Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0002 | 1/0 | 669 | 60 | 4 | 13 | 31 | 1 | 10 | 23 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0003 | 0/0 | 669 | 31 | 0 | 4 | 23 | 1 | 3 | 19 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0004 | 0/0 | 669 | 11 | 0 | 1 | 10 | 0 | 0 | 8 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0005 | 0/0 | 669 | 8 | 0 | 4 | 0 | 3 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0006 | 0/0 | 669 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0007 | 0/0 | 669 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0008 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0009 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0010 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0011 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0012 | 0/0 | 669 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0013 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0014 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0015 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| a0016 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | MAYYQ others(664): Show |
chr2 | 30717771 | 30812446 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2007 | 163 | 69 | 17 | 50 | 7 | 19 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0001c0002 | 0/0 | 2007 | 94 | 12 | 25 | 47 | 4 | 6 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0001c0013 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0001c0020 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0001c0021 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0002c0003 | 1/0 | 2007 | 60 | 4 | 13 | 31 | 1 | 10 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0003c0004 | 0/0 | 2007 | 30 | 0 | 4 | 22 | 1 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0003c0010 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0004c0005 | 0/0 | 2007 | 11 | 0 | 1 | 10 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0005c0006 | 0/0 | 2007 | 8 | 0 | 4 | 0 | 3 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0006c0007 | 0/0 | 2007 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0007c0008 | 0/0 | 2007 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0008c0014 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0009c0018 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0010c0017 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0011c0015 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0012c0009 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0013c0012 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0014c0011 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0015c0016 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
chr2 | 30717771 | 30812446 | ||
| a0016c0019 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | ATGGC others(2002): Show |
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 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0002 | 0/1 | 2683 | 51 | 28 | 5 | 9 | 3 | 5 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0003 | 0/0 | 2683 | 24 | 7 | 2 | 13 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0004 | 0/0 | 2683 | 9 | 1 | 4 | 0 | 0 | 4 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0005 | 0/0 | 2683 | 7 | 3 | 0 | 2 | 1 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0006 | 0/0 | 2683 | 4 | 1 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0007 | 0/0 | 2683 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0001t0008 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0001 | 0/0 | 2683 | 29 | 1 | 10 | 14 | 2 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0002 | 0/0 | 2683 | 46 | 7 | 12 | 23 | 2 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0003 | 0/0 | 2683 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0004 | 0/0 | 2683 | 3 | 0 | 2 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0005 | 0/0 | 2683 | 10 | 3 | 1 | 5 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0006 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0010 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0002t0012 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0013t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0020t0004 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0001c0021t0001 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0002c0003t0001 | 1/0 | 2683 | 46 | 3 | 12 | 24 | 0 | 6 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0002c0003t0002 | 0/0 | 2683 | 4 | 1 | 0 | 2 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0002c0003t0004 | 0/0 | 2683 | 9 | 0 | 1 | 4 | 1 | 3 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0002c0003t0011 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0003c0004t0002 | 0/0 | 2683 | 26 | 0 | 4 | 20 | 0 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0003c0004t0005 | 0/0 | 2683 | 4 | 0 | 0 | 2 | 1 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0003c0010t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0004c0005t0001 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0004c0005t0002 | 0/0 | 2683 | 9 | 0 | 0 | 9 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0004c0005t0009 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0005c0006t0001 | 0/0 | 2683 | 7 | 0 | 3 | 0 | 3 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0005c0006t0004 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0006c0007t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0006c0007t0005 | 0/0 | 2683 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0007c0008t0001 | 0/0 | 2683 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0008c0014t0002 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0009c0018t0001 | 0/0 | 2683 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0010c0017t0002 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0011c0015t0001 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0012c0009t0004 | 0/0 | 2683 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0013c0012t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0014c0011t0002 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0015c0016t0001 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| a0016c0019t0001 | 0/0 | 2683 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | AAGCA others(2678): Show |
chr2 | 30717771 | 30812446 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0109 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0137 | 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 |
| a0001c0001t0001g0143 | 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 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0209 | 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 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0272 | 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 |
| a0001c0001t0001g0275 | 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 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0289 | 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 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0119 | 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 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0226 | 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 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0250 | 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 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0283 | 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 |
| a0001c0001t0002g0306 | 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 |
| a0001c0001t0002g0341 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0014 | 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 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0087 | 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 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0140 | 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 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0195 | 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 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0259 | 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 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0312 | 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 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0002g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0003g0031 | 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 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0010g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0002t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0013t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0020t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0001c0021t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0200 | 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 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0003t0001g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0002g0024 | 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 |
| a0002c0003t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0011 | 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 |
| a0002c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0002c0003t0011g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0196 | 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 |
| a0003c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0220 | 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 |
| a0003c0004t0002g0253 | 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 |
| a0003c0004t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0004t0005g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0003c0010t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0004c0005t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0111 | 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 |
| a0005c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0005c0006t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0006c0007t0002g0324 | 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 |
| a0006c0007t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0007c0008t0001g0277 | 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 |
| a0008c0014t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0009c0018t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0010c0017t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0011c0015t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0012c0009t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0013c0012t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0014c0011t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0015c0016t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| a0016c0019t0001g0139 | 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 | g0175 | EUR | GBR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0182 | EUR | GBR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0217 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00280 | hp2 | a0005 | c0006 | t0001 | g0070 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00323 | hp1 | a0003 | c0004 | t0005 | g0118 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0366 | 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 | g0302 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0178 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00597 | hp1 | a0004 | c0005 | t0002 | g0354 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00621 | hp1 | a0004 | c0005 | t0002 | g0044 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00621 | hp2 | a0003 | c0004 | t0002 | g0060 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0365 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00735 | hp1 | a0002 | c0003 | t0004 | g0286 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00735 | hp2 | a0005 | c0006 | t0004 | g0152 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0295 | 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 | g0370 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG00741 | hp2 | a0008 | c0014 | t0002 | g0058 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0305 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0200 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01168 | hp2 | a0003 | c0004 | t0002 | g0004 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01169 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0357 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0314 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01256 | hp2 | a0003 | c0004 | t0002 | g0136 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01258 | hp1 | a0003 | c0004 | t0002 | g0066 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01261 | hp1 | a0009 | c0018 | t0001 | g0313 | 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 | g0188 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0359 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0038 | 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 | g0171 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01433 | hp2 | a0004 | c0005 | t0001 | g0105 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0339 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01516 | hp2 | a0005 | c0006 | t0001 | g0069 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0353 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0114 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0328 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0312 | 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 | g0247 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0350 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0311 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0351 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0073 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02015 | hp2 | a0003 | c0004 | t0002 | g0196 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02027 | hp1 | a0003 | c0010 | t0002 | g0059 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02027 | hp2 | a0002 | c0003 | t0004 | g0198 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0304 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0046 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02129 | hp2 | a0010 | c0017 | t0002 | g0016 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0204 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02132 | hp2 | a0001 | c0002 | t0006 | g0179 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02135 | hp1 | a0003 | c0004 | t0005 | g0342 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0344 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02148 | hp1 | a0005 | c0006 | t0001 | g0307 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0218 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0343 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02155 | hp2 | a0011 | c0015 | t0001 | g0082 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CDX | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02258 | hp1 | a0001 | c0013 | t0002 | g0093 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0371 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PEL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0349 | 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 | g0225 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0309 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | KHV | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0145 | 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 | g0023 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0219 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02622 | hp1 | a0001 | c0002 | t0012 | g0240 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02647 | hp2 | a0007 | c0008 | t0001 | g0277 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02698 | hp1 | a0012 | c0009 | t0004 | g0221 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02735 | hp1 | a0003 | c0004 | t0002 | g0055 | 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 | g0211 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02738 | hp2 | a0005 | c0006 | t0001 | g0267 | 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 | g0364 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0347 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02895 | hp1 | a0013 | c0012 | t0002 | g0269 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0372 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0345 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0280 | 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 | g0226 | 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 | g0274 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0138 | 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 | g0141 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0338 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0373 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03491 | hp1 | a0002 | c0003 | t0004 | g0155 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0276 | 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 | g0146 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0029 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0062 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0333 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03710 | hp1 | a0001 | c0002 | t0010 | g0358 | 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 | g0360 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0068 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0369 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0191 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0361 | SAS | BEB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04199 | hp1 | a0002 | c0003 | t0004 | g0180 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04199 | hp2 | a0002 | c0003 | t0004 | g0303 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04204 | hp1 | a0003 | c0004 | t0005 | g0030 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0308 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | STU | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0316 | 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 | g0275 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | CHB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CHB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0142 | 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 | g0018 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0321 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18942 | hp2 | a0001 | c0020 | t0004 | g0054 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0265 | 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 | g0253 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18949 | hp1 | a0004 | c0005 | t0002 | g0205 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18951 | hp2 | a0003 | c0004 | t0002 | g0165 | 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 | g0019 | 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 | g0053 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0160 | 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 | g0158 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18961 | hp1 | a0003 | c0004 | t0002 | g0101 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18962 | hp2 | a0004 | c0005 | t0009 | g0210 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0346 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18964 | hp2 | a0003 | c0004 | t0002 | g0293 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18965 | hp1 | a0003 | c0004 | t0002 | g0164 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18966 | hp2 | a0002 | c0003 | t0004 | g0106 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18971 | hp1 | a0003 | c0004 | t0002 | g0102 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18973 | hp2 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18974 | hp1 | a0004 | c0005 | t0002 | g0227 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18975 | hp1 | a0002 | c0003 | t0011 | g0320 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0099 | 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 | g0206 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18986 | hp1 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18988 | hp2 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18990 | hp2 | a0006 | c0007 | t0005 | g0264 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18991 | hp1 | a0004 | c0005 | t0002 | g0260 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0296 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18995 | hp2 | a0004 | c0005 | t0002 | g0254 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18997 | hp2 | a0004 | c0005 | t0002 | g0096 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA18999 | hp2 | a0001 | c0002 | t0005 | g0336 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19000 | hp2 | a0015 | c0016 | t0001 | g0363 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0317 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19009 | hp2 | a0002 | c0003 | t0004 | g0151 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0327 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19010 | hp2 | a0003 | c0004 | t0002 | g0100 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19011 | hp2 | a0003 | c0004 | t0002 | g0262 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0050 | 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 | g0251 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0032 | 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 | g0220 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19065 | hp1 | a0003 | c0004 | t0002 | g0133 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19067 | hp1 | a0003 | c0004 | t0002 | g0176 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19070 | hp1 | a0003 | c0004 | t0002 | g0098 | 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 | g0367 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19081 | hp1 | a0003 | c0004 | t0002 | g0035 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0356 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19084 | hp2 | a0004 | c0005 | t0002 | g0258 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19089 | hp1 | a0006 | c0007 | t0002 | g0324 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19090 | hp1 | a0003 | c0004 | t0002 | g0329 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19091 | hp2 | a0003 | c0004 | t0002 | g0207 | EAS | JPT | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | YRI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20129 | hp1 | a0016 | c0019 | t0001 | g0139 | AFR | ASW | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0279 | AFR | ASW | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0011 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20805 | hp1 | a0005 | c0006 | t0001 | g0266 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | TSI | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20905 | hp1 | a0003 | c0004 | t0002 | g0075 | SAS | GIH | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20905 | hp2 | a0002 | c0003 | t0002 | g0334 | SAS | GIH | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0181 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG01123 | hp2 | a0005 | c0006 | t0001 | g0111 | AMR | CLM | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0124 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | 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 | g0001 | AFR | ACB | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0129 | 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 | a0014 | c0011 | t0002 | g0132 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG06807 | hp1 | a0001 | c0021 | t0001 | g0278 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | 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 | g0224 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | LWK | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0341 | REF | REF | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0319 | REF | REF | CAPN13_chr2_30717771_30812446 | CAPN13 | chr2 | 30717771 | 30812446 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30734460 | A | G | 4 | a0003 a0006 a0008 others(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 | a0014 | 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 | a0011 | 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 | a0010 | 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 | a0005 a0008 |
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 | a0001 a0003 a0004 others(6): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): 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 | a0004 a0006 a0009 others(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 | a0012 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30753192 | C | T | 8 | a0001c0002 a0001c0013 a0003c0004 others(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 | a0001c0013 a0016c0019 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30722795 | T | C | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(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 | a0001c0001t0002 a0001c0001t0005 a0001c0002t0002 others(14): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): 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 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(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 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:30723360 | A | C | 33 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0004c0005t0009g0210 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0002t0012g0240 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0280 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0002t0010g0358 | 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 | a0001c0001t0001g0117 a0001c0001t0004g0043 |
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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0021t0001g0278 |
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 | 36 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(33): Show |
39 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(36): 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0002t0002g0259 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0272 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0002t0012g0240 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | 194 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(191): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0108 others(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 | a0001c0002t0002g0311 | 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 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0002t0001g0085 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0131 a0001c0001t0001g0135 others(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 | 208 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): 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 | a0001c0002t0004g0040 | 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 | a0014c0011t0002g0132 | 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 | 161 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(158): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0225 a0001c0001t0004g0087 |
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 | 35 | a0001c0001t0002g0216 a0001c0001t0002g0361 a0003c0004t0002g0004 others(32): 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 | a0001c0001t0004g0159 | 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 | 194 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(191): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.*31-2982G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726218 | |||||||
| chr2:30726349 | A | T | 195 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.*31-3113T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726349 | |||||||
| chr2:30726357 | A | G | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.*31-3121T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726357 | |||||||
| chr2:30726385 | A | G | 196 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): 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 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0110 |
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 | 195 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0272 others(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 | a0002c0003t0001g0204 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0352 |
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 | a0001c0001t0002g0079 | 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 | 210 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(207): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.*31-3490A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726726 | |||||||
| chr2:30726768 | T | C | 210 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(207): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.*31-3532A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726768 | |||||||
| chr2:30726801 | G | C | 202 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): 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 | a0002c0003t0001g0296 a0002c0003t0001g0321 a0002c0003t0011g0320 |
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 | 201 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(198): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): 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 | a0001c0001t0002g0168 | 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 | 162 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(159): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): 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 | a0001c0001t0003g0126 a0001c0001t0003g0245 a0001c0001t0003g0323 others(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 | 168 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(165): Show |
172 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.*31-3686G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30726922 | |||||||
| chr2:30727043 | T | C | 211 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): 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 | a0003c0004t0002g0035 | 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 | a0001c0001t0002g0079 a0001c0001t0002g0128 a0001c0001t0002g0171 others(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 | a0001c0002t0002g0312 | 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0108 others(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 | a0001c0001t0005g0243 | 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 | a0001c0001t0003g0145 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0002c0003t0001g0038 a0002c0003t0001g0124 a0002c0003t0001g0181 others(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 | a0001c0002t0002g0190 | 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0230 a0001c0001t0002g0237 others(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 | a0002c0003t0002g0018 | 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 | a0001c0001t0002g0071 | 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 | 113 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0002g0064 others(110): 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 | a0002c0003t0001g0371 | 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 | a0001c0002t0001g0085 | 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 | 197 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(194): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0272 others(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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0002c0003t0001g0265 | 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0006c0007t0002g0324 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0280 others(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 | a0003c0004t0005g0118 | 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 | 165 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(162): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.*30+1677T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729053 | |||||||
| chr2:30729066 | G | C | 158 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(155): Show |
162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.*30+1664C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729066 | |||||||
| chr2:30729118 | T | C | 214 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): 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 | a0001c0002t0005g0029 | 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 | a0003c0004t0002g0253 a0003c0004t0002g0329 |
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 | a0001c0001t0003g0086 a0001c0001t0003g0107 a0001c0001t0003g0187 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0097 a0001c0001t0006g0343 |
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 | 285 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.*30+1106A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 22/22 | chr2 | 30729624 | |||||||
| chr2:30729688 | G | A | 20 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(17): Show |
23 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(20): 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 | a0002c0003t0004g0155 | 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 | a0001c0002t0005g0336 a0001c0002t0005g0346 |
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 | 114 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0002g0064 others(111): 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 | a0001c0002t0001g0085 | 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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | 111 | a0001c0001t0002g0050 a0001c0001t0002g0064 a0001c0001t0002g0199 others(108): 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 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0275 |
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 | a0003c0010t0002g0059 | 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 | a0016c0019t0001g0139 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0003g0340 a0001c0001t0003g0372 |
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 | a0004c0005t0002g0044 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0275 |
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 | a0001c0002t0010g0358 | 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 | a0001c0001t0002g0168 | 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 | a0001c0001t0002g0134 | 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 | a0001c0001t0003g0340 a0001c0001t0003g0372 |
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 | a0001c0002t0002g0156 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0272 |
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 | 284 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0005c0006t0001g0069 a0005c0006t0001g0307 |
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 | a0002c0003t0001g0068 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0352 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0162 a0001c0001t0002g0050 a0001c0001t0002g0064 others(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 | 40 | a0001c0001t0001g0183 a0001c0001t0001g0272 a0001c0001t0002g0001 others(37): Show |
43 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1927+182C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732256 | |||||||
| chr2:30732288 | A | G | 207 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1927+150T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 20/22 | chr2 | 30732288 | |||||||
| chr2:30732310 | A | G | 151 | a0001c0001t0001g0183 a0001c0001t0001g0272 a0001c0001t0002g0001 others(148): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): 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 | a0012c0009t0004g0221 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0129 others(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 | a0001c0002t0002g0297 a0003c0004t0005g0342 |
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 | 283 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): 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 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0110 |
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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0002g0064 others(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 |
283 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): 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 | 35 | a0001c0001t0002g0361 a0003c0004t0002g0004 a0003c0004t0002g0035 others(32): 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 | 164 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(161): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0003c0004t0002g0206 | 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 | a0001c0002t0002g0113 | 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 | a0001c0002t0001g0295 | 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 | a0001c0001t0002g0216 a0001c0001t0003g0014 a0001c0001t0003g0036 others(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 | 35 | a0001c0001t0001g0272 a0003c0004t0002g0004 a0003c0004t0002g0035 others(32): 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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0352 |
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 | a0001c0001t0001g0285 a0001c0002t0001g0007 a0001c0002t0001g0034 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | a0001c0001t0002g0119 a0001c0001t0002g0223 a0001c0001t0002g0235 |
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 | 42 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(39): Show |
45 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(42): 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 | a0001c0002t0001g0027 a0001c0002t0001g0257 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0280 a0001c0001t0002g0090 a0001c0001t0002g0091 others(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 | a0001c0002t0001g0167 | 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 | 208 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(205): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0108 others(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 | 284 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): 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 | a0001c0002t0002g0122 a0001c0002t0002g0195 a0001c0002t0002g0288 others(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 | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0108 others(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 | a0001c0001t0002g0134 a0001c0001t0002g0231 a0001c0001t0002g0232 others(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 | a0016c0019t0001g0139 | 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 | a0001c0001t0001g0247 | 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 | a0001c0002t0002g0163 | 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 | a0001c0001t0003g0138 | 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 | 178 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0183 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | a0001c0002t0006g0179 | 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 | a0001c0002t0002g0188 a0001c0002t0002g0190 a0001c0002t0002g0297 others(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 | a0001c0002t0005g0279 | 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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(226): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): 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 | a0001c0001t0001g0189 a0001c0001t0001g0316 a0001c0001t0002g0361 others(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 | a0001c0002t0005g0279 | 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 | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1654-125C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30736696 | |||||||
| chr2:30736961 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(187): 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 | 37 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(34): Show |
40 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(37): 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 | a0001c0001t0002g0373 | 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 | a0001c0002t0005g0029 | 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 | a0002c0003t0001g0081 | 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 | a0001c0001t0003g0045 a0001c0001t0006g0343 |
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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0108 others(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 | a0001c0021t0001g0278 | 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 | 39 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(36): Show |
42 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(39): 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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0352 others(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 | a0001c0001t0001g0137 | 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 | 38 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0005 others(35): Show |
41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): 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 | a0016c0019t0001g0139 | 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 | a0001c0001t0001g0282 | 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 | 249 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1653+430G>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 17/22 | chr2 | 30737805 | |||||||
| chr2:30737966 | G | GAC | 40 | a0001c0001t0001g0142 a0001c0001t0001g0183 a0001c0001t0001g0192 others(37): 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 | 18 | a0001c0001t0001g0148 a0001c0001t0001g0280 a0001c0001t0002g0001 others(15): Show |
20 | HG01071.hp1 HG01106.hp2 HG01109.hp2 others(17): 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 | 99 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0072 others(96): 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 | 10 | a0001c0001t0001g0052 a0001c0001t0001g0316 a0001c0001t0002g0121 others(7): 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 | a0001c0001t0001g0285 a0001c0001t0002g0050 a0001c0001t0002g0064 others(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 | a0001c0001t0003g0245 a0001c0001t0003g0323 a0001c0001t0003g0325 |
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 | a0001c0002t0002g0113 | 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 | 37 | a0001c0001t0001g0282 a0001c0001t0002g0361 a0003c0004t0002g0004 others(34): 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 | 38 | a0001c0001t0001g0280 a0001c0001t0002g0001 a0001c0001t0002g0005 others(35): Show |
41 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(38): 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 | a0001c0001t0001g0272 a0001c0001t0001g0285 a0001c0001t0002g0276 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0168 a0001c0001t0002g0223 others(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 | a0003c0004t0002g0035 | 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 | a0001c0002t0002g0084 | 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 | a0001c0001t0002g0241 | 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 | 181 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(178): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | 57 | a0001c0001t0001g0183 a0001c0001t0001g0272 a0001c0001t0001g0280 others(54): Show |
61 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1537-420delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30738876 | |||||||
| chr2:30738877 | T | TG | 4 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0282 others(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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | 50 | a0001c0001t0001g0183 a0001c0001t0001g0272 a0001c0001t0001g0285 others(47): Show |
54 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(51): 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 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
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 | a0001c0001t0001g0316 a0001c0001t0004g0370 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0148 | 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 | a0003c0004t0002g0206 a0003c0004t0002g0293 a0003c0004t0005g0367 others(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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(180): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0001c0002t0001g0027 a0001c0002t0001g0257 a0001c0002t0002g0020 others(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 | a0001c0002t0012g0240 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0001c0013t0002g0093 a0005c0006t0001g0069 a0005c0006t0001g0070 others(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 | a0001c0001t0002g0276 | 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 | 30 | a0001c0001t0002g0361 a0001c0002t0002g0013 a0001c0002t0002g0208 others(27): 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 | a0002c0003t0001g0203 a0002c0003t0001g0344 a0002c0003t0001g0348 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0280 a0001c0001t0003g0045 a0001c0002t0002g0112 others(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 | 187 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(184): Show |
194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): 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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(4): 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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0212 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0247 a0001c0001t0002g0119 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0109 others(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 | a0001c0001t0003g0045 a0001c0002t0002g0150 a0001c0002t0002g0163 others(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 | 187 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(184): Show |
194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): 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 | a0001c0002t0005g0028 a0003c0004t0002g0196 |
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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(86): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): 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 | a0001c0002t0001g0292 | 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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | a0001c0021t0001g0278 | 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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0005c0006t0001g0111 a0005c0006t0004g0152 |
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 | a0001c0002t0001g0085 | 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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(85): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1536+1573G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 15/22 | chr2 | 30740335 | |||||||
| chr2:30740498 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(90): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): 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 | a0001c0001t0001g0366 | 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 | a0002c0003t0001g0038 | 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 | a0003c0004t0002g0220 | 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 | a0002c0003t0001g0191 a0012c0009t0004g0221 |
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 | a0002c0003t0002g0024 | 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 | a0001c0013t0002g0093 | 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 | a0001c0002t0002g0084 a0001c0002t0002g0364 |
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 | a0001c0002t0001g0300 | 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 | a0001c0001t0002g0128 a0001c0001t0002g0230 |
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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0001g0015 | 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 | 31 | a0001c0002t0002g0013 a0001c0002t0002g0208 a0001c0002t0002g0259 others(28): 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 | a0016c0019t0001g0139 | 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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | a0001c0001t0002g0362 | 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0003g0372 |
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 | a0001c0001t0001g0282 | 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 | a0001c0013t0002g0093 | 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0015 | 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 | a0003c0004t0002g0133 | 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 | a0001c0001t0001g0366 | 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 | a0001c0001t0003g0123 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0109 | 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 | a0002c0003t0001g0308 a0002c0003t0004g0303 |
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 | a0001c0002t0001g0167 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0192 a0001c0020t0004g0054 |
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 | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(83): Show |
91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): 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 | a0001c0002t0001g0103 a0001c0002t0001g0295 a0001c0002t0002g0284 others(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 | a0007c0008t0001g0277 a0007c0008t0001g0281 |
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 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0034 others(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 | 302 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(299): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0001c0001t0001g0015 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(223): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0001c0002t0001g0103 a0001c0002t0001g0295 a0001c0002t0010g0358 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0090 a0001c0001t0002g0091 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0184 a0002c0003t0001g0032 a0002c0003t0001g0315 others(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 | 29 | a0001c0002t0002g0013 a0001c0002t0002g0208 a0001c0002t0002g0259 others(26): 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 | a0016c0019t0001g0139 | 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 | 6 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(3): 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 | a0003c0004t0002g0251 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0129 others(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 | 90 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(87): 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 | a0001c0001t0001g0137 | 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 | a0002c0003t0001g0344 | 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0120 a0001c0001t0001g0261 |
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 | a0002c0003t0001g0308 a0002c0003t0004g0303 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(87): Show |
95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): 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 | a0001c0001t0002g0128 a0001c0001t0002g0306 a0001c0001t0005g0202 others(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 | a0001c0001t0003g0287 a0001c0001t0003g0340 a0001c0001t0006g0127 others(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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(5): 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 | a0001c0001t0002g0244 a0001c0002t0001g0085 a0001c0002t0002g0048 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0171 a0001c0001t0002g0276 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | a0001c0001t0002g0276 | 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 | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(117): Show |
125 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(122): 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 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0034 others(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 | a0001c0002t0002g0020 a0004c0005t0002g0019 a0004c0005t0009g0210 |
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 | a0001c0002t0001g0103 a0001c0002t0001g0295 a0001c0002t0010g0358 |
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 | a0002c0003t0001g0081 | 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 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0034 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | 255 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(252): Show |
264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): 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 | a0001c0001t0001g0280 | 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 | 102 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0034 others(99): 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 | a0001c0001t0002g0276 | 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 | 7 | a0002c0003t0001g0002 a0002c0003t0001g0218 a0002c0003t0001g0327 others(4): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0007c0008t0001g0277 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0244 a0001c0001t0002g0276 others(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 | a0001c0001t0002g0276 | 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 | a0001c0001t0001g0154 | 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 | a0001c0002t0001g0103 a0001c0002t0001g0295 a0001c0002t0010g0358 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0129 others(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 | 22 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0009 others(19): 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 | a0001c0001t0002g0119 a0001c0001t0002g0244 a0001c0001t0002g0276 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0129 a0001c0001t0001g0148 others(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 | a0001c0013t0002g0093 | 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 | a0003c0004t0005g0030 | 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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0002c0003t0001g0344 | 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 | a0001c0001t0002g0119 a0001c0001t0002g0244 |
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 | a0003c0004t0002g0165 | 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 | a0003c0004t0002g0207 | 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0012g0240 | 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 | 145 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(142): Show |
152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): 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 | a0001c0001t0002g0274 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | a0001c0002t0001g0103 a0001c0002t0001g0295 a0001c0002t0010g0358 |
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 | 6 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(3): 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 | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(182): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): 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 | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(182): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1236+1343A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 11/22 | chr2 | 30749760 | |||||||
| chr2:30749803 | C | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(182): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): 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 | a0007c0008t0001g0277 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0079 a0001c0001t0002g0090 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0079 a0001c0001t0002g0090 others(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 | 21 | a0001c0001t0001g0280 a0001c0001t0002g0001 a0001c0001t0002g0234 others(18): 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 | a0001c0001t0002g0274 | 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 | 112 | a0001c0001t0002g0276 a0001c0001t0008g0080 a0001c0002t0001g0007 others(109): 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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(198): Show |
208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): 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 | a0001c0013t0002g0093 a0016c0019t0001g0139 |
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 | a0001c0001t0001g0135 a0001c0001t0002g0079 a0001c0001t0002g0090 others(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 | a0001c0001t0001g0061 | 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 | a0002c0003t0001g0371 | 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 | 6 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(3): 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 | 155 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(152): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0001c0001t0002g0274 | 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0241 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | 55 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0009 others(52): 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 | a0003c0004t0005g0367 | 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 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0034 others(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 | 127 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(124): 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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | 136 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(133): 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 | 129 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(126): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0001t0001g0142 | 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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(301): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0002t0002g0062 | 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 | 10 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0280 others(7): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0002c0003t0001g0081 | 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 | a0001c0001t0001g0366 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | 76 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0109 others(73): 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 | a0001c0002t0002g0084 a0001c0002t0002g0364 |
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 | a0001c0013t0002g0093 a0016c0019t0001g0139 |
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 | 60 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0002t0001g0006 others(57): 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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0130 others(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 | a0001c0013t0002g0093 a0016c0019t0001g0139 |
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 | a0001c0001t0003g0323 a0001c0001t0003g0325 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | a0004c0005t0002g0044 | 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 | a0003c0004t0002g0100 a0003c0004t0002g0101 a0003c0004t0002g0102 others(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 | a0001c0002t0012g0240 | 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 | 52 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0135 others(49): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0003g0372 |
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 | 12 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0142 others(9): 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 | 303 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(300): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | a0001c0001t0002g0119 a0001c0001t0002g0244 |
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 | 303 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(300): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): 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 | a0010c0017t0002g0016 | 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 | 30 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0002g0001 others(27): 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 | a0001c0001t0003g0365 | 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 | a0001c0001t0002g0223 a0001c0001t0002g0235 |
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 | 203 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(200): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): 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 | a0001c0001t0008g0080 | 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 | a0002c0003t0002g0334 | 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 | a0001c0001t0001g0280 a0001c0001t0007g0228 a0001c0001t0007g0229 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0141 others(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 | a0001c0001t0003g0372 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0275 a0001c0001t0003g0104 a0001c0001t0003g0138 others(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 | a0001c0002t0001g0027 a0001c0002t0001g0257 a0001c0002t0002g0020 others(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 | a0001c0001t0001g0141 | 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 | 69 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(66): Show |
71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): 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 | a0001c0002t0002g0369 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0130 others(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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(301): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0002t0005g0346 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0108 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0005g0353 |
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 | 308 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(305): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | a0005c0006t0001g0069 a0005c0006t0001g0070 a0005c0006t0001g0111 others(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 | 300 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(297): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.866+1425A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 8/22 | chr2 | 30756621 | |||||||
| chr2:30756799 | G | A | 54 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0009 others(51): 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 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0004g0095 |
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 | a0001c0001t0002g0355 | 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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(72): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0007c0008t0001g0277 others(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 | a0001c0001t0001g0174 | 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 | a0003c0004t0002g0101 | 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 | 54 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0009 others(51): 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 | a0001c0002t0005g0345 | 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 | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(137): Show |
148 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(145): 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 | a0002c0003t0002g0024 | 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 | a0001c0001t0001g0117 a0001c0001t0004g0043 |
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 | a0001c0001t0006g0304 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0275 a0001c0001t0002g0079 others(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 | a0001c0001t0001g0003 | 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 | a0002c0003t0001g0022 a0002c0003t0001g0099 a0002c0003t0001g0178 others(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 | a0002c0003t0004g0155 | 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 | 57 | a0001c0001t0002g0119 a0001c0001t0002g0244 a0001c0002t0001g0006 others(54): 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 | 57 | a0001c0001t0002g0119 a0001c0001t0002g0244 a0001c0002t0001g0006 others(54): 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 | a0001c0001t0001g0225 | 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 | 70 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0142 others(67): 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 | a0001c0001t0002g0232 | 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 | 55 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0009 others(52): 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 | a0001c0001t0003g0014 | 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 | a0001c0001t0008g0080 | 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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0276 others(4): 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 | a0001c0001t0002g0134 a0001c0001t0002g0231 a0001c0001t0002g0232 others(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 | a0001c0001t0008g0080 | 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 | a0001c0001t0001g0285 | 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 | a0003c0004t0002g0100 a0003c0004t0002g0101 a0003c0004t0002g0102 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0225 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0272 a0001c0001t0007g0228 a0001c0001t0007g0229 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0199 a0001c0001t0002g0250 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0199 a0001c0001t0002g0250 others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.775-650delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30758786 | |||||||
| chr2:30758787 | T | C | 47 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): 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 | a0001c0002t0003g0031 a0001c0002t0003g0033 a0001c0002t0005g0017 others(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 |
57 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0272 others(54): 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 | a0003c0004t0002g0164 | 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 | a0001c0001t0002g0050 a0001c0001t0002g0199 a0001c0001t0002g0250 others(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 | a0003c0004t0002g0206 a0003c0004t0002g0293 a0003c0004t0005g0367 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | a0001c0001t0002g0071 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | a0001c0001t0003g0138 a0001c0001t0003g0145 a0001c0001t0003g0271 others(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 | 23 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0135 others(20): Show |
24 | HG00099.hp1 HG00408.hp2 HG01169.hp2 others(21): 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 | a0001c0002t0003g0158 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0282 |
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 | 21 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0276 others(18): 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 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0004g0095 |
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 | a0001c0001t0003g0014 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0078 others(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 | a0002c0003t0001g0038 | 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 | a0001c0001t0003g0036 a0002c0003t0001g0022 a0002c0003t0001g0099 others(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 | a0001c0001t0003g0036 a0002c0003t0001g0022 a0002c0003t0001g0099 others(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 | 22 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0276 others(19): 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 | a0001c0001t0003g0036 a0002c0003t0001g0022 a0002c0003t0001g0099 others(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 | 20 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0276 others(17): 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 | 22 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0276 others(19): 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 | 48 | a0001c0001t0002g0001 a0001c0001t0002g0050 a0001c0001t0002g0090 others(45): 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 | 61 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0002g0064 others(58): 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 | a0001c0001t0003g0086 | 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0083 others(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 | 96 | a0001c0001t0001g0078 a0001c0001t0001g0135 a0001c0001t0001g0142 others(93): 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 | a0001c0001t0003g0014 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0247 a0001c0001t0002g0185 a0001c0001t0002g0223 others(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 | a0003c0004t0002g0176 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0282 a0001c0002t0002g0172 others(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 | a0001c0001t0002g0276 | 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 | a0002c0003t0001g0194 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0146 others(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 | 30 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0135 others(27): Show |
31 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(28): 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 | a0001c0001t0004g0144 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0280 a0001c0001t0002g0226 a0001c0001t0002g0306 others(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 | a0001c0002t0002g0065 | 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 | 31 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0135 others(28): Show |
32 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(29): 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 | 9 | a0001c0001t0002g0001 a0001c0001t0002g0231 a0001c0001t0002g0232 others(6): 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 | a0001c0001t0002g0079 | 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 | a0003c0004t0005g0030 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0154 others(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 | a0001c0001t0003g0086 | 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 | 66 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0247 others(63): 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 | a0001c0001t0004g0159 | 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 | 124 | a0001c0001t0001g0078 a0001c0001t0001g0129 a0001c0001t0001g0131 others(121): 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 | a0002c0003t0001g0204 a0011c0015t0001g0082 |
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 | 51 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0135 others(48): Show |
51 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(48): 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 | a0001c0001t0001g0273 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0146 a0001c0001t0002g0276 a0001c0001t0004g0144 others(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 | a0001c0001t0002g0216 a0001c0001t0003g0014 a0001c0001t0003g0036 others(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 | a0001c0001t0003g0086 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0013c0012t0002g0269 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0002g0108 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0154 others(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 | 231 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(228): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): 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 | a0002c0003t0001g0170 | 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 | a0001c0001t0003g0086 | 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 | 18 | a0001c0001t0001g0110 a0001c0001t0001g0183 a0001c0001t0002g0005 others(15): Show |
19 | HG00099.hp1 HG00423.hp2 HG01169.hp2 others(16): 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | 235 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0002g0216 a0001c0001t0003g0036 a0001c0001t0003g0045 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0149 | 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 | a0003c0004t0002g0101 | 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 | a0001c0002t0001g0249 | 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 | a0001c0001t0008g0080 | 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 | 15 | a0001c0001t0001g0110 a0001c0001t0001g0183 a0001c0001t0002g0005 others(12): Show |
16 | HG00099.hp1 HG00423.hp2 HG01169.hp2 others(13): 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0109 others(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 | a0001c0002t0001g0103 a0001c0002t0001g0295 |
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 | 40 | a0001c0001t0001g0110 a0001c0001t0001g0129 a0001c0001t0001g0183 others(37): Show |
41 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(38): 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 | a0001c0001t0001g0129 a0001c0001t0001g0224 a0001c0001t0001g0242 others(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 | a0001c0001t0002g0047 a0001c0002t0001g0027 a0001c0002t0002g0026 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0226 a0001c0001t0002g0231 others(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 | a0001c0001t0002g0216 a0001c0001t0002g0223 a0001c0001t0002g0276 others(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 | 234 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(231): 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 |
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 | a0001c0001t0002g0223 a0001c0013t0002g0093 a0007c0008t0001g0277 others(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 | a0002c0003t0001g0051 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0057 others(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 | 151 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0001c0001t0001g0109 others(148): Show |
152 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.775-1956delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760092 | |||||||
| chr2:30760146 | G | T | 48 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0001c0001t0001g0115 others(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 | a0001c0001t0002g0079 | 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 | 255 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(252): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.775-2084G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30760221 | |||||||
| chr2:30760257 | T | C | 5 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(2): 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 | 211 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(208): 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 | a0001c0002t0005g0279 | 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 | a0001c0001t0006g0343 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0129 others(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 | 109 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(106): 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 | a0001c0001t0002g0168 a0001c0001t0002g0239 a0014c0011t0002g0132 |
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 | 179 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0052 others(176): 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 | a0001c0001t0001g0247 a0001c0001t0001g0282 a0001c0002t0012g0240 |
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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(301): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): 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 | a0001c0002t0001g0027 | 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 | a0001c0002t0002g0284 a0001c0002t0005g0114 |
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 | 268 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(265): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0141 others(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 | 254 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(251): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): 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 | a0001c0002t0004g0073 | 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 | a0001c0001t0008g0080 | 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 | a0001c0002t0002g0084 | 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 | a0001c0002t0005g0336 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0368 a0001c0002t0002g0074 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0238 a0001c0001t0002g0223 a0001c0001t0003g0372 |
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 | 41 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0238 others(38): 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 | a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | 89 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0130 others(86): 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 | a0003c0004t0005g0342 | 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 | 263 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): 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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0238 others(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 | a0001c0001t0002g0244 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0247 others(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 | a0001c0002t0004g0073 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0247 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0235 a0001c0001t0002g0244 others(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 | a0001c0002t0002g0012 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0238 others(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 | 2 | a0001c0001t0002g0005 a0002c0003t0001g0338 |
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 | 282 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(279): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.774+174C>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 7/22 | chr2 | 30762908 | |||||||
| chr2:30762963 | C | T | 321 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(318): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): 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 | a0001c0002t0002g0150 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0275 a0001c0001t0002g0079 a0001c0001t0002g0090 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(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 | a0001c0001t0002g0250 a0001c0001t0006g0304 a0001c0001t0006g0343 others(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 | a0002c0003t0001g0305 | 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 | 2 | a0003c0004t0002g0004 a0003c0004t0002g0055 |
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 | 8 | a0001c0001t0001g0275 a0001c0001t0002g0005 a0001c0001t0002g0071 others(5): 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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0146 others(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 | 327 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(324): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0001g0352 a0001c0001t0002g0171 a0001c0001t0002g0235 others(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 | a0001c0001t0001g0272 a0001c0001t0002g0079 a0001c0001t0007g0228 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | a0002c0003t0001g0081 | 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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0352 a0001c0001t0002g0235 a0001c0001t0002g0244 others(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 | a0003c0004t0002g0196 | 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 | a0001c0002t0002g0012 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | a0003c0004t0005g0367 | 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 | 98 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0057 others(95): 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 | 165 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(162): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): 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 | a0001c0001t0001g0129 a0001c0001t0002g0128 a0001c0001t0002g0230 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0142 others(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 | 153 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(150): Show |
156 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.525-928A>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765234 | |||||||
| chr2:30765235 | T | G | 163 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(160): Show |
166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.525-929A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765235 | |||||||
| chr2:30765282 | G | A | 161 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(158): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.525-976C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765282 | |||||||
| chr2:30765509 | A | G | 303 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0042 others(300): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0001g0092 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0226 a0001c0001t0002g0306 others(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 | 2 | a0001c0001t0002g0185 a0001c0002t0002g0201 |
2 | HG03654.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.525-1406C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30765712 | |||||||
| chr2:30765795 | A | G | 2 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0001g0129 a0001c0001t0002g0128 a0001c0001t0002g0230 others(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 | a0001c0002t0001g0292 a0001c0002t0001g0298 a0001c0002t0001g0299 others(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 | a0001c0002t0002g0369 a0001c0002t0004g0359 a0001c0002t0005g0314 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0137 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | 110 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0057 others(107): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0282 a0001c0001t0003g0287 |
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 | a0001c0002t0002g0012 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0002t0002g0012 | 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 | a0001c0001t0002g0349 | 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 | a0007c0008t0001g0277 | 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 | 13 | a0001c0001t0001g0352 a0001c0001t0002g0001 a0001c0001t0002g0234 others(10): 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 | 299 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0042 others(296): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.524+2851C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30767462 | |||||||
| chr2:30767530 | C | T | 11 | a0001c0001t0001g0352 a0001c0001t0002g0001 a0001c0001t0002g0234 others(8): 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 | 6 | a0001c0002t0002g0297 a0002c0003t0001g0002 a0002c0003t0001g0218 others(3): 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 | 303 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0042 others(300): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): 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 | a0001c0001t0001g0146 a0001c0001t0001g0236 a0001c0001t0001g0282 others(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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(4): 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 | 35 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0352 others(32): 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 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0142 others(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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0352 a0001c0001t0002g0079 others(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 | a0014c0011t0002g0132 | 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 | 304 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0042 others(301): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): 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 | a0001c0001t0001g0149 a0001c0001t0001g0352 a0001c0001t0002g0079 others(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 | a0014c0011t0002g0132 | 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 | a0001c0001t0003g0116 a0002c0003t0001g0181 a0002c0003t0001g0211 others(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 | 18 | a0001c0001t0001g0149 a0001c0001t0001g0352 a0001c0001t0002g0001 others(15): 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 | a0016c0019t0001g0139 | 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | a0001c0013t0002g0093 | 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 | 8 | a0001c0001t0001g0010 a0001c0001t0002g0001 a0001c0001t0002g0234 others(5): 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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0001c0001t0001g0352 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0231 a0001c0001t0002g0232 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0272 a0001c0001t0002g0128 others(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 | a0002c0003t0001g0305 a0005c0006t0001g0069 a0005c0006t0001g0070 others(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 | a0001c0001t0001g0189 | 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 | a0014c0011t0002g0132 | 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 | 100 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(97): 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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | a0001c0001t0001g0275 a0001c0001t0002g0134 a0001c0001t0002g0239 others(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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0368 a0001c0001t0002g0186 others(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 | a0014c0011t0002g0132 | 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 | a0001c0001t0002g0244 | 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 | a0003c0004t0002g0098 | 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 | a0001c0002t0002g0190 | 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 | a0001c0001t0008g0080 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0002t0003g0031 | 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 | a0001c0001t0002g0050 a0001c0001t0002g0216 a0001c0001t0002g0355 others(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 | 251 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(248): Show |
259 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(256): 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 | a0003c0004t0002g0165 | 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 | a0002c0003t0001g0219 | 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 | 53 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(50): Show |
55 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.524+358T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 5/22 | chr2 | 30769955 | |||||||
| chr2:30769992 | G | A | 8 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(5): 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 | a0001c0001t0001g0352 a0001c0001t0002g0235 a0001c0001t0002g0244 others(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 | 266 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(263): Show |
274 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(271): 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 | a0002c0003t0001g0204 | 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 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0242 a0001c0001t0004g0095 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0002g0239 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | a0001c0001t0002g0134 | 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 | a0003c0004t0002g0176 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0154 others(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 | 102 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(99): 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0002g0250 a0001c0001t0002g0252 |
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 | 17 | a0001c0001t0001g0149 a0001c0001t0001g0352 a0001c0001t0002g0001 others(14): 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 | a0001c0001t0004g0370 a0001c0001t0008g0080 a0001c0002t0002g0147 |
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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0149 a0001c0001t0002g0079 a0001c0001t0002g0226 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0120 |
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 | 235 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(232): Show |
245 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(242): 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0003g0372 | 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 | a0001c0002t0002g0067 | 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 | a0001c0001t0005g0353 | 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 | a0001c0002t0003g0031 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 |
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 | 301 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(298): Show |
311 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(308): 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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0352 a0001c0001t0002g0079 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0008g0080 | 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 | a0001c0001t0001g0149 | 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 | 211 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(208): Show |
219 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(216): 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 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0224 others(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 | 277 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(274): Show |
285 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.388-2374delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772822 | |||||||
| chr2:30772835 | T | C | 1 | a0001c0001t0006g0046 | 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 | 223 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(220): Show |
233 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.388-2404G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 4/22 | chr2 | 30772853 | |||||||
| chr2:30773014 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(241): Show |
254 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(251): 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 | a0002c0003t0001g0204 | 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 | a0001c0020t0004g0054 | 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 | 299 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(296): Show |
309 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(306): 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 | a0002c0003t0001g0305 | 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 | a0002c0003t0001g0197 | 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 | 73 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(70): Show |
75 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(72): 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 | a0001c0001t0001g0149 a0001c0001t0002g0079 a0001c0001t0002g0226 others(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 | 23 | a0001c0001t0001g0149 a0001c0001t0001g0238 a0001c0001t0001g0280 others(20): 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 | a0014c0011t0002g0132 | 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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | 8 | a0001c0001t0001g0189 a0001c0002t0002g0188 a0001c0002t0002g0190 others(5): 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 | a0001c0001t0004g0125 a0001c0001t0004g0159 a0002c0003t0004g0155 others(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 | a0001c0001t0006g0304 a0001c0001t0006g0343 a0003c0004t0005g0342 |
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 | a0001c0002t0001g0034 a0005c0006t0001g0069 a0005c0006t0001g0070 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0079 a0001c0001t0002g0226 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | 235 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(232): Show |
245 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(242): 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 | a0001c0020t0004g0054 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0149 a0001c0001t0002g0079 |
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 | a0001c0001t0002g0168 a0001c0002t0001g0167 |
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 | 100 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(97): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(5): 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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(5): 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 | a0001c0002t0005g0029 | 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 | a0001c0001t0003g0045 a0001c0002t0003g0033 |
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 | 100 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(97): Show |
102 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(99): 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 | a0001c0020t0004g0054 | 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 | a0001c0001t0002g0239 a0001c0001t0004g0087 a0001c0001t0005g0088 others(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 | 9 | a0001c0001t0001g0174 a0001c0001t0002g0001 a0001c0001t0002g0234 others(6): 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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | 8 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(5): 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 | a0001c0001t0002g0349 a0001c0001t0005g0360 a0002c0003t0004g0025 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0142 |
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 | a0002c0003t0001g0371 | 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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(136): Show |
143 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.272-113delA | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776157 | |||||||
| chr2:30776325 | G | A | 1 | a0001c0001t0008g0080 | 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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0280 a0001c0001t0002g0223 others(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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(4): 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 | a0001c0001t0001g0280 | 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 | 7 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 others(4): 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 | 33 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0352 others(30): 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 | a0001c0001t0001g0316 | 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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0002g0079 others(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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(95): Show |
100 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.271+600C>T | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 3/22 | chr2 | 30776967 | |||||||
| chr2:30776994 | G | C | 17 | a0001c0001t0001g0248 a0001c0002t0001g0006 a0001c0002t0001g0007 others(14): 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 | a0001c0001t0001g0242 a0001c0001t0004g0095 |
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 | a0001c0021t0001g0278 | 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 | a0001c0001t0001g0137 a0001c0001t0002g0231 a0001c0001t0002g0232 others(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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | 20 | a0001c0001t0001g0149 a0001c0001t0001g0238 a0001c0001t0001g0280 others(17): 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 | a0001c0001t0001g0117 | 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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0129 a0001c0001t0002g0128 a0001c0001t0002g0230 others(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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0002c0003t0011g0320 | 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 | a0002c0003t0004g0011 a0005c0006t0004g0152 |
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 | a0001c0001t0001g0115 a0001c0001t0002g0226 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0242 a0001c0001t0004g0095 |
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 | a0001c0001t0008g0080 a0014c0011t0002g0132 |
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 | 260 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(257): Show |
270 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(267): 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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0241 |
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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0008g0080 a0014c0011t0002g0132 |
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 | 234 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(231): Show |
244 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(241): 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 | a0001c0001t0001g0089 a0001c0001t0001g0120 a0001c0001t0001g0142 others(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 | a0002c0003t0002g0334 | 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 | a0001c0001t0002g0373 a0002c0003t0001g0371 a0016c0019t0001g0139 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0137 others(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 | a0002c0003t0001g0032 a0002c0003t0001g0051 a0002c0003t0001g0160 others(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 | a0001c0002t0002g0259 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0002g0239 a0001c0001t0004g0087 a0001c0001t0005g0088 others(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 | 141 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(138): Show |
145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): 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 | a0005c0006t0001g0111 | 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 | a0001c0001t0002g0047 a0001c0002t0001g0027 a0001c0002t0002g0113 others(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 | 236 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(233): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): 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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0014c0011t0002g0132 | 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 | a0014c0011t0002g0132 | 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 | a0001c0001t0001g0192 | 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 | a0003c0004t0002g0102 | 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 | 141 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(138): Show |
145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-2346T>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30779985 | |||||||
| chr2:30780097 | C | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(74): Show |
81 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.199-2458G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780097 | |||||||
| chr2:30780153 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(135): Show |
142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | 139 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(136): Show |
143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-2940T>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780579 | |||||||
| chr2:30780580 | AC | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(136): Show |
143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.199-2942delG | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30780580 | |||||||
| chr2:30780821 | C | T | 1 | a0003c0004t0005g0118 | 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 | 138 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(135): Show |
142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): 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 | a0001c0001t0001g0109 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0352 | 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 | 138 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(135): Show |
142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): 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 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0076 others(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 | a0003c0004t0005g0030 | 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 | a0002c0003t0001g0308 | 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 | 6 | a0001c0002t0001g0310 a0001c0002t0002g0297 a0002c0003t0001g0002 others(3): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0001t0008g0080 others(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 | 87 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0130 others(84): 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 | a0001c0002t0002g0255 | 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 | 300 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(297): Show |
310 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.199-4573A>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782212 | |||||||
| chr2:30782213 | T | G | 300 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(297): Show |
310 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(307): 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 | a0001c0001t0001g0352 a0001c0001t0002g0235 a0001c0001t0002g0244 others(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 | 294 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(291): Show |
304 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(301): 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 | 173 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(170): Show |
177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | 137 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(134): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.198+4697A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30782431 | |||||||
| chr2:30782546 | G | A | 277 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(274): Show |
287 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(284): 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 | a0002c0003t0001g0308 | 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 | 173 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(170): Show |
177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): 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 | a0001c0002t0001g0021 | 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 | a0002c0003t0001g0302 | 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 | 124 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0129 others(121): 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 | a0001c0001t0002g0349 | 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 | a0002c0003t0001g0032 | 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 | 294 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(291): Show |
304 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(301): 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 | a0001c0002t0001g0167 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | 97 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(94): 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 | 99 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(96): 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 | 102 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0077 others(99): 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 | a0001c0002t0001g0167 | 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 | 295 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(292): Show |
305 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(302): 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 | a0002c0003t0004g0286 | 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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0003c0004t0005g0367 | 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 | a0003c0004t0005g0367 | 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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0001t0002g0349 a0001c0001t0005g0360 a0002c0003t0004g0025 others(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 | 291 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(288): Show |
301 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.198+3270G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30783858 | |||||||
| chr2:30783902 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(169): Show |
176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): 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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.198+2859A>G | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784269 | |||||||
| chr2:30784272 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0001t0001g0242 a0001c0001t0001g0275 a0001c0001t0002g0239 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0001t0008g0080 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0001c0001t0002g0223 | 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 | 169 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(166): Show |
173 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.198+2315G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30784813 | |||||||
| chr2:30784926 | C | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(128): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): 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 | a0001c0001t0002g0226 a0001c0001t0002g0306 a0001c0002t0002g0222 |
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 | 43 | a0001c0001t0001g0189 a0001c0001t0001g0275 a0001c0001t0001g0285 others(40): 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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | a0001c0001t0004g0125 a0001c0001t0004g0159 a0002c0003t0004g0155 others(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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0234 a0001c0001t0002g0294 |
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 | a0004c0005t0001g0105 | 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 | 90 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0174 others(87): 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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | 120 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0129 others(117): 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 | a0001c0001t0002g0239 a0001c0001t0004g0087 a0001c0001t0004g0144 others(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 | a0001c0002t0004g0359 a0001c0002t0005g0314 a0002c0003t0004g0286 |
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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | 44 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(41): 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 | 120 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0129 others(117): 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 | 147 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(144): Show |
151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.198+783C>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786345 | |||||||
| chr2:30786440 | C | G | 324 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(321): Show |
335 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.198+688G>C | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 2/22 | chr2 | 30786440 | |||||||
| chr2:30786534 | A | G | 42 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0135 others(39): 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 | a0005c0006t0001g0267 | 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 | 121 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0129 others(118): 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 | 41 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0137 others(38): 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 | 19 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0236 others(16): 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 | a0001c0001t0008g0080 | 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 | a0002c0003t0001g0371 | 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 | 346 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(343): Show |
357 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(354): 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 | 339 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0042 others(336): Show |
350 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(347): 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 | a0001c0002t0002g0094 | 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 | a0001c0001t0001g0149 | 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 | a0001c0021t0001g0278 | 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 | a0016c0019t0001g0139 | 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 | a0001c0001t0002g0128 a0001c0001t0004g0087 a0001c0001t0004g0144 others(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 | a0001c0001t0003g0014 | 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 | a0001c0002t0005g0314 | 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 | a0001c0001t0001g0290 a0002c0003t0001g0037 |
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 | 69 | a0001c0001t0001g0057 a0001c0001t0001g0072 a0001c0001t0001g0076 others(66): 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 | a0001c0001t0001g0149 a0001c0001t0008g0080 |
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 | 158 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0072 others(155): 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 | a0001c0002t0001g0310 a0001c0002t0002g0312 a0001c0002t0002g0351 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0149 a0001c0001t0001g0224 others(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 | a0004c0005t0002g0260 | 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 | a0001c0001t0001g0148 a0001c0002t0002g0147 |
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 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0001c0001t0002g0230 a0001c0001t0002g0235 a0001c0001t0002g0244 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0247 a0001c0001t0005g0353 |
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 | a0001c0002t0002g0288 a0003c0004t0005g0367 |
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 | a0001c0001t0001g0135 a0001c0002t0005g0114 |
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 | a0001c0001t0002g0373 | 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 | a0001c0001t0005g0202 a0001c0002t0002g0201 a0001c0002t0005g0017 others(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 | a0001c0001t0003g0340 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0002c0003t0001g0219 | 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 | a0001c0002t0001g0085 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0224 | 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 | a0001c0002t0002g0140 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0261 others(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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0280 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | 61 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(58): 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 | a0001c0001t0001g0117 a0001c0002t0002g0065 |
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 | a0001c0001t0001g0129 a0001c0001t0002g0108 a0001c0001t0002g0128 others(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 | a0001c0002t0002g0311 | 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 | a0001c0002t0004g0359 a0001c0002t0005g0314 a0003c0004t0005g0118 others(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 | a0001c0002t0002g0163 | 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 | a0001c0001t0001g0280 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | a0013c0012t0002g0269 | 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 | 76 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0001c0001t0001g0077 others(73): Show |
79 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(76): 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0272 others(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 | a0001c0001t0004g0161 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | a0001c0001t0005g0243 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
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 | 3 | a0001c0002t0002g0357 a0002c0003t0001g0002 a0002c0003t0001g0328 |
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 | a0001c0001t0002g0223 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0002c0003t0001g0317 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0002t0005g0279 others(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 | 329 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(326): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0003g0107 a0001c0001t0003g0123 a0002c0003t0004g0106 |
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 | 261 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(258): Show |
270 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(267): 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(52): 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 | 166 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0072 others(163): Show |
171 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(168): 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0261 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0280 a0001c0001t0002g0226 others(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 | a0002c0003t0001g0371 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0352 a0001c0001t0002g0276 a0007c0008t0001g0277 |
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 | a0001c0002t0005g0314 a0003c0004t0005g0118 a0009c0018t0001g0313 |
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 | a0012c0009t0004g0221 | 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 | a0002c0003t0002g0334 | 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 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0149 | 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 | a0001c0002t0002g0140 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | 42 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(39): 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0001g0135 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | 189 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(186): Show |
196 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(193): 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 | a0001c0001t0001g0072 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0001t0004g0161 | 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 | a0001c0001t0002g0226 | 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 | a0001c0001t0001g0209 | 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 | 48 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(45): 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 | a0001c0001t0001g0109 a0001c0001t0002g0064 a0001c0001t0002g0108 others(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 | a0001c0002t0002g0140 | 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 | 159 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0072 others(156): Show |
164 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(161): 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 | a0001c0001t0002g0186 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0261 a0001c0001t0002g0250 others(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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 |
3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0002g0230 a0001c0001t0002g0235 a0001c0001t0002g0244 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | a0001c0001t0005g0243 a0001c0002t0012g0240 |
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 | a0001c0001t0001g0149 | 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 | a0001c0002t0012g0240 | 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 | a0001c0001t0005g0243 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | a0001c0001t0001g0149 a0001c0001t0002g0373 a0001c0001t0003g0372 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | 43 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(40): 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 | a0001c0001t0005g0202 a0001c0002t0002g0201 |
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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 |
3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0001c0001t0005g0353 a0001c0002t0002g0270 a0001c0013t0002g0093 |
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 | a0001c0001t0001g0268 a0001c0001t0001g0282 a0001c0001t0002g0064 others(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 | a0003c0004t0005g0342 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0001g0109 a0001c0001t0002g0064 a0001c0001t0002g0108 others(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 | a0001c0002t0002g0311 | 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 | a0001c0001t0004g0159 | 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 | |||||||
| chr2:30796499 | T | G | 12 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0268 others(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 | 2 | a0001c0001t0002g0001 a0001c0001t0002g0294 |
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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0001g0268 a0001c0001t0002g0283 a0001c0002t0005g0279 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0002c0003t0004g0151 | 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 | a0001c0001t0001g0273 a0001c0001t0002g0274 |
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 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0003 a0001c0002t0010g0358 |
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 | a0001c0001t0001g0109 a0001c0001t0002g0064 a0001c0001t0002g0108 others(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 | a0001c0002t0003g0158 | 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 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0282 others(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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | a0001c0002t0004g0073 | 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 | a0001c0002t0002g0332 | 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 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0001g0078 a0001c0001t0002g0079 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0316 others(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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0280 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 a0016c0019t0001g0139 |
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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0268 a0001c0001t0001g0272 others(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 | 59 | a0001c0001t0001g0052 a0001c0001t0001g0246 a0001c0001t0001g0248 others(56): 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 | a0002c0003t0002g0334 | 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 | a0002c0003t0002g0334 | 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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0373 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | 116 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0072 others(113): Show |
121 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(118): 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 | a0001c0001t0002g0108 | 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 | 72 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(69): 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0268 others(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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(68): 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 | a0001c0001t0003g0045 | 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 | a0001c0002t0004g0040 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0268 others(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 | a0001c0001t0003g0116 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0224 a0001c0002t0005g0314 |
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 | a0001c0001t0001g0129 a0001c0001t0002g0128 a0001c0001t0006g0127 |
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 | 67 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(64): 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0268 others(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 | a0004c0005t0002g0205 | 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 | 97 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0146 others(94): Show |
100 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(97): 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 | a0001c0001t0001g0109 | 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 | 67 | a0001c0001t0001g0052 a0001c0001t0001g0246 a0001c0001t0001g0248 others(64): Show |
70 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.-33+7304G>A | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30799998 | |||||||
| chr2:30800030 | C | T | 80 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0246 others(77): Show |
83 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(80): 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0001g0296 | 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 | a0001c0002t0004g0359 | 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0001g0296 | 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 | a0002c0003t0004g0286 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0209 | 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 | 63 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0057 others(60): Show |
65 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(62): 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 | a0001c0001t0001g0015 a0001c0001t0001g0130 a0001c0001t0001g0142 others(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 | a0001c0001t0002g0355 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0117 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0247 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0061 a0001c0001t0002g0108 a0001c0001t0002g0274 others(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 | a0001c0001t0002g0362 a0001c0002t0002g0153 |
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 | a0003c0004t0002g0133 a0004c0005t0009g0210 |
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 | a0001c0001t0002g0283 | 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 | a0001c0001t0001g0282 | 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 | a0001c0002t0001g0249 | 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 | a0005c0006t0001g0267 | 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 | a0002c0003t0004g0155 | 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 | a0001c0002t0002g0255 | 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 | a0001c0001t0002g0250 | 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 | a0001c0002t0001g0257 a0004c0005t0002g0260 |
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 | a0003c0004t0002g0251 | 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 | a0002c0003t0001g0265 | 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 | a0005c0006t0001g0266 | 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0280 a0002c0003t0001g0204 a0015c0016t0001g0363 |
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 | a0001c0002t0001g0008 | 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 | a0001c0002t0005g0345 a0003c0004t0002g0102 |
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 | a0001c0001t0003g0138 | 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 | a0001c0001t0003g0325 | 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 | a0001c0001t0002g0119 a0003c0004t0002g0035 |
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 | a0004c0005t0002g0258 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0352 a0001c0001t0002g0276 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0001t0002g0079 others(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 | a0001c0001t0003g0107 a0001c0001t0003g0123 a0001c0002t0001g0085 others(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 | a0001c0001t0003g0245 a0001c0021t0001g0278 |
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 | a0001c0002t0002g0259 | 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 | a0003c0004t0002g0253 | 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 | a0004c0005t0002g0258 | 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 | a0004c0005t0002g0254 | 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 | a0001c0001t0001g0209 a0001c0001t0004g0087 |
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 | a0003c0004t0002g0262 | 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 | a0006c0007t0005g0264 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0268 a0001c0002t0002g0147 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0003g0372 | 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 | a0016c0019t0001g0139 | 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 | a0007c0008t0001g0277 | 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 | a0001c0001t0002g0373 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0162 others(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 | a0001c0002t0001g0295 | 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 | 3 | a0001c0001t0002g0001 a0001c0001t0002g0294 a0001c0001t0003g0340 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0261 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0247 others(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 | a0001c0002t0004g0040 | 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 | a0001c0001t0005g0360 a0001c0002t0001g0333 a0002c0003t0002g0334 |
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 | 1 | a0001c0001t0002g0005 | 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 | a0001c0021t0001g0278 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0268 others(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 | a0001c0001t0002g0064 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0002c0003t0001g0124 | 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 | a0003c0004t0002g0220 | 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 | a0003c0004t0002g0293 | 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 | 46 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(43): 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0003c0004t0002g0293 | 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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0002g0226 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0042 a0001c0002t0002g0041 |
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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0209 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0115 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0002g0274 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0268 others(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 | 271 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(268): 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 | a0001c0001t0001g0272 | 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 | a0004c0005t0002g0258 | 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 | a0001c0001t0001g0282 a0001c0001t0002g0283 a0007c0008t0001g0281 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0004g0144 a0001c0002t0002g0113 |
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 | a0001c0001t0001g0261 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | a0001c0001t0003g0045 a0001c0001t0006g0046 |
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 | a0003c0004t0005g0367 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0002g0230 others(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 | a0001c0001t0002g0276 a0007c0008t0001g0277 |
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 | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(55): 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
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 | a0001c0001t0001g0247 | 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 | 32 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0355 others(29): Show |
33 | HG00597.hp1 HG00741.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+4759dupC | CAPN13 | ENSG00000162949.16 | transcript | ENST00000295055.12 | protein_coding | 1/22 | chr2 | 30802542 | |||||||
| chr2:30802542 | TG | T | 179 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(176): 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 | 57 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(54): 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 | a0001c0001t0002g0230 | 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 | a0001c0002t0002g0284 | 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 | 46 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(43): 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 | a0001c0002t0002g0062 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0002g0373 a0001c0001t0003g0138 a0001c0001t0003g0372 others(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 | a0001c0001t0001g0282 a0001c0001t0002g0283 a0007c0008t0001g0281 |
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 | a0001c0001t0002g0283 | 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 | a0001c0002t0002g0288 a0003c0004t0005g0367 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0242 a0001c0001t0002g0241 |
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 | a0001c0001t0007g0228 a0001c0001t0007g0229 |
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 | a0014c0011t0002g0132 | 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 | a0003c0004t0002g0133 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0006c0007t0005g0263 a0006c0007t0005g0264 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | 51 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(48): 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 | a0001c0001t0002g0244 a0001c0001t0003g0145 a0001c0001t0005g0243 |
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 | a0001c0002t0005g0279 a0001c0021t0001g0278 |
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 | a0001c0001t0001g0261 a0001c0001t0002g0250 a0001c0001t0002g0252 others(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 | 202 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(199): 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 | a0001c0001t0002g0223 | 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 | 205 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(202): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0002t0005g0279 a0001c0021t0001g0278 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | 199 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(196): 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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0153 | 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 | 173 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(170): 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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0153 | 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 | 91 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(88): 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 | 276 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(273): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | 49 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(46): 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 | 86 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(83): 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 |
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 | a0001c0001t0001g0282 a0001c0001t0002g0283 a0007c0008t0001g0281 |
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 | a0001c0001t0001g0247 | 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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(52): 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0242 others(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 | 186 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(183): 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 | a0016c0019t0001g0139 | 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 | a0001c0001t0003g0138 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 |
128 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0042 others(125): 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 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0261 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0248 a0005c0006t0001g0266 a0005c0006t0001g0267 |
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 | a0002c0003t0001g0265 | 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 | a0001c0002t0005g0279 a0001c0021t0001g0278 |
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 | 186 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(183): 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 | a0001c0001t0001g0057 | 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 | 276 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(273): 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 | a0001c0001t0001g0280 a0001c0001t0002g0373 a0001c0001t0003g0372 others(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 | 240 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(237): 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 | a0001c0001t0001g0366 | 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 | a0003c0004t0005g0367 | 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 | a0001c0001t0001g0247 | 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 | 248 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(245): 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 | a0001c0001t0001g0003 a0001c0001t0001g0268 a0001c0001t0002g0373 others(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 | a0001c0001t0001g0248 a0001c0001t0001g0261 a0001c0001t0002g0250 others(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 | 86 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0076 others(83): 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 | a0001c0001t0001g0248 a0001c0001t0001g0261 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0282 a0001c0001t0002g0283 a0001c0002t0002g0284 others(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 | a0001c0001t0001g0248 a0001c0001t0001g0261 a0001c0001t0001g0268 others(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 | a0001c0001t0003g0271 a0001c0002t0002g0270 a0013c0012t0002g0269 |
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 | a0001c0001t0001g0368 a0001c0001t0004g0370 a0001c0002t0002g0369 others(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 | a0001c0021t0001g0278 | 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 | a0001c0001t0001g0272 | 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 | 51 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(48): 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0002g0274 |
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 | 275 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(272): 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 | a0001c0001t0002g0276 a0007c0008t0001g0277 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0002g0373 a0001c0001t0003g0372 |
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 | 270 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(267): 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 |