142C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741766 | ||||||
| chr2:30741833
|
C | T | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1536+75G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30741833 | ||||||
| chr2:30741994
|
G | C | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1480-30C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30741994 | ||||||
| chr2:30742012
|
C | T | 1 | a0001c0001t0002g0368 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1480-48G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742012 | ||||||
| chr2:30742034
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1480-70C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742034 | ||||||
| chr2:30742040
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0003g0380 | 3 | HG02922.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1480-76G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742040 | ||||||
| chr2:30742176
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1479+150T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742176 | ||||||
| chr2:30742200
|
G | A | 1 | a0001c0013t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1479+126C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742200 | ||||||
| chr2:30742240
|
C | T | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1479+86G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742240 | ||||||
| chr2:30742282
|
T | G | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1479+44A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742282 | ||||||
| chr2:30742283
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1479+43C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 14/22 | chr2 | 30742283 | ||||||
| chr2:30742413
|
G | A | 1 | a0003c0004t0002g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1446-54C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742413 | ||||||
| chr2:30742516
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1446-157G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742516 | ||||||
| chr2:30742593
|
G | A | 1 | a0001c0001t0003g0122 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1446-234C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742593 | ||||||
| chr2:30742643
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0208 | 2 | NA18984.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1446-284G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742643 | ||||||
| chr2:30742739
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1446-380A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742739 | ||||||
| chr2:30742786
|
G | A | 2 | a0002c0003t0001g0325a0002c0003t0004g0307 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1446-427C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742786 | ||||||
| chr2:30742909
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1445+474A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742909 | ||||||
| chr2:30742968
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1445+415G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30742968 | ||||||
| chr2:30743028
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1445+355G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30743028 | ||||||
| chr2:30743043
|
C | T | 2 | a0001c0001t0001g0195a0001c0020t0004g0051 | 2 | NA18942.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1445+340G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30743043 | ||||||
| chr2:30743126
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(87): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1445+257G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 13/22 | chr2 | 30743126 | ||||||
| chr2:30743638
|
T | A | 5 | a0001c0002t0001g0098a0001c0002t0001g0297a0001c0002t0002g0283others(2): Show | 5 | HG00738.hp1 HG01891.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-59A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30743638 | ||||||
| chr2:30743702
|
A | G | 2 | a0007c0008t0001g0276a0007c0008t0001g0281 | 2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1249-123T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30743702 | ||||||
| chr2:30743821
|
G | A | 74 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0017others(71): Show | 75 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1249-242C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30743821 | ||||||
| chr2:30743871
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1249-292C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30743871 | ||||||
| chr2:30744036
|
C | A | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1249-457G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744036 | ||||||
| chr2:30744208
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1249-629A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744208 | ||||||
| chr2:30744222
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1249-643G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744222 | ||||||
| chr2:30744246
|
A | G | 2 | a0001c0001t0002g0301a0001c0001t0005g0350 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1249-667T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744246 | ||||||
| chr2:30744354
|
C | T | 3 | a0001c0002t0001g0098a0001c0002t0001g0297a0001c0002t0010g0364 | 3 | HG00738.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1249-775G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744354 | ||||||
| chr2:30744556
|
G | C | 6 | a0001c0001t0001g0134a0001c0001t0002g0071a0001c0001t0002g0079others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1249-977C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744556 | ||||||
| chr2:30744581
|
T | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0229 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1249-1002A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744581 | ||||||
| chr2:30744627
|
CT | C | 4 | a0001c0002t0001g0192a0002c0003t0001g0027a0002c0003t0001g0310others(1): Show | 4 | NA18948.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-1049delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744627 | ||||||
| chr2:30744721
|
T | C | 30 | a0001c0002t0002g0008a0001c0002t0002g0207a0001c0002t0002g0258others(27): Show | 30 | HG00323.hp1 HG00621.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1248+1002A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744721 | ||||||
| chr2:30744726
|
G | A | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1248+997C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30744726 | ||||||
| chr2:30745073
|
C | T | 8 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+650G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745073 | ||||||
| chr2:30745122
|
T | A | 1 | a0003c0004t0002g0255 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1248+601A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745122 | ||||||
| chr2:30745148
|
T | C | 41 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0127others(38): Show | 41 | HG00408.hp2 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1248+575A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745148 | ||||||
| chr2:30745362
|
A | G | 93 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(90): Show | 93 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1248+361T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745362 | ||||||
| chr2:30745508
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1248+215G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745508 | ||||||
| chr2:30745535
|
A | G | 1 | a0002c0003t0001g0360 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1248+188T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745535 | ||||||
| chr2:30745571
|
T | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1248+152A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745571 | ||||||
| chr2:30745627
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0153others(2): Show | 5 | NA18954.hp2 NA18993.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+96T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745627 | ||||||
| chr2:30745694
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0118a0001c0001t0001g0260 | 3 | NA18944.hp1 NA18978.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1248+29G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 12/22 | chr2 | 30745694 | ||||||
| chr2:30745822
|
C | T | 2 | a0002c0003t0001g0325a0002c0003t0004g0307 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1237-88G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745822 | ||||||
| chr2:30745894
|
A | AT | 33 | a0001c0001t0001g0110a0001c0001t0001g0129a0001c0001t0001g0130others(30): Show | 33 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1237-161dupA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
A | ATT | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(91): Show | 96 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1237-162_1237-161d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
A | ATTT | 9 | a0001c0001t0002g0126a0001c0001t0002g0301a0001c0001t0005g0158others(6): Show | 9 | HG00639.hp1 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-163_1237-161d others(5): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
AT | A | 13 | a0001c0001t0003g0286a0001c0001t0003g0345a0001c0001t0006g0128others(10): Show | 13 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1237-161delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
ATT | A | 10 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(7): Show | 10 | HG02071.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-162_1237-161d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
ATTT | A | 12 | a0001c0001t0002g0243a0001c0002t0001g0106a0001c0002t0002g0045others(9): Show | 12 | HG00280.hp1 HG01192.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1237-163_1237-161d others(5): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
ATTTT | A | 62 | a0001c0001t0002g0115a0001c0001t0002g0176a0001c0001t0002g0275others(59): Show | 63 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1237-164_1237-161d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745894
|
ATTTTT | A | 47 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1237-165_1237-161d others(7): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745894 | ||||||
| chr2:30745932
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1237-198C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745932 | ||||||
| chr2:30745982
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(121): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1237-248G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30745982 | ||||||
| chr2:30746063
|
G | C | 71 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0017others(68): Show | 72 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1237-329C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746063 | ||||||
| chr2:30746126
|
C | T | 3 | a0001c0002t0002g0029a0004c0005t0002g0034a0004c0005t0009g0209 | 3 | NA18953.hp1 NA18962.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1237-392G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746126 | ||||||
| chr2:30746186
|
T | G | 3 | a0001c0002t0001g0098a0001c0002t0001g0297a0001c0002t0010g0364 | 3 | HG00738.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1237-452A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746186 | ||||||
| chr2:30746426
|
T | C | 1 | a0002c0003t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1237-692A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746426 | ||||||
| chr2:30746519
|
G | A | 73 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0017others(70): Show | 74 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1237-785C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746519 | ||||||
| chr2:30746596
|
T | C | 48 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(45): Show | 48 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1237-862A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746596 | ||||||
| chr2:30746602
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(259): Show | 265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1237-868A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746602 | ||||||
| chr2:30746603
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1237-869T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746603 | ||||||
| chr2:30746935
|
G | T | 103 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0017others(100): Show | 104 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1237-1201C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30746935 | ||||||
| chr2:30747138
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1237-1404C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747138 | ||||||
| chr2:30747277
|
T | TGA | 8 | a0002c0003t0001g0004a0002c0003t0001g0217a0002c0003t0001g0312others(5): Show | 9 | HG01074.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-1545_1237-154 others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747277 | ||||||
| chr2:30747417
|
A | C | 4 | a0001c0001t0007g0227a0001c0001t0007g0228a0007c0008t0001g0276others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-1683T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747417 | ||||||
| chr2:30747437
|
C | T | 6 | a0001c0001t0002g0115a0001c0001t0002g0243a0001c0001t0002g0275others(3): Show | 6 | HG01891.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237-1703G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747437 | ||||||
| chr2:30747705
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1237-1971A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747705 | ||||||
| chr2:30747712
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1237-1978G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747712 | ||||||
| chr2:30747782
|
C | T | 3 | a0001c0002t0001g0098a0001c0002t0001g0297a0001c0002t0010g0364 | 3 | HG00738.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1237-2048G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747782 | ||||||
| chr2:30747866
|
G | C | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1237-2132C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747866 | ||||||
| chr2:30747867
|
G | T | 27 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0127others(24): Show | 27 | HG00408.hp2 HG01109.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1237-2133C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747867 | ||||||
| chr2:30747871
|
C | A | 24 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0046others(21): Show | 25 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237-2137G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747871 | ||||||
| chr2:30747968
|
T | C | 15 | a0001c0001t0002g0115a0001c0001t0002g0243a0001c0001t0002g0275others(12): Show | 15 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1237-2234A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30747968 | ||||||
| chr2:30748082
|
G | A | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1237-2348C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748082 | ||||||
| chr2:30748091
|
G | T | 48 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(45): Show | 48 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1237-2357C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748091 | ||||||
| chr2:30748202
|
G | T | 5 | a0001c0001t0001g0094a0001c0001t0001g0127a0001c0001t0001g0146others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-2468C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748202 | ||||||
| chr2:30748284
|
G | A | 1 | a0001c0013t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1237-2550C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748284 | ||||||
| chr2:30748291
|
A | G | 1 | a0003c0004t0005g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1237-2557T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748291 | ||||||
| chr2:30748398
|
C | G | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237-2664G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748398 | ||||||
| chr2:30748440
|
G | A | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1236+2663C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748440 | ||||||
| chr2:30748730
|
A | G | 1 | a0002c0003t0001g0360 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1236+2373T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748730 | ||||||
| chr2:30748798
|
C | T | 2 | a0001c0001t0002g0115a0001c0001t0002g0243 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1236+2305G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748798 | ||||||
| chr2:30748839
|
G | A | 1 | a0003c0004t0002g0168 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1236+2264C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748839 | ||||||
| chr2:30748901
|
C | T | 1 | a0003c0004t0002g0206 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1236+2202G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30748901 | ||||||
| chr2:30749045
|
G | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1236+2058C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749045 | ||||||
| chr2:30749166
|
G | A | 1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1236+1937C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749166 | ||||||
| chr2:30749351
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1236+1752C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749351 | ||||||
| chr2:30749361
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1236+1742A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749361 | ||||||
| chr2:30749473
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1236+1630C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749473 | ||||||
| chr2:30749500
|
C | A | 3 | a0001c0002t0001g0098a0001c0002t0001g0297a0001c0002t0010g0364 | 3 | HG00738.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1236+1603G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749500 | ||||||
| chr2:30749750
|
G | T | 8 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1236+1353C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749750 | ||||||
| chr2:30749758
|
C | CATGTGAT | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1236+1344_1236+134 others(11): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749758 | ||||||
| chr2:30749760
|
T | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1236+1343A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749760 | ||||||
| chr2:30749803
|
C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1236+1300G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749803 | ||||||
| chr2:30749922
|
A | T | 1 | a0007c0008t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1236+1181T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749922 | ||||||
| chr2:30750007
|
G | A | 14 | a0001c0001t0001g0134a0001c0001t0002g0071a0001c0001t0002g0079others(11): Show | 14 | HG01433.hp1 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1236+1096C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750007 | ||||||
| chr2:30750018
|
T | C | 14 | a0001c0001t0001g0134a0001c0001t0002g0071a0001c0001t0002g0079others(11): Show | 14 | HG01433.hp1 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1236+1085A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750018 | ||||||
| chr2:30750065
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1236+1038G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750065 | ||||||
| chr2:30750066
|
C | A | 23 | a0001c0001t0001g0279a0001c0001t0002g0234a0001c0001t0002g0293others(20): Show | 23 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1236+1037G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750066 | ||||||
| chr2:30750147
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1236+956A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750147 | ||||||
| chr2:30750228
|
C | T | 113 | a0001c0001t0002g0275a0001c0001t0008g0078a0001c0002t0001g0003others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1236+875G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750228 | ||||||
| chr2:30750357
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(203): Show | 209 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1236+746G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750357 | ||||||
| chr2:30750362
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1236+741G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750362 | ||||||
| chr2:30750477
|
T | C | 2 | a0001c0013t0002g0075a0016c0019t0001g0138 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1236+626A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750477 | ||||||
| chr2:30750490
|
A | C | 13 | a0001c0001t0001g0134a0001c0001t0002g0071a0001c0001t0002g0079others(10): Show | 13 | HG01433.hp1 HG01496.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1236+613T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750490 | ||||||
| chr2:30750873
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1236+230G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750873 | ||||||
| chr2:30750936
|
T | C | 1 | a0002c0003t0001g0378 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1236+167A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750936 | ||||||
| chr2:30750946
|
A | G | 8 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1236+157T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750946 | ||||||
| chr2:30750959
|
C | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1236+144G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30750959 | ||||||
| chr2:30751013
|
A | C | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1236+90T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30751013 | ||||||
| chr2:30751047
|
A | C | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1236+56T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30751047 | ||||||
| chr2:30751065
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1236+38T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30751065 | ||||||
| chr2:30751291
|
C | T | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-40G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751291 | ||||||
| chr2:30751330
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-79A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751330 | ||||||
| chr2:30751401
|
T | C | 3 | a0001c0001t0002g0071a0001c0001t0002g0079a0001c0001t0002g0240 | 3 | HG02257.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1088-150A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751401 | ||||||
| chr2:30751458
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-207A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751458 | ||||||
| chr2:30751472
|
C | T | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-221G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751472 | ||||||
| chr2:30751635
|
G | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-384C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751635 | ||||||
| chr2:30751636
|
C | G | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-385G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751636 | ||||||
| chr2:30751709
|
A | C | 58 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0046others(55): Show | 59 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1088-458T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751709 | ||||||
| chr2:30751829
|
C | T | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1088-578G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751829 | ||||||
| chr2:30751851
|
G | C | 74 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0017others(71): Show | 75 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1088-600C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751851 | ||||||
| chr2:30751869
|
G | A | 130 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(127): Show | 132 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1088-618C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751869 | ||||||
| chr2:30751910
|
G | T | 43 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1088-659C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751910 | ||||||
| chr2:30751928
|
T | C | 139 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(136): Show | 141 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1088-677A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751928 | ||||||
| chr2:30751950
|
G | A | 132 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0014others(129): Show | 134 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1088-699C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30751950 | ||||||
| chr2:30752235
|
G | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+818C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752235 | ||||||
| chr2:30752358
|
G | C | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+695C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752358 | ||||||
| chr2:30752397
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1087+656G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752397 | ||||||
| chr2:30752417
|
G | C | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1087+636C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752417 | ||||||
| chr2:30752481
|
G | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+572C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752481 | ||||||
| chr2:30752590
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1087+463T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752590 | ||||||
| chr2:30752600
|
T | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+453A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752600 | ||||||
| chr2:30752615
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1087+438G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752615 | ||||||
| chr2:30752800
|
G | A | 12 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0001g0279others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1087+253C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752800 | ||||||
| chr2:30752920
|
G | A | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+133C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30752920 | ||||||
| chr2:30753015
|
T | A | 1 | a0002c0003t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1087+38A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 10/22 | chr2 | 30753015 | ||||||
| chr2:30753220
|
C | T | 1 | a0001c0001t0001g0373 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.942-22G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753220 | ||||||
| chr2:30753246
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.942-48G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753246 | ||||||
| chr2:30753302
|
T | C | 78 | a0001c0001t0001g0054a0001c0001t0001g0090a0001c0001t0001g0094others(75): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.942-104A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753302 | ||||||
| chr2:30753404
|
G | T | 2 | a0001c0002t0002g0069a0001c0002t0002g0371 | 2 | HG02004.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.942-206C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753404 | ||||||
| chr2:30753465
|
G | A | 2 | a0001c0013t0002g0075a0016c0019t0001g0138 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.942-267C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753465 | ||||||
| chr2:30753613
|
C | CT | 63 | a0001c0001t0007g0227a0001c0001t0007g0228a0001c0002t0001g0002others(60): Show | 64 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.942-416dupA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753613 | ||||||
| chr2:30753673
|
T | A | 20 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0130others(17): Show | 20 | HG00408.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.942-475A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753673 | ||||||
| chr2:30753726
|
A | G | 2 | a0001c0013t0002g0075a0016c0019t0001g0138 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.942-528T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753726 | ||||||
| chr2:30753768
|
A | G | 2 | a0001c0001t0003g0298a0001c0001t0003g0321 | 2 | HG00558.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.941+522T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753768 | ||||||
| chr2:30753786
|
A | C | 43 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.941+504T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753786 | ||||||
| chr2:30753901
|
C | T | 1 | a0004c0005t0002g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.941+389G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753901 | ||||||
| chr2:30753902
|
C | T | 5 | a0003c0004t0002g0065a0003c0004t0002g0067a0003c0004t0002g0097others(2): Show | 5 | NA18961.hp1 NA18971.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.941+388G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753902 | ||||||
| chr2:30753913
|
T | C | 1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.941+377A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753913 | ||||||
| chr2:30753925
|
C | A | 54 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0134others(51): Show | 54 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.941+365G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753925 | ||||||
| chr2:30753980
|
C | G | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.941+310G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30753980 | ||||||
| chr2:30754058
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0003g0380 | 3 | HG02922.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.941+232T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30754058 | ||||||
| chr2:30754078
|
A | G | 14 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0001g0140others(11): Show | 14 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.941+212T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30754078 | ||||||
| chr2:30754207
|
G | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.941+83C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 9/22 | chr2 | 30754207 | ||||||
| chr2:30754379
|
A | G | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.867-15T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754379 | ||||||
| chr2:30754427
|
T | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0243 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.867-63A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754427 | ||||||
| chr2:30754488
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.867-124G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754488 | ||||||
| chr2:30754578
|
G | A | 1 | a0015c0017t0002g0012 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.867-214C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754578 | ||||||
| chr2:30754611
|
G | T | 32 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0002g0234others(29): Show | 32 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.867-247C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754611 | ||||||
| chr2:30754613
|
G | C | 1 | a0001c0001t0003g0372 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.867-249C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754613 | ||||||
| chr2:30754623
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0235 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.867-259C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754623 | ||||||
| chr2:30754766
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(207): Show | 212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.867-402G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754766 | ||||||
| chr2:30754945
|
T | C | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.867-581A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30754945 | ||||||
| chr2:30755037
|
C | T | 1 | a0002c0003t0002g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.867-673G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755037 | ||||||
| chr2:30755059
|
T | C | 29 | a0001c0001t0001g0279a0001c0001t0007g0227a0001c0001t0007g0228others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.867-695A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755059 | ||||||
| chr2:30755108
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0273 | 3 | HG02486.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.867-744G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755108 | ||||||
| chr2:30755132
|
C | G | 43 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0142others(40): Show | 43 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.867-768G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755132 | ||||||
| chr2:30755297
|
G | T | 1 | a0001c0001t0003g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.867-933C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755297 | ||||||
| chr2:30755345
|
G | C | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0129others(21): Show | 24 | HG00408.hp2 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.867-981C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755345 | ||||||
| chr2:30755504
|
T | G | 28 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0129others(25): Show | 28 | HG00408.hp2 HG01109.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.867-1140A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755504 | ||||||
| chr2:30755620
|
T | C | 6 | a0001c0001t0001g0274a0001c0001t0003g0074a0001c0001t0003g0137others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-1256A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755620 | ||||||
| chr2:30755739
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.867-1375G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755739 | ||||||
| chr2:30755857
|
C | A | 20 | a0001c0002t0001g0017a0001c0002t0001g0253a0001c0002t0002g0021others(17): Show | 20 | HG00597.hp1 HG00621.hp1 NA18612.hp1 others(17): Show |
intron_variant | MODIFIER | c.867-1493G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755857 | ||||||
| chr2:30755857
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.867-1493G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755857 | ||||||
| chr2:30755858
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(68): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.867-1494C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755858 | ||||||
| chr2:30755880
|
C | T | 1 | a0001c0002t0002g0375 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.867-1516G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755880 | ||||||
| chr2:30755894
|
C | T | 25 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0130others(22): Show | 25 | HG00408.hp2 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.867-1530G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755894 | ||||||
| chr2:30755934
|
T | G | 26 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0130others(23): Show | 26 | HG00408.hp2 HG01109.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.867-1570A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30755934 | ||||||
| chr2:30756050
|
C | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.867-1686G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756050 | ||||||
| chr2:30756098
|
G | T | 1 | a0001c0002t0005g0347 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.867-1734C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756098 | ||||||
| chr2:30756177
|
C | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0002g0068others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1813G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756177 | ||||||
| chr2:30756191
|
A | G | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0005g0350 | 3 | HG01884.hp1 HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.867-1827T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756191 | ||||||
| chr2:30756217
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.866+1829G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756217 | ||||||
| chr2:30756279
|
G | A | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.866+1767C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756279 | ||||||
| chr2:30756433
|
C | T | 9 | a0005c0006t0001g0085a0005c0006t0001g0092a0005c0006t0001g0109others(6): Show | 9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.866+1613G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756433 | ||||||
| chr2:30756621
|
T | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.866+1425A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756621 | ||||||
| chr2:30756799
|
G | A | 57 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0046others(54): Show | 58 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.866+1247C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756799 | ||||||
| chr2:30756799
|
G | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0004g0095 | 3 | HG02451.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.866+1247C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756799 | ||||||
| chr2:30756806
|
C | T | 1 | a0001c0001t0002g0356 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.866+1240G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756806 | ||||||
| chr2:30756854
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(74): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.866+1192A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756854 | ||||||
| chr2:30756899
|
C | T | 4 | a0001c0001t0007g0227a0001c0001t0007g0228a0007c0008t0001g0276others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+1147G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756899 | ||||||
| chr2:30756973
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.866+1073C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756973 | ||||||
| chr2:30756981
|
CACAGCTT others(14): Show |
C | 1 | a0003c0004t0002g0067 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.866+1044_866+1064d others(23): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756981 | ||||||
| chr2:30756992
|
C | G | 57 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0046others(54): Show | 58 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.866+1054G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756992 | ||||||
| chr2:30757001
|
C | A | 1 | a0001c0002t0005g0346 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.866+1045G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757001 | ||||||
| chr2:30757005
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.866+1041G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757005 | ||||||
| chr2:30757016
|
C | T | 1 | a0002c0003t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.866+1030G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757016 | ||||||
| chr2:30757073
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0004g0041 | 2 | HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.866+973A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757073 | ||||||
| chr2:30757118
|
TCATGTTC others(4): Show |
T | 1 | a0001c0001t0006g0308 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.866+917_866+927del others(11): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757118 | ||||||
| chr2:30757171
|
C | T | 38 | a0001c0001t0001g0134a0001c0001t0001g0274a0001c0001t0002g0071others(35): Show | 38 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.866+875G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757171 | ||||||
| chr2:30757236
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.866+810G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757236 | ||||||
| chr2:30757260
|
G | C | 11 | a0002c0003t0001g0035a0002c0003t0001g0073a0002c0003t0001g0171others(8): Show | 11 | HG00558.hp1 NA18939.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.866+786C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757260 | ||||||
| chr2:30757316
|
G | C | 1 | a0002c0003t0004g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.866+730C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757316 | ||||||
| chr2:30757363
|
C | T | 60 | a0001c0001t0002g0115a0001c0001t0002g0243a0001c0002t0001g0002others(57): Show | 61 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.866+683G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757363 | ||||||
| chr2:30757393
|
C | T | 60 | a0001c0001t0002g0115a0001c0001t0002g0243a0001c0002t0001g0002others(57): Show | 61 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.866+653G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757393 | ||||||
| chr2:30757542
|
C | T | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.866+504G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757542 | ||||||
| chr2:30757552
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.866+494C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757552 | ||||||
| chr2:30757713
|
C | G | 75 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0001g0140others(72): Show | 76 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.866+333G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757713 | ||||||
| chr2:30757758
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.866+288A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757758 | ||||||
| chr2:30757783
|
G | A | 58 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0046others(55): Show | 59 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.866+263C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757783 | ||||||
| chr2:30757875
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.866+171G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30757875 | ||||||
| chr2:30758006
|
C | T | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.866+40G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30758006 | ||||||
| chr2:30758280
|
GA | G | 9 | a0001c0001t0002g0234a0001c0001t0002g0275a0001c0001t0002g0293others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-144delT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758280 | ||||||
| chr2:30758406
|
T | A | 4 | a0001c0001t0002g0133a0001c0001t0002g0230a0001c0001t0002g0231others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-269A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758406 | ||||||
| chr2:30758418
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.775-281T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758418 | ||||||
| chr2:30758458
|
T | C | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-321A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758458 | ||||||
| chr2:30758554
|
G | C | 1 | a0001c0001t0001g0284 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-417C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758554 | ||||||
| chr2:30758596
|
CGTGA | C | 5 | a0003c0004t0002g0065a0003c0004t0002g0067a0003c0004t0002g0097others(2): Show | 5 | NA18961.hp1 NA18971.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-463_775-460del others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758596 | ||||||
| chr2:30758746
|
CCCTCCCT others(19): Show |
C | 8 | a0001c0001t0001g0145a0001c0001t0001g0224a0001c0001t0001g0236others(5): Show | 8 | HG01109.hp2 HG01358.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-635_775-610del others(26): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758746 | ||||||
| chr2:30758752
|
C | G | 29 | a0001c0001t0001g0271a0001c0001t0007g0227a0001c0001t0007g0228others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.775-615G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758752 | ||||||
| chr2:30758759
|
T | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(45): Show | 49 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.775-622A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758759 | ||||||
| chr2:30758765
|
CT | C | 6 | a0001c0001t0002g0047a0001c0001t0002g0183a0001c0001t0002g0249others(3): Show | 6 | HG00423.hp2 NA18963.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-629delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758765 | ||||||
| chr2:30758772
|
T | C | 6 | a0001c0001t0002g0047a0001c0001t0002g0183a0001c0001t0002g0249others(3): Show | 6 | HG00423.hp2 NA18963.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-635A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758772 | ||||||
| chr2:30758774
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.775-637G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758774 | ||||||
| chr2:30758784
|
C | T | 47 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(44): Show | 48 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.775-647G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758784 | ||||||
| chr2:30758786
|
CT | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.775-650delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758786 | ||||||
| chr2:30758787
|
T | C | 47 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(44): Show | 48 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.775-650A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758787 | ||||||
| chr2:30758789
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.775-652A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758789 | ||||||
| chr2:30758789
|
T | TCCTTTCC others(10): Show |
4 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0005g0011others(1): Show | 4 | NA18950.hp1 NA18954.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-653_775-652ins others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758789 | ||||||
| chr2:30758789
|
T | TCCTTTCC others(18): Show |
60 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0271others(57): Show | 61 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.775-653_775-652ins others(25): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758789 | ||||||
| chr2:30758789
|
T | TCCTTTCC others(43): Show |
1 | a0003c0004t0002g0167 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.775-653_775-652ins others(50): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758789 | ||||||
| chr2:30758789
|
TCCTTTCC others(23): Show |
T | 6 | a0001c0001t0002g0047a0001c0001t0002g0183a0001c0001t0002g0249others(3): Show | 6 | HG00423.hp2 NA18963.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-682_775-653del others(30): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758789 | ||||||
| chr2:30758790
|
C | CCTTTCCT others(18): Show |
3 | a0003c0004t0002g0205a0003c0004t0002g0292a0003c0004t0005g0374 | 3 | NA18964.hp2 NA18982.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.775-654_775-653ins others(25): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758790 | ||||||
| chr2:30758791
|
CT | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(46): Show | 50 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.775-655delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758791 | ||||||
| chr2:30758792
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.775-655A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758792 | ||||||
| chr2:30758792
|
T | TCCCTCCC others(29): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0280 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.775-656_775-655ins others(36): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758792 | ||||||
| chr2:30758794
|
T | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(42): Show | 46 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.775-657A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758794 | ||||||
| chr2:30758794
|
TCCTTCCT others(18): Show |
T | 1 | a0001c0001t0002g0093 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.775-682_775-658del others(25): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758794 | ||||||
| chr2:30758798
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(48): Show | 52 | HG00438.hp1 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.775-661A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758798 | ||||||
| chr2:30758802
|
CCCTCCCT others(6): Show |
C | 25 | a0001c0001t0003g0137a0001c0001t0003g0144a0001c0001t0003g0269others(22): Show | 25 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.775-678_775-666del others(13): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758802 | ||||||
| chr2:30758802
|
CCCTCCCT others(18): Show |
C | 25 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0134others(22): Show | 25 | HG00099.hp1 HG00408.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.775-690_775-666del others(25): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758802 | ||||||
| chr2:30758804
|
C | T | 1 | a0001c0002t0003g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.775-667G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758804 | ||||||
| chr2:30758806
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0280 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.775-669G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758806 | ||||||
| chr2:30758808
|
CT | C | 23 | a0001c0001t0002g0234a0001c0001t0002g0275a0001c0001t0002g0293others(20): Show | 23 | HG00544.hp1 HG00558.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.775-672delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758808 | ||||||
| chr2:30758809
|
T | TCCCTCCC others(42): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0004g0095 | 3 | HG02451.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.775-673_775-672ins others(49): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758809 | ||||||
| chr2:30758809
|
T | TCCCTCCC others(67): Show |
1 | a0001c0001t0003g0009 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.775-673_775-672ins others(74): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758809 | ||||||
| chr2:30758809
|
T | TTCCCTTC others(1): Show |
43 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0094others(40): Show | 44 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.775-680_775-673dup others(8): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758809 | ||||||
| chr2:30758809
|
T | TTCCCTTC others(26): Show |
1 | a0002c0003t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.775-673_775-672ins others(33): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758809 | ||||||
| chr2:30758810
|
T | C | 6 | a0001c0001t0003g0036a0002c0003t0001g0035a0002c0003t0001g0073others(3): Show | 6 | HG00438.hp1 NA18939.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-673A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758810 | ||||||
| chr2:30758813
|
C | T | 6 | a0001c0001t0003g0036a0002c0003t0001g0035a0002c0003t0001g0073others(3): Show | 6 | HG00438.hp1 NA18939.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-676G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758813 | ||||||
| chr2:30758815
|
T | C | 24 | a0001c0001t0002g0234a0001c0001t0002g0275a0001c0001t0002g0293others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.775-678A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758815 | ||||||
| chr2:30758815
|
TCCTC | T | 6 | a0001c0001t0003g0036a0002c0003t0001g0035a0002c0003t0001g0073others(3): Show | 6 | HG00438.hp1 NA18939.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-682_775-679del others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758815 | ||||||
| chr2:30758817
|
C | CT | 22 | a0001c0001t0002g0234a0001c0001t0002g0275a0001c0001t0002g0293others(19): Show | 22 | HG00558.hp2 HG02040.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.775-681dupA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758817 | ||||||
| chr2:30758819
|
C | T | 24 | a0001c0001t0002g0234a0001c0001t0002g0275a0001c0001t0002g0293others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.775-682G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758819 | ||||||
| chr2:30758827
|
T | C | 50 | a0001c0001t0002g0047a0001c0001t0002g0071a0001c0001t0002g0079others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.775-690A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758827 | ||||||
| chr2:30758827
|
T | TCCTC | 64 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0002g0061others(61): Show | 65 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.775-694_775-691dup others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758827 | ||||||
| chr2:30758847
|
T | A | 1 | a0001c0001t0003g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775-710A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758847 | ||||||
| chr2:30758912
|
CTTCT | C | 40 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0100others(37): Show | 40 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.775-779_775-776del others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758912 | ||||||
| chr2:30758963
|
TTC | T | 101 | a0001c0001t0001g0094a0001c0001t0001g0134a0001c0001t0001g0140others(98): Show | 103 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.775-828_775-827del others(2): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758963 | ||||||
| chr2:30758982
|
T | A | 20 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0043others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-845A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758982 | ||||||
| chr2:30758983
|
C | T | 18 | a0001c0001t0001g0246a0001c0001t0002g0170a0001c0001t0002g0222others(15): Show | 18 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.775-846G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758983 | ||||||
| chr2:30758986
|
C | T | 1 | a0003c0004t0002g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.775-849G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758986 | ||||||
| chr2:30758989
|
T | G | 5 | a0001c0001t0001g0238a0001c0001t0001g0280a0001c0002t0002g0186others(2): Show | 5 | HG01884.hp2 HG03209.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-852A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758989 | ||||||
| chr2:30759020
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-883T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759020 | ||||||
| chr2:30759022
|
T | TCTTCCTT others(17): Show |
1 | a0002c0003t0001g0196 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.775-909_775-886dup others(24): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759022 | ||||||
| chr2:30759022
|
TCTTCCTT others(17): Show |
T | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.775-909_775-886del others(24): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759022 | ||||||
| chr2:30759022
|
TCTTCCTT others(21): Show |
T | 9 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0145others(6): Show | 9 | HG03209.hp2 HG03225.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-913_775-886del others(28): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759022 | ||||||
| chr2:30759024
|
TTCCTTCC others(1): Show |
T | 32 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0134others(29): Show | 32 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.775-895_775-888del others(8): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759024 | ||||||
| chr2:30759024
|
TTCCTTCC others(25): Show |
T | 1 | a0001c0001t0004g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.775-919_775-888del others(32): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759024 | ||||||
| chr2:30759028
|
T | C | 55 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0153others(52): Show | 55 | HG00642.hp1 HG01069.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.775-891A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759028 | ||||||
| chr2:30759028
|
TTCCCTCC others(21): Show |
T | 4 | a0001c0001t0001g0279a0001c0001t0002g0223a0001c0001t0002g0301others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-919_775-892del others(28): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759028 | ||||||
| chr2:30759032
|
CTCCCTCC others(13): Show |
C | 1 | a0001c0002t0002g0082 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.775-915_775-896del others(20): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759032 | ||||||
| chr2:30759040
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-903G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759040 | ||||||
| chr2:30759044
|
T | C | 33 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0134others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.775-907A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759044 | ||||||
| chr2:30759045
|
TCCTTCCT others(21): Show |
T | 11 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0234others(8): Show | 11 | HG00738.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.775-936_775-909del others(28): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759045 | ||||||
| chr2:30759045
|
TCCTTCCT others(25): Show |
T | 1 | a0001c0001t0002g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-940_775-909del others(32): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759045 | ||||||
| chr2:30759048
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-911A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759048 | ||||||
| chr2:30759048
|
TTCCTTCC others(5): Show |
T | 1 | a0003c0004t0005g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.775-923_775-912del others(12): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759048 | ||||||
| chr2:30759049
|
TCCTTCCC others(21): Show |
T | 46 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0153others(43): Show | 47 | HG00642.hp1 HG01069.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.775-940_775-913del others(28): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759049 | ||||||
| chr2:30759050
|
CCTTCCCT others(4): Show |
C | 1 | a0001c0001t0003g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775-924_775-914del others(11): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759050 | ||||||
| chr2:30759052
|
T | C | 69 | a0001c0001t0001g0058a0001c0001t0001g0094a0001c0001t0001g0246others(66): Show | 70 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.775-915A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759052 | ||||||
| chr2:30759052
|
TTCCCTCC others(12): Show |
T | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.775-934_775-916del others(19): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759052 | ||||||
| chr2:30759053
|
TCCCTCCC others(17): Show |
T | 1 | a0001c0001t0004g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775-940_775-917del others(24): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759053 | ||||||
| chr2:30759054
|
CCCTCCCT others(8): Show |
C | 127 | a0001c0001t0001g0094a0001c0001t0001g0127a0001c0001t0001g0129others(124): Show | 128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.775-932_775-918del others(15): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759054 | ||||||
| chr2:30759056
|
C | CTCCCTCC others(28): Show |
2 | a0002c0003t0001g0156a0010c0015t0001g0081 | 2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.775-920_775-919ins others(35): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759056 | ||||||
| chr2:30759058
|
CCCTCCCT others(4): Show |
C | 52 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0134others(49): Show | 52 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.775-932_775-922del others(11): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759058 | ||||||
| chr2:30759064
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0003g0103 | 2 | HG02486.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.775-927G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759064 | ||||||
| chr2:30759066
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.775-929G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759066 | ||||||
| chr2:30759067
|
CCTCCTCC others(10): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.775-947_775-931del others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759067 | ||||||
| chr2:30759068
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-931G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759068 | ||||||
| chr2:30759073
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0002g0275a0001c0001t0004g0143others(1): Show | 4 | HG01496.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-936G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759073 | ||||||
| chr2:30759077
|
C | T | 46 | a0001c0001t0002g0216a0001c0001t0003g0009a0001c0001t0003g0036others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.775-940G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759077 | ||||||
| chr2:30759078
|
C | T | 1 | a0001c0001t0003g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775-941G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759078 | ||||||
| chr2:30759118
|
CCT | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0141a0013c0012t0002g0268 | 3 | HG02559.hp2 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.775-983_775-982del others(2): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759118 | ||||||
| chr2:30759120
|
T | TCTCTTC | 5 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0002g0068others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-984_775-983ins others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759120 | ||||||
| chr2:30759140
|
T | C | 56 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0153others(53): Show | 57 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.775-1003A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759140 | ||||||
| chr2:30759150
|
C | CCTTAT | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.775-1014_775-1013i others(7): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759150 | ||||||
| chr2:30759155
|
T | G | 1 | a0002c0003t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.775-1018A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759155 | ||||||
| chr2:30759187
|
A | T | 1 | a0001c0001t0003g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775-1050T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759187 | ||||||
| chr2:30759206
|
A | C | 20 | a0001c0001t0001g0110a0001c0001t0001g0191a0001c0001t0002g0023others(17): Show | 20 | HG00099.hp1 HG00423.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-1069T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759206 | ||||||
| chr2:30759207
|
C | T | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.775-1070G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759207 | ||||||
| chr2:30759252
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.775-1115A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759252 | ||||||
| chr2:30759269
|
CCT | C | 16 | a0001c0001t0002g0216a0001c0001t0003g0036a0001c0001t0003g0043others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.775-1134_775-1133d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759269 | ||||||
| chr2:30759289
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.775-1152C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759289 | ||||||
| chr2:30759311
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775-1174C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759311 | ||||||
| chr2:30759316
|
C | A | 1 | a0003c0004t0002g0067 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.775-1179G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759316 | ||||||
| chr2:30759336
|
G | T | 1 | a0001c0002t0001g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.775-1199C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759336 | ||||||
| chr2:30759525
|
G | A | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-1388C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759525 | ||||||
| chr2:30759543
|
T | C | 17 | a0001c0001t0001g0110a0001c0001t0001g0191a0001c0001t0002g0023others(14): Show | 17 | HG00099.hp1 HG00423.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.775-1406A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759543 | ||||||
| chr2:30759545
|
C | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0090others(39): Show | 43 | HG00438.hp2 HG01192.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.775-1408G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759545 | ||||||
| chr2:30759602
|
A | G | 2 | a0001c0002t0001g0098a0001c0002t0001g0297 | 2 | HG00738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.775-1465T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759602 | ||||||
| chr2:30759606
|
C | A | 42 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0191others(39): Show | 42 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.775-1469G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759606 | ||||||
| chr2:30759616
|
C | G | 85 | a0001c0001t0001g0127a0001c0001t0001g0225a0001c0001t0001g0241others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.775-1479G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759616 | ||||||
| chr2:30759701
|
A | C | 18 | a0001c0001t0002g0044a0001c0002t0001g0017a0001c0002t0002g0021others(15): Show | 18 | HG00597.hp1 HG00621.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.775-1564T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759701 | ||||||
| chr2:30759754
|
G | T | 7 | a0001c0001t0002g0176a0001c0001t0002g0223a0001c0001t0002g0230others(4): Show | 7 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-1617C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759754 | ||||||
| chr2:30759860
|
G | C | 41 | a0001c0001t0002g0216a0001c0001t0002g0222a0001c0001t0002g0275others(38): Show | 41 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.775-1723C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759860 | ||||||
| chr2:30759860
|
G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(236): Show | 242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.775-1723C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759860 | ||||||
| chr2:30759864
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0142 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.775-1727A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759864 | ||||||
| chr2:30759866
|
G | C | 4 | a0001c0001t0002g0222a0001c0013t0002g0075a0007c0008t0001g0276others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1729C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759866 | ||||||
| chr2:30759920
|
G | A | 1 | a0002c0003t0001g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.775-1783C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759920 | ||||||
| chr2:30759929
|
T | C | 80 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0090others(77): Show | 81 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.775-1792A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30759929 | ||||||
| chr2:30760017
|
G | A | 84 | a0001c0001t0001g0054a0001c0001t0001g0088a0001c0001t0001g0090others(81): Show | 84 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.775-1880C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760017 | ||||||
| chr2:30760018
|
A | G | 137 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0054others(134): Show | 138 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.775-1881T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760018 | ||||||
| chr2:30760092
|
AT | A | 153 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0094others(150): Show | 153 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.775-1956delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760092 | ||||||
| chr2:30760146
|
G | T | 48 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0114others(45): Show | 48 | HG00408.hp1 HG00673.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.775-2009C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760146 | ||||||
| chr2:30760187
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-2050C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760187 | ||||||
| chr2:30760221
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.775-2084G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760221 | ||||||
| chr2:30760257
|
T | C | 7 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-2120A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760257 | ||||||
| chr2:30760300
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(211): Show | 216 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.775-2163A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760300 | ||||||
| chr2:30760364
|
A | G | 1 | a0001c0002t0005g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.775-2227T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760364 | ||||||
| chr2:30760391
|
A | G | 1 | a0001c0001t0006g0359 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.775-2254T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760391 | ||||||
| chr2:30760439
|
A | G | 67 | a0001c0001t0001g0090a0001c0001t0001g0114a0001c0001t0001g0127others(64): Show | 67 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.775-2302T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760439 | ||||||
| chr2:30760442
|
G | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(108): Show | 113 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.775-2305C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760442 | ||||||
| chr2:30760442
|
GT | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0237a0012c0011t0002g0131 | 3 | HG02818.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.775-2306delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760442 | ||||||
| chr2:30760443
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0049others(178): Show | 183 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.775-2306A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760443 | ||||||
| chr2:30760445
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0280a0001c0002t0012g0239 | 3 | HG01934.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.775-2308C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760445 | ||||||
| chr2:30760568
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.775-2431C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760568 | ||||||
| chr2:30760590
|
G | A | 1 | a0001c0001t0002g0331 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.775-2453C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760590 | ||||||
| chr2:30760628
|
G | A | 1 | a0001c0002t0001g0017 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.774+2454C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760628 | ||||||
| chr2:30760724
|
T | C | 2 | a0001c0002t0002g0283a0001c0002t0005g0113 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.774+2358A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760724 | ||||||
| chr2:30760830
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.774+2252C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760830 | ||||||
| chr2:30760965
|
G | A | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.774+2117C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760965 | ||||||
| chr2:30760966
|
A | G | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.774+2116T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760966 | ||||||
| chr2:30760979
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0142 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.774+2103C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760979 | ||||||
| chr2:30761021
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0142others(3): Show | 6 | HG02257.hp1 HG02559.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+2061C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761021 | ||||||
| chr2:30761048
|
C | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.774+2034G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761048 | ||||||
| chr2:30761060
|
G | A | 1 | a0001c0002t0004g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.774+2022C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761060 | ||||||
| chr2:30761222
|
G | A | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+1860C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761222 | ||||||
| chr2:30761333
|
G | A | 1 | a0001c0002t0002g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.774+1749C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761333 | ||||||
| chr2:30761416
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.774+1666G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761416 | ||||||
| chr2:30761419
|
G | A | 1 | a0001c0002t0005g0340 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.774+1663C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761419 | ||||||
| chr2:30761420
|
C | T | 40 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0238others(37): Show | 40 | HG01433.hp1 HG01884.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.774+1662G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761420 | ||||||
| chr2:30761424
|
C | G | 4 | a0001c0001t0001g0173a0001c0001t0001g0376a0001c0002t0002g0099others(1): Show | 4 | HG01069.hp1 HG01109.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1658G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761424 | ||||||
| chr2:30761459
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0246others(2): Show | 5 | HG01891.hp2 HG01934.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1623G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761459 | ||||||
| chr2:30761498
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.774+1584G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761498 | ||||||
| chr2:30761533
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0002g0222a0001c0001t0003g0380 | 3 | HG02922.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.774+1549C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761533 | ||||||
| chr2:30761667
|
A | T | 42 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0238others(39): Show | 42 | HG01433.hp1 HG01516.hp1 HG01517.hp1 others(39): Show |
intron_variant | MODIFIER | c.774+1415T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761667 | ||||||
| chr2:30761789
|
T | C | 2 | a0001c0021t0001g0277a0016c0019t0001g0138 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.774+1293A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761789 | ||||||
| chr2:30761805
|
C | A | 91 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0130others(88): Show | 91 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(88): Show |
intron_variant | MODIFIER | c.774+1277G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761805 | ||||||
| chr2:30761906
|
A | G | 1 | a0003c0004t0005g0353 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.774+1176T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761906 | ||||||
| chr2:30761984
|
G | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.774+1098C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30761984 | ||||||
| chr2:30762031
|
A | G | 13 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0238others(10): Show | 13 | HG01106.hp2 HG02572.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.774+1051T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762031 | ||||||
| chr2:30762126
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.774+956G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762126 | ||||||
| chr2:30762175
|
T | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0246others(2): Show | 5 | HG01891.hp2 HG01934.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+907A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762175 | ||||||
| chr2:30762323
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0246others(1): Show | 4 | HG01891.hp2 HG01934.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+759G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762323 | ||||||
| chr2:30762480
|
A | T | 1 | a0001c0002t0004g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.774+602T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762480 | ||||||
| chr2:30762556
|
T | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.774+526A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762556 | ||||||
| chr2:30762582
|
C | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0148a0001c0001t0001g0246others(1): Show | 4 | HG01891.hp2 HG01934.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+500G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762582 | ||||||
| chr2:30762610
|
T | C | 4 | a0001c0001t0002g0176a0001c0001t0002g0235a0001c0001t0002g0243others(1): Show | 4 | HG01433.hp1 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+472A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762610 | ||||||
| chr2:30762630
|
CCTGGCAT others(14): Show |
C | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.774+431_774+451del others(21): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762630 | ||||||
| chr2:30762719
|
C | T | 8 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0238others(5): Show | 8 | HG01106.hp2 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.774+363G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762719 | ||||||
| chr2:30762791
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0002c0003t0001g0343 | 3 | HG01516.hp1 HG01517.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.774+291G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762791 | ||||||
| chr2:30762908
|
G | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.774+174C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762908 | ||||||
| chr2:30762963
|
C | T | 328 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(325): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.774+119G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762963 | ||||||
| chr2:30763419
|
C | G | 1 | a0001c0002t0002g0149 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.700-263G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763419 | ||||||
| chr2:30763430
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0002g0133 | 3 | HG01106.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.700-274A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763430 | ||||||
| chr2:30763476
|
G | A | 39 | a0001c0001t0001g0274a0001c0001t0002g0071a0001c0001t0002g0079others(36): Show | 39 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.700-320C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763476 | ||||||
| chr2:30763779
|
C | T | 62 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(59): Show | 62 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.699+353G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763779 | ||||||
| chr2:30763879
|
T | C | 7 | a0001c0001t0002g0249a0001c0001t0006g0308a0001c0001t0006g0359others(4): Show | 7 | HG02040.hp1 HG02135.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.699+253A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763879 | ||||||
| chr2:30763885
|
G | A | 1 | a0002c0003t0001g0333 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.699+247C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763885 | ||||||
| chr2:30763886
|
T | C | 3 | a0003c0004t0002g0016a0003c0004t0002g0018a0003c0004t0002g0052 | 3 | HG01168.hp2 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.699+246A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763886 | ||||||
| chr2:30763987
|
A | G | 9 | a0001c0001t0001g0274a0001c0001t0002g0062a0001c0001t0002g0063others(6): Show | 9 | HG01515.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+145T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30763987 | ||||||
| chr2:30764044
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0145others(13): Show | 16 | HG01106.hp2 HG01109.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.699+88G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30764044 | ||||||
| chr2:30764123
|
G | T | 335 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.699+9C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30764123 | ||||||
| chr2:30764124
|
T | C | 5 | a0001c0001t0001g0365a0001c0001t0002g0176a0001c0001t0002g0235others(2): Show | 5 | HG01433.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.699+8A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 6/22 | chr2 | 30764124 | ||||||
| chr2:30764379
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0002g0104a0001c0001t0007g0227others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-73T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764379 | ||||||
| chr2:30764468
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.525-162G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764468 | ||||||
| chr2:30764511
|
C | T | 1 | a0002c0003t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.525-205G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764511 | ||||||
| chr2:30764526
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.525-220G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764526 | ||||||
| chr2:30764543
|
A | T | 6 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-237T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764543 | ||||||
| chr2:30764560
|
C | T | 7 | a0001c0001t0001g0365a0001c0001t0002g0235a0001c0001t0002g0243others(4): Show | 7 | HG01884.hp1 HG02040.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.525-254G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764560 | ||||||
| chr2:30764601
|
C | G | 1 | a0003c0004t0002g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.525-295G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764601 | ||||||
| chr2:30764768
|
T | A | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-462A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764768 | ||||||
| chr2:30764779
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.525-473C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764779 | ||||||
| chr2:30764798
|
A | G | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.525-492T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764798 | ||||||
| chr2:30764828
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0054others(98): Show | 104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.525-522C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764828 | ||||||
| chr2:30764835
|
T | C | 169 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(166): Show | 169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.525-529A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764835 | ||||||
| chr2:30764930
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0002g0229others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-624C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30764930 | ||||||
| chr2:30765105
|
G | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0140others(7): Show | 10 | HG01106.hp2 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.525-799C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765105 | ||||||
| chr2:30765234
|
T | A | 157 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(154): Show | 157 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.525-928A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765234 | ||||||
| chr2:30765235
|
T | G | 167 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(164): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.525-929A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765235 | ||||||
| chr2:30765282
|
G | A | 165 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(162): Show | 165 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.525-976C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765282 | ||||||
| chr2:30765509
|
A | G | 310 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0038others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.525-1203T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765509 | ||||||
| chr2:30765539
|
T | A | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-1233A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765539 | ||||||
| chr2:30765583
|
G | A | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.525-1277C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765583 | ||||||
| chr2:30765605
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.525-1299C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765605 | ||||||
| chr2:30765612
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0002g0223a0001c0001t0002g0301others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1306A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765612 | ||||||
| chr2:30765712
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0358a0001c0002t0002g0162 | 3 | HG03654.hp2 NA18971.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.525-1406C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765712 | ||||||
| chr2:30765795
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.525-1489T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765795 | ||||||
| chr2:30765992
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0002g0229others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1686G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765992 | ||||||
| chr2:30766028
|
A | C | 5 | a0001c0002t0001g0291a0001c0002t0001g0300a0001c0002t0001g0304others(2): Show | 5 | NA18941.hp2 NA18966.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.525-1722T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766028 | ||||||
| chr2:30766049
|
C | T | 4 | a0001c0002t0002g0375a0001c0002t0004g0366a0001c0002t0005g0319others(1): Show | 4 | HG00735.hp1 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1743G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766049 | ||||||
| chr2:30766164
|
G | A | 54 | a0001c0001t0001g0094a0001c0001t0001g0136a0001c0001t0001g0145others(51): Show | 54 | HG00438.hp2 HG00558.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.525-1858C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766164 | ||||||
| chr2:30766287
|
G | A | 15 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.525-1981C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766287 | ||||||
| chr2:30766306
|
C | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0054others(110): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.525-2000G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766306 | ||||||
| chr2:30766480
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.525-2174T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766480 | ||||||
| chr2:30766489
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0003g0286 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525-2183G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766489 | ||||||
| chr2:30766697
|
A | T | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2391T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766697 | ||||||
| chr2:30766743
|
T | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(3): Show | 6 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-2437A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766743 | ||||||
| chr2:30766916
|
T | G | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2610A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766916 | ||||||
| chr2:30766917
|
T | A | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2611A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766917 | ||||||
| chr2:30766918
|
C | A | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2612G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766918 | ||||||
| chr2:30766931
|
C | G | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2625G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766931 | ||||||
| chr2:30766941
|
T | G | 1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2635A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766941 | ||||||
| chr2:30766973
|
A | ATGGGCTA others(12): Show |
1 | a0001c0002t0002g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.525-2668_525-2667i others(21): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30766973 | ||||||
| chr2:30767015
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.525-2709C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767015 | ||||||
| chr2:30767082
|
G | A | 1 | a0007c0008t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.525-2776C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767082 | ||||||
| chr2:30767099
|
C | T | 15 | a0001c0001t0001g0365a0001c0001t0002g0234a0001c0001t0002g0235others(12): Show | 15 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-2793G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767099 | ||||||
| chr2:30767462
|
G | T | 306 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0038others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.524+2851C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767462 | ||||||
| chr2:30767530
|
C | T | 13 | a0001c0001t0001g0365a0001c0001t0002g0234a0001c0001t0002g0235others(10): Show | 13 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.524+2783G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767530 | ||||||
| chr2:30767558
|
C | T | 7 | a0001c0002t0002g0316a0002c0003t0001g0004a0002c0003t0001g0217others(4): Show | 8 | HG01074.hp1 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.524+2755G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767558 | ||||||
| chr2:30767714
|
A | C | 310 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0038others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.524+2599T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767714 | ||||||
| chr2:30767723
|
T | C | 7 | a0001c0001t0001g0145a0001c0001t0001g0236a0001c0001t0001g0280others(4): Show | 7 | HG02615.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.524+2590A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767723 | ||||||
| chr2:30767767
|
T | C | 9 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+2546A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767767 | ||||||
| chr2:30767781
|
T | C | 37 | a0001c0001t0001g0114a0001c0001t0001g0148a0001c0001t0001g0365others(34): Show | 37 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.524+2532A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767781 | ||||||
| chr2:30767877
|
C | T | 33 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0140others(30): Show | 33 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.524+2436G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767877 | ||||||
| chr2:30767895
|
C | T | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+2418G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767895 | ||||||
| chr2:30768043
|
G | A | 9 | a0001c0001t0001g0148a0001c0001t0001g0365a0001c0001t0002g0104others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+2270C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768043 | ||||||
| chr2:30768047
|
T | C | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+2266A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768047 | ||||||
| chr2:30768075
|
A | G | 311 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0038others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.524+2238T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768075 | ||||||
| chr2:30768112
|
G | A | 9 | a0001c0001t0001g0148a0001c0001t0001g0365a0001c0001t0002g0104others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+2201C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768112 | ||||||
| chr2:30768123
|
C | T | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+2190G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768123 | ||||||
| chr2:30768210
|
C | T | 5 | a0001c0001t0003g0119a0002c0003t0001g0164a0002c0003t0001g0210others(2): Show | 5 | HG00544.hp1 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+2103G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768210 | ||||||
| chr2:30768278
|
A | G | 20 | a0001c0001t0001g0148a0001c0001t0001g0365a0001c0001t0002g0104others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.524+2035T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768278 | ||||||
| chr2:30768430
|
G | A | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.524+1883C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768430 | ||||||
| chr2:30768509
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.524+1804G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768509 | ||||||
| chr2:30768565
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.524+1748G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768565 | ||||||
| chr2:30768599
|
T | G | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.524+1714A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768599 | ||||||
| chr2:30768673
|
T | G | 1 | a0001c0013t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.524+1640A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768673 | ||||||
| chr2:30768678
|
T | TTTCC | 10 | a0001c0001t0001g0005a0001c0001t0002g0234a0001c0001t0002g0293others(7): Show | 10 | HG01074.hp2 HG02015.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.524+1631_524+1634d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(1): Show |
17 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(14): Show | 17 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.524+1627_524+1634d others(10): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(5): Show |
1 | a0001c0001t0001g0365 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.524+1623_524+1634d others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(9): Show |
3 | a0001c0001t0001g0148a0001c0001t0002g0230a0001c0001t0002g0231 | 3 | HG00738.hp2 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.524+1619_524+1634d others(18): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(13): Show |
11 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG01106.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.524+1615_524+1634d others(22): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(17): Show |
20 | a0001c0001t0001g0127a0001c0001t0001g0145a0001c0001t0001g0236others(17): Show | 20 | HG01109.hp2 HG01433.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.524+1611_524+1634d others(26): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
T | TTTCCTTC others(21): Show |
9 | a0001c0001t0001g0246a0001c0001t0001g0271a0001c0001t0002g0126others(6): Show | 9 | HG01934.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+1607_524+1634d others(30): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768678
|
TTTCC | T | 4 | a0002c0003t0001g0333a0005c0006t0001g0085a0005c0006t0001g0092others(1): Show | 4 | HG00280.hp2 HG01106.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+1631_524+1634d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768678 | ||||||
| chr2:30768703
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.524+1610A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768703 | ||||||
| chr2:30768704
|
T | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+1609A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30768704 | ||||||
| chr2:30769204
|
C | T | 103 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(100): Show | 106 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.524+1109G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769204 | ||||||
| chr2:30769284
|
T | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+1029A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769284 | ||||||
| chr2:30769365
|
C | T | 50 | a0001c0001t0001g0274a0001c0001t0002g0133a0001c0001t0002g0237others(47): Show | 50 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.524+948G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769365 | ||||||
| chr2:30769410
|
C | T | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+903G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769410 | ||||||
| chr2:30769411
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0376a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01109.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+902C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769411 | ||||||
| chr2:30769482
|
G | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524+831C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769482 | ||||||
| chr2:30769522
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.524+791C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769522 | ||||||
| chr2:30769590
|
C | A | 1 | a0003c0004t0002g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.524+723G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769590 | ||||||
| chr2:30769597
|
A | G | 1 | a0002c0003t0002g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.524+716T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769597 | ||||||
| chr2:30769703
|
T | A | 1 | a0001c0002t0002g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.524+610A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769703 | ||||||
| chr2:30769726
|
T | A | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.524+587A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769726 | ||||||
| chr2:30769773
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.524+540G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769773 | ||||||
| chr2:30769795
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.524+518G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769795 | ||||||
| chr2:30769806
|
C | T | 1 | a0001c0002t0003g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.524+507G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769806 | ||||||
| chr2:30769809
|
C | A | 9 | a0001c0001t0002g0047a0001c0001t0002g0216a0001c0001t0002g0356others(6): Show | 9 | HG00423.hp1 HG02071.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+504G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769809 | ||||||
| chr2:30769853
|
G | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(253): Show | 260 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.524+460C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769853 | ||||||
| chr2:30769893
|
C | T | 1 | a0003c0004t0002g0168 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.524+420G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769893 | ||||||
| chr2:30769951
|
C | T | 1 | a0002c0003t0001g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.524+362G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769951 | ||||||
| chr2:30769955
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(52): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.524+358T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769955 | ||||||
| chr2:30769992
|
G | A | 10 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.524+321C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769992 | ||||||
| chr2:30770008
|
C | T | 4 | a0001c0001t0001g0365a0001c0001t0002g0235a0001c0001t0002g0243others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+305G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30770008 | ||||||
| chr2:30770011
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(268): Show | 275 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.524+302C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30770011 | ||||||
| chr2:30770020
|
G | A | 1 | a0002c0003t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.524+293C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30770020 | ||||||
| chr2:30770266
|
G | T | 16 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0001g0236others(13): Show | 16 | HG00738.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.524+47C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30770266 | ||||||
| chr2:30770296
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0004g0095 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.524+17C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30770296 | ||||||
| chr2:30770462
|
C | G | 11 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(8): Show | 11 | HG01433.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-13G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770462 | ||||||
| chr2:30770540
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.388-91G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770540 | ||||||
| chr2:30770588
|
G | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.388-139C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770588 | ||||||
| chr2:30770615
|
T | G | 1 | a0001c0001t0002g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.388-166A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770615 | ||||||
| chr2:30770734
|
G | T | 1 | a0003c0004t0002g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.388-285C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770734 | ||||||
| chr2:30770912
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.388-463C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770912 | ||||||
| chr2:30770942
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0153others(4): Show | 7 | HG00597.hp2 NA18954.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-493G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770942 | ||||||
| chr2:30770952
|
A | G | 105 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(102): Show | 108 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.388-503T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770952 | ||||||
| chr2:30770964
|
G | T | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-515C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30770964 | ||||||
| chr2:30771002
|
G | A | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-553C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771002 | ||||||
| chr2:30771177
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0252 | 2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.388-728C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771177 | ||||||
| chr2:30771272
|
A | G | 19 | a0001c0001t0001g0148a0001c0001t0001g0365a0001c0001t0002g0104others(16): Show | 19 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.388-823T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771272 | ||||||
| chr2:30771356
|
G | A | 3 | a0001c0001t0004g0377a0001c0001t0008g0078a0001c0002t0002g0147 | 3 | HG00741.hp1 HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.388-907C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771356 | ||||||
| chr2:30771431
|
A | G | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-982T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771431 | ||||||
| chr2:30771438
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0002g0104a0001c0001t0002g0223others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-989A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771438 | ||||||
| chr2:30771448
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0118 | 2 | NA18944.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.388-999A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771448 | ||||||
| chr2:30771510
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(239): Show | 246 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.388-1061T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771510 | ||||||
| chr2:30771611
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.388-1162A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771611 | ||||||
| chr2:30771633
|
G | A | 1 | a0001c0001t0003g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-1184C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771633 | ||||||
| chr2:30771760
|
C | T | 1 | a0001c0002t0002g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.388-1311G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771760 | ||||||
| chr2:30771856
|
T | C | 1 | a0001c0001t0005g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.388-1407A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771856 | ||||||
| chr2:30771890
|
G | A | 1 | a0001c0002t0003g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.388-1441C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30771890 | ||||||
| chr2:30772056
|
T | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1607A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772056 | ||||||
| chr2:30772096
|
C | T | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232 | 3 | HG00738.hp2 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.388-1647G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772096 | ||||||
| chr2:30772161
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(305): Show | 312 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.388-1712A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772161 | ||||||
| chr2:30772304
|
C | T | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-1855G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772304 | ||||||
| chr2:30772363
|
C | A | 14 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-1914G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772363 | ||||||
| chr2:30772377
|
C | G | 9 | a0001c0001t0001g0148a0001c0001t0001g0365a0001c0001t0002g0104others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-1928G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772377 | ||||||
| chr2:30772403
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.388-1954G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772403 | ||||||
| chr2:30772621
|
A | T | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.388-2172T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772621 | ||||||
| chr2:30772682
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.388-2233G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772682 | ||||||
| chr2:30772713
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(213): Show | 220 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.388-2264A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772713 | ||||||
| chr2:30772723
|
T | C | 6 | a0001c0001t0001g0090a0001c0001t0001g0142a0001c0001t0001g0224others(3): Show | 6 | HG02451.hp2 HG02622.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-2274A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772723 | ||||||
| chr2:30772786
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.388-2337T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772786 | ||||||
| chr2:30772822
|
CT | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(279): Show | 286 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.388-2374delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772822 | ||||||
| chr2:30772835
|
T | C | 1 | a0001c0001t0006g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.388-2386A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772835 | ||||||
| chr2:30772853
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(227): Show | 234 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.388-2404G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772853 | ||||||
| chr2:30773014
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(248): Show | 255 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.388-2565A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773014 | ||||||
| chr2:30773027
|
T | G | 1 | a0002c0003t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.388-2578A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773027 | ||||||
| chr2:30773052
|
C | A | 1 | a0001c0020t0004g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.388-2603G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773052 | ||||||
| chr2:30773104
|
G | A | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-2655C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773104 | ||||||
| chr2:30773113
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(303): Show | 310 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.388-2664A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773113 | ||||||
| chr2:30773221
|
G | A | 1 | a0002c0003t0001g0333 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.387+2709C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773221 | ||||||
| chr2:30773272
|
G | A | 1 | a0002c0003t0001g0171 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.387+2658C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773272 | ||||||
| chr2:30773327
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(72): Show | 76 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.387+2603T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773327 | ||||||
| chr2:30773331
|
ACT | A | 5 | a0001c0001t0001g0148a0001c0001t0002g0104a0001c0001t0002g0223others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2597_387+2598d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773331 | ||||||
| chr2:30773349
|
G | GA | 25 | a0001c0001t0001g0148a0001c0001t0001g0238a0001c0001t0001g0279others(22): Show | 25 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.387+2580dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773349 | ||||||
| chr2:30773362
|
A | C | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.387+2568T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773362 | ||||||
| chr2:30773476
|
A | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.387+2454T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773476 | ||||||
| chr2:30773614
|
T | C | 9 | a0001c0001t0001g0199a0001c0002t0002g0193a0001c0002t0002g0194others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.387+2316A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773614 | ||||||
| chr2:30773698
|
G | A | 4 | a0001c0001t0004g0124a0001c0001t0004g0157a0002c0003t0004g0154others(1): Show | 4 | HG03017.hp1 HG03491.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+2232C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773698 | ||||||
| chr2:30773733
|
C | T | 3 | a0001c0001t0006g0308a0001c0001t0006g0359a0003c0004t0005g0353 | 3 | HG02040.hp1 HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.387+2197G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773733 | ||||||
| chr2:30773836
|
T | C | 4 | a0001c0002t0001g0014a0005c0006t0001g0085a0005c0006t0001g0092others(1): Show | 4 | HG00280.hp2 HG01192.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2094A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30773836 | ||||||
| chr2:30774004
|
A | G | 5 | a0001c0001t0001g0148a0001c0001t0002g0104a0001c0001t0002g0223others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1926T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774004 | ||||||
| chr2:30774017
|
CAG | C | 26 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0136others(23): Show | 26 | HG00738.hp2 HG01433.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.387+1911_387+1912d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774017 | ||||||
| chr2:30774073
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(239): Show | 246 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.387+1857C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774073 | ||||||
| chr2:30774121
|
A | T | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.387+1809T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774121 | ||||||
| chr2:30774385
|
A | C | 1 | a0001c0020t0004g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.387+1545T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774385 | ||||||
| chr2:30774427
|
G | A | 28 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0136others(25): Show | 28 | HG00738.hp2 HG01433.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.387+1503C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774427 | ||||||
| chr2:30774447
|
A | T | 2 | a0001c0001t0001g0148a0001c0001t0002g0104 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.387+1483T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774447 | ||||||
| chr2:30774906
|
T | G | 2 | a0001c0001t0002g0185a0001c0002t0001g0169 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.387+1024A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30774906 | ||||||
| chr2:30775032
|
A | G | 103 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(100): Show | 106 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.387+898T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775032 | ||||||
| chr2:30775119
|
T | C | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.387+811A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775119 | ||||||
| chr2:30775159
|
T | G | 10 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+771A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775159 | ||||||
| chr2:30775289
|
A | T | 10 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+641T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775289 | ||||||
| chr2:30775353
|
G | A | 1 | a0001c0002t0005g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.387+577C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775353 | ||||||
| chr2:30775405
|
A | C | 2 | a0001c0001t0003g0043a0001c0002t0003g0033 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.387+525T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775405 | ||||||
| chr2:30775456
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(99): Show | 103 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.387+474G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775456 | ||||||
| chr2:30775458
|
G | T | 1 | a0001c0020t0004g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.387+472C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775458 | ||||||
| chr2:30775469
|
T | TA | 6 | a0001c0001t0002g0237a0001c0001t0004g0064a0001c0001t0005g0101others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+460dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775469 | ||||||
| chr2:30775469
|
TA | T | 11 | a0001c0001t0001g0187a0001c0001t0002g0234a0001c0001t0002g0293others(8): Show | 11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.387+460delT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775469 | ||||||
| chr2:30775470
|
A | T | 5 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(2): Show | 5 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+460T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775470 | ||||||
| chr2:30775484
|
A | G | 10 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+446T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775484 | ||||||
| chr2:30775532
|
A | G | 5 | a0001c0001t0002g0357a0001c0001t0005g0367a0002c0003t0004g0025others(2): Show | 5 | HG02300.hp2 HG03831.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+398T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775532 | ||||||
| chr2:30775910
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0140 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.387+20G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30775910 | ||||||
| chr2:30776151
|
T | A | 1 | a0002c0003t0001g0378 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.272-106A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776151 | ||||||
| chr2:30776157
|
AT | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(140): Show | 144 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.272-113delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776157 | ||||||
| chr2:30776325
|
G | A | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.272-280C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776325 | ||||||
| chr2:30776402
|
A | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-357T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776402 | ||||||
| chr2:30776422
|
A | C | 4 | a0001c0001t0001g0238a0001c0001t0001g0279a0001c0001t0002g0222others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-377T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776422 | ||||||
| chr2:30776482
|
A | G | 9 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.272-437T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776482 | ||||||
| chr2:30776586
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.272-541T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776586 | ||||||
| chr2:30776610
|
T | C | 9 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.272-565A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776610 | ||||||
| chr2:30776702
|
G | C | 35 | a0001c0001t0001g0114a0001c0001t0001g0148a0001c0001t0001g0365others(32): Show | 35 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.272-657C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776702 | ||||||
| chr2:30776874
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.271+693C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776874 | ||||||
| chr2:30776941
|
G | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.271+626C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776941 | ||||||
| chr2:30776944
|
G | C | 20 | a0001c0001t0001g0114a0001c0001t0001g0148a0001c0001t0002g0104others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.271+623C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776944 | ||||||
| chr2:30776967
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(97): Show | 101 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.271+600C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776967 | ||||||
| chr2:30776994
|
G | C | 19 | a0001c0001t0001g0247a0001c0002t0001g0002a0001c0002t0001g0003others(16): Show | 21 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.271+573C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776994 | ||||||
| chr2:30777145
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0004g0095 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.271+422G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777145 | ||||||
| chr2:30777229
|
G | A | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.271+338C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777229 | ||||||
| chr2:30777350
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0002g0230a0001c0001t0002g0231others(1): Show | 4 | HG00738.hp2 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+217C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777350 | ||||||
| chr2:30777350
|
G | T | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.271+217C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777350 | ||||||
| chr2:30777377
|
T | G | 22 | a0001c0001t0001g0148a0001c0001t0001g0238a0001c0001t0001g0279others(19): Show | 22 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.271+190A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777377 | ||||||
| chr2:30777442
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.271+125A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777442 | ||||||
| chr2:30777467
|
C | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.271+100G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777467 | ||||||
| chr2:30777471
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.271+96G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777471 | ||||||
| chr2:30777504
|
G | C | 59 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0130others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.271+63C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30777504 | ||||||
| chr2:30777673
|
GT | G | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0002g0229others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-35delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30777673 | ||||||
| chr2:30777696
|
C | T | 18 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-57G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30777696 | ||||||
| chr2:30777747
|
G | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0271 | 2 | HG01934.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.199-108C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30777747 | ||||||
| chr2:30777777
|
C | T | 17 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(14): Show | 17 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.199-138G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30777777 | ||||||
| chr2:30777841
|
A | G | 1 | a0002c0003t0011g0335 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.199-202T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30777841 | ||||||
| chr2:30778028
|
A | G | 2 | a0002c0003t0004g0006a0005c0006t0004g0151 | 2 | HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.199-389T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778028 | ||||||
| chr2:30778041
|
T | C | 20 | a0001c0001t0001g0114a0001c0001t0002g0223a0001c0001t0002g0249others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.199-402A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778041 | ||||||
| chr2:30778234
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0004g0095 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.199-595G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778234 | ||||||
| chr2:30778283
|
G | GTGGTTAT others(3): Show |
2 | a0001c0001t0008g0078a0012c0011t0002g0131 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.199-654_199-645dup others(10): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778283 | ||||||
| chr2:30778301
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(264): Show | 271 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.199-662T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778301 | ||||||
| chr2:30778334
|
A | T | 3 | a0001c0001t0002g0071a0001c0001t0002g0079a0001c0001t0002g0240 | 3 | HG02257.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.199-695T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778334 | ||||||
| chr2:30778372
|
G | C | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.199-733C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778372 | ||||||
| chr2:30778539
|
T | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0130others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.199-900A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778539 | ||||||
| chr2:30778568
|
C | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0130others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.199-929G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778568 | ||||||
| chr2:30778672
|
G | C | 2 | a0001c0001t0008g0078a0012c0011t0002g0131 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.199-1033C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778672 | ||||||
| chr2:30778739
|
G | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(238): Show | 245 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.199-1100C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778739 | ||||||
| chr2:30778796
|
C | T | 9 | a0001c0001t0001g0088a0001c0001t0001g0118a0001c0001t0001g0140others(6): Show | 9 | NA18906.hp1 NA18939.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-1157G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778796 | ||||||
| chr2:30778831
|
T | C | 1 | a0002c0003t0002g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.199-1192A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778831 | ||||||
| chr2:30778891
|
C | T | 3 | a0001c0001t0002g0379a0002c0003t0001g0378a0016c0019t0001g0138 | 3 | HG02258.hp2 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.199-1252G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778891 | ||||||
| chr2:30778933
|
G | A | 31 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0136others(28): Show | 31 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-1294C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30778933 | ||||||
| chr2:30779049
|
C | T | 4 | a0002c0003t0001g0027a0002c0003t0001g0048a0002c0003t0001g0165others(1): Show | 4 | NA18939.hp2 NA18956.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1410G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779049 | ||||||
| chr2:30779077
|
C | G | 1 | a0001c0002t0002g0258 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.199-1438G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779077 | ||||||
| chr2:30779232
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.199-1593G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779232 | ||||||
| chr2:30779256
|
C | T | 6 | a0001c0001t0002g0237a0001c0001t0004g0064a0001c0001t0005g0101others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1617G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779256 | ||||||
| chr2:30779264
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(142): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.199-1625G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779264 | ||||||
| chr2:30779317
|
C | T | 1 | a0005c0006t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.199-1678G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779317 | ||||||
| chr2:30779318
|
G | A | 4 | a0001c0001t0002g0044a0001c0002t0001g0017a0001c0002t0002g0112others(1): Show | 4 | HG02083.hp2 NA18948.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1679C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779318 | ||||||
| chr2:30779355
|
T | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(240): Show | 247 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.199-1716A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779355 | ||||||
| chr2:30779366
|
T | C | 15 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1727A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779366 | ||||||
| chr2:30779461
|
G | T | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-1822C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779461 | ||||||
| chr2:30779546
|
G | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.199-1907C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779546 | ||||||
| chr2:30779587
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199-1948G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779587 | ||||||
| chr2:30779889
|
T | C | 1 | a0003c0004t0002g0065 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.199-2250A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779889 | ||||||
| chr2:30779985
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(142): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.199-2346T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779985 | ||||||
| chr2:30780097
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(78): Show | 82 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.199-2458G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780097 | ||||||
| chr2:30780153
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-2514C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780153 | ||||||
| chr2:30780411
|
G | C | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.199-2772C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780411 | ||||||
| chr2:30780454
|
G | C | 64 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0130others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.199-2815C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780454 | ||||||
| chr2:30780579
|
A | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(140): Show | 144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.199-2940T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780579 | ||||||
| chr2:30780580
|
AC | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(140): Show | 144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.199-2942delG | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780580 | ||||||
| chr2:30780821
|
C | T | 1 | a0003c0004t0005g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.199-3182G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780821 | ||||||
| chr2:30780932
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-3293A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780932 | ||||||
| chr2:30780933
|
G | A | 63 | a0001c0001t0001g0090a0001c0001t0001g0129a0001c0001t0001g0130others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-3294C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780933 | ||||||
| chr2:30781187
|
C | A | 1 | a0001c0001t0001g0365 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199-3548G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781187 | ||||||
| chr2:30781343
|
C | T | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-3704G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781343 | ||||||
| chr2:30781499
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-3860C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781499 | ||||||
| chr2:30781500
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0086others(13): Show | 16 | HG00597.hp2 HG01928.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-3861G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781500 | ||||||
| chr2:30781602
|
G | A | 1 | a0003c0004t0005g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.199-3963C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781602 | ||||||
| chr2:30781615
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.199-3976C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781615 | ||||||
| chr2:30781716
|
G | A | 1 | a0002c0003t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-4077C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781716 | ||||||
| chr2:30781758
|
C | T | 7 | a0001c0002t0001g0309a0001c0002t0002g0316a0002c0003t0001g0004others(4): Show | 8 | HG00639.hp1 HG01074.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-4119G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781758 | ||||||
| chr2:30781885
|
T | C | 4 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0001t0008g0078others(1): Show | 4 | HG02055.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-4246A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30781885 | ||||||
| chr2:30782037
|
G | T | 89 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0129others(86): Show | 89 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.199-4398C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782037 | ||||||
| chr2:30782168
|
G | A | 1 | a0001c0002t0002g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.199-4529C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782168 | ||||||
| chr2:30782212
|
T | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(304): Show | 311 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.199-4573A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782212 | ||||||
| chr2:30782213
|
T | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(304): Show | 311 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.199-4574A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782213 | ||||||
| chr2:30782255
|
C | T | 4 | a0001c0001t0001g0365a0001c0001t0002g0235a0001c0001t0002g0243others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-4616G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782255 | ||||||
| chr2:30782263
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(298): Show | 305 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.199-4624G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782263 | ||||||
| chr2:30782293
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199-4654G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782293 | ||||||
| chr2:30782310
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(174): Show | 178 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.199-4671A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782310 | ||||||
| chr2:30782407
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.198+4721G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782407 | ||||||
| chr2:30782431
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+4697A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782431 | ||||||
| chr2:30782546
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(281): Show | 288 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.198+4582C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782546 | ||||||
| chr2:30782582
|
T | A | 1 | a0002c0003t0001g0325 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.198+4546A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782582 | ||||||
| chr2:30782618
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(174): Show | 178 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.198+4510T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782618 | ||||||
| chr2:30782642
|
C | T | 1 | a0001c0002t0001g0015 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.198+4486G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782642 | ||||||
| chr2:30782730
|
C | A | 1 | a0002c0003t0001g0317 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.198+4398G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782730 | ||||||
| chr2:30782757
|
C | G | 126 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0127others(123): Show | 126 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+4371G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782757 | ||||||
| chr2:30782779
|
A | G | 1 | a0001c0001t0002g0357 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+4349T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782779 | ||||||
| chr2:30782917
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.198+4211A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782917 | ||||||
| chr2:30782973
|
C | T | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+4155G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782973 | ||||||
| chr2:30782974
|
G | A | 1 | a0002c0003t0001g0027 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.198+4154C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782974 | ||||||
| chr2:30783005
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(298): Show | 305 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.198+4123T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783005 | ||||||
| chr2:30783116
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+4012A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783116 | ||||||
| chr2:30783161
|
T | G | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.198+3967A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783161 | ||||||
| chr2:30783198
|
G | T | 100 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(97): Show | 103 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.198+3930C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783198 | ||||||
| chr2:30783200
|
G | C | 102 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(99): Show | 105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.198+3928C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783200 | ||||||
| chr2:30783203
|
C | T | 105 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0087others(102): Show | 108 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.198+3925G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783203 | ||||||
| chr2:30783233
|
A | G | 1 | a0001c0002t0001g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+3895T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783233 | ||||||
| chr2:30783267
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(299): Show | 306 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.198+3861A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783267 | ||||||
| chr2:30783327
|
G | A | 1 | a0002c0003t0004g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.198+3801C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783327 | ||||||
| chr2:30783373
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+3755G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783373 | ||||||
| chr2:30783510
|
T | C | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+3618A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783510 | ||||||
| chr2:30783561
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+3567C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783561 | ||||||
| chr2:30783582
|
C | A | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.198+3546G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783582 | ||||||
| chr2:30783583
|
T | C | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.198+3545A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783583 | ||||||
| chr2:30783768
|
C | T | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+3360G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783768 | ||||||
| chr2:30783770
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+3358G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783770 | ||||||
| chr2:30783835
|
G | A | 5 | a0001c0001t0002g0357a0001c0001t0005g0367a0002c0003t0004g0025others(2): Show | 5 | HG02300.hp2 HG03831.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+3293C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783835 | ||||||
| chr2:30783858
|
C | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(295): Show | 302 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.198+3270G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783858 | ||||||
| chr2:30783902
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(173): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.198+3226A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783902 | ||||||
| chr2:30783906
|
T | C | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+3222A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783906 | ||||||
| chr2:30784022
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+3106C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784022 | ||||||
| chr2:30784057
|
G | T | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+3071C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784057 | ||||||
| chr2:30784095
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+3033C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784095 | ||||||
| chr2:30784188
|
G | GA | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+2939dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784188 | ||||||
| chr2:30784269
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+2859A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784269 | ||||||
| chr2:30784272
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+2856G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784272 | ||||||
| chr2:30784457
|
C | T | 53 | a0001c0001t0001g0241a0001c0001t0001g0274a0001c0001t0002g0237others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.198+2671G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784457 | ||||||
| chr2:30784468
|
C | T | 41 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(38): Show | 41 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.198+2660G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784468 | ||||||
| chr2:30784523
|
A | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(129): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+2605T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784523 | ||||||
| chr2:30784534
|
T | C | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.198+2594A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784534 | ||||||
| chr2:30784625
|
G | A | 37 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(34): Show | 37 | HG01433.hp1 HG01884.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.198+2503C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784625 | ||||||
| chr2:30784658
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.198+2470G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784658 | ||||||
| chr2:30784761
|
C | A | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+2367G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784761 | ||||||
| chr2:30784813
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(170): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.198+2315G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784813 | ||||||
| chr2:30784926
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(130): Show | 134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.198+2202G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784926 | ||||||
| chr2:30784962
|
A | T | 3 | a0001c0001t0002g0223a0001c0001t0002g0301a0001c0002t0002g0221 | 3 | HG02055.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.198+2166T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784962 | ||||||
| chr2:30785096
|
T | C | 44 | a0001c0001t0001g0199a0001c0001t0001g0274a0001c0001t0001g0284others(41): Show | 44 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.198+2032A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785096 | ||||||
| chr2:30785108
|
A | C | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+2020T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785108 | ||||||
| chr2:30785128
|
T | A | 4 | a0001c0001t0004g0124a0001c0001t0004g0157a0002c0003t0004g0154others(1): Show | 4 | HG03017.hp1 HG03491.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+2000A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785128 | ||||||
| chr2:30785173
|
C | A | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+1955G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785173 | ||||||
| chr2:30785185
|
C | A | 5 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0294others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+1943G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785185 | ||||||
| chr2:30785222
|
A | G | 1 | a0004c0005t0001g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198+1906T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785222 | ||||||
| chr2:30785268
|
T | G | 93 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0179others(90): Show | 96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.198+1860A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785268 | ||||||
| chr2:30785276
|
T | C | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+1852A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785276 | ||||||
| chr2:30785380
|
G | C | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+1748C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785380 | ||||||
| chr2:30785465
|
G | A | 122 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0127others(119): Show | 122 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.198+1663C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785465 | ||||||
| chr2:30785704
|
C | T | 7 | a0001c0001t0002g0237a0001c0001t0004g0064a0001c0001t0004g0143others(4): Show | 7 | HG01109.hp2 HG01496.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1424G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785704 | ||||||
| chr2:30785876
|
G | A | 3 | a0001c0002t0004g0366a0001c0002t0005g0319a0002c0003t0004g0285 | 3 | HG00735.hp1 HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.198+1252C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785876 | ||||||
| chr2:30785899
|
T | TA | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+1228dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30785899 | ||||||
| chr2:30786021
|
A | G | 46 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(43): Show | 46 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.198+1107T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786021 | ||||||
| chr2:30786034
|
GGT | G | 122 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0127others(119): Show | 122 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.198+1092_198+1093d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786034 | ||||||
| chr2:30786345
|
G | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(148): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.198+783C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786345 | ||||||
| chr2:30786440
|
C | G | 332 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(329): Show | 336 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.198+688G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786440 | ||||||
| chr2:30786534
|
A | G | 44 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0134others(41): Show | 44 | HG00738.hp2 HG01433.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.198+594T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786534 | ||||||
| chr2:30786612
|
C | T | 1 | a0005c0006t0001g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.198+516G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786612 | ||||||
| chr2:30786613
|
G | A | 123 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0127others(120): Show | 123 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.198+515C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786613 | ||||||
| chr2:30786729
|
G | C | 43 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0136others(40): Show | 43 | HG00738.hp2 HG01433.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.198+399C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786729 | ||||||
| chr2:30786830
|
C | T | 21 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0001g0236others(18): Show | 21 | HG00738.hp2 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.198+298G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786830 | ||||||
| chr2:30786905
|
A | G | 1 | a0005c0006t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.198+223T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786905 | ||||||
| chr2:30786921
|
G | T | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.198+207C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786921 | ||||||
| chr2:30787006
|
T | C | 1 | a0002c0003t0001g0378 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.198+122A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30787006 | ||||||
| chr2:30787010
|
T | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(351): Show | 358 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.198+118A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30787010 | ||||||
| chr2:30787047
|
C | T | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+81G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30787047 | ||||||
| chr2:30787111
|
G | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0038others(344): Show | 351 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.198+17C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30787111 | ||||||
| chr2:30787361
|
T | C | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.-32-4A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787361 | ||||||
| chr2:30787395
|
A | G | 1 | a0001c0002t0002g0066 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-32-38T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787395 | ||||||
| chr2:30787586
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-32-229G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787586 | ||||||
| chr2:30787613
|
T | C | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-32-256A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787613 | ||||||
| chr2:30787764
|
G | A | 1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32-407C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787764 | ||||||
| chr2:30787767
|
C | T | 6 | a0001c0001t0002g0126a0001c0001t0004g0064a0001c0001t0004g0143others(3): Show | 6 | HG01109.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-410G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787767 | ||||||
| chr2:30787824
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-32-467A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787824 | ||||||
| chr2:30787850
|
T | A | 1 | a0001c0002t0005g0319 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-32-493A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787850 | ||||||
| chr2:30787923
|
C | A | 2 | a0001c0001t0001g0290a0002c0003t0001g0028 | 2 | HG00597.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-32-566G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787923 | ||||||
| chr2:30787946
|
G | C | 70 | a0001c0001t0001g0054a0001c0001t0001g0070a0001c0001t0001g0086others(67): Show | 71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-32-589C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787946 | ||||||
| chr2:30787955
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0008g0078 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-32-598A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30787955 | ||||||
| chr2:30788058
|
C | T | 162 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0070others(159): Show | 163 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.-32-701G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788058 | ||||||
| chr2:30788061
|
T | C | 7 | a0001c0002t0001g0309a0001c0002t0002g0336a0001c0002t0002g0352others(4): Show | 7 | HG00639.hp1 HG01168.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-704A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788061 | ||||||
| chr2:30788116
|
A | G | 15 | a0001c0001t0001g0094a0001c0001t0001g0148a0001c0001t0001g0224others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-759T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788116 | ||||||
| chr2:30788164
|
T | C | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-807A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788164 | ||||||
| chr2:30788198
|
G | A | 1 | a0004c0005t0002g0259 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-32-841C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788198 | ||||||
| chr2:30788247
|
A | G | 2 | a0001c0001t0001g0146a0001c0002t0002g0147 | 2 | HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-32-890T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788247 | ||||||
| chr2:30788258
|
A | G | 25 | a0001c0001t0001g0114a0001c0001t0002g0249a0001c0001t0002g0252others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32-901T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788258 | ||||||
| chr2:30788269
|
G | A | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-32-912C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788269 | ||||||
| chr2:30788273
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0002g0235a0001c0001t0002g0243 | 3 | HG03041.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-916A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788273 | ||||||
| chr2:30788349
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0246a0001c0001t0005g0350 | 3 | HG01884.hp1 HG01934.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-32-992T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788349 | ||||||
| chr2:30788363
|
G | A | 2 | a0001c0002t0002g0287a0003c0004t0005g0374 | 2 | NA18978.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-32-1006C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788363 | ||||||
| chr2:30788406
|
G | A | 2 | a0001c0001t0001g0134a0001c0002t0005g0113 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-32-1049C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788406 | ||||||
| chr2:30788421
|
T | C | 1 | a0001c0001t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-32-1064A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788421 | ||||||
| chr2:30788430
|
T | C | 4 | a0001c0001t0005g0158a0001c0002t0002g0162a0001c0002t0005g0011others(1): Show | 4 | NA18954.hp1 NA18957.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-1073A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788430 | ||||||
| chr2:30788495
|
T | C | 1 | a0005c0006t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-32-1138A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788495 | ||||||
| chr2:30788964
|
G | T | 1 | a0001c0001t0003g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-32-1607C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30788964 | ||||||
| chr2:30789131
|
G | A | 1 | a0002c0003t0002g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-32-1774C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789131 | ||||||
| chr2:30789196
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-1839A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789196 | ||||||
| chr2:30789290
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-32-1933C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789290 | ||||||
| chr2:30789306
|
G | C | 1 | a0002c0003t0001g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-32-1949C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789306 | ||||||
| chr2:30789340
|
A | C | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-32-1983T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789340 | ||||||
| chr2:30789417
|
T | C | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-2060A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789417 | ||||||
| chr2:30789614
|
T | C | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-32-2257A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789614 | ||||||
| chr2:30789625
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-32-2268A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789625 | ||||||
| chr2:30789701
|
G | C | 1 | a0001c0002t0002g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32-2344C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789701 | ||||||
| chr2:30789754
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32-2397C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789754 | ||||||
| chr2:30789945
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-32-2588C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789945 | ||||||
| chr2:30789971
|
G | A | 22 | a0001c0001t0001g0114a0001c0001t0001g0148a0001c0001t0001g0260others(19): Show | 22 | HG00423.hp2 HG00673.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-2614C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30789971 | ||||||
| chr2:30790063
|
G | A | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-2706C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790063 | ||||||
| chr2:30790078
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32-2721C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790078 | ||||||
| chr2:30790178
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32-2821G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790178 | ||||||
| chr2:30790275
|
C | T | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-2918G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790275 | ||||||
| chr2:30790504
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(59): Show | 63 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-32-3147T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790504 | ||||||
| chr2:30790572
|
C | T | 2 | a0001c0001t0001g0116a0001c0002t0002g0082 | 2 | HG00323.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-32-3215G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790572 | ||||||
| chr2:30790773
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0002g0068a0001c0001t0002g0126others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-3416C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790773 | ||||||
| chr2:30790852
|
G | C | 1 | a0001c0002t0002g0324 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-32-3495C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790852 | ||||||
| chr2:30790984
|
C | T | 4 | a0001c0002t0004g0366a0001c0002t0005g0319a0003c0004t0005g0117others(1): Show | 4 | HG00323.hp1 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-3627G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790984 | ||||||
| chr2:30790991
|
C | G | 1 | a0001c0002t0002g0174 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-32-3634G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30790991 | ||||||
| chr2:30791000
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32-3643T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791000 | ||||||
| chr2:30791064
|
T | A | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-3707A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791064 | ||||||
| chr2:30791084
|
C | T | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-3727G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791084 | ||||||
| chr2:30791217
|
A | C | 1 | a0013c0012t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-32-3860T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791217 | ||||||
| chr2:30791300
|
A | C | 79 | a0001c0001t0001g0049a0001c0001t0001g0086a0001c0001t0001g0087others(76): Show | 80 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-32-3943T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791300 | ||||||
| chr2:30791356
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0271others(1): Show | 4 | HG02976.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-3999G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791356 | ||||||
| chr2:30791369
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-4012T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791369 | ||||||
| chr2:30791596
|
T | A | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-4239A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791596 | ||||||
| chr2:30791665
|
A | G | 1 | a0001c0001t0005g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-32-4308T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791665 | ||||||
| chr2:30791760
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-32-4403A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791760 | ||||||
| chr2:30791997
|
C | T | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-4640G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30791997 | ||||||
| chr2:30792147
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-32-4790A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792147 | ||||||
| chr2:30792165
|
T | A | 4 | a0001c0002t0002g0352a0002c0003t0001g0004a0002c0003t0001g0312others(1): Show | 5 | HG01074.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-4808A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792165 | ||||||
| chr2:30792257
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-32-4900C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792257 | ||||||
| chr2:30792423
|
A | G | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-5066T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792423 | ||||||
| chr2:30792734
|
G | A | 1 | a0002c0003t0001g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-32-5377C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792734 | ||||||
| chr2:30792789
|
C | T | 1 | a0002c0003t0001g0334 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-32-5432G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792789 | ||||||
| chr2:30792790
|
G | A | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-5433C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792790 | ||||||
| chr2:30792890
|
T | C | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0002t0005g0278others(2): Show | 5 | HG02451.hp2 HG06807.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-5533A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792890 | ||||||
| chr2:30792981
|
G | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(333): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-32-5624C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30792981 | ||||||
| chr2:30793068
|
G | A | 3 | a0001c0001t0003g0108a0001c0001t0003g0122a0002c0003t0004g0107 | 3 | NA18966.hp2 NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-32-5711C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793068 | ||||||
| chr2:30793218
|
G | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(265): Show | 271 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.-32-5861C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793218 | ||||||
| chr2:30793219
|
G | T | 10 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(7): Show | 10 | HG01496.hp2 HG02572.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-5862C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793219 | ||||||
| chr2:30793327
|
A | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 57 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-32-5970T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793327 | ||||||
| chr2:30793373
|
A | C | 170 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0070others(167): Show | 172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.-32-6016T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793373 | ||||||
| chr2:30793393
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-32-6036C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793393 | ||||||
| chr2:30793468
|
C | T | 21 | a0001c0001t0001g0114a0001c0001t0001g0260a0001c0001t0002g0249others(18): Show | 21 | HG00423.hp2 HG00673.hp1 HG02738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32-6111G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793468 | ||||||
| chr2:30793599
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32-6242T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793599 | ||||||
| chr2:30793616
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0271others(1): Show | 4 | HG02976.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-6259G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793616 | ||||||
| chr2:30793725
|
T | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0279a0001c0001t0002g0223others(1): Show | 4 | HG02886.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-6368A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793725 | ||||||
| chr2:30793896
|
T | C | 1 | a0002c0003t0001g0378 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-32-6539A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793896 | ||||||
| chr2:30793924
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-32-6567T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30793924 | ||||||
| chr2:30794149
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32-6792C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794149 | ||||||
| chr2:30794198
|
A | G | 3 | a0001c0001t0001g0365a0001c0001t0002g0275a0007c0008t0001g0276 | 3 | HG02647.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-32-6841T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794198 | ||||||
| chr2:30794320
|
G | A | 3 | a0001c0002t0005g0319a0003c0004t0005g0117a0014c0018t0001g0326 | 3 | HG00323.hp1 HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-32-6963C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794320 | ||||||
| chr2:30794390
|
G | C | 1 | a0008c0009t0004g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-32-7033C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794390 | ||||||
| chr2:30794475
|
GAAAACAG others(14): Show |
G | 1 | a0002c0003t0002g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-32-7139_-32-7119d others(23): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794475 | ||||||
| chr2:30794596
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-32-7239T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794596 | ||||||
| chr2:30794712
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-32-7355C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794712 | ||||||
| chr2:30794868
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32-7511G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794868 | ||||||
| chr2:30794938
|
TTGAG | T | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-7585_-32-7582d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30794938 | ||||||
| chr2:30795068
|
T | C | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-7711A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795068 | ||||||
| chr2:30795222
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(40): Show | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-32-7865T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795222 | ||||||
| chr2:30795347
|
G | T | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-7990C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795347 | ||||||
| chr2:30795385
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32-8028A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795385 | ||||||
| chr2:30795530
|
T | C | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-8173A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795530 | ||||||
| chr2:30795731
|
T | C | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-8374A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795731 | ||||||
| chr2:30795736
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 197 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-32-8379C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795736 | ||||||
| chr2:30795801
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-32-8444A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795801 | ||||||
| chr2:30795820
|
C | T | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-32-8463G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30795820 | ||||||
| chr2:30796017
|
A | C | 1 | a0001c0001t0004g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-8660T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796017 | ||||||
| chr2:30796041
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-32-8684T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796041 | ||||||
| chr2:30796093
|
C | A | 1 | a0001c0001t0002g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-32-8736G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796093 | ||||||
| chr2:30796131
|
TATATATA others(21): Show |
T | 1 | a0001c0001t0001g0208 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-32-8802_-32-8775d others(30): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796131 | ||||||
| chr2:30796144
|
G | GTA | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(46): Show | 50 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-32-8789_-32-8788d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796144 | ||||||
| chr2:30796146
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0002g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-32-8790_-32-8789i others(52): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796146 | ||||||
| chr2:30796146
|
A | ATATATAT others(45): Show |
6 | a0001c0001t0001g0090a0001c0001t0002g0061a0001c0001t0002g0068others(3): Show | 6 | HG02622.hp2 HG02897.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-8841_-32-8790d others(54): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796146 | ||||||
| chr2:30796146
|
A | ATATATAT others(25): Show |
1 | a0001c0002t0002g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32-8790_-32-8789i others(34): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796146 | ||||||
| chr2:30796146
|
A | G | 163 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0070others(160): Show | 165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-32-8789T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796146 | ||||||
| chr2:30796157
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-32-8800A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796157 | ||||||
| chr2:30796172
|
G | GTA | 21 | a0001c0001t0001g0114a0001c0001t0001g0260a0001c0001t0002g0249others(18): Show | 21 | HG00423.hp2 HG00673.hp1 HG02738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32-8817_-32-8816d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796172 | ||||||
| chr2:30796173
|
T | TATATATA others(5): Show |
2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-32-8817_-32-8816i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796173 | ||||||
| chr2:30796173
|
T | TATATATA others(17): Show |
5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-8817_-32-8816i others(26): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796173 | ||||||
| chr2:30796175
|
T | TATATATA others(5): Show |
3 | a0001c0001t0002g0229a0001c0001t0002g0235a0001c0001t0002g0243 | 3 | HG03041.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-8819_-32-8818i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796175 | ||||||
| chr2:30796177
|
T | TATATACA others(5): Show |
7 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(4): Show | 7 | HG02257.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-8821_-32-8820i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796177 | ||||||
| chr2:30796183
|
T | C | 2 | a0001c0001t0005g0242a0001c0002t0012g0239 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-32-8826A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796183 | ||||||
| chr2:30796185
|
C | CATATATA others(45): Show |
1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-32-8829_-32-8828i others(54): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796185 | ||||||
| chr2:30796186
|
A | ACACATAT others(5): Show |
1 | a0001c0002t0012g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-32-8830_-32-8829i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796186 | ||||||
| chr2:30796186
|
A | ACATATAT others(45): Show |
1 | a0001c0001t0005g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-32-8830_-32-8829i others(54): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796186 | ||||||
| chr2:30796186
|
A | ATATATAT others(41): Show |
2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-8830_-32-8829i others(50): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796186 | ||||||
| chr2:30796194
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0002g0379a0001c0001t0003g0380others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-8837C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796194 | ||||||
| chr2:30796200
|
G | GTA | 13 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(10): Show | 13 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32-8845_-32-8844d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796200 | ||||||
| chr2:30796200
|
GTATATAT others(19): Show |
G | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(41): Show | 45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-32-8869_-32-8844d others(28): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796200 | ||||||
| chr2:30796202
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0005g0158a0001c0002t0002g0162 | 2 | NA18957.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-32-8867_-32-8846d others(24): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796202 | ||||||
| chr2:30796217
|
T | C | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-8860A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796217 | ||||||
| chr2:30796222
|
A | ATATGTAT others(9): Show |
5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-8866_-32-8865i others(18): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796222 | ||||||
| chr2:30796223
|
T | TGTATATA others(61): Show |
11 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(8): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32-8867_-32-8866i others(70): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796223 | ||||||
| chr2:30796223
|
T | TGTATATA others(101): Show |
2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-32-8867_-32-8866i others(110): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796223 | ||||||
| chr2:30796224
|
G | GTA | 3 | a0001c0001t0005g0350a0001c0002t0002g0270a0001c0013t0002g0075 | 3 | HG01884.hp1 HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-32-8869_-32-8868d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796224 | ||||||
| chr2:30796224
|
GTA | G | 9 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0002g0061others(6): Show | 9 | HG02280.hp2 HG02622.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-8869_-32-8868d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796224 | ||||||
| chr2:30796234
|
A | G | 1 | a0003c0004t0005g0353 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-32-8877T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796234 | ||||||
| chr2:30796250
|
A | G | 1 | a0001c0001t0003g0244 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-32-8893T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796250 | ||||||
| chr2:30796251
|
TAC | T | 7 | a0001c0001t0001g0090a0001c0001t0002g0061a0001c0001t0002g0068others(4): Show | 7 | HG02572.hp2 HG02622.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-8896_-32-8895d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796251 | ||||||
| chr2:30796253
|
C | T | 1 | a0001c0002t0002g0324 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-32-8896G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796253 | ||||||
| chr2:30796359
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-32-9002G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796359 | ||||||
| chr2:30796362
|
C | T | 1 | a0005c0006t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-32-9005G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796362 | ||||||
| chr2:30796363
|
G | A | 1 | a0001c0001t0002g0358 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-32-9006C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796363 | ||||||
| chr2:30796499
|
T | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0148a0001c0001t0001g0267others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32-9142A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796499 | ||||||
| chr2:30796766
|
G | A | 4 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-9409C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796766 | ||||||
| chr2:30796883
|
A | C | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-9526T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30796883 | ||||||
| chr2:30797288
|
C | T | 6 | a0001c0001t0001g0267a0001c0001t0002g0282a0001c0002t0005g0278others(3): Show | 6 | HG02280.hp2 HG03130.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-9931G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797288 | ||||||
| chr2:30797463
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01106.hp2 HG01496.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+9839G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797463 | ||||||
| chr2:30797472
|
C | T | 1 | a0002c0003t0004g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-33+9830G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797472 | ||||||
| chr2:30797510
|
T | A | 2 | a0001c0001t0001g0273a0001c0001t0002g0272 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-33+9792A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797510 | ||||||
| chr2:30797568
|
TG | T | 8 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0280others(5): Show | 8 | HG02280.hp2 HG02976.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+9733delC | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797568 | ||||||
| chr2:30797588
|
G | A | 2 | a0001c0001t0001g0001a0001c0002t0010g0364 | 3 | HG03491.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-33+9714C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797588 | ||||||
| chr2:30797759
|
C | T | 7 | a0001c0001t0001g0090a0001c0001t0002g0061a0001c0001t0002g0068others(4): Show | 7 | HG02572.hp2 HG02622.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+9543G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797759 | ||||||
| chr2:30797779
|
C | T | 1 | a0001c0002t0003g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-33+9523G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797779 | ||||||
| chr2:30797797
|
T | C | 8 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0280others(5): Show | 8 | HG02280.hp2 HG02976.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+9505A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797797 | ||||||
| chr2:30797936
|
C | T | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+9366G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797936 | ||||||
| chr2:30797939
|
T | C | 1 | a0001c0002t0004g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-33+9363A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30797939 | ||||||
| chr2:30798153
|
T | C | 1 | a0001c0002t0002g0315 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-33+9149A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798153 | ||||||
| chr2:30798224
|
A | G | 8 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0280others(5): Show | 8 | HG02280.hp2 HG02976.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+9078T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798224 | ||||||
| chr2:30798232
|
G | A | 14 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(11): Show | 14 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+9070C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798232 | ||||||
| chr2:30798276
|
T | C | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+9026A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798276 | ||||||
| chr2:30798394
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0002g0104 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-33+8908G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798394 | ||||||
| chr2:30798447
|
C | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0327others(3): Show | 6 | HG01069.hp1 HG03490.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+8855G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798447 | ||||||
| chr2:30798473
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-33+8829C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798473 | ||||||
| chr2:30798521
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-33+8781A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798521 | ||||||
| chr2:30798526
|
G | A | 3 | a0001c0002t0005g0278a0001c0021t0001g0277a0016c0019t0001g0138 | 3 | HG06807.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+8776C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798526 | ||||||
| chr2:30798543
|
T | C | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+8759A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798543 | ||||||
| chr2:30798718
|
C | T | 10 | a0001c0001t0001g0134a0001c0001t0001g0267a0001c0001t0001g0271others(7): Show | 10 | HG02280.hp2 HG02976.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33+8584G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798718 | ||||||
| chr2:30798910
|
C | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0245a0001c0001t0001g0247others(58): Show | 62 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-33+8392G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30798910 | ||||||
| chr2:30799062
|
T | TCCTCACT others(72): Show |
1 | a0002c0003t0002g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-33+8239_-33+8240i others(81): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799062 | ||||||
| chr2:30799065
|
CTCAGGGC others(50): Show |
C | 1 | a0002c0003t0002g0339 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-33+8180_-33+8236d others(59): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799065 | ||||||
| chr2:30799206
|
G | A | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0379others(1): Show | 4 | HG02451.hp2 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+8096C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799206 | ||||||
| chr2:30799264
|
CAT | C | 14 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(11): Show | 14 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+8036_-33+8037d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799264 | ||||||
| chr2:30799618
|
C | T | 120 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0070others(117): Show | 122 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.-33+7684G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799618 | ||||||
| chr2:30799619
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-33+7683C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799619 | ||||||
| chr2:30799647
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(72): Show | 76 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-33+7655A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799647 | ||||||
| chr2:30799746
|
ATGAAG | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0267others(1): Show | 4 | HG02280.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+7551_-33+7555d others(7): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799746 | ||||||
| chr2:30799751
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(71): Show | 75 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-33+7551C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799751 | ||||||
| chr2:30799799
|
C | T | 1 | a0001c0001t0003g0043 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33+7503G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799799 | ||||||
| chr2:30799844
|
T | C | 1 | a0001c0002t0004g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-33+7458A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799844 | ||||||
| chr2:30799844
|
T | G | 2 | a0001c0002t0005g0278a0001c0021t0001g0277 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+7458A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799844 | ||||||
| chr2:30799863
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0267others(1): Show | 4 | HG02280.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+7439C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799863 | ||||||
| chr2:30799869
|
C | T | 1 | a0001c0001t0003g0119 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-33+7433G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799869 | ||||||
| chr2:30799881
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0225a0001c0002t0005g0319 | 3 | HG01255.hp1 HG03017.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-33+7421T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799881 | ||||||
| chr2:30799884
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0006g0128 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-33+7418A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799884 | ||||||
| chr2:30799889
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 71 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-33+7413G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799889 | ||||||
| chr2:30799901
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-33+7401C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799901 | ||||||
| chr2:30799902
|
T | C | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0267others(2): Show | 5 | HG02280.hp2 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+7400A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799902 | ||||||
| chr2:30799925
|
T | A | 1 | a0004c0005t0002g0204 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-33+7377A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799925 | ||||||
| chr2:30799952
|
C | T | 100 | a0001c0001t0001g0049a0001c0001t0001g0114a0001c0001t0001g0145others(97): Show | 101 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-33+7350G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799952 | ||||||
| chr2:30799971
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-33+7331C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799971 | ||||||
| chr2:30799998
|
C | T | 70 | a0001c0001t0001g0049a0001c0001t0001g0245a0001c0001t0001g0247others(67): Show | 71 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.-33+7304G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799998 | ||||||
| chr2:30800030
|
C | T | 83 | a0001c0001t0001g0049a0001c0001t0001g0114a0001c0001t0001g0245others(80): Show | 84 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.-33+7272G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800030 | ||||||
| chr2:30800063
|
G | A | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7239C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800063 | ||||||
| chr2:30800073
|
C | G | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7229G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800073 | ||||||
| chr2:30800077
|
A | G | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7225T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800077 | ||||||
| chr2:30800077
|
AAAAGAAA others(76): Show |
A | 1 | a0001c0002t0004g0366 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-33+7142_-33+7224d others(85): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800077 | ||||||
| chr2:30800089
|
G | A | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7213C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800089 | ||||||
| chr2:30800091
|
A | G | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7211T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800091 | ||||||
| chr2:30800093
|
G | A | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7209C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800093 | ||||||
| chr2:30800094
|
A | G | 1 | a0002c0003t0001g0323 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-33+7208T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800094 | ||||||
| chr2:30800103
|
AAAGAAAA others(22): Show |
A | 1 | a0002c0003t0004g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-33+7170_-33+7198d others(31): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800103 | ||||||
| chr2:30800110
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-33+7192T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800110 | ||||||
| chr2:30800111
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-33+7191C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800111 | ||||||
| chr2:30800116
|
A | AAAAG | 64 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0054others(61): Show | 66 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-33+7182_-33+7185d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(1): Show |
67 | a0001c0001t0001g0010a0001c0001t0001g0130a0001c0001t0001g0140others(64): Show | 67 | HG00621.hp1 HG00639.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-33+7178_-33+7185d others(10): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(10): Show |
1 | a0001c0001t0002g0356 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(19): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(5): Show |
38 | a0001c0001t0001g0070a0001c0001t0001g0116a0001c0001t0001g0118others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-33+7174_-33+7185d others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(9): Show |
17 | a0001c0001t0001g0129a0001c0001t0001g0246a0001c0001t0001g0288others(14): Show | 17 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+7170_-33+7185d others(18): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(13): Show |
8 | a0001c0001t0001g0058a0001c0001t0002g0068a0001c0001t0002g0272others(5): Show | 8 | HG01192.hp1 HG02145.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+7166_-33+7185d others(22): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(17): Show |
2 | a0001c0001t0002g0368a0001c0002t0002g0152 | 2 | NA18945.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.-33+7162_-33+7185d others(26): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(21): Show |
2 | a0003c0004t0002g0132a0004c0005t0009g0209 | 2 | NA18962.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-33+7158_-33+7185d others(30): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(55): Show |
1 | a0007c0008t0001g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(64): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(67): Show |
1 | a0001c0001t0002g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(76): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(69): Show |
1 | a0001c0001t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(78): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(55): Show |
1 | a0001c0002t0001g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(64): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(53): Show |
1 | a0005c0006t0001g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(62): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(56): Show |
1 | a0002c0003t0004g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(65): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(55): Show |
1 | a0001c0002t0002g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(64): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(71): Show |
1 | a0003c0004t0002g0256 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(80): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(58): Show |
1 | a0001c0001t0002g0249 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(67): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(59): Show |
2 | a0001c0002t0001g0253a0004c0005t0002g0259 | 2 | NA18991.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-33+7185_-33+7186i others(68): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(67): Show |
1 | a0003c0004t0002g0255 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(76): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(62): Show |
1 | a0002c0003t0001g0264 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(71): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(57): Show |
1 | a0005c0006t0001g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(66): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAAGAAA others(39): Show |
1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(48): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAGAAAG | 3 | a0001c0001t0001g0279a0002c0003t0001g0156a0011c0016t0001g0369 | 3 | HG02132.hp1 HG03098.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-33+7185_-33+7186i others(9): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAGAAAG others(4): Show |
1 | a0001c0002t0001g0299 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(13): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAGAAAG others(8): Show |
2 | a0001c0002t0005g0346a0003c0004t0002g0065 | 2 | HG03041.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-33+7185_-33+7186i others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0003g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(21): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0003g0298 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(12): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAGAAAGA others(11): Show |
2 | a0001c0001t0002g0115a0003c0004t0002g0013 | 2 | NA19030.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-33+7185_-33+7186i others(20): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
A | AAGAAAGA others(63): Show |
1 | a0004c0005t0002g0257 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33+7185_-33+7186i others(72): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
AAAAG | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0199others(25): Show | 29 | HG00099.hp1 HG00438.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-33+7182_-33+7185d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
AAAAGAAA others(1): Show |
A | 16 | a0001c0001t0001g0365a0001c0001t0002g0275a0001c0001t0002g0370others(13): Show | 17 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+7178_-33+7185d others(10): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0001g0134a0001c0001t0001g0238a0001c0001t0002g0104others(10): Show | 13 | HG01928.hp2 HG02027.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33+7174_-33+7185d others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
AAAAGAAA others(9): Show |
A | 4 | a0001c0001t0003g0108a0001c0001t0003g0122a0001c0002t0001g0106others(1): Show | 4 | HG02965.hp1 NA18966.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+7170_-33+7185d others(18): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800116
|
AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0003g0244a0001c0021t0001g0277 | 2 | HG06807.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-33+7166_-33+7185d others(22): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800116 | ||||||
| chr2:30800118
|
A | AAGAAAGA others(47): Show |
1 | a0001c0002t0002g0258 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-33+7183_-33+7184i others(56): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800118 | ||||||
| chr2:30800118
|
A | AAGAAAGA others(49): Show |
1 | a0006c0007t0005g0263 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-33+7183_-33+7184i others(58): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800118 | ||||||
| chr2:30800118
|
A | AAGAAAGA others(55): Show |
1 | a0001c0001t0002g0252 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-33+7183_-33+7184i others(64): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800118 | ||||||
| chr2:30800118
|
A | AAGAAAGA others(63): Show |
1 | a0003c0004t0002g0251 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-33+7183_-33+7184i others(72): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800118 | ||||||
| chr2:30800118
|
A | G | 1 | a0004c0005t0002g0257 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33+7184T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800118 | ||||||
| chr2:30800121
|
A | AAAGAAAG others(52): Show |
1 | a0004c0005t0002g0250 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-33+7180_-33+7181i others(61): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800121 | ||||||
| chr2:30800121
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0004g0064 | 2 | HG01109.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-33+7181T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800121 | ||||||
| chr2:30800122
|
A | AAGAAAGA others(45): Show |
1 | a0003c0004t0002g0261 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-33+7179_-33+7180i others(54): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800122 | ||||||
| chr2:30800122
|
A | AAGAAAGA others(51): Show |
1 | a0006c0007t0005g0262 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-33+7179_-33+7180i others(60): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800122 | ||||||
| chr2:30800122
|
A | AAGAAAGA others(53): Show |
1 | a0001c0001t0001g0260 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-33+7179_-33+7180i others(62): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800122 | ||||||
| chr2:30800124
|
G | GAAAAGAA others(12): Show |
1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-33+7177_-33+7178i others(21): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800124 | ||||||
| chr2:30800126
|
A | AAGAAAGA others(46): Show |
1 | a0001c0001t0001g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-33+7175_-33+7176i others(55): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800126 | ||||||
| chr2:30800132
|
G | GA | 3 | a0001c0001t0001g0146a0001c0001t0001g0267a0001c0002t0002g0147 | 3 | HG02280.hp2 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-33+7169dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800132 | ||||||
| chr2:30800133
|
A | AAAGAAAG others(29): Show |
1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33+7168_-33+7169i others(38): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800133 | ||||||
| chr2:30800144
|
G | A | 1 | a0001c0002t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+7158C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800144 | ||||||
| chr2:30800149
|
A | AAAGAAAG others(29): Show |
1 | a0001c0001t0003g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-33+7152_-33+7153i others(38): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800149 | ||||||
| chr2:30800149
|
A | AAAGAAAG others(17): Show |
1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+7152_-33+7153i others(26): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800149 | ||||||
| chr2:30800149
|
AAAGAAAG others(8): Show |
A | 1 | a0007c0008t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-33+7138_-33+7152d others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800149 | ||||||
| chr2:30800153
|
A | AAAGAAAG others(29): Show |
1 | a0001c0001t0002g0379 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-33+7148_-33+7149i others(38): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800153 | ||||||
| chr2:30800196
|
C | T | 75 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0001t0001g0173others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.-33+7106G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800196 | ||||||
| chr2:30800242
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-33+7060G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800242 | ||||||
| chr2:30800330
|
A | G | 5 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+6972T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800330 | ||||||
| chr2:30800345
|
A | T | 21 | a0001c0001t0001g0114a0001c0001t0001g0260a0001c0001t0002g0249others(18): Show | 21 | HG00423.hp2 HG00673.hp1 HG02738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-33+6957T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800345 | ||||||
| chr2:30800372
|
C | G | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0246others(2): Show | 5 | HG01934.hp2 HG02280.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+6930G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800372 | ||||||
| chr2:30800417
|
T | C | 1 | a0001c0002t0004g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-33+6885A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800417 | ||||||
| chr2:30800418
|
G | A | 3 | a0001c0001t0005g0367a0001c0002t0001g0338a0002c0003t0002g0339 | 3 | HG03704.hp1 HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-33+6884C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800418 | ||||||
| chr2:30800546
|
C | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-33+6756G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800546 | ||||||
| chr2:30800645
|
T | C | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+6657A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800645 | ||||||
| chr2:30800651
|
A | G | 9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0267others(6): Show | 9 | HG02280.hp2 HG02922.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+6651T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800651 | ||||||
| chr2:30800673
|
A | G | 1 | a0001c0002t0002g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+6629T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800673 | ||||||
| chr2:30800736
|
G | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0267others(6): Show | 9 | HG02280.hp2 HG02922.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33+6566C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800736 | ||||||
| chr2:30800796
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-33+6506G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800796 | ||||||
| chr2:30800814
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-33+6488C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800814 | ||||||
| chr2:30800864
|
T | C | 1 | a0002c0003t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-33+6438A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800864 | ||||||
| chr2:30800944
|
A | T | 1 | a0003c0004t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-33+6358T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30800944 | ||||||
| chr2:30801013
|
A | T | 1 | a0003c0004t0002g0292 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-33+6289T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801013 | ||||||
| chr2:30801016
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(44): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-33+6286A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801016 | ||||||
| chr2:30801171
|
C | T | 11 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33+6131G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801171 | ||||||
| chr2:30801176
|
A | C | 1 | a0003c0004t0002g0292 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-33+6126T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801176 | ||||||
| chr2:30801278
|
C | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0223 | 3 | HG02451.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-33+6024G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801278 | ||||||
| chr2:30801324
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-33+5978T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801324 | ||||||
| chr2:30801344
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-33+5958C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801344 | ||||||
| chr2:30801439
|
C | A | 2 | a0001c0001t0001g0038a0001c0002t0002g0039 | 2 | NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-33+5863G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801439 | ||||||
| chr2:30801467
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-33+5835A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801467 | ||||||
| chr2:30801604
|
T | TA | 14 | a0001c0001t0001g0058a0001c0001t0001g0208a0001c0001t0001g0247others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+5697dupT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801604 | ||||||
| chr2:30801604
|
TA | T | 31 | a0001c0001t0001g0054a0001c0001t0001g0114a0001c0001t0001g0246others(28): Show | 31 | HG00423.hp2 HG00673.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+5697delT | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801604 | ||||||
| chr2:30801605
|
A | C | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0272others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+5697T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801605 | ||||||
| chr2:30801621
|
AAAAAAAG | A | 11 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33+5674_-33+5680d others(9): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801621 | ||||||
| chr2:30801625
|
A | G | 19 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(16): Show | 19 | HG00738.hp2 HG02257.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+5677T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801625 | ||||||
| chr2:30801640
|
GAAA | G | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0267others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+5659_-33+5661d others(5): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801640 | ||||||
| chr2:30801643
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-33+5659T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801643 | ||||||
| chr2:30801697
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33+5605C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801697 | ||||||
| chr2:30801925
|
G | A | 1 | a0004c0005t0002g0257 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33+5377C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30801925 | ||||||
| chr2:30802019
|
G | C | 3 | a0001c0001t0001g0280a0001c0001t0002g0282a0007c0008t0001g0281 | 3 | HG03130.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-33+5283C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802019 | ||||||
| chr2:30802030
|
A | G | 17 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(14): Show | 17 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+5272T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802030 | ||||||
| chr2:30802056
|
G | A | 2 | a0001c0001t0004g0143a0001c0002t0002g0112 | 2 | HG01496.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-33+5246C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802056 | ||||||
| chr2:30802066
|
G | C | 19 | a0001c0001t0001g0260a0001c0001t0002g0249a0001c0001t0002g0252others(16): Show | 19 | HG00423.hp2 HG02738.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+5236C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802066 | ||||||
| chr2:30802122
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0006g0042 | 2 | HG02083.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-33+5180C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802122 | ||||||
| chr2:30802124
|
A | G | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-33+5178T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802124 | ||||||
| chr2:30802129
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-33+5173G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802129 | ||||||
| chr2:30802381
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-33+4921A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802381 | ||||||
| chr2:30802402
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-33+4900G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802402 | ||||||
| chr2:30802403
|
T | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+4899A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802403 | ||||||
| chr2:30802463
|
A | ATG | 34 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(31): Show | 34 | HG00423.hp2 HG01081.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+4837_-33+4838d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802463
|
A | ATGTG | 77 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0001t0001g0173others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-33+4835_-33+4838d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802463
|
A | ATGTGTG | 16 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0002g0229others(13): Show | 16 | HG00738.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33+4833_-33+4838d others(8): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802463
|
A | G | 2 | a0001c0001t0002g0275a0007c0008t0001g0276 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-33+4839T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802463
|
ATG | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 60 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33+4837_-33+4838d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802463
|
ATGTG | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0002t0002g0147 | 3 | HG03471.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-33+4835_-33+4838d others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802463 | ||||||
| chr2:30802529
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-33+4773C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802529 | ||||||
| chr2:30802542
|
T | TG | 34 | a0001c0001t0001g0365a0001c0001t0002g0356a0001c0001t0002g0357others(31): Show | 34 | HG00597.hp1 HG00741.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+4759dupC | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802542 | ||||||
| chr2:30802542
|
TG | T | 180 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.-33+4759delC | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802542 | ||||||
| chr2:30802542
|
TGG | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(55): Show | 59 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-33+4758_-33+4759d others(4): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802542 | ||||||
| chr2:30802544
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33+4758C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802544 | ||||||
| chr2:30802546
|
G | T | 1 | a0001c0002t0002g0283 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-33+4756C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802546 | ||||||
| chr2:30802547
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(44): Show | 48 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-33+4755C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802547 | ||||||
| chr2:30802548
|
G | T | 1 | a0001c0002t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-33+4754C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802548 | ||||||
| chr2:30802549
|
G | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+4753C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802549 | ||||||
| chr2:30802552
|
G | C | 4 | a0001c0001t0002g0379a0001c0001t0003g0137a0001c0001t0003g0380others(1): Show | 4 | HG02922.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+4750C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802552 | ||||||
| chr2:30802755
|
C | T | 3 | a0001c0001t0001g0280a0001c0001t0002g0282a0007c0008t0001g0281 | 3 | HG03130.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-33+4547G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802755 | ||||||
| chr2:30802839
|
T | C | 1 | a0001c0001t0002g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-33+4463A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802839 | ||||||
| chr2:30802885
|
C | T | 2 | a0001c0002t0002g0287a0003c0004t0005g0374 | 2 | NA18978.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-33+4417G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802885 | ||||||
| chr2:30802886
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-33+4416C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802886 | ||||||
| chr2:30802891
|
C | T | 18 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(15): Show | 18 | HG00738.hp2 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33+4411G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802891 | ||||||
| chr2:30802914
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-33+4388C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802914 | ||||||
| chr2:30802954
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0002g0240 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-33+4348A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802954 | ||||||
| chr2:30802970
|
C | G | 2 | a0001c0001t0007g0227a0001c0001t0007g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-33+4332G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802970 | ||||||
| chr2:30803007
|
T | A | 1 | a0012c0011t0002g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-33+4295A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803007 | ||||||
| chr2:30803117
|
G | A | 1 | a0003c0004t0002g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-33+4185C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803117 | ||||||
| chr2:30803257
|
C | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+4045G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803257 | ||||||
| chr2:30803283
|
G | A | 2 | a0006c0007t0005g0262a0006c0007t0005g0263 | 2 | NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-33+4019C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803283 | ||||||
| chr2:30803309
|
A | G | 14 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+3993T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803309 | ||||||
| chr2:30803404
|
G | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(49): Show | 53 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-33+3898C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803404 | ||||||
| chr2:30803567
|
G | A | 3 | a0001c0001t0002g0243a0001c0001t0003g0144a0001c0001t0005g0242 | 3 | HG02572.hp1 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-33+3735C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803567 | ||||||
| chr2:30803648
|
G | A | 2 | a0001c0002t0005g0278a0001c0021t0001g0277 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+3654C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803648 | ||||||
| chr2:30803735
|
G | C | 19 | a0001c0001t0001g0260a0001c0001t0002g0249a0001c0001t0002g0252others(16): Show | 19 | HG00423.hp2 HG02738.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+3567C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803735 | ||||||
| chr2:30803737
|
A | C | 203 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-33+3565T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803737 | ||||||
| chr2:30803786
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-33+3516T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803786 | ||||||
| chr2:30803871
|
T | C | 206 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-33+3431A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803871 | ||||||
| chr2:30803979
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-33+3323G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30803979 | ||||||
| chr2:30804023
|
T | C | 14 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+3279A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804023 | ||||||
| chr2:30804265
|
A | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+3037T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804265 | ||||||
| chr2:30804269
|
C | T | 2 | a0001c0002t0005g0278a0001c0021t0001g0277 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+3033G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804269 | ||||||
| chr2:30804364
|
C | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01106.hp2 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+2938G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804364 | ||||||
| chr2:30804386
|
A | G | 200 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-33+2916T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804386 | ||||||
| chr2:30804517
|
A | C | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2785T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804517 | ||||||
| chr2:30804523
|
C | G | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2779G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804523 | ||||||
| chr2:30804524
|
T | C | 174 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-33+2778A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804524 | ||||||
| chr2:30804528
|
G | T | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2774C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804528 | ||||||
| chr2:30804530
|
G | T | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2772C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804530 | ||||||
| chr2:30804531
|
G | T | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2771C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804531 | ||||||
| chr2:30804578
|
T | A | 1 | a0001c0002t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33+2724A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804578 | ||||||
| chr2:30804644
|
A | G | 92 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(89): Show | 93 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-33+2658T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804644 | ||||||
| chr2:30804710
|
C | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-33+2592G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804710 | ||||||
| chr2:30804811
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-33+2491T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804811 | ||||||
| chr2:30804895
|
A | T | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-33+2407T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30804895 | ||||||
| chr2:30805096
|
A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(47): Show | 51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-33+2206T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805096 | ||||||
| chr2:30805147
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 88 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-33+2155A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805147 | ||||||
| chr2:30805220
|
T | C | 2 | a0001c0002t0005g0278a0001c0021t0001g0277 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+2082A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805220 | ||||||
| chr2:30805274
|
C | T | 3 | a0001c0001t0001g0280a0001c0001t0002g0282a0007c0008t0001g0281 | 3 | HG03130.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-33+2028G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805274 | ||||||
| chr2:30805523
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-33+1779T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805523 | ||||||
| chr2:30805665
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 57 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-33+1637C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805665 | ||||||
| chr2:30805717
|
C | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 8 | HG01496.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+1585G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805717 | ||||||
| chr2:30805718
|
G | A | 17 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(14): Show | 17 | HG00738.hp2 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-33+1584C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805718 | ||||||
| chr2:30805739
|
A | G | 187 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-33+1563T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805739 | ||||||
| chr2:30805747
|
C | CTTTATTT others(5): Show |
1 | a0016c0019t0001g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33+1554_-33+1555i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTATTT others(7): Show |
1 | a0001c0001t0003g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33+1554_-33+1555i others(16): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0245others(3): Show | 6 | HG02976.hp1 HG03471.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+1545_-33+1554d others(12): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(4): Show |
99 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0160others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-33+1554_-33+1555i others(13): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(5): Show |
130 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0038others(127): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-33+1554_-33+1555i others(14): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(6): Show |
14 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0140others(11): Show | 15 | HG00621.hp2 HG01496.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.-33+1554_-33+1555i others(15): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(7): Show |
19 | a0001c0001t0001g0246a0001c0001t0001g0260a0001c0001t0002g0249others(16): Show | 19 | HG00423.hp2 HG01934.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+1554_-33+1555i others(16): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805747
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0247a0005c0006t0001g0265a0005c0006t0001g0266 | 3 | HG02738.hp2 NA19090.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-33+1554_-33+1555i others(17): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805747 | ||||||
| chr2:30805829
|
T | G | 1 | a0002c0003t0001g0264 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-33+1473A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805829 | ||||||
| chr2:30805895
|
T | G | 2 | a0001c0002t0005g0278a0001c0021t0001g0277 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+1407A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805895 | ||||||
| chr2:30805981
|
T | C | 187 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-33+1321A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30805981 | ||||||
| chr2:30806050
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-33+1252C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806050 | ||||||
| chr2:30806079
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(275): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-33+1223A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806079 | ||||||
| chr2:30806103
|
A | G | 5 | a0001c0001t0001g0279a0001c0001t0002g0379a0001c0001t0003g0380others(2): Show | 5 | HG02922.hp2 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+1199T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806103 | ||||||
| chr2:30806230
|
T | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-33+1072A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806230 | ||||||
| chr2:30806231
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-33+1071C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806231 | ||||||
| chr2:30806234
|
G | A | 1 | a0003c0004t0005g0374 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-33+1068C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806234 | ||||||
| chr2:30806300
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-33+1002A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806300 | ||||||
| chr2:30806370
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-33+932G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806370 | ||||||
| chr2:30806402
|
TAAC | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0267a0001c0001t0002g0379others(5): Show | 9 | HG02280.hp2 HG02738.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33+897_-33+899del others(3): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806402 | ||||||
| chr2:30806402
|
TAACAAC | T | 19 | a0001c0001t0001g0247a0001c0001t0001g0260a0001c0001t0002g0249others(16): Show | 19 | HG00423.hp2 HG02886.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.-33+894_-33+899del others(6): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806402 | ||||||
| chr2:30806402
|
TAACAACA others(2): Show |
T | 87 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0086others(84): Show | 88 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-33+891_-33+899del others(9): Show |
CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806402 | ||||||
| chr2:30806430
|
A | T | 25 | a0001c0001t0001g0247a0001c0001t0001g0260a0001c0001t0001g0267others(22): Show | 25 | HG00423.hp2 HG02280.hp2 HG02738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-33+872T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806430 | ||||||
| chr2:30806519
|
G | T | 4 | a0001c0001t0001g0280a0001c0001t0002g0282a0001c0002t0002g0283others(1): Show | 4 | HG02922.hp1 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+783C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806519 | ||||||
| chr2:30806523
|
C | A | 26 | a0001c0001t0001g0247a0001c0001t0001g0260a0001c0001t0001g0267others(23): Show | 26 | HG00423.hp2 HG02280.hp2 HG02738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-33+779G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806523 | ||||||
| chr2:30806554
|
G | A | 3 | a0001c0001t0003g0269a0001c0002t0002g0270a0013c0012t0002g0268 | 3 | HG02615.hp2 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-33+748C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806554 | ||||||
| chr2:30806588
|
T | C | 5 | a0001c0001t0001g0376a0001c0001t0004g0377a0001c0002t0002g0375others(2): Show | 5 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+714A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806588 | ||||||
| chr2:30806605
|
C | G | 1 | a0001c0021t0001g0277 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33+697G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806605 | ||||||
| chr2:30806662
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-33+640C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806662 | ||||||
| chr2:30806812
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(49): Show | 53 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-33+490G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806812 | ||||||
| chr2:30806822
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-33+480T>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806822 | ||||||
| chr2:30806871
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0272 | 3 | HG02486.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-33+431A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806871 | ||||||
| chr2:30806969
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-33+333G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806969 | ||||||
| chr2:30806987
|
A | G | 2 | a0001c0001t0002g0275a0007c0008t0001g0276 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-33+315T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30806987 | ||||||
| chr2:30807045
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-33+257G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30807045 | ||||||
| chr2:30807133
|
G | A | 2 | a0001c0001t0002g0379a0001c0001t0003g0380 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-33+169C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30807133 | ||||||
| chr2:30807158
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-33+144G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30807158 |