Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 726 |
| ensemblid | ENSG00000149260.18 |
| hgncid | 1482 |
| symbol | CAPN5 |
| name | calpain 5 |
| refseq_nuc | NM_004055.5 |
| refseq_prot | NP_004046.2 |
| ensembl_nuc | ENST00000648180.1 |
| ensembl_prot | ENSP00000498132.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 77066971 |
| end | 77126155 |
| strand | + |
| ver | v1.2 |
| region | chr11:77066971-77126155 |
| region5000 | chr11:77061971-77131155 |
| regionname0 | CAPN5_chr11_77066971_77126155 |
| regionname5000 | CAPN5_chr11_77061971_77131155 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 640 | 355 | 78 | 71 | 151 | 12 | 41 | 109 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0002 | 0/0 | 640 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0003 | 0/0 | 640 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0004 | 0/0 | 640 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0005 | 0/0 | 640 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0006 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0007 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0008 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0009 | 0/0 | 640 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0010 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0011 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0012 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| a0013 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | MFSCV others(635): Show |
chr11 | 77061971 | 77131155 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1920 | 335 | 63 | 69 | 150 | 10 | 41 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0002 | 0/0 | 1920 | 13 | 13 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0007 | 0/0 | 1920 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0011 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0012 | 0/0 | 1920 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0015 | 0/0 | 1920 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0019 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0001c0020 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0002c0003 | 0/0 | 1920 | 8 | 7 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0002c0021 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0003c0004 | 0/0 | 1920 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0003c0009 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0004c0005 | 0/0 | 1920 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0005c0006 | 0/0 | 1920 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0006c0013 | 0/0 | 1920 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0007c0022 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0008c0016 | 0/0 | 1920 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0009c0008 | 0/0 | 1920 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0010c0017 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0011c0014 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0012c0018 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 | ||
| a0013c0010 | 0/0 | 1920 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | ATGTT others(1915): Show |
chr11 | 77061971 | 77131155 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4367 | 92 | 10 | 23 | 36 | 3 | 18 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0002 | 0/0 | 4359 | 54 | 5 | 6 | 36 | 1 | 6 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0003 | 0/0 | 4367 | 43 | 3 | 7 | 28 | 0 | 5 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0004 | 0/0 | 4367 | 16 | 0 | 4 | 9 | 0 | 3 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0005 | 0/0 | 4367 | 15 | 4 | 6 | 0 | 4 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0006 | 0/0 | 4359 | 11 | 8 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0007 | 0/0 | 4369 | 11 | 7 | 2 | 0 | 0 | 2 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0008 | 0/0 | 4369 | 10 | 0 | 0 | 10 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0009 | 0/0 | 4371 | 10 | 0 | 2 | 8 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0010 | 0/0 | 4371 | 8 | 0 | 1 | 6 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0011 | 0/0 | 4369 | 5 | 2 | 3 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0012 | 0/0 | 4371 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0013 | 0/0 | 4367 | 4 | 0 | 3 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0014 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0015 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4358): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0016 | 0/0 | 4365 | 3 | 2 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4360): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0017 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4356): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0018 | 0/0 | 4369 | 3 | 0 | 0 | 2 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0019 | 0/0 | 4367 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0020 | 0/0 | 4375 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4370): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0022 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0023 | 0/0 | 4367 | 2 | 0 | 0 | 1 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0024 | 0/0 | 4371 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0025 | 0/0 | 4375 | 2 | 0 | 1 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4370): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0027 | 0/0 | 4373 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4368): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0028 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0029 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0030 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0032 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0033 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0034 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0035 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0036 | 0/0 | 4373 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4368): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0037 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0038 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4360): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0039 | 0/0 | 4395 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4390): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0041 | 0/0 | 4377 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4372): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0042 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4372): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0043 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4378): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0045 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4360): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0046 | 0/0 | 4371 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0047 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0048 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0049 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0051 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0052 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4358): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0053 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0054 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0055 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0056 | 0/0 | 4371 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0057 | 0/0 | 4371 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0001t0058 | 0/0 | 4375 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4370): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0006 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0012 | 0/0 | 4371 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4366): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0014 | 0/0 | 4369 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0015 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4358): Show |
chr11 | 77061971 | 77131155 |
| a0001c0002t0050 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4356): Show |
chr11 | 77061971 | 77131155 |
| a0001c0007t0026 | 0/0 | 4367 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0011t0031 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0012t0013 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0015t0003 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0001c0019t0044 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4380): Show |
chr11 | 77061971 | 77131155 |
| a0001c0020t0002 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0001 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0006 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0007 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0011 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0015 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4358): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0017 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4356): Show |
chr11 | 77061971 | 77131155 |
| a0002c0003t0028 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0002c0021t0019 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0003c0004t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0003c0004t0021 | 0/0 | 4379 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4374): Show |
chr11 | 77061971 | 77131155 |
| a0003c0009t0029 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0004c0005t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0004c0005t0004 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0004c0005t0040 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4370): Show |
chr11 | 77061971 | 77131155 |
| a0005c0006t0011 | 0/0 | 4369 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4364): Show |
chr11 | 77061971 | 77131155 |
| a0006c0013t0013 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | GGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0007c0022t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0008c0016t0001 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0009c0008t0003 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0010c0017t0016 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4360): Show |
chr11 | 77061971 | 77131155 |
| a0011c0014t0002 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4354): Show |
chr11 | 77061971 | 77131155 |
| a0012c0018t0004 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| a0013c0010t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | AGTCC others(4362): Show |
chr11 | 77061971 | 77131155 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0006g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0008g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0010g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0011g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0012g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0013g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0013g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0014g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0015g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0016g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0018g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0019g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0020g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0020g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0022g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0022g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0023g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0023g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0024g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0025g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0025g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0027g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0027g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0028g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0029g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0030g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0032g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0033g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0034g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0035g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0036g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0037g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0038g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0039g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0041g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0042g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0043g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0045g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0046g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0047g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0048g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0049g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0051g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0052g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0053g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0054g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0055g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0056g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0057g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0001t0058g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0014g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0015g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0002t0050g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0007t0026g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0007t0026g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0011t0031g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0012t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0015t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0019t0044g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0001c0020t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0017g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0003t0028g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0002c0021t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0003c0004t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0003c0004t0021g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0003c0004t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0003c0009t0029g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0004c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0004c0005t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0004c0005t0040g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0005c0006t0011g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0005c0006t0011g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0006c0013t0013g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0007c0022t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0008c0016t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0009c0008t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0010c0017t0016g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0011c0014t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0012c0018t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| a0013c0010t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00099 | hp2 | a0001 | c0001 | t0049 | g0113 | EUR | GBR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0339 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00323 | hp1 | a0001 | c0001 | t0047 | g0137 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0302 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0343 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00438 | hp2 | a0001 | c0001 | t0023 | g0139 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00597 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00597 | hp2 | a0004 | c0005 | t0004 | g0028 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0147 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00639 | hp2 | a0002 | c0003 | t0007 | g0296 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00741 | hp1 | a0001 | c0001 | t0035 | g0312 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0261 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01071 | hp2 | a0001 | c0001 | t0039 | g0158 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01074 | hp1 | a0001 | c0001 | t0034 | g0317 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0232 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0001 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01081 | hp2 | a0005 | c0006 | t0011 | g0354 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01099 | hp1 | a0006 | c0013 | t0013 | g0048 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01175 | hp1 | a0001 | c0001 | t0013 | g0001 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01243 | hp1 | a0001 | c0001 | t0019 | g0186 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0344 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01255 | hp1 | a0001 | c0001 | t0011 | g0295 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0286 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0282 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01358 | hp2 | a0001 | c0015 | t0003 | g0313 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0265 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01496 | hp1 | a0001 | c0001 | t0041 | g0316 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0292 | EUR | IBS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01515 | hp2 | a0001 | c0007 | t0026 | g0018 | EUR | IBS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0340 | EUR | IBS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01517 | hp2 | a0001 | c0007 | t0026 | g0017 | EUR | IBS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0210 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01884 | hp2 | a0001 | c0001 | t0029 | g0361 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01928 | hp1 | a0001 | c0012 | t0013 | g0001 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01943 | hp1 | a0001 | c0001 | t0055 | g0066 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0051 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01952 | hp1 | a0001 | c0001 | t0058 | g0047 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0262 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01975 | hp2 | a0001 | c0001 | t0013 | g0001 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02004 | hp1 | a0001 | c0001 | t0036 | g0304 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02004 | hp2 | a0001 | c0001 | t0057 | g0062 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02015 | hp2 | a0001 | c0001 | t0042 | g0189 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0064 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02055 | hp1 | a0007 | c0022 | t0003 | g0176 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02055 | hp2 | a0001 | c0002 | t0006 | g0212 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02056 | hp2 | a0004 | c0005 | t0001 | g0240 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0201 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02132 | hp2 | a0001 | c0001 | t0030 | g0079 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0213 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02145 | hp2 | a0003 | c0004 | t0021 | g0009 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0065 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0078 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02165 | hp2 | a0001 | c0001 | t0009 | g0030 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02258 | hp1 | a0005 | c0006 | t0011 | g0355 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0162 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02273 | hp1 | a0001 | c0001 | t0056 | g0044 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02280 | hp1 | a0002 | c0003 | t0017 | g0198 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0293 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02300 | hp2 | a0001 | c0001 | t0025 | g0242 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02451 | hp2 | a0003 | c0004 | t0021 | g0009 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02523 | hp1 | a0001 | c0001 | t0053 | g0323 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0141 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02602 | hp1 | a0001 | c0001 | t0023 | g0093 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0173 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02615 | hp2 | a0001 | c0001 | t0046 | g0181 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02630 | hp1 | a0002 | c0003 | t0011 | g0233 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02647 | hp1 | a0001 | c0002 | t0014 | g0183 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02647 | hp2 | a0002 | c0003 | t0028 | g0334 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02717 | hp1 | a0001 | c0002 | t0012 | g0184 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02717 | hp2 | a0001 | c0001 | t0051 | g0363 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02723 | hp1 | a0002 | c0003 | t0015 | g0195 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02723 | hp2 | a0001 | c0019 | t0044 | g0227 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0241 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02738 | hp2 | a0009 | c0008 | t0003 | g0019 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02809 | hp2 | a0001 | c0001 | t0052 | g0362 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02818 | hp1 | a0002 | c0021 | t0019 | g0197 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0231 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02886 | hp2 | a0001 | c0002 | t0014 | g0220 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0207 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02922 | hp1 | a0001 | c0002 | t0015 | g0349 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02922 | hp2 | a0001 | c0001 | t0022 | g0222 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02965 | hp1 | a0001 | c0002 | t0012 | g0193 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0276 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02976 | hp2 | a0003 | c0009 | t0029 | g0359 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0332 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0338 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0175 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0163 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03130 | hp1 | a0001 | c0001 | t0033 | g0225 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03139 | hp1 | a0001 | c0001 | t0022 | g0270 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03195 | hp1 | a0001 | c0001 | t0043 | g0097 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03209 | hp1 | a0003 | c0004 | t0021 | g0234 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03225 | hp1 | a0001 | c0011 | t0031 | g0230 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0274 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03486 | hp1 | a0003 | c0004 | t0002 | g0353 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0297 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03491 | hp2 | a0001 | c0001 | t0016 | g0305 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03516 | hp1 | a0001 | c0002 | t0014 | g0211 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0228 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0187 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0244 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0086 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0347 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0273 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0283 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0131 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0178 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0342 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CHB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0257 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0337 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0128 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18940 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18947 | hp2 | a0001 | c0001 | t0010 | g0289 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18948 | hp1 | a0001 | c0001 | t0027 | g0134 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18959 | hp2 | a0001 | c0001 | t0032 | g0073 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18965 | hp1 | a0001 | c0001 | t0027 | g0161 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18965 | hp2 | a0010 | c0017 | t0016 | g0120 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18973 | hp1 | a0001 | c0001 | t0054 | g0307 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18980 | hp2 | a0004 | c0005 | t0040 | g0076 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0280 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18986 | hp2 | a0001 | c0001 | t0018 | g0063 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18995 | hp2 | a0001 | c0001 | t0018 | g0049 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19002 | hp2 | a0001 | c0001 | t0025 | g0110 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0172 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0100 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19057 | hp2 | a0001 | c0001 | t0028 | g0169 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19068 | hp2 | a0011 | c0014 | t0002 | g0203 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0278 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19076 | hp1 | a0012 | c0018 | t0004 | g0106 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0303 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19079 | hp2 | a0001 | c0020 | t0002 | g0284 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0264 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19080 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19085 | hp1 | a0001 | c0001 | t0008 | g0148 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19085 | hp2 | a0013 | c0010 | t0001 | g0310 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA19240 | hp2 | a0002 | c0003 | t0006 | g0042 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | ASW | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20129 | hp2 | a0001 | c0002 | t0014 | g0208 | AFR | ASW | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0055 | EUR | TSI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0026 | SAS | GIH | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0119 | SAS | GIH | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01123 | hp1 | a0001 | c0001 | t0037 | g0109 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0341 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0352 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02559 | hp1 | a0008 | c0016 | t0001 | g0036 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0356 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG06807 | hp1 | a0001 | c0001 | t0045 | g0350 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0165 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA18955 | hp2 | a0001 | c0001 | t0008 | g0256 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20300 | hp1 | a0001 | c0001 | t0048 | g0266 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA20300 | hp2 | a0001 | c0002 | t0050 | g0360 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0159 | REF | REF | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0050 | REF | REF | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77084916 | C | G | 2 | a0002 a0007 |
10 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(7): Show |
missense_variant | MODERATE | c.30C>G | p.Asp10Glu | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/13 | 189/4367 | 30/1923 | 10/640 | chr11 | 77084916 | |||
| chr11:77084939 | G | A | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.53G>A | p.Arg18Gln | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/13 | 212/4367 | 53/1923 | 18/640 | chr11 | 77084939 | |||
| chr11:77085031 | G | A | 1 | a0004 | 3 | HG00597.hp2 HG02056.hp2 NA18980.hp2 |
missense_variant | MODERATE | c.145G>A | p.Val49Ile | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/13 | 304/4367 | 145/1923 | 49/640 | chr11 | 77085031 | |||
| chr11:77093683 | G | A | 2 | a0003 a0007 |
6 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.167G>A | p.Gly56Asp | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/13 | 326/4367 | 167/1923 | 56/640 | chr11 | 77093683 | |||
| chr11:77114313 | T | G | 1 | a0013 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.578T>G | p.Val193Gly | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/13 | 737/4367 | 578/1923 | 193/640 | chr11 | 77114313 | |||
| chr11:77119085 | G | A | 1 | a0006 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1223G>A | p.Arg408Gln | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/13 | 1382/4367 | 1223/1923 | 408/640 | chr11 | 77119085 | |||
| chr11:77120713 | G | A | 1 | a0011 | 1 | NA19068.hp2 | missense_variant&splice_region_variant | MODERATE | c.1291G>A | p.Val431Met | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/13 | 1450/4367 | 1291/1923 | 431/640 | chr11 | 77120713 | |||
| chr11:77120755 | A | G | 1 | a0012 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.1333A>G | p.Lys445Glu | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/13 | 1492/4367 | 1333/1923 | 445/640 | chr11 | 77120755 | |||
| chr11:77122665 | A | C | 1 | a0010 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.1693A>C | p.Lys565Gln | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/13 | 1852/4367 | 1693/1923 | 565/640 | chr11 | 77122665 | |||
| chr11:77123791 | G | A | 1 | a0005 | 2 | HG01081.hp2 HG02258.hp1 |
missense_variant | MODERATE | c.1844G>A | p.Arg615Gln | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2003/4367 | 1844/1923 | 615/640 | chr11 | 77123791 | |||
| chr11:77123841 | C | A | 1 | a0008 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1894C>A | p.Leu632Ile | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2053/4367 | 1894/1923 | 632/640 | chr11 | 77123841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77084976 | C | A | 2 | a0001c0002 a0002c0021 |
14 | HG02055.hp2 HG02145.hp1 HG02647.hp1 others(11): Show |
synonymous_variant | LOW | c.90C>A | p.Pro30Pro | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/13 | 249/4367 | 90/1923 | 30/640 | chr11 | 77084976 | |||
| chr11:77112627 | A | G | 1 | a0001c0020 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.336A>G | p.Glu112Glu | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/13 | 495/4367 | 336/1923 | 112/640 | chr11 | 77112627 | |||
| chr11:77114317 | T | C | 1 | a0001c0011 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.582T>C | p.Ser194Ser | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/13 | 741/4367 | 582/1923 | 194/640 | chr11 | 77114317 | |||
| chr11:77114353 | C | T | 1 | a0001c0019 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.618C>T | p.Asn206Asn | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/13 | 777/4367 | 618/1923 | 206/640 | chr11 | 77114353 | |||
| chr11:77118265 | T | C | 1 | a0001c0012 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.1080T>C | p.His360His | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 8/13 | 1239/4367 | 1080/1923 | 360/640 | chr11 | 77118265 | |||
| chr11:77120847 | C | T | 1 | a0001c0007 | 2 | HG01515.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.1425C>T | p.Phe475Phe | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/13 | 1584/4367 | 1425/1923 | 475/640 | chr11 | 77120847 | |||
| chr11:77122598 | C | T | 1 | a0003c0009 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1626C>T | p.Ile542Ile | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/13 | 1785/4367 | 1626/1923 | 542/640 | chr11 | 77122598 | |||
| chr11:77122625 | G | A | 1 | a0001c0015 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1653G>A | p.Ser551Ser | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/13 | 1812/4367 | 1653/1923 | 551/640 | chr11 | 77122625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77066971 | A | G | 7 | a0001c0001t0013 a0001c0001t0055 a0001c0001t0056 others(4): Show |
10 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-159A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/13 | 17916 | chr11 | 77066971 | ||||||
| chr11:77066988 | C | T | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG02523.hp1 NA18973.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-142C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/13 | chr11 | 77066988 | |||||||
| chr11:77067050 | G | A | 1 | a0001c0001t0030 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/13 | 17837 | chr11 | 77067050 | ||||||
| chr11:77067052 | C | T | 5 | a0001c0001t0029 a0001c0001t0051 a0001c0001t0052 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-78C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/13 | 17835 | chr11 | 77067052 | ||||||
| chr11:77124047 | G | A | 1 | a0001c0011t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 177 | chr11 | 77124047 | ||||||
| chr11:77124181 | G | A | 1 | a0001c0001t0022 | 2 | HG02922.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*311G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 311 | chr11 | 77124181 | ||||||
| chr11:77124231 | C | T | 2 | a0001c0001t0014 a0001c0002t0014 |
5 | HG02647.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 361 | chr11 | 77124231 | ||||||
| chr11:77124337 | C | T | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*467C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 467 | chr11 | 77124337 | ||||||
| chr11:77124794 | A | G | 4 | a0001c0001t0016 a0001c0001t0028 a0002c0003t0028 others(1): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*924A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 924 | chr11 | 77124794 | ||||||
| chr11:77124848 | C | T | 1 | a0001c0001t0058 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*978C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 978 | chr11 | 77124848 | ||||||
| chr11:77124884 | C | T | 1 | a0001c0001t0048 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1014C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1014 | chr11 | 77124884 | ||||||
| chr11:77124924 | G | A | 1 | a0001c0001t0032 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1054 | chr11 | 77124924 | ||||||
| chr11:77124938 | C | T | 1 | a0001c0001t0047 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1068 | chr11 | 77124938 | ||||||
| chr11:77125304 | T | C | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(41): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1434T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1434 | chr11 | 77125304 | ||||||
| chr11:77125393 | A | G | 20 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(17): Show |
79 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1523A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1523 | chr11 | 77125393 | ||||||
| chr11:77125415 | G | A | 1 | a0001c0007t0026 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1545G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1545 | chr11 | 77125415 | ||||||
| chr11:77125515 | T | A | 20 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(17): Show |
79 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1645T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1645 | chr11 | 77125515 | ||||||
| chr11:77125541 | C | T | 1 | a0001c0001t0045 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1671 | chr11 | 77125541 | ||||||
| chr11:77125604 | T | C | 1 | a0001c0001t0037 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1734 | chr11 | 77125604 | ||||||
| chr11:77125611 | G | A | 4 | a0001c0001t0015 a0001c0001t0052 a0001c0002t0015 others(1): Show |
5 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1741G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1741 | chr11 | 77125611 | ||||||
| chr11:77125614 | C | CTA | 15 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(12): Show |
45 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1769_*1770dupTA | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATA | 8 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(5): Show |
29 | HG00597.hp1 HG00609.hp2 HG01071.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1767_*1770dupTATA | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATA | 2 | a0001c0001t0027 a0001c0001t0036 |
3 | HG02004.hp1 NA18948.hp1 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1765_*1770dupTATA others(2): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATAT others(1): Show |
3 | a0001c0001t0025 a0001c0001t0058 a0004c0005t0040 |
4 | HG01952.hp1 HG02300.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1763_*1770dupTATA others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATAT others(3): Show |
2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG01496.hp1 HG02015.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1761_*1770dupTATA others(6): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATAT others(5): Show |
1 | a0003c0004t0021 | 3 | HG02145.hp2 HG02451.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1759_*1770dupTATA others(8): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATAT others(9): Show |
1 | a0001c0001t0043 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1755_*1770dupTATA others(12): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | C | CTATATAT others(11): Show |
1 | a0001c0019t0044 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753_*1770dupTATA others(14): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | CTA | C | 4 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0045 others(1): Show |
6 | HG03491.hp2 HG03579.hp2 HG03942.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1769_*1770delTA | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1769 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | CTATA | C | 4 | a0001c0001t0015 a0001c0001t0052 a0001c0002t0015 others(1): Show |
5 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1767_*1770delTATA | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1767 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | CTATATA | C | 3 | a0001c0001t0017 a0001c0002t0050 a0002c0003t0017 |
4 | HG02280.hp1 HG02818.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1765_*1770delTATA others(2): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1765 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125614 | CTATATAT others(1): Show |
C | 14 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0029 others(11): Show |
77 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1763_*1770delTATA others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1763 | INFO_REALIGN_3_PRIME | chr11 | 77125614 | |||||
| chr11:77125639 | T | C | 1 | a0001c0001t0034 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1769 | chr11 | 77125639 | ||||||
| chr11:77125639 | T | TATATATA others(1): Show |
1 | a0001c0001t0020 | 3 | HG02258.hp2 HG03098.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770_*1771insTATA others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1771 | INFO_REALIGN_3_PRIME | chr11 | 77125639 | |||||
| chr11:77125818 | G | A | 57 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(54): Show |
220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1948G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1948 | chr11 | 77125818 | ||||||
| chr11:77125818 | G | C | 4 | a0001c0001t0041 a0001c0001t0043 a0001c0019t0044 others(1): Show |
6 | HG01496.hp1 HG02145.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1948G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 1948 | chr11 | 77125818 | ||||||
| chr11:77125909 | A | C | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2039A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2039 | chr11 | 77125909 | ||||||
| chr11:77125910 | T | C | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2040 | chr11 | 77125910 | ||||||
| chr11:77125911 | G | T | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2041G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2041 | chr11 | 77125911 | ||||||
| chr11:77125924 | G | A | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2054 | chr11 | 77125924 | ||||||
| chr11:77125934 | G | C | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2064G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2064 | chr11 | 77125934 | ||||||
| chr11:77125935 | A | C | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2065 | chr11 | 77125935 | ||||||
| chr11:77125945 | C | A | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2075C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2075 | chr11 | 77125945 | ||||||
| chr11:77125948 | G | T | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2078 | chr11 | 77125948 | ||||||
| chr11:77125949 | G | A | 1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2079 | chr11 | 77125949 | ||||||
| chr11:77125950 | C | CCCTCTTC others(21): Show |
1 | a0001c0001t0039 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2080_*2081insCCTC others(24): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2081 | chr11 | 77125950 | ||||||
| chr11:77126003 | A | C | 2 | a0001c0001t0019 a0002c0021t0019 |
3 | HG01243.hp1 HG02615.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2133A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2133 | chr11 | 77126003 | ||||||
| chr11:77126087 | G | C | 1 | a0001c0001t0033 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2217G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 13/13 | 2217 | chr11 | 77126087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77067126 | C | CTG | 3 | a0001c0001t0001g0016 a0001c0007t0026g0017 a0001c0007t0026g0018 |
3 | HG01257.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-36+52_-36+53dupGT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067126 | ||||||
| chr11:77067126 | CTG | C | 197 | a0001c0001t0001g0014 a0001c0001t0001g0174 a0001c0001t0001g0179 others(194): Show |
204 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-36+52_-36+53delGT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067126 | ||||||
| chr11:77067126 | CTGTG | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+50_-36+53delGT others(2): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067126 | ||||||
| chr11:77067145 | TG | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0358 a0001c0001t0002g0166 |
3 | HG02056.hp1 HG03654.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-36+52delG | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067145 | |||||||
| chr11:77067149 | T | C | 3 | a0001c0001t0001g0167 a0001c0001t0002g0166 a0009c0008t0003g0019 |
3 | HG02056.hp1 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-36+55T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067149 | |||||||
| chr11:77067150 | C | G | 3 | a0001c0001t0001g0167 a0001c0001t0002g0166 a0009c0008t0003g0019 |
3 | HG02056.hp1 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-36+56C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067150 | |||||||
| chr11:77067201 | G | A | 1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-36+107G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067201 | |||||||
| chr11:77067237 | G | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+143G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067237 | |||||||
| chr11:77067269 | G | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+175G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067269 | |||||||
| chr11:77067269 | G | C | 1 | a0001c0001t0028g0169 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-36+175G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067269 | |||||||
| chr11:77067333 | C | CT | 166 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0101 others(163): Show |
173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-36+246dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067333 | ||||||
| chr11:77067345 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-36+251T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067345 | |||||||
| chr11:77067352 | G | A | 1 | a0001c0001t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-36+258G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067352 | |||||||
| chr11:77067469 | C | T | 1 | a0001c0001t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-36+375C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067469 | |||||||
| chr11:77067524 | C | T | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+430C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067524 | |||||||
| chr11:77067535 | G | T | 28 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(25): Show |
29 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.-36+441G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067535 | |||||||
| chr11:77067552 | A | G | 210 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(207): Show |
219 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-36+458A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067552 | |||||||
| chr11:77067562 | C | G | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+468C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067562 | |||||||
| chr11:77067582 | A | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+488A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067582 | |||||||
| chr11:77067632 | C | CGT | 25 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0035 others(22): Show |
26 | HG00597.hp2 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-36+575_-36+576dup others(2): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGT | 32 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0255 others(29): Show |
35 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.-36+573_-36+576dup others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGT | 57 | a0001c0001t0001g0167 a0001c0001t0001g0245 a0001c0001t0001g0248 others(54): Show |
60 | HG00323.hp2 HG00621.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-36+571_-36+576dup others(6): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(1): Show |
30 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(27): Show |
30 | HG00544.hp1 HG00639.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-36+569_-36+576dup others(8): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(3): Show |
43 | a0001c0001t0001g0016 a0001c0001t0001g0150 a0001c0001t0001g0151 others(40): Show |
43 | HG01071.hp2 HG01257.hp1 HG01515.hp2 others(40): Show |
intron_variant | MODIFIER | c.-36+567_-36+576dup others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(5): Show |
47 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0124 others(44): Show |
48 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-36+565_-36+576dup others(12): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(7): Show |
22 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(19): Show |
22 | HG00099.hp2 HG00621.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-36+563_-36+576dup others(14): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(9): Show |
9 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0003g0107 others(6): Show |
9 | HG00642.hp1 HG00673.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+561_-36+576dup others(16): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(11): Show |
10 | a0001c0001t0001g0174 a0001c0001t0002g0104 a0001c0001t0002g0105 others(7): Show |
10 | HG00609.hp1 HG00673.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36+559_-36+576dup others(18): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0003g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-36+557_-36+576dup others(20): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | C | CGTGTGTG others(15): Show |
2 | a0001c0001t0002g0170 a0001c0001t0003g0102 |
2 | HG02165.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-36+555_-36+576dup others(22): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067632 | CGTGTGTG others(3): Show |
C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+567_-36+576del others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067632 | ||||||
| chr11:77067670 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0101 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-36+576_-36+577ins others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067670 | |||||||
| chr11:77067685 | G | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+591G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067685 | |||||||
| chr11:77067876 | A | G | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-36+782A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067876 | |||||||
| chr11:77067892 | G | T | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+798G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77067892 | |||||||
| chr11:77068081 | C | T | 1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-36+987C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068081 | |||||||
| chr11:77068083 | G | T | 53 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(50): Show |
53 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-36+989G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068083 | |||||||
| chr11:77068212 | T | G | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-36+1118T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068212 | |||||||
| chr11:77068216 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0037 |
2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-36+1122G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068216 | |||||||
| chr11:77068306 | C | T | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+1212C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068306 | |||||||
| chr11:77068473 | A | G | 35 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(32): Show |
37 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.-36+1379A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068473 | |||||||
| chr11:77068484 | G | A | 94 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0167 others(91): Show |
98 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-36+1390G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068484 | |||||||
| chr11:77068500 | A | T | 2 | a0001c0002t0014g0220 a0001c0019t0044g0227 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-36+1406A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068500 | |||||||
| chr11:77068524 | G | A | 3 | a0001c0001t0022g0270 a0001c0001t0048g0266 a0002c0003t0028g0334 |
3 | HG02647.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-36+1430G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068524 | |||||||
| chr11:77068576 | G | T | 2 | a0001c0001t0007g0262 a0001c0001t0010g0261 |
2 | HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-36+1482G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068576 | |||||||
| chr11:77068659 | G | A | 1 | a0001c0001t0017g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-36+1565G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068659 | |||||||
| chr11:77068740 | A | G | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+1646A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068740 | |||||||
| chr11:77068752 | T | G | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+1658T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068752 | |||||||
| chr11:77068783 | G | A | 1 | a0001c0001t0017g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-36+1689G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068783 | |||||||
| chr11:77068815 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0011g0232 a0002c0003t0011g0233 |
3 | HG01074.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-36+1721C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068815 | |||||||
| chr11:77068889 | T | TAAGTTGA others(1): Show |
5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+1796_-36+1803d others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77068889 | ||||||
| chr11:77068960 | C | T | 4 | a0001c0001t0006g0226 a0001c0001t0017g0231 a0001c0001t0033g0225 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+1866C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77068960 | |||||||
| chr11:77069012 | G | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+1918G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069012 | |||||||
| chr11:77069167 | G | A | 91 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0167 others(88): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-36+2073G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069167 | |||||||
| chr11:77069194 | T | G | 1 | a0001c0001t0003g0122 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-36+2100T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069194 | |||||||
| chr11:77069205 | G | A | 53 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(50): Show |
53 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-36+2111G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069205 | |||||||
| chr11:77069321 | A | C | 21 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0224 others(18): Show |
21 | HG00621.hp2 HG00673.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36+2227A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069321 | |||||||
| chr11:77069725 | C | T | 1 | a0001c0001t0004g0333 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-36+2631C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069725 | |||||||
| chr11:77069762 | C | T | 2 | a0002c0003t0002g0356 a0005c0006t0011g0355 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-36+2668C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069762 | |||||||
| chr11:77069778 | A | G | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+2684A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069778 | |||||||
| chr11:77069815 | G | A | 1 | a0001c0001t0008g0148 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-36+2721G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069815 | |||||||
| chr11:77069845 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-36+2751C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069845 | |||||||
| chr11:77069856 | G | A | 70 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(67): Show |
72 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-36+2762G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069856 | |||||||
| chr11:77069878 | C | T | 2 | a0001c0001t0001g0281 a0001c0001t0010g0280 |
2 | NA18983.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-36+2784C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069878 | |||||||
| chr11:77069897 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0005g0171 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-36+2803G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069897 | |||||||
| chr11:77069929 | T | C | 210 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(207): Show |
219 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-36+2835T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069929 | |||||||
| chr11:77069957 | A | G | 277 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(274): Show |
286 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-36+2863A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069957 | |||||||
| chr11:77069960 | A | G | 277 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(274): Show |
286 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-36+2866A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069960 | |||||||
| chr11:77069961 | A | C | 277 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(274): Show |
286 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-36+2867A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069961 | |||||||
| chr11:77070090 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-36+2996G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070090 | |||||||
| chr11:77070153 | T | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3059T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070153 | |||||||
| chr11:77070158 | C | T | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3064C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070158 | |||||||
| chr11:77070196 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-36+3102C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070196 | |||||||
| chr11:77070325 | G | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3231G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070325 | |||||||
| chr11:77070410 | C | T | 17 | a0001c0001t0001g0174 a0001c0001t0001g0185 a0001c0001t0001g0214 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36+3316C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070410 | |||||||
| chr11:77070716 | G | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3622G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070716 | |||||||
| chr11:77070742 | A | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(68): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-36+3648A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070742 | |||||||
| chr11:77070747 | A | G | 183 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(180): Show |
191 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-36+3653A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070747 | |||||||
| chr11:77070781 | T | C | 1 | a0001c0001t0022g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-36+3687T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070781 | |||||||
| chr11:77070901 | T | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3807T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070901 | |||||||
| chr11:77070943 | G | T | 2 | a0001c0002t0014g0220 a0001c0019t0044g0227 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-36+3849G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070943 | |||||||
| chr11:77070971 | C | T | 1 | a0001c0001t0006g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-36+3877C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070971 | |||||||
| chr11:77070974 | T | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+3880T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070974 | |||||||
| chr11:77071050 | G | A | 1 | a0001c0001t0004g0025 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-36+3956G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071050 | |||||||
| chr11:77071070 | C | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(67): Show |
72 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-36+3976C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071070 | |||||||
| chr11:77071332 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(261): Show |
273 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-36+4238A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071332 | |||||||
| chr11:77071371 | C | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+4277C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071371 | |||||||
| chr11:77071381 | G | A | 91 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0167 others(88): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-36+4287G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071381 | |||||||
| chr11:77071396 | G | C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(68): Show |
73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-36+4302G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071396 | |||||||
| chr11:77071403 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-36+4309G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071403 | |||||||
| chr11:77071427 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-36+4333G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071427 | |||||||
| chr11:77071529 | A | G | 1 | a0008c0016t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-36+4435A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071529 | |||||||
| chr11:77071606 | A | T | 1 | a0001c0019t0044g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-36+4512A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071606 | |||||||
| chr11:77071652 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0011g0232 a0002c0003t0011g0233 |
3 | HG01074.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-36+4558C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071652 | |||||||
| chr11:77071766 | T | G | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-36+4672T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071766 | |||||||
| chr11:77071826 | T | C | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+4732T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071826 | |||||||
| chr11:77071864 | G | C | 1 | a0001c0001t0002g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-36+4770G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071864 | |||||||
| chr11:77071880 | C | T | 2 | a0001c0001t0003g0095 a0001c0001t0003g0096 |
2 | HG02135.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-36+4786C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071880 | |||||||
| chr11:77071940 | C | T | 11 | a0001c0001t0001g0221 a0001c0002t0002g0209 a0001c0002t0003g0213 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36+4846C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071940 | |||||||
| chr11:77071995 | G | A | 1 | a0001c0001t0003g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-36+4901G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071995 | |||||||
| chr11:77072157 | T | A | 5 | a0001c0001t0029g0361 a0001c0001t0051g0363 a0001c0001t0052g0362 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+5063T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072157 | |||||||
| chr11:77072231 | C | A | 46 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(43): Show |
46 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-36+5137C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072231 | |||||||
| chr11:77072317 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0011g0232 a0002c0003t0011g0233 |
3 | HG01074.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-36+5223G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072317 | |||||||
| chr11:77072415 | G | A | 50 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(47): Show |
50 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-36+5321G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072415 | |||||||
| chr11:77072422 | T | G | 1 | a0001c0001t0002g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-36+5328T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072422 | |||||||
| chr11:77072489 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-36+5395G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072489 | |||||||
| chr11:77072580 | G | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(67): Show |
72 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-36+5486G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072580 | |||||||
| chr11:77072705 | A | T | 1 | a0001c0001t0003g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-36+5611A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072705 | |||||||
| chr11:77072916 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0045g0350 a0005c0006t0011g0354 |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+5822G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072916 | |||||||
| chr11:77072927 | G | A | 1 | a0002c0003t0028g0334 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-36+5833G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77072927 | |||||||
| chr11:77073001 | C | T | 9 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(6): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36+5907C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073001 | |||||||
| chr11:77073249 | C | T | 2 | a0001c0001t0011g0147 a0001c0001t0039g0158 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-36+6155C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073249 | |||||||
| chr11:77073316 | G | A | 1 | a0001c0001t0007g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-36+6222G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073316 | |||||||
| chr11:77073371 | G | A | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36+6277G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073371 | |||||||
| chr11:77073398 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0040 |
3 | HG00408.hp2 HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-36+6304G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073398 | |||||||
| chr11:77073399 | C | T | 50 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(47): Show |
50 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-36+6305C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073399 | |||||||
| chr11:77073445 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-36+6351C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073445 | |||||||
| chr11:77073482 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-36+6388C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073482 | |||||||
| chr11:77073487 | C | G | 1 | a0001c0001t0023g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36+6393C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073487 | |||||||
| chr11:77073509 | C | G | 3 | a0001c0001t0022g0270 a0001c0001t0048g0266 a0002c0003t0028g0334 |
3 | HG02647.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-36+6415C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073509 | |||||||
| chr11:77073634 | G | A | 2 | a0001c0001t0003g0180 a0001c0001t0046g0181 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-36+6540G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073634 | |||||||
| chr11:77073715 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0003g0023 |
2 | HG00738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-36+6621C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073715 | |||||||
| chr11:77073759 | G | C | 95 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0167 others(92): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-36+6665G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073759 | |||||||
| chr11:77073848 | G | A | 1 | a0001c0020t0002g0284 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-36+6754G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073848 | |||||||
| chr11:77073857 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-36+6763G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073857 | |||||||
| chr11:77073912 | G | A | 1 | a0001c0001t0017g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36+6818G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073912 | |||||||
| chr11:77073982 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(261): Show |
273 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-36+6888A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073982 | |||||||
| chr11:77074046 | C | A | 214 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(211): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-36+6952C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074046 | |||||||
| chr11:77074148 | G | A | 264 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(261): Show |
273 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-36+7054G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074148 | |||||||
| chr11:77074323 | A | ATCCCCAG others(25): Show |
1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-36+7235_-36+7266d others(34): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77074323 | ||||||
| chr11:77074406 | G | A | 92 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0001g0167 others(89): Show |
96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-36+7312G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074406 | |||||||
| chr11:77074412 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-36+7318C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074412 | |||||||
| chr11:77074478 | G | A | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-36+7384G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074478 | |||||||
| chr11:77074542 | G | A | 1 | a0001c0002t0014g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-36+7448G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074542 | |||||||
| chr11:77074649 | G | A | 8 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(5): Show |
9 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-36+7555G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074649 | |||||||
| chr11:77074770 | C | T | 1 | a0001c0001t0004g0025 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-36+7676C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074770 | |||||||
| chr11:77074786 | C | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0146 a0001c0001t0003g0143 others(4): Show |
7 | NA18963.hp1 NA18965.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+7692C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074786 | |||||||
| chr11:77074825 | G | T | 2 | a0001c0001t0001g0142 a0001c0001t0037g0109 |
2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-36+7731G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074825 | |||||||
| chr11:77074922 | C | T | 202 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0101 others(199): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-36+7828C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074922 | |||||||
| chr11:77074980 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-36+7886C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074980 | |||||||
| chr11:77075043 | C | G | 277 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(274): Show |
286 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-36+7949C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075043 | |||||||
| chr11:77075054 | G | C | 264 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(261): Show |
273 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-36+7960G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075054 | |||||||
| chr11:77075081 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0002g0177 a0001c0001t0002g0216 |
3 | HG00673.hp1 NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-36+7987G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075081 | |||||||
| chr11:77075130 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-36+8036C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075130 | |||||||
| chr11:77075131 | G | T | 275 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0099 others(272): Show |
284 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-36+8037G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075131 | |||||||
| chr11:77075148 | G | T | 3 | a0001c0001t0002g0011 a0001c0001t0045g0350 a0005c0006t0011g0354 |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8054G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075148 | |||||||
| chr11:77075160 | G | A | 3 | a0001c0001t0002g0011 a0001c0001t0045g0350 a0005c0006t0011g0354 |
4 | HG01081.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8066G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075160 | |||||||
| chr11:77075417 | C | T | 2 | a0001c0001t0007g0098 a0001c0001t0043g0097 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-36+8323C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075417 | |||||||
| chr11:77075455 | T | C | 11 | a0001c0001t0001g0185 a0001c0001t0001g0214 a0001c0001t0005g0171 others(8): Show |
11 | HG01243.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36+8361T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075455 | |||||||
| chr11:77075486 | G | A | 2 | a0001c0001t0001g0335 a0001c0001t0002g0301 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-36+8392G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075486 | |||||||
| chr11:77075536 | G | T | 2 | a0001c0001t0005g0118 a0001c0001t0018g0119 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-36+8442G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075536 | |||||||
| chr11:77075713 | A | C | 1 | a0001c0001t0001g0330 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-36+8619A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075713 | |||||||
| chr11:77075812 | C | T | 2 | a0002c0003t0002g0356 a0005c0006t0011g0355 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-36+8718C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075812 | |||||||
| chr11:77075860 | A | G | 1 | a0007c0022t0003g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-36+8766A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075860 | |||||||
| chr11:77075932 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-36+8838T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075932 | |||||||
| chr11:77076037 | C | T | 50 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0185 others(47): Show |
50 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-35-8815C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076037 | |||||||
| chr11:77076064 | C | T | 1 | a0001c0001t0010g0034 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-35-8788C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076064 | |||||||
| chr11:77076136 | CAGATCAC others(3): Show |
C | 11 | a0001c0001t0001g0221 a0001c0002t0002g0209 a0001c0002t0003g0213 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-8709_-35-8700d others(12): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77076136 | ||||||
| chr11:77076263 | G | A | 2 | a0001c0001t0006g0043 a0002c0003t0006g0042 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-35-8589G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076263 | |||||||
| chr11:77076421 | T | A | 2 | a0001c0001t0003g0180 a0001c0001t0046g0181 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-35-8431T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076421 | |||||||
| chr11:77076425 | A | G | 1 | a0001c0002t0012g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-35-8427A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076425 | |||||||
| chr11:77076646 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-35-8206C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076646 | |||||||
| chr11:77076983 | A | G | 25 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(22): Show |
26 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-35-7869A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77076983 | |||||||
| chr11:77077186 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18956.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-35-7666G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077186 | |||||||
| chr11:77077208 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-35-7644T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077208 | |||||||
| chr11:77077371 | T | A | 2 | a0001c0001t0022g0270 a0001c0001t0048g0266 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-35-7481T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077371 | |||||||
| chr11:77077405 | TG | T | 11 | a0001c0001t0001g0221 a0001c0002t0002g0209 a0001c0002t0003g0213 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-7446delG | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077405 | |||||||
| chr11:77077416 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35-7436A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077416 | |||||||
| chr11:77077457 | G | T | 1 | a0001c0001t0006g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-35-7395G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077457 | |||||||
| chr11:77077488 | T | C | 1 | a0001c0001t0002g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-35-7364T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077488 | |||||||
| chr11:77077512 | A | AT | 64 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0179 others(61): Show |
66 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.-35-7339dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77077512 | ||||||
| chr11:77077514 | G | T | 64 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0179 others(61): Show |
66 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.-35-7338G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077514 | |||||||
| chr11:77077527 | AT | A | 65 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0179 others(62): Show |
67 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-35-7313delT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77077527 | ||||||
| chr11:77077584 | C | T | 3 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35-7268C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077584 | |||||||
| chr11:77077607 | G | A | 1 | a0001c0001t0003g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-35-7245G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077607 | |||||||
| chr11:77077646 | C | G | 26 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(23): Show |
27 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-35-7206C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077646 | |||||||
| chr11:77077699 | G | A | 1 | a0003c0009t0029g0359 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-7153G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077699 | |||||||
| chr11:77077853 | G | T | 1 | a0001c0001t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-35-6999G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077853 | |||||||
| chr11:77077917 | G | GT | 3 | a0001c0001t0003g0269 a0003c0004t0021g0009 a0003c0004t0021g0234 |
4 | HG02145.hp2 HG02451.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-6928dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77077917 | ||||||
| chr11:77078023 | G | A | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-35-6829G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078023 | |||||||
| chr11:77078063 | A | G | 11 | a0001c0001t0001g0221 a0001c0002t0002g0209 a0001c0002t0003g0213 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-6789A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078063 | |||||||
| chr11:77078233 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(163): Show |
171 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-35-6619T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078233 | |||||||
| chr11:77078786 | CTT | C | 93 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0164 others(90): Show |
97 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-35-6063_-35-6062d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77078786 | ||||||
| chr11:77078901 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-35-5951G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078901 | |||||||
| chr11:77078984 | T | G | 1 | a0001c0001t0042g0189 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-35-5868T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078984 | |||||||
| chr11:77078996 | A | G | 1 | a0001c0001t0005g0344 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-35-5856A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77078996 | |||||||
| chr11:77079112 | G | A | 3 | a0001c0001t0001g0016 a0001c0007t0026g0017 a0001c0007t0026g0018 |
3 | HG01257.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-35-5740G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079112 | |||||||
| chr11:77079149 | C | CTTA | 66 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0179 others(63): Show |
68 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.-35-5682_-35-5680d others(5): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079149 | ||||||
| chr11:77079314 | A | G | 26 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(23): Show |
27 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-35-5538A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079314 | |||||||
| chr11:77079420 | T | A | 3 | a0001c0001t0006g0236 a0003c0004t0021g0009 a0003c0004t0021g0234 |
4 | HG02145.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-5432T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079420 | |||||||
| chr11:77079460 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-35-5392A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079460 | |||||||
| chr11:77079496 | A | G | 5 | a0001c0001t0003g0180 a0001c0001t0006g0236 a0001c0001t0046g0181 others(2): Show |
6 | HG02145.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35-5356A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079496 | |||||||
| chr11:77079625 | C | G | 277 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(274): Show |
288 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-35-5227C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079625 | |||||||
| chr11:77079723 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0090 |
3 | HG01928.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-35-5129C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079723 | |||||||
| chr11:77079735 | A | T | 26 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0255 others(23): Show |
27 | HG00438.hp1 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-35-5117A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079735 | |||||||
| chr11:77079783 | T | TTG | 105 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0039 others(102): Show |
109 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-35-5039_-35-5038d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | T | TTGTG | 25 | a0001c0001t0001g0221 a0001c0001t0001g0299 a0001c0001t0002g0010 others(22): Show |
27 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-35-5041_-35-5038d others(6): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | T | TTGTGTG | 69 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0108 others(66): Show |
71 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-35-5043_-35-5038d others(8): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | T | TTGTGTGT others(1): Show |
17 | a0001c0001t0001g0101 a0001c0001t0001g0116 a0001c0001t0001g0133 others(14): Show |
17 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35-5045_-35-5038d others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0001g0140 a0001c0001t0008g0141 |
2 | HG02523.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-35-5047_-35-5038d others(12): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-35-5053_-35-5038d others(18): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | TTG | T | 5 | a0001c0001t0004g0271 a0001c0001t0006g0043 a0001c0001t0012g0228 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-5039_-35-5038d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0002g0011 a0001c0001t0002g0235 a0001c0001t0002g0237 others(6): Show |
10 | HG01884.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35-5045_-35-5038d others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079783 | TTGTGTGT others(5): Show |
T | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-35-5049_-35-5038d others(14): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77079783 | ||||||
| chr11:77079969 | A | G | 65 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0179 others(62): Show |
67 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-35-4883A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77079969 | |||||||
| chr11:77080001 | T | A | 1 | a0001c0001t0004g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-35-4851T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77080001 | |||||||
| chr11:77080208 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-35-4644A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77080208 | |||||||
| chr11:77080296 | A | T | 5 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35-4556A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77080296 | |||||||
| chr11:77080377 | C | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0235 a0001c0001t0002g0237 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-4475C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77080377 | |||||||
| chr11:77081198 | A | G | 1 | a0001c0001t0019g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-35-3654A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081198 | |||||||
| chr11:77081213 | T | A | 1 | a0001c0002t0012g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-35-3639T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081213 | |||||||
| chr11:77081249 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0101 others(72): Show |
77 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-35-3603G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081249 | |||||||
| chr11:77081385 | C | A | 167 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(164): Show |
173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-35-3467C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081385 | |||||||
| chr11:77081424 | C | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0235 a0001c0001t0002g0237 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-3428C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081424 | |||||||
| chr11:77081454 | C | G | 10 | a0001c0001t0002g0011 a0001c0001t0002g0235 a0001c0001t0002g0237 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-3398C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081454 | |||||||
| chr11:77081801 | G | C | 1 | a0002c0003t0028g0334 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-35-3051G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081801 | |||||||
| chr11:77081864 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0027g0134 |
2 | NA18948.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-35-2988G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081864 | |||||||
| chr11:77081976 | A | G | 279 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(276): Show |
290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-35-2876A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081976 | |||||||
| chr11:77081979 | C | A | 225 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(222): Show |
234 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-35-2873C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081979 | |||||||
| chr11:77081984 | A | G | 226 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0039 others(223): Show |
235 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-35-2868A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081984 | |||||||
| chr11:77082182 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-35-2670G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082182 | |||||||
| chr11:77082188 | C | T | 6 | a0001c0001t0001g0248 a0001c0001t0003g0180 a0001c0001t0006g0236 others(3): Show |
7 | HG01106.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35-2664C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082188 | |||||||
| chr11:77082198 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-35-2654C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082198 | |||||||
| chr11:77082473 | A | G | 1 | a0001c0001t0008g0031 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-35-2379A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082473 | |||||||
| chr11:77082474 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0011g0175 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-35-2378C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082474 | |||||||
| chr11:77082539 | T | C | 1 | a0001c0001t0002g0287 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-35-2313T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082539 | |||||||
| chr11:77082578 | A | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0003g0149 |
3 | NA18956.hp2 NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-35-2274A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082578 | |||||||
| chr11:77082652 | T | C | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-35-2200T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082652 | |||||||
| chr11:77082688 | C | T | 25 | a0001c0001t0001g0245 a0001c0001t0001g0255 a0001c0001t0001g0259 others(22): Show |
26 | HG00438.hp1 HG01071.hp1 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35-2164C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77082688 | |||||||
| chr11:77083333 | C | T | 1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-35-1519C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77083333 | |||||||
| chr11:77083688 | C | A | 1 | a0001c0001t0009g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-35-1164C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77083688 | |||||||
| chr11:77083706 | G | C | 96 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0164 others(93): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-35-1146G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77083706 | |||||||
| chr11:77084056 | G | A | 1 | a0001c0001t0009g0032 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-35-796G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084056 | |||||||
| chr11:77084074 | C | T | 1 | a0001c0001t0006g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-35-778C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084074 | |||||||
| chr11:77084119 | C | T | 2 | a0001c0001t0029g0361 a0001c0001t0052g0362 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-35-733C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084119 | |||||||
| chr11:77084213 | G | C | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-35-639G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084213 | |||||||
| chr11:77084234 | G | GCTGGGCC others(3): Show |
64 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0108 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-35-609_-35-600dup others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77084234 | ||||||
| chr11:77084287 | C | T | 2 | a0001c0001t0012g0352 a0003c0004t0002g0353 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-35-565C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084287 | |||||||
| chr11:77084367 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-35-485A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084367 | |||||||
| chr11:77084391 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-35-461T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084391 | |||||||
| chr11:77084699 | C | G | 1 | a0001c0001t0004g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-35-153C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084699 | |||||||
| chr11:77084700 | T | G | 3 | a0001c0001t0006g0239 a0001c0001t0007g0008 a0002c0003t0001g0210 |
4 | HG01884.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-152T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084700 | |||||||
| chr11:77084793 | A | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0035 others(154): Show |
166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-35-59A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084793 | |||||||
| chr11:77084829 | C | T | 2 | a0001c0001t0001g0285 a0001c0001t0027g0134 |
2 | NA18948.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-35-23C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77084829 | |||||||
| chr11:77085100 | CCACAAGG others(3): Show |
C | 1 | a0001c0001t0009g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.165+50_165+59delCA others(8): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085100 | |||||||
| chr11:77085113 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0033 others(109): Show |
120 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+62C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085113 | |||||||
| chr11:77085176 | G | C | 4 | a0001c0001t0001g0099 a0001c0001t0007g0098 a0001c0001t0011g0297 others(1): Show |
4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+125G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085176 | |||||||
| chr11:77085202 | G | A | 1 | a0001c0002t0050g0360 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+151G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085202 | |||||||
| chr11:77085216 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.165+165G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085216 | |||||||
| chr11:77085745 | G | A | 1 | a0011c0014t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+694G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085745 | |||||||
| chr11:77085774 | G | A | 2 | a0001c0001t0004g0273 a0001c0001t0005g0168 |
2 | HG01261.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.165+723G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085774 | |||||||
| chr11:77085781 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.165+730G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085781 | |||||||
| chr11:77085805 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.165+754T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085805 | |||||||
| chr11:77085894 | C | T | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+843C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77085894 | |||||||
| chr11:77086163 | G | A | 2 | a0001c0001t0002g0302 a0001c0001t0005g0055 |
2 | HG00323.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.165+1112G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086163 | |||||||
| chr11:77086188 | T | A | 1 | a0001c0001t0002g0301 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.165+1137T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086188 | |||||||
| chr11:77086315 | C | T | 232 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.165+1264C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086315 | |||||||
| chr11:77086318 | A | T | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+1267A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086318 | |||||||
| chr11:77086564 | A | C | 1 | a0001c0001t0001g0298 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.165+1513A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086564 | |||||||
| chr11:77086736 | G | A | 66 | a0001c0001t0001g0348 a0001c0001t0001g0357 a0001c0001t0002g0037 others(63): Show |
69 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.165+1685G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086736 | |||||||
| chr11:77086792 | C | T | 3 | a0001c0001t0020g0162 a0001c0001t0020g0163 a0001c0001t0020g0165 |
3 | HG02258.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.165+1741C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086792 | |||||||
| chr11:77086852 | G | A | 1 | a0001c0002t0014g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165+1801G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086852 | |||||||
| chr11:77086953 | A | T | 1 | a0002c0003t0007g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.165+1902A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77086953 | |||||||
| chr11:77087057 | G | C | 2 | a0001c0001t0014g0274 a0001c0002t0007g0207 |
2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.165+2006G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087057 | |||||||
| chr11:77087094 | G | A | 7 | a0001c0001t0006g0226 a0001c0001t0012g0199 a0001c0001t0012g0352 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+2043G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087094 | |||||||
| chr11:77087147 | C | T | 1 | a0001c0001t0045g0350 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165+2096C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087147 | |||||||
| chr11:77087454 | C | G | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.165+2403C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087454 | |||||||
| chr11:77087496 | TCCTCAGC others(5): Show |
T | 1 | a0001c0002t0014g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.165+2446_165+2457d others(14): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087496 | |||||||
| chr11:77087874 | C | T | 1 | a0001c0001t0023g0139 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.165+2823C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087874 | |||||||
| chr11:77087915 | G | A | 7 | a0001c0001t0006g0226 a0001c0001t0012g0199 a0001c0001t0012g0352 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+2864G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087915 | |||||||
| chr11:77087955 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.165+2904C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087955 | |||||||
| chr11:77087958 | T | C | 314 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(311): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.165+2907T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77087958 | |||||||
| chr11:77088038 | T | C | 6 | a0001c0001t0001g0174 a0001c0001t0001g0277 a0001c0001t0007g0276 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+2987T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088038 | |||||||
| chr11:77088073 | C | G | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.165+3022C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088073 | |||||||
| chr11:77088106 | C | T | 7 | a0001c0001t0006g0226 a0001c0001t0012g0199 a0001c0001t0012g0352 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+3055C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088106 | |||||||
| chr11:77088177 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(106): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.165+3126G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088177 | |||||||
| chr11:77088346 | G | A | 309 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(306): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.165+3295G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088346 | |||||||
| chr11:77088401 | G | A | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.165+3350G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088401 | |||||||
| chr11:77088452 | A | C | 7 | a0001c0001t0006g0226 a0001c0001t0012g0199 a0001c0001t0012g0352 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+3401A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088452 | |||||||
| chr11:77088638 | A | C | 314 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(311): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.165+3587A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088638 | |||||||
| chr11:77088665 | T | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(95): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.165+3614T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088665 | |||||||
| chr11:77088699 | G | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(66): Show |
72 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+3648G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088699 | |||||||
| chr11:77088903 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.165+3852C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088903 | |||||||
| chr11:77088969 | C | T | 76 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0185 others(73): Show |
81 | HG00408.hp1 HG00621.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.165+3918C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088969 | |||||||
| chr11:77089069 | G | C | 1 | a0001c0001t0002g0216 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.165+4018G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089069 | |||||||
| chr11:77089081 | A | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(66): Show |
72 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+4030A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089081 | |||||||
| chr11:77089324 | A | G | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+4273A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089324 | |||||||
| chr11:77089335 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.165+4284G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089335 | |||||||
| chr11:77089904 | C | A | 2 | a0001c0001t0048g0266 a0001c0011t0031g0230 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.166-3778C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089904 | |||||||
| chr11:77089998 | C | A | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3684C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77089998 | |||||||
| chr11:77090000 | T | C | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3682T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090000 | |||||||
| chr11:77090001 | T | A | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3681T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090001 | |||||||
| chr11:77090005 | G | T | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3677G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090005 | |||||||
| chr11:77090006 | T | A | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3676T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090006 | |||||||
| chr11:77090007 | G | C | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3675G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090007 | |||||||
| chr11:77090008 | C | G | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3674C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090008 | |||||||
| chr11:77090009 | C | G | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3673C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090009 | |||||||
| chr11:77090010 | T | A | 13 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(10): Show |
13 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3672T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090010 | |||||||
| chr11:77090208 | A | T | 2 | a0001c0001t0005g0168 a0001c0002t0014g0220 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.166-3474A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090208 | |||||||
| chr11:77090209 | G | C | 2 | a0001c0001t0005g0168 a0001c0002t0014g0220 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.166-3473G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090209 | |||||||
| chr11:77090210 | A | T | 2 | a0001c0001t0005g0168 a0001c0002t0014g0220 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.166-3472A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090210 | |||||||
| chr11:77090212 | C | T | 2 | a0001c0001t0005g0168 a0001c0002t0014g0220 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.166-3470C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090212 | |||||||
| chr11:77090216 | T | A | 2 | a0001c0001t0005g0168 a0001c0002t0014g0220 |
2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.166-3466T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090216 | |||||||
| chr11:77090262 | C | T | 4 | a0001c0001t0007g0008 a0001c0001t0020g0162 a0001c0001t0020g0163 others(1): Show |
5 | HG01891.hp1 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3420C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090262 | |||||||
| chr11:77090364 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0146 |
2 | NA18975.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.166-3318G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090364 | |||||||
| chr11:77090482 | C | G | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.166-3200C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090482 | |||||||
| chr11:77090614 | C | T | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.166-3068C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090614 | |||||||
| chr11:77090738 | G | A | 1 | a0001c0001t0052g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.166-2944G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090738 | |||||||
| chr11:77090877 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0074 a0001c0001t0001g0164 others(3): Show |
6 | HG00735.hp2 HG01257.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-2805G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090877 | |||||||
| chr11:77090936 | G | A | 1 | a0001c0001t0011g0147 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.166-2746G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090936 | |||||||
| chr11:77090936 | G | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0067 others(102): Show |
113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.166-2746G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090936 | |||||||
| chr11:77091069 | C | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0067 others(102): Show |
113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.166-2613C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091069 | |||||||
| chr11:77091280 | T | C | 1 | a0001c0001t0035g0312 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-2402T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091280 | |||||||
| chr11:77091310 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.166-2372G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091310 | |||||||
| chr11:77091391 | G | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0074 others(29): Show |
35 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.166-2291G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091391 | |||||||
| chr11:77091428 | T | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0074 others(29): Show |
35 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.166-2254T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091428 | |||||||
| chr11:77091459 | T | A | 1 | a0010c0017t0016g0120 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.166-2223T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091459 | |||||||
| chr11:77091490 | T | C | 1 | a0001c0001t0010g0303 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.166-2192T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091490 | |||||||
| chr11:77091564 | A | G | 2 | a0001c0002t0012g0178 a0001c0002t0012g0184 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.166-2118A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091564 | |||||||
| chr11:77091654 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.166-2028G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091654 | |||||||
| chr11:77091734 | T | C | 1 | a0001c0001t0022g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-1948T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091734 | |||||||
| chr11:77091740 | A | C | 73 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0185 others(70): Show |
78 | HG00408.hp1 HG00621.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.166-1942A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091740 | |||||||
| chr11:77091778 | C | A | 1 | a0001c0002t0014g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.166-1904C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091778 | |||||||
| chr11:77091869 | C | A | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-1813C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091869 | |||||||
| chr11:77091870 | G | A | 1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-1812G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091870 | |||||||
| chr11:77091960 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.166-1722C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091960 | |||||||
| chr11:77092013 | A | T | 1 | a0001c0001t0008g0155 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.166-1669A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092013 | |||||||
| chr11:77092126 | A | G | 1 | a0001c0001t0017g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.166-1556A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092126 | |||||||
| chr11:77092164 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0277 a0001c0019t0044g0227 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1518A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092164 | |||||||
| chr11:77092259 | A | G | 2 | a0001c0001t0007g0276 a0001c0001t0007g0329 |
2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.166-1423A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092259 | |||||||
| chr11:77092265 | A | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0074 others(29): Show |
35 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.166-1417A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092265 | |||||||
| chr11:77092282 | A | G | 109 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0067 others(106): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.166-1400A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092282 | |||||||
| chr11:77092402 | G | T | 42 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(39): Show |
46 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.166-1280G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092402 | |||||||
| chr11:77092409 | A | C | 1 | a0001c0001t0005g0340 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.166-1273A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092409 | |||||||
| chr11:77092702 | C | T | 232 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0067 others(229): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.166-980C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092702 | |||||||
| chr11:77092891 | C | T | 1 | a0001c0001t0004g0025 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.166-791C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092891 | |||||||
| chr11:77092947 | G | A | 1 | a0009c0008t0003g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.166-735G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092947 | |||||||
| chr11:77093025 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0002g0117 others(2): Show |
5 | HG00280.hp2 HG00323.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-657A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093025 | |||||||
| chr11:77093068 | C | G | 11 | a0001c0001t0001g0275 a0001c0001t0022g0222 a0001c0001t0022g0270 others(8): Show |
11 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-614C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093068 | |||||||
| chr11:77093085 | G | A | 222 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0070 others(219): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.166-597G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093085 | |||||||
| chr11:77093149 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.166-533G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093149 | |||||||
| chr11:77093175 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0011g0175 a0001c0001t0012g0228 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-507C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093175 | |||||||
| chr11:77093265 | G | C | 9 | a0001c0001t0022g0222 a0001c0001t0022g0270 a0001c0002t0002g0209 others(6): Show |
9 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-417G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093265 | |||||||
| chr11:77093319 | A | T | 63 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0140 others(60): Show |
67 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.166-363A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093319 | |||||||
| chr11:77093400 | C | T | 2 | a0001c0001t0006g0226 a0001c0001t0033g0225 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.166-282C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093400 | |||||||
| chr11:77093440 | A | G | 3 | a0001c0001t0003g0059 a0001c0001t0003g0085 a0001c0001t0003g0191 |
3 | HG02135.hp2 NA18747.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.166-242A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093440 | |||||||
| chr11:77093489 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.166-193G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093489 | |||||||
| chr11:77093563 | A | G | 1 | a0001c0001t0006g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.166-119A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093563 | |||||||
| chr11:77093583 | A | AGTCTGTG others(8): Show |
2 | a0003c0004t0021g0009 a0003c0004t0021g0234 |
3 | HG02145.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.166-84_166-70dupCG others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093583 | ||||||
| chr11:77093583 | AGTCTGTG others(8): Show |
A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0060 others(73): Show |
78 | HG00423.hp2 HG00639.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.166-84_166-70delCG others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093583 | ||||||
| chr11:77093585 | TCTGTGTC others(5): Show |
T | 8 | a0001c0001t0001g0074 a0001c0001t0001g0108 a0001c0001t0005g0075 others(5): Show |
8 | HG00280.hp1 HG01168.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-95_166-84delTG others(10): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093585 | ||||||
| chr11:77093586 | CTGTGTCT others(4): Show |
C | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.166-95_166-85delTG others(9): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093586 | |||||||
| chr11:77093592 | CTGTCACG others(4): Show |
C | 1 | a0001c0001t0023g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.166-85_166-75delAC others(9): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093592 | ||||||
| chr11:77093597 | ACGTCTGT others(4): Show |
A | 2 | a0001c0001t0015g0172 a0001c0002t0015g0349 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.166-84_166-74delCG others(9): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093597 | |||||||
| chr11:77093598 | CGTCTGTG others(3): Show |
C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0331 |
2 | NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.166-80_166-71delTG others(8): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093598 | ||||||
| chr11:77093598 | CGTCTGTG others(8): Show |
C | 3 | a0001c0001t0001g0214 a0001c0001t0002g0315 a0005c0006t0011g0355 |
3 | HG01496.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.166-79_166-65delGT others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 77093598 | ||||||
| chr11:77093613 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.166-69T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093613 | |||||||
| chr11:77093617 | T | C | 21 | a0001c0001t0001g0174 a0001c0001t0001g0277 a0001c0001t0002g0011 others(18): Show |
23 | HG01074.hp2 HG01496.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.166-65T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77093617 | |||||||
| chr11:77093965 | G | A | 1 | a0001c0001t0051g0363 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.297+152G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77093965 | |||||||
| chr11:77093985 | C | T | 6 | a0001c0001t0001g0275 a0001c0001t0017g0100 a0001c0001t0017g0231 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+172C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77093985 | |||||||
| chr11:77093997 | G | C | 3 | a0001c0001t0006g0239 a0001c0002t0003g0213 a0001c0002t0006g0212 |
3 | HG02055.hp2 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.297+184G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77093997 | |||||||
| chr11:77094123 | T | C | 2 | a0001c0001t0007g0008 a0001c0001t0046g0181 |
3 | HG01891.hp1 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.297+310T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094123 | |||||||
| chr11:77094336 | GGGCTCTG others(87): Show |
G | 2 | a0001c0001t0008g0128 a0001c0001t0008g0155 |
2 | NA18940.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.297+561_297+654del others(94): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77094336 | ||||||
| chr11:77094366 | C | T | 46 | a0001c0001t0001g0070 a0001c0001t0002g0302 a0001c0001t0004g0002 others(43): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.297+553C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094366 | |||||||
| chr11:77094377 | T | C | 1 | a0001c0001t0002g0013 | 2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.297+564T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094377 | |||||||
| chr11:77094584 | C | A | 1 | a0001c0001t0006g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.297+771C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094584 | |||||||
| chr11:77094731 | A | G | 234 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(231): Show |
247 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.297+918A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094731 | |||||||
| chr11:77094756 | C | T | 4 | a0001c0001t0017g0100 a0001c0001t0017g0231 a0001c0002t0050g0360 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+943C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094756 | |||||||
| chr11:77094757 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+944G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094757 | |||||||
| chr11:77094962 | A | G | 1 | a0001c0001t0006g0229 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.297+1149A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77094962 | |||||||
| chr11:77095107 | C | T | 2 | a0001c0001t0003g0023 a0002c0003t0007g0296 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.297+1294C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095107 | |||||||
| chr11:77095172 | G | A | 3 | a0001c0001t0010g0029 a0001c0001t0010g0034 a0004c0005t0001g0240 |
3 | HG02056.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.297+1359G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095172 | |||||||
| chr11:77095190 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0008g0130 a0001c0001t0008g0148 others(1): Show |
4 | NA18965.hp1 NA18986.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+1377C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095190 | |||||||
| chr11:77095255 | G | GCCACCAC others(2): Show |
138 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(135): Show |
146 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.297+1445_297+1446i others(11): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77095255 | ||||||
| chr11:77095261 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.297+1448C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095261 | |||||||
| chr11:77095321 | G | C | 4 | a0001c0001t0002g0011 a0001c0019t0044g0227 a0005c0006t0011g0354 others(1): Show |
5 | HG01081.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+1508G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095321 | |||||||
| chr11:77095476 | C | T | 135 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(132): Show |
142 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.297+1663C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095476 | |||||||
| chr11:77095495 | C | A | 1 | a0001c0001t0009g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.297+1682C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095495 | |||||||
| chr11:77095504 | C | T | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.297+1691C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095504 | |||||||
| chr11:77095748 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.297+1935C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095748 | |||||||
| chr11:77095941 | G | T | 6 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(3): Show |
7 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+2128G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77095941 | |||||||
| chr11:77096024 | G | A | 1 | a0001c0001t0017g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.297+2211G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096024 | |||||||
| chr11:77096039 | G | A | 8 | a0001c0001t0001g0275 a0001c0001t0005g0196 a0001c0001t0020g0162 others(5): Show |
8 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+2226G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096039 | |||||||
| chr11:77096051 | T | G | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.297+2238T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096051 | |||||||
| chr11:77096330 | C | T | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.297+2517C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096330 | |||||||
| chr11:77096331 | G | A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+2518G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096331 | |||||||
| chr11:77096436 | C | T | 20 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(17): Show |
20 | HG00558.hp2 HG00741.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.297+2623C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096436 | |||||||
| chr11:77096472 | C | A | 6 | a0001c0001t0001g0275 a0001c0001t0005g0196 a0001c0001t0020g0162 others(3): Show |
6 | HG02258.hp2 HG02897.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+2659C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096472 | |||||||
| chr11:77096479 | A | G | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.297+2666A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096479 | |||||||
| chr11:77096487 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0185 a0001c0001t0001g0214 others(6): Show |
9 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+2674C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096487 | |||||||
| chr11:77096488 | C | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0185 a0001c0001t0001g0214 others(6): Show |
9 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+2675C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096488 | |||||||
| chr11:77096503 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+2690G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096503 | |||||||
| chr11:77096697 | A | G | 235 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(232): Show |
248 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.297+2884A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096697 | |||||||
| chr11:77096930 | A | G | 162 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(159): Show |
170 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.297+3117A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096930 | |||||||
| chr11:77096948 | C | T | 17 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+3135C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096948 | |||||||
| chr11:77096951 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0011g0297 |
2 | HG00558.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.297+3138G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77096951 | |||||||
| chr11:77097067 | A | T | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.297+3254A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097067 | |||||||
| chr11:77097094 | C | T | 17 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+3281C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097094 | |||||||
| chr11:77097208 | C | T | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0272 |
3 | HG01257.hp2 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.297+3395C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097208 | |||||||
| chr11:77097263 | C | T | 2 | a0001c0001t0003g0059 a0001c0001t0003g0085 |
2 | HG02135.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.297+3450C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097263 | |||||||
| chr11:77097382 | A | C | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+3569A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097382 | |||||||
| chr11:77097428 | C | T | 3 | a0001c0001t0002g0117 a0001c0001t0002g0136 a0001c0001t0002g0216 |
3 | NA18945.hp2 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.297+3615C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097428 | |||||||
| chr11:77097464 | G | GT | 22 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0116 others(19): Show |
23 | HG01257.hp2 HG01993.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.297+3676dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | G | GTT | 38 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0058 others(35): Show |
40 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.297+3675_297+3676d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | G | GTTT | 98 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0358 others(95): Show |
103 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.297+3674_297+3676d others(5): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | G | GTTTT | 40 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0224 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+3673_297+3676d others(6): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | G | GTTTTT | 21 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0004g0002 others(18): Show |
25 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.297+3672_297+3676d others(7): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | GT | G | 21 | a0001c0001t0001g0054 a0001c0001t0001g0082 a0001c0001t0001g0091 others(18): Show |
23 | HG00738.hp2 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.297+3676delT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097464 | GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+3666_297+3676d others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097464 | ||||||
| chr11:77097472 | T | G | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+3659T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097472 | |||||||
| chr11:77097580 | C | G | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.297+3767C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097580 | |||||||
| chr11:77097587 | C | G | 136 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(133): Show |
143 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.297+3774C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097587 | |||||||
| chr11:77097602 | G | A | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(48): Show |
55 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.297+3789G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097602 | |||||||
| chr11:77097614 | G | T | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(48): Show |
55 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.297+3801G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097614 | |||||||
| chr11:77097721 | T | C | 235 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(232): Show |
248 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.297+3908T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097721 | |||||||
| chr11:77097791 | G | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0325 a0001c0001t0027g0134 |
3 | NA18948.hp1 NA18993.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.297+3978G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097791 | |||||||
| chr11:77097837 | C | T | 52 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(49): Show |
56 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.297+4024C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097837 | |||||||
| chr11:77097848 | GAA | G | 3 | a0001c0001t0043g0097 a0001c0002t0003g0213 a0001c0002t0006g0212 |
3 | HG02055.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.297+4038_297+4039d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77097848 | ||||||
| chr11:77097965 | C | G | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+4152C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77097965 | |||||||
| chr11:77098000 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.297+4187G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098000 | |||||||
| chr11:77098040 | G | A | 1 | a0001c0001t0037g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.297+4227G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098040 | |||||||
| chr11:77098066 | A | ACCTCCCG others(350): Show |
1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(359): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098066 | ||||||
| chr11:77098067 | C | A | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+4254C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098067 | |||||||
| chr11:77098068 | C | CTCCCGGA others(123): Show |
11 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(8): Show |
11 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+4276_297+4277i others(132): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(123): Show |
1 | a0001c0001t0012g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(132): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(172): Show |
184 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(181): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.297+4280_297+4281i others(181): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(173): Show |
4 | a0001c0001t0001g0072 a0001c0001t0007g0283 a0001c0001t0048g0266 others(1): Show |
4 | HG00597.hp2 HG01192.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+4280_297+4281i others(182): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(172): Show |
1 | a0001c0001t0032g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(181): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(173): Show |
1 | a0001c0001t0001g0259 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(182): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(174): Show |
1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(183): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(172): Show |
2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4280_297+4281i others(181): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(172): Show |
1 | a0001c0001t0003g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(181): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(173): Show |
1 | a0009c0008t0003g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(182): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098068 | C | CTCCCGGA others(172): Show |
1 | a0001c0001t0011g0295 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.297+4324_297+4325i others(181): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098068 | ||||||
| chr11:77098093 | C | CAGGGGGC others(173): Show |
1 | a0001c0001t0002g0117 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.297+4280_297+4281i others(182): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098093 | |||||||
| chr11:77098094 | G | A | 25 | a0001c0001t0002g0217 a0001c0001t0002g0290 a0001c0001t0003g0021 others(22): Show |
25 | HG00544.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+4281G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098094 | |||||||
| chr11:77098103 | A | ACCCCCCC others(173): Show |
1 | a0001c0001t0003g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.297+4324_297+4325i others(182): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098103 | ||||||
| chr11:77098110 | C | G | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.297+4297C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098110 | |||||||
| chr11:77098115 | C | A | 1 | a0001c0001t0032g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.297+4302C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098115 | |||||||
| chr11:77098117 | C | CTCCCGGA others(123): Show |
7 | a0001c0001t0002g0290 a0001c0001t0003g0021 a0001c0001t0003g0053 others(4): Show |
7 | HG00544.hp1 HG01123.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+4324_297+4325i others(132): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098117 | ||||||
| chr11:77098138 | T | C | 66 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
70 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.297+4325T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098138 | |||||||
| chr11:77098139 | G | A | 17 | a0001c0001t0002g0217 a0001c0001t0003g0311 a0001c0001t0003g0328 others(14): Show |
17 | HG01071.hp1 HG01074.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.297+4326G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098139 | |||||||
| chr11:77098166 | A | AG | 17 | a0001c0001t0002g0217 a0001c0001t0003g0311 a0001c0001t0003g0328 others(14): Show |
17 | HG01071.hp1 HG01074.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.297+4357dupG | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098166 | ||||||
| chr11:77098176 | G | A | 17 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+4363G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098176 | |||||||
| chr11:77098185 | C | T | 46 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(43): Show |
50 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.297+4372C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098185 | |||||||
| chr11:77098187 | T | C | 235 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(232): Show |
248 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.297+4374T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098187 | |||||||
| chr11:77098221 | A | C | 47 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(44): Show |
51 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.297+4408A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098221 | |||||||
| chr11:77098221 | A | G | 17 | a0001c0001t0003g0311 a0001c0001t0003g0328 a0001c0001t0003g0338 others(14): Show |
17 | HG01071.hp1 HG01074.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+4408A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098221 | |||||||
| chr11:77098231 | A | AC | 16 | a0001c0001t0001g0071 a0001c0001t0001g0112 a0001c0001t0001g0151 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+4426dupC | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098231 | ||||||
| chr11:77098246 | C | T | 16 | a0001c0001t0003g0311 a0001c0001t0003g0328 a0001c0001t0003g0338 others(13): Show |
16 | HG01071.hp1 HG01074.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+4433C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098246 | |||||||
| chr11:77098261 | T | G | 64 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(61): Show |
68 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.297+4448T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098261 | |||||||
| chr11:77098267 | C | T | 2 | a0001c0001t0010g0280 a0001c0001t0010g0289 |
2 | NA18947.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.297+4454C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098267 | |||||||
| chr11:77098268 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.297+4455G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098268 | |||||||
| chr11:77098281 | A | ACCCCCCC others(122): Show |
2 | a0001c0001t0003g0328 a0001c0001t0004g0273 |
2 | HG03834.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.297+4495_297+4496i others(131): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098281 | ||||||
| chr11:77098304 | G | C | 1 | a0007c0022t0003g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+4491G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098304 | |||||||
| chr11:77098309 | A | G | 15 | a0001c0001t0003g0311 a0001c0001t0003g0328 a0001c0001t0004g0273 others(12): Show |
15 | HG01071.hp1 HG01074.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+4496A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098309 | |||||||
| chr11:77098310 | G | GCTGGCTG others(122): Show |
8 | a0001c0001t0003g0311 a0001c0001t0007g0262 a0001c0001t0010g0261 others(5): Show |
8 | HG01071.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+4502_297+4503i others(131): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098310 | ||||||
| chr11:77098310 | G | GCTGGCTG others(122): Show |
1 | a0001c0001t0056g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.297+4502_297+4503i others(131): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098310 | ||||||
| chr11:77098320 | C | CAGAGGGG others(72): Show |
2 | a0001c0001t0011g0232 a0002c0003t0011g0233 |
2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.297+4507_297+4508i others(81): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098320 | |||||||
| chr11:77098322 | G | A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4509G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098322 | |||||||
| chr11:77098323 | G | A | 53 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.297+4510G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098323 | |||||||
| chr11:77098323 | G | GGGGCTGA others(120): Show |
1 | a0001c0001t0008g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.297+4534_297+4535i others(129): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098323 | ||||||
| chr11:77098328 | T | TCCTCACT others(25): Show |
1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4515_297+4516i others(34): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098328 | |||||||
| chr11:77098330 | A | AC | 10 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0260 others(7): Show |
10 | HG01074.hp2 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+4524dupC | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098330 | ||||||
| chr11:77098330 | A | C | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4517A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098330 | |||||||
| chr11:77098330 | AC | A | 47 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0004g0002 others(44): Show |
51 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.297+4524delC | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098330 | ||||||
| chr11:77098331 | C | G | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4518C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098331 | |||||||
| chr11:77098336 | C | T | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4523C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098336 | |||||||
| chr11:77098344 | C | T | 2 | a0001c0001t0011g0232 a0002c0003t0011g0233 |
2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.297+4531C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098344 | |||||||
| chr11:77098348 | G | C | 115 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(112): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.297+4535G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098348 | |||||||
| chr11:77098353 | G | A | 54 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(51): Show |
58 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.297+4540G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098353 | |||||||
| chr11:77098358 | A | G | 57 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(54): Show |
61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.297+4545A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098358 | |||||||
| chr11:77098397 | C | T | 2 | a0001c0001t0007g0008 a0001c0001t0048g0266 |
3 | HG01891.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.297+4584C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098397 | |||||||
| chr11:77098402 | C | G | 57 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(54): Show |
61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.297+4589C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098402 | |||||||
| chr11:77098403 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4590G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098403 | |||||||
| chr11:77098433 | C | T | 1 | a0004c0005t0001g0240 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+4620C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098433 | |||||||
| chr11:77098436 | C | T | 53 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.297+4623C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098436 | |||||||
| chr11:77098443 | G | T | 11 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+4630G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098443 | |||||||
| chr11:77098476 | A | G | 2 | a0001c0001t0011g0232 a0002c0003t0011g0233 |
2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.297+4663A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098476 | |||||||
| chr11:77098483 | G | A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4670G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098483 | |||||||
| chr11:77098493 | A | G | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4680A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098493 | |||||||
| chr11:77098499 | AGGGCTGA others(42): Show |
A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4716_297+4764d others(51): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098499 | ||||||
| chr11:77098529 | A | G | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4716A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098529 | |||||||
| chr11:77098542 | G | A | 5 | a0001c0001t0008g0141 a0001c0001t0009g0081 a0001c0001t0011g0232 others(2): Show |
5 | HG00597.hp1 HG01074.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+4729G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098542 | |||||||
| chr11:77098573 | C | T | 53 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.297+4760C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098573 | |||||||
| chr11:77098574 | G | GGACTGGG others(43): Show |
1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4764_297+4765i others(52): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098574 | ||||||
| chr11:77098582 | C | CGGCTGGC others(43): Show |
54 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(51): Show |
58 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.297+4780_297+4781i others(52): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098582 | ||||||
| chr11:77098582 | C | CGGCTGGC others(44): Show |
3 | a0001c0001t0002g0088 a0001c0001t0002g0217 a0001c0001t0009g0081 |
3 | HG00597.hp1 HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.297+4780_297+4781i others(53): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098582 | ||||||
| chr11:77098582 | C | T | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4769C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098582 | |||||||
| chr11:77098583 | G | A | 1 | a0001c0001t0010g0261 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.297+4770G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098583 | |||||||
| chr11:77098590 | C | T | 2 | a0001c0002t0003g0213 a0001c0002t0006g0212 |
2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.297+4777C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098590 | |||||||
| chr11:77098595 | A | T | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4782A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098595 | |||||||
| chr11:77098600 | G | C | 1 | a0001c0001t0002g0250 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.297+4787G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098600 | |||||||
| chr11:77098612 | C | T | 124 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(121): Show |
128 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.297+4799C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098612 | |||||||
| chr11:77098626 | C | G | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4813C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098626 | |||||||
| chr11:77098628 | G | A | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.297+4815G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098628 | |||||||
| chr11:77098638 | G | A | 4 | a0001c0001t0017g0100 a0001c0001t0017g0231 a0001c0002t0050g0360 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+4825G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098638 | |||||||
| chr11:77098651 | C | T | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4838C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098651 | |||||||
| chr11:77098652 | A | G | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4839A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098652 | |||||||
| chr11:77098673 | G | A | 57 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(54): Show |
61 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.297+4860G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098673 | |||||||
| chr11:77098675 | A | G | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4862A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098675 | |||||||
| chr11:77098677 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.297+4864G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098677 | |||||||
| chr11:77098678 | G | T | 2 | a0001c0001t0001g0351 a0001c0001t0023g0093 |
2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.297+4865G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098678 | |||||||
| chr11:77098704 | C | T | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4891C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098704 | |||||||
| chr11:77098707 | G | C | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4894G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098707 | |||||||
| chr11:77098708 | G | A | 58 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(55): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.297+4895G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098708 | |||||||
| chr11:77098708 | G | GCGGCTGG others(297): Show |
1 | a0001c0001t0004g0273 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(306): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(220): Show |
1 | a0001c0001t0001g0071 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(219): Show |
1 | a0001c0001t0005g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(219): Show |
1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(219): Show |
244 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(241): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(220): Show |
1 | a0001c0001t0008g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(220): Show |
1 | a0001c0001t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(220): Show |
4 | a0001c0001t0001g0299 a0001c0001t0001g0327 a0001c0001t0003g0095 others(1): Show |
4 | HG00741.hp2 HG02135.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(221): Show |
1 | a0006c0013t0013g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.297+4910_297+4911i others(230): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(221): Show |
1 | a0009c0008t0003g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(230): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(219): Show |
20 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 others(17): Show |
21 | HG00673.hp2 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GCGGCTGG others(220): Show |
3 | a0001c0001t0001g0067 a0001c0001t0003g0144 a0001c0001t0003g0152 |
3 | HG03239.hp2 NA18993.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098708 | ||||||
| chr11:77098708 | G | GTGGCTGG others(219): Show |
1 | a0001c0001t0019g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.297+4895_297+4896i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098708 | |||||||
| chr11:77098709 | C | CGGCTGGC others(221): Show |
1 | a0001c0001t0001g0112 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.297+4910_297+4911i others(230): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098709 | ||||||
| chr11:77098718 | A | AGGCGGGG others(219): Show |
4 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(1): Show |
5 | HG02109.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098718 | ||||||
| chr11:77098718 | A | AGGCGGGG others(219): Show |
2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.297+4910_297+4911i others(228): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098718 | ||||||
| chr11:77098721 | C | CGGGGGGC others(220): Show |
1 | a0001c0001t0001g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+4910_297+4911i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098721 | ||||||
| chr11:77098728 | G | GCTGACCC others(220): Show |
1 | a0001c0001t0003g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.297+4915_297+4916i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098728 | |||||||
| chr11:77098731 | A | ACCCCCCC others(220): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0124 a0001c0001t0020g0162 |
3 | HG00408.hp2 HG02258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.297+4925_297+4926i others(229): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098731 | ||||||
| chr11:77098731 | A | ACCCCCCC others(221): Show |
2 | a0001c0001t0007g0008 a0001c0001t0048g0266 |
3 | HG01891.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.297+4925_297+4926i others(230): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098731 | ||||||
| chr11:77098731 | A | ACCCCCCC others(221): Show |
1 | a0001c0001t0005g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.297+4940_297+4941i others(230): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098731 | ||||||
| chr11:77098731 | A | ACCCCCCC others(222): Show |
2 | a0001c0001t0005g0118 a0004c0005t0004g0028 |
2 | HG00597.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.297+4940_297+4941i others(231): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098731 | ||||||
| chr11:77098732 | C | CCCCCCCA others(169): Show |
3 | a0001c0001t0005g0196 a0001c0001t0007g0241 a0001c0001t0045g0350 |
3 | HG02735.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4925_297+4926i others(178): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098732 | ||||||
| chr11:77098732 | C | CCCCCCCA others(218): Show |
1 | a0001c0001t0022g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.297+4925_297+4926i others(227): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098732 | ||||||
| chr11:77098754 | T | C | 5 | a0001c0001t0005g0196 a0001c0001t0007g0241 a0001c0001t0011g0297 others(2): Show |
5 | HG02735.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+4941T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098754 | |||||||
| chr11:77098757 | C | G | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+4944C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098757 | |||||||
| chr11:77098758 | A | G | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+4945A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098758 | |||||||
| chr11:77098768 | G | A | 3 | a0001c0001t0005g0196 a0001c0001t0007g0241 a0001c0001t0045g0350 |
3 | HG02735.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+4955G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098768 | |||||||
| chr11:77098771 | C | T | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+4958C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098771 | |||||||
| chr11:77098782 | A | ACCCCCCC others(121): Show |
1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+4975_297+4976i others(130): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098782 | ||||||
| chr11:77098782 | ACCCCCCA others(43): Show |
A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+4990_297+5039d others(52): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098782 | ||||||
| chr11:77098803 | T | C | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+4990T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098803 | |||||||
| chr11:77098806 | G | C | 4 | a0001c0001t0005g0196 a0001c0001t0007g0241 a0001c0001t0045g0350 others(1): Show |
4 | HG02735.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+4993G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098806 | |||||||
| chr11:77098807 | G | A | 4 | a0001c0001t0005g0196 a0001c0001t0007g0241 a0001c0001t0045g0350 others(1): Show |
4 | HG02735.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+4994G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098807 | |||||||
| chr11:77098817 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+5004G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098817 | |||||||
| chr11:77098849 | C | T | 1 | a0001c0001t0012g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.297+5036C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098849 | |||||||
| chr11:77098853 | C | T | 1 | a0001c0001t0007g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+5040C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098853 | |||||||
| chr11:77098858 | T | C | 1 | a0001c0001t0007g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+5045T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098858 | |||||||
| chr11:77098869 | C | T | 103 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(100): Show |
108 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.297+5056C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098869 | |||||||
| chr11:77098914 | AGGCTCCT others(33): Show |
A | 2 | a0001c0001t0014g0274 a0001c0002t0014g0220 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.297+5125_297+5164d others(42): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77098914 | ||||||
| chr11:77098942 | T | G | 5 | a0001c0001t0001g0082 a0001c0001t0001g0112 a0001c0001t0013g0001 others(2): Show |
7 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+5129T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098942 | |||||||
| chr11:77098966 | T | A | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(48): Show |
55 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.297+5153T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098966 | |||||||
| chr11:77099014 | G | A | 2 | a0001c0001t0007g0241 a0001c0001t0047g0137 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.297+5201G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099014 | |||||||
| chr11:77099033 | G | A | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.297+5220G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099033 | |||||||
| chr11:77099039 | C | T | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+5226C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099039 | |||||||
| chr11:77099072 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+5259C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099072 | |||||||
| chr11:77099098 | C | T | 74 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(71): Show |
79 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.297+5285C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099098 | |||||||
| chr11:77099108 | GCGCTCCC others(32): Show |
G | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.297+5302_297+5340d others(41): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77099108 | ||||||
| chr11:77099139 | G | A | 68 | a0001c0001t0001g0357 a0001c0001t0002g0290 a0001c0001t0003g0012 others(65): Show |
70 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.297+5326G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099139 | |||||||
| chr11:77099189 | G | A | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.297+5376G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099189 | |||||||
| chr11:77099302 | G | A | 2 | a0001c0001t0003g0023 a0002c0003t0007g0296 |
2 | HG00639.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.297+5489G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099302 | |||||||
| chr11:77099322 | C | CG | 11 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0260 others(8): Show |
11 | HG01261.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+5513dupG | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77099322 | ||||||
| chr11:77099330 | C | T | 16 | a0001c0001t0006g0043 a0001c0001t0006g0182 a0001c0001t0006g0205 others(13): Show |
17 | HG00673.hp2 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+5517C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099330 | |||||||
| chr11:77099402 | G | GAGCCGAG others(18): Show |
1 | a0001c0001t0003g0311 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.297+5594_297+5618d others(27): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77099402 | ||||||
| chr11:77099449 | T | G | 3 | a0001c0001t0020g0162 a0001c0001t0020g0163 a0001c0001t0020g0165 |
3 | HG02258.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.297+5636T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099449 | |||||||
| chr11:77099456 | A | G | 52 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(49): Show |
56 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.297+5643A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099456 | |||||||
| chr11:77099473 | A | C | 3 | a0001c0001t0002g0166 a0001c0001t0002g0217 a0001c0001t0002g0301 |
3 | HG02698.hp1 HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.297+5660A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099473 | |||||||
| chr11:77099486 | G | T | 1 | a0001c0001t0049g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.297+5673G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099486 | |||||||
| chr11:77099505 | A | T | 2 | a0001c0001t0002g0263 a0001c0020t0002g0284 |
2 | NA18942.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.297+5692A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099505 | |||||||
| chr11:77099532 | G | A | 2 | a0001c0001t0016g0244 a0001c0001t0016g0257 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+5719G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099532 | |||||||
| chr11:77099556 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.297+5743C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099556 | |||||||
| chr11:77099611 | T | C | 3 | a0001c0001t0005g0196 a0001c0001t0045g0350 a0001c0002t0007g0207 |
3 | HG02895.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.297+5798T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099611 | |||||||
| chr11:77099638 | A | G | 235 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(232): Show |
248 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.297+5825A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099638 | |||||||
| chr11:77099655 | C | G | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.297+5842C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099655 | |||||||
| chr11:77099706 | G | A | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.297+5893G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099706 | |||||||
| chr11:77099717 | G | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0217 |
2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.297+5904G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099717 | |||||||
| chr11:77099733 | G | A | 1 | a0003c0009t0029g0359 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+5920G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099733 | |||||||
| chr11:77099763 | C | CGGAGAGG others(5): Show |
2 | a0001c0001t0024g0005 a0001c0001t0025g0110 |
3 | NA18940.hp2 NA19002.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.297+5967_297+5978d others(14): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77099763 | ||||||
| chr11:77099878 | C | T | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+6065C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099878 | |||||||
| chr11:77099930 | G | A | 49 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(46): Show |
53 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.297+6117G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77099930 | |||||||
| chr11:77100067 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(1): Show |
5 | HG02109.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+6254C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100067 | |||||||
| chr11:77100096 | C | T | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+6283C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100096 | |||||||
| chr11:77100156 | G | A | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+6343G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100156 | |||||||
| chr11:77100206 | A | T | 12 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+6393A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100206 | |||||||
| chr11:77100311 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(3): Show |
7 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+6498A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100311 | |||||||
| chr11:77100359 | C | T | 17 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.297+6546C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100359 | |||||||
| chr11:77100871 | A | G | 3 | a0001c0001t0020g0162 a0001c0001t0020g0163 a0001c0001t0020g0165 |
3 | HG02258.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.297+7058A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77100871 | |||||||
| chr11:77101025 | C | A | 66 | a0001c0001t0001g0357 a0001c0001t0002g0290 a0001c0001t0003g0012 others(63): Show |
68 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.297+7212C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101025 | |||||||
| chr11:77101232 | G | A | 1 | a0001c0001t0007g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.297+7419G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101232 | |||||||
| chr11:77101372 | A | T | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+7559A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101372 | |||||||
| chr11:77101544 | C | A | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.297+7731C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101544 | |||||||
| chr11:77101650 | A | G | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+7837A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101650 | |||||||
| chr11:77101652 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.297+7839T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101652 | |||||||
| chr11:77101673 | C | G | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.297+7860C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101673 | |||||||
| chr11:77101757 | A | G | 82 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(79): Show |
88 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.297+7944A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101757 | |||||||
| chr11:77101773 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+7960C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101773 | |||||||
| chr11:77101781 | C | G | 78 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.297+7968C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101781 | |||||||
| chr11:77101837 | C | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0174 a0001c0001t0001g0185 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+8024C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101837 | |||||||
| chr11:77101910 | G | A | 24 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0004g0002 others(21): Show |
28 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.297+8097G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101910 | |||||||
| chr11:77101922 | G | T | 53 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(50): Show |
55 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.297+8109G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77101922 | |||||||
| chr11:77102001 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+8188C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102001 | |||||||
| chr11:77102099 | A | G | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.297+8286A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102099 | |||||||
| chr11:77102408 | C | T | 4 | a0001c0001t0002g0011 a0001c0019t0044g0227 a0005c0006t0011g0354 others(1): Show |
5 | HG01081.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+8595C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102408 | |||||||
| chr11:77102731 | G | A | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.297+8918G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102731 | |||||||
| chr11:77102915 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0112 a0001c0001t0001g0114 others(4): Show |
9 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+9102C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102915 | |||||||
| chr11:77102922 | G | A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.297+9109G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102922 | |||||||
| chr11:77102945 | G | A | 4 | a0001c0001t0017g0100 a0001c0001t0017g0231 a0001c0002t0050g0360 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+9132G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77102945 | |||||||
| chr11:77103064 | G | A | 69 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(66): Show |
72 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.297+9251G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103064 | |||||||
| chr11:77103222 | G | A | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.298-9367G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103222 | |||||||
| chr11:77103246 | G | T | 1 | a0001c0001t0019g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.298-9343G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103246 | |||||||
| chr11:77103310 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0279 a0001c0001t0033g0225 |
3 | HG03130.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298-9279C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103310 | |||||||
| chr11:77103355 | C | T | 1 | a0001c0001t0008g0031 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.298-9234C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103355 | |||||||
| chr11:77103425 | G | A | 62 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(59): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.298-9164G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103425 | |||||||
| chr11:77103433 | G | C | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.298-9156G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103433 | |||||||
| chr11:77103470 | A | G | 50 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(47): Show |
54 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.298-9119A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103470 | |||||||
| chr11:77103586 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.298-9003G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103586 | |||||||
| chr11:77103685 | C | A | 22 | a0001c0001t0005g0055 a0001c0001t0005g0075 a0001c0001t0005g0118 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-8904C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103685 | |||||||
| chr11:77103739 | CAG | C | 13 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(10): Show |
13 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-8846_298-8845d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77103739 | ||||||
| chr11:77103814 | C | T | 13 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(10): Show |
13 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-8775C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103814 | |||||||
| chr11:77103815 | G | A | 17 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.298-8774G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103815 | |||||||
| chr11:77103928 | C | T | 1 | a0001c0001t0008g0031 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.298-8661C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103928 | |||||||
| chr11:77103944 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.298-8645G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77103944 | |||||||
| chr11:77104079 | C | G | 1 | a0001c0001t0002g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298-8510C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104079 | |||||||
| chr11:77104159 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.298-8430G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104159 | |||||||
| chr11:77104163 | G | A | 1 | a0005c0006t0011g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.298-8426G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104163 | |||||||
| chr11:77104182 | G | C | 99 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(96): Show |
104 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.298-8407G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104182 | |||||||
| chr11:77104182 | G | T | 1 | a0001c0020t0002g0284 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.298-8407G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104182 | |||||||
| chr11:77104282 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(4): Show |
8 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-8307T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104282 | |||||||
| chr11:77104352 | T | C | 82 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(79): Show |
86 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.298-8237T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104352 | |||||||
| chr11:77104669 | TAC | T | 62 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(59): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.298-7918_298-7917d others(4): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77104669 | ||||||
| chr11:77104790 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-7799G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104790 | |||||||
| chr11:77104955 | G | T | 1 | a0001c0001t0003g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.298-7634G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77104955 | |||||||
| chr11:77105012 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.298-7577G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105012 | |||||||
| chr11:77105037 | G | A | 4 | a0001c0001t0002g0290 a0001c0001t0003g0053 a0001c0001t0003g0095 others(1): Show |
4 | HG00544.hp1 HG01123.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-7552G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105037 | |||||||
| chr11:77105072 | C | T | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.298-7517C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105072 | |||||||
| chr11:77105139 | A | G | 62 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(59): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.298-7450A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105139 | |||||||
| chr11:77105227 | C | A | 1 | a0001c0002t0006g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.298-7362C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105227 | |||||||
| chr11:77105227 | C | T | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.298-7362C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105227 | |||||||
| chr11:77105241 | A | T | 1 | a0001c0001t0002g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.298-7348A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105241 | |||||||
| chr11:77105261 | C | T | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-7328C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105261 | |||||||
| chr11:77105268 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.298-7321G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105268 | |||||||
| chr11:77105305 | G | C | 5 | a0001c0001t0002g0011 a0001c0001t0046g0181 a0001c0019t0044g0227 others(2): Show |
6 | HG01081.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-7284G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105305 | |||||||
| chr11:77105437 | G | A | 1 | a0001c0001t0006g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.298-7152G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105437 | |||||||
| chr11:77105449 | G | A | 22 | a0001c0001t0005g0055 a0001c0001t0005g0075 a0001c0001t0005g0118 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-7140G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105449 | |||||||
| chr11:77105469 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-7120G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105469 | |||||||
| chr11:77105494 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.298-7095G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105494 | |||||||
| chr11:77105525 | T | C | 23 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-7064T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105525 | |||||||
| chr11:77105546 | A | C | 4 | a0001c0001t0002g0011 a0001c0001t0007g0276 a0001c0001t0007g0329 others(1): Show |
5 | HG02109.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-7043A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105546 | |||||||
| chr11:77105664 | C | T | 1 | a0001c0001t0043g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.298-6925C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105664 | |||||||
| chr11:77105810 | A | T | 7 | a0001c0001t0003g0180 a0001c0001t0007g0241 a0001c0001t0011g0175 others(4): Show |
7 | HG00323.hp1 HG02055.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-6779A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105810 | |||||||
| chr11:77105859 | T | A | 1 | a0010c0017t0016g0120 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.298-6730T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77105859 | |||||||
| chr11:77106069 | ACCAAGTC others(4): Show |
A | 62 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(59): Show |
66 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.298-6517_298-6507d others(13): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77106069 | ||||||
| chr11:77106163 | A | G | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.298-6426A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106163 | |||||||
| chr11:77106233 | A | C | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298-6356A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106233 | |||||||
| chr11:77106246 | T | C | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-6343T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106246 | |||||||
| chr11:77106248 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.298-6341C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106248 | |||||||
| chr11:77106267 | C | T | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298-6322C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106267 | |||||||
| chr11:77106276 | C | T | 1 | a0001c0001t0055g0066 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.298-6313C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106276 | |||||||
| chr11:77106504 | TGTG | T | 3 | a0001c0001t0006g0182 a0001c0001t0006g0205 a0001c0001t0006g0218 |
3 | HG00673.hp2 NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.298-6081_298-6079d others(5): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77106504 | ||||||
| chr11:77106575 | A | G | 12 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.298-6014A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106575 | |||||||
| chr11:77106837 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.298-5752G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106837 | |||||||
| chr11:77106938 | G | A | 2 | a0001c0001t0007g0241 a0001c0001t0047g0137 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.298-5651G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106938 | |||||||
| chr11:77106990 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.298-5599G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77106990 | |||||||
| chr11:77107003 | C | T | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-5586C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107003 | |||||||
| chr11:77107007 | C | G | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.298-5582C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107007 | |||||||
| chr11:77107040 | A | G | 353 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(350): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.298-5549A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107040 | |||||||
| chr11:77107370 | G | A | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.298-5219G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107370 | |||||||
| chr11:77107452 | C | T | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298-5137C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107452 | |||||||
| chr11:77107524 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.298-5065C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107524 | |||||||
| chr11:77107616 | C | T | 78 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.298-4973C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107616 | |||||||
| chr11:77107690 | C | T | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-4899C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107690 | |||||||
| chr11:77107691 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.298-4898G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107691 | |||||||
| chr11:77107697 | G | A | 54 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(51): Show |
56 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.298-4892G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107697 | |||||||
| chr11:77107699 | A | C | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-4890A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107699 | |||||||
| chr11:77107782 | C | T | 1 | a0001c0001t0007g0008 | 2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.298-4807C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107782 | |||||||
| chr11:77107910 | C | A | 2 | a0001c0001t0003g0246 a0001c0001t0003g0258 |
2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.298-4679C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107910 | |||||||
| chr11:77107975 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-4614G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77107975 | |||||||
| chr11:77108125 | C | T | 78 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.298-4464C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108125 | |||||||
| chr11:77108294 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-4295G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108294 | |||||||
| chr11:77108526 | G | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0174 a0001c0001t0001g0185 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-4063G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108526 | |||||||
| chr11:77108630 | A | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-3959A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108630 | |||||||
| chr11:77108736 | CA | C | 124 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(121): Show |
131 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.298-3841delA | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77108736 | ||||||
| chr11:77108775 | T | C | 230 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(227): Show |
243 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.298-3814T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108775 | |||||||
| chr11:77108846 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.298-3743G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108846 | |||||||
| chr11:77108952 | G | A | 1 | a0004c0005t0040g0076 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.298-3637G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77108952 | |||||||
| chr11:77109091 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.298-3498T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109091 | |||||||
| chr11:77109139 | C | T | 1 | a0001c0001t0005g0293 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.298-3450C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109139 | |||||||
| chr11:77109383 | A | C | 231 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(228): Show |
244 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.298-3206A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109383 | |||||||
| chr11:77109384 | A | C | 1 | a0001c0001t0005g0292 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.298-3205A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109384 | |||||||
| chr11:77109393 | T | C | 1 | a0001c0001t0009g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.298-3196T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109393 | |||||||
| chr11:77109447 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.298-3142T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109447 | |||||||
| chr11:77109505 | C | T | 1 | a0001c0001t0011g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.298-3084C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109505 | |||||||
| chr11:77109613 | C | T | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298-2976C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109613 | |||||||
| chr11:77109712 | A | G | 12 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.298-2877A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109712 | |||||||
| chr11:77109753 | C | T | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-2836C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109753 | |||||||
| chr11:77109825 | T | C | 5 | a0001c0001t0002g0011 a0001c0001t0046g0181 a0001c0019t0044g0227 others(2): Show |
6 | HG01081.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-2764T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109825 | |||||||
| chr11:77109900 | G | C | 4 | a0001c0001t0002g0011 a0001c0019t0044g0227 a0005c0006t0011g0354 others(1): Show |
5 | HG01081.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-2689G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77109900 | |||||||
| chr11:77110109 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.298-2480G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110109 | |||||||
| chr11:77110110 | A | T | 1 | a0001c0001t0003g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.298-2479A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110110 | |||||||
| chr11:77110117 | C | CT | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(48): Show |
55 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.298-2458dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77110117 | ||||||
| chr11:77110117 | CT | C | 15 | a0001c0001t0001g0224 a0001c0001t0001g0357 a0001c0001t0002g0024 others(12): Show |
15 | HG02155.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.298-2458delT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77110117 | ||||||
| chr11:77110159 | C | A | 73 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(70): Show |
77 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.298-2430C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110159 | |||||||
| chr11:77110234 | C | T | 61 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(58): Show |
65 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.298-2355C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110234 | |||||||
| chr11:77110289 | A | T | 19 | a0001c0001t0001g0357 a0001c0001t0002g0011 a0001c0001t0011g0297 others(16): Show |
20 | HG01081.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-2300A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110289 | |||||||
| chr11:77110557 | G | A | 97 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(94): Show |
102 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.298-2032G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110557 | |||||||
| chr11:77110593 | C | T | 16 | a0001c0001t0006g0043 a0001c0001t0006g0182 a0001c0001t0006g0205 others(13): Show |
17 | HG00673.hp2 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.298-1996C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110593 | |||||||
| chr11:77110665 | C | G | 1 | a0001c0001t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298-1924C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110665 | |||||||
| chr11:77110668 | C | T | 1 | a0001c0019t0044g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.298-1921C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110668 | |||||||
| chr11:77110878 | C | T | 19 | a0001c0001t0001g0357 a0001c0001t0002g0011 a0001c0001t0011g0297 others(16): Show |
20 | HG01081.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-1711C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110878 | |||||||
| chr11:77110992 | G | A | 4 | a0001c0001t0017g0100 a0001c0001t0017g0231 a0001c0002t0050g0360 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1597G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77110992 | |||||||
| chr11:77111090 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298-1499G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111090 | |||||||
| chr11:77111113 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.298-1476A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111113 | |||||||
| chr11:77111240 | G | A | 19 | a0001c0001t0001g0357 a0001c0001t0002g0011 a0001c0001t0011g0297 others(16): Show |
20 | HG01081.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.298-1349G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111240 | |||||||
| chr11:77111541 | G | A | 1 | a0001c0002t0007g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298-1048G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111541 | |||||||
| chr11:77111602 | T | G | 63 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(60): Show |
67 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.298-987T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111602 | |||||||
| chr11:77111637 | G | A | 1 | a0001c0001t0039g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.298-952G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111637 | |||||||
| chr11:77111652 | T | C | 1 | a0001c0001t0002g0250 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.298-937T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111652 | |||||||
| chr11:77111714 | TC | T | 97 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(94): Show |
102 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.298-872delC | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 77111714 | ||||||
| chr11:77111855 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0046g0181 a0001c0019t0044g0227 others(2): Show |
6 | HG01081.hp2 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-734C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111855 | |||||||
| chr11:77111915 | G | A | 2 | a0001c0001t0014g0274 a0001c0002t0014g0220 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.298-674G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111915 | |||||||
| chr11:77111954 | G | C | 12 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.298-635G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77111954 | |||||||
| chr11:77112167 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-422G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77112167 | |||||||
| chr11:77112181 | G | A | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.298-408G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77112181 | |||||||
| chr11:77112241 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-348G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77112241 | |||||||
| chr11:77112438 | C | T | 61 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(58): Show |
65 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.298-151C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77112438 | |||||||
| chr11:77112580 | C | G | 2 | a0001c0001t0009g0077 a0001c0001t0009g0078 |
2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.298-9C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77112580 | |||||||
| chr11:77112933 | A | G | 1 | a0001c0001t0002g0287 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.506+136A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77112933 | |||||||
| chr11:77112936 | G | A | 24 | a0001c0001t0005g0055 a0001c0001t0005g0075 a0001c0001t0005g0118 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.506+139G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77112936 | |||||||
| chr11:77113032 | G | A | 51 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(48): Show |
55 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.506+235G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113032 | |||||||
| chr11:77113194 | G | A | 12 | a0001c0001t0001g0357 a0001c0001t0011g0297 a0001c0001t0012g0199 others(9): Show |
12 | HG02280.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.506+397G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113194 | |||||||
| chr11:77113212 | T | A | 2 | a0003c0004t0021g0009 a0003c0004t0021g0234 |
3 | HG02145.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.506+415T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113212 | |||||||
| chr11:77113240 | G | A | 1 | a0001c0001t0008g0343 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.506+443G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113240 | |||||||
| chr11:77113398 | C | T | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.506+601C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113398 | |||||||
| chr11:77113407 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.506+610C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113407 | |||||||
| chr11:77113610 | G | A | 1 | a0001c0001t0003g0103 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.507-632G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113610 | |||||||
| chr11:77113701 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.507-541C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113701 | |||||||
| chr11:77113723 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0054g0307 |
2 | NA18973.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.507-519C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77113723 | |||||||
| chr11:77113736 | G | GGCTTGTC others(17): Show |
229 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(226): Show |
242 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.507-505_507-504ins others(24): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 77113736 | ||||||
| chr11:77114000 | C | CT | 10 | a0001c0001t0001g0255 a0001c0001t0007g0008 a0001c0001t0007g0276 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.507-230dupT | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 77114000 | ||||||
| chr11:77114100 | A | G | 74 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(71): Show |
77 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.507-142A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77114100 | |||||||
| chr11:77114114 | C | T | 1 | a0001c0001t0004g0291 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.507-128C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77114114 | |||||||
| chr11:77114194 | C | G | 1 | a0001c0001t0001g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.507-48C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77114194 | |||||||
| chr11:77114218 | A | C | 4 | a0001c0001t0002g0011 a0001c0019t0044g0227 a0005c0006t0011g0354 others(1): Show |
5 | HG01081.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.507-24A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 4/12 | chr11 | 77114218 | |||||||
| chr11:77114623 | C | T | 2 | a0001c0001t0003g0103 a0001c0001t0003g0192 |
2 | NA18978.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.699+189C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77114623 | |||||||
| chr11:77114835 | T | C | 1 | a0001c0001t0006g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.699+401T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77114835 | |||||||
| chr11:77114880 | ACC | A | 50 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(47): Show |
54 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.699+448_699+449del others(2): Show |
CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 77114880 | ||||||
| chr11:77114987 | C | G | 7 | a0001c0001t0002g0011 a0001c0001t0007g0008 a0001c0001t0007g0276 others(4): Show |
9 | HG01081.hp2 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-408C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77114987 | |||||||
| chr11:77114987 | C | T | 3 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0238 |
3 | HG02257.hp1 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.700-408C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77114987 | |||||||
| chr11:77115072 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.700-323A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77115072 | |||||||
| chr11:77115127 | T | C | 53 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.700-268T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77115127 | |||||||
| chr11:77115203 | A | G | 73 | a0001c0001t0002g0290 a0001c0001t0003g0012 a0001c0001t0003g0015 others(70): Show |
76 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.700-192A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77115203 | |||||||
| chr11:77115343 | G | A | 1 | a0001c0001t0027g0161 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.700-52G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77115343 | |||||||
| chr11:77115349 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0277 a0002c0003t0001g0210 |
3 | HG01884.hp1 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.700-46G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 5/12 | chr11 | 77115349 | |||||||
| chr11:77115710 | G | A | 66 | a0001c0001t0001g0224 a0001c0001t0002g0003 a0001c0001t0002g0010 others(63): Show |
70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.893+122G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77115710 | |||||||
| chr11:77115827 | G | A | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893+239G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77115827 | |||||||
| chr11:77115868 | G | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0259 others(13): Show |
16 | HG00558.hp2 HG00741.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.893+280G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77115868 | |||||||
| chr11:77115939 | A | G | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.894-287A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77115939 | |||||||
| chr11:77115966 | C | G | 1 | a0001c0001t0011g0147 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.894-260C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77115966 | |||||||
| chr11:77116078 | G | T | 2 | a0005c0006t0011g0354 a0005c0006t0011g0355 |
2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.894-148G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77116078 | |||||||
| chr11:77116106 | C | T | 1 | a0001c0001t0038g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.894-120C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77116106 | |||||||
| chr11:77116177 | G | C | 153 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(150): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.894-49G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77116177 | |||||||
| chr11:77116221 | C | G | 2 | a0001c0001t0024g0005 a0001c0001t0025g0110 |
3 | NA18940.hp2 NA19002.hp2 NA19080.hp2 |
splice_region_variant&intron_variant | LOW | c.894-5C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 6/12 | chr11 | 77116221 | |||||||
| chr11:77116314 | A | G | 145 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0070 others(142): Show |
154 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.971+11A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116314 | |||||||
| chr11:77116450 | C | T | 1 | a0002c0003t0002g0356 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.971+147C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116450 | |||||||
| chr11:77116621 | C | T | 1 | a0001c0011t0031g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+318C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116621 | |||||||
| chr11:77116670 | G | A | 1 | a0001c0001t0015g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.971+367G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116670 | |||||||
| chr11:77116796 | T | C | 4 | a0001c0001t0007g0008 a0001c0001t0007g0276 a0001c0001t0007g0329 others(1): Show |
5 | HG01891.hp1 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+493T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116796 | |||||||
| chr11:77116831 | G | A | 2 | a0001c0001t0009g0030 a0001c0001t0009g0278 |
2 | HG02165.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.971+528G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116831 | |||||||
| chr11:77116849 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.971+546C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116849 | |||||||
| chr11:77116856 | C | T | 2 | a0001c0001t0002g0011 a0001c0019t0044g0227 |
3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.971+553C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116856 | |||||||
| chr11:77116946 | C | T | 96 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0224 others(93): Show |
101 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.971+643C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116946 | |||||||
| chr11:77116950 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.971+647G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77116950 | |||||||
| chr11:77117021 | T | G | 58 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(55): Show |
63 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.971+718T>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117021 | |||||||
| chr11:77117134 | G | T | 1 | a0001c0001t0003g0249 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.971+831G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117134 | |||||||
| chr11:77117190 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.971+887C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117190 | |||||||
| chr11:77117409 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.972-748G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117409 | |||||||
| chr11:77117603 | T | A | 1 | a0001c0001t0004g0022 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.972-554T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117603 | |||||||
| chr11:77117799 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.972-358C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117799 | |||||||
| chr11:77117823 | A | G | 1 | a0001c0001t0007g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.972-334A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117823 | |||||||
| chr11:77117885 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.972-272G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117885 | |||||||
| chr11:77117987 | G | T | 1 | a0001c0001t0002g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.972-170G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 7/12 | chr11 | 77117987 | |||||||
| chr11:77118358 | C | T | 2 | a0001c0001t0024g0005 a0001c0001t0025g0110 |
3 | NA18940.hp2 NA19002.hp2 NA19080.hp2 |
splice_region_variant&intron_variant | LOW | c.1167+6C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 8/12 | chr11 | 77118358 | |||||||
| chr11:77118569 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1167+217G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 8/12 | chr11 | 77118569 | |||||||
| chr11:77118578 | G | A | 1 | a0001c0019t0044g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1167+226G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 8/12 | chr11 | 77118578 | |||||||
| chr11:77118753 | G | T | 2 | a0001c0001t0006g0229 a0001c0001t0006g0337 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1168-277G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 8/12 | chr11 | 77118753 | |||||||
| chr11:77119274 | T | C | 6 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0001c0001t0016g0305 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+122T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119274 | |||||||
| chr11:77119295 | C | T | 6 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0001c0001t0016g0305 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+143C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119295 | |||||||
| chr11:77119461 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1290+309G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119461 | |||||||
| chr11:77119521 | C | T | 1 | a0001c0001t0008g0343 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1290+369C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119521 | |||||||
| chr11:77119539 | T | C | 59 | a0001c0001t0003g0328 a0001c0001t0004g0002 a0001c0001t0004g0004 others(56): Show |
63 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1290+387T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119539 | |||||||
| chr11:77119581 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1290+429T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119581 | |||||||
| chr11:77119595 | C | T | 1 | a0001c0001t0043g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1290+443C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119595 | |||||||
| chr11:77119606 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1290+454G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119606 | |||||||
| chr11:77119624 | C | A | 3 | a0001c0001t0003g0319 a0001c0001t0007g0282 a0001c0015t0003g0313 |
3 | HG01261.hp1 HG01358.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1290+472C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119624 | |||||||
| chr11:77119667 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0045g0350 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1290+515G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119667 | |||||||
| chr11:77119686 | A | C | 1 | a0001c0001t0003g0345 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1290+534A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119686 | |||||||
| chr11:77119732 | C | T | 1 | a0013c0010t0001g0310 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1290+580C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119732 | |||||||
| chr11:77119862 | A | T | 1 | a0001c0019t0044g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1290+710A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119862 | |||||||
| chr11:77119982 | G | A | 6 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0001c0001t0016g0305 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291-731G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77119982 | |||||||
| chr11:77120028 | G | A | 1 | a0001c0001t0048g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1291-685G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120028 | |||||||
| chr11:77120047 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1291-666T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120047 | |||||||
| chr11:77120136 | C | G | 4 | a0001c0001t0003g0180 a0001c0001t0007g0241 a0001c0001t0047g0137 others(1): Show |
4 | HG00323.hp1 HG02055.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291-577C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120136 | |||||||
| chr11:77120313 | G | A | 21 | a0001c0001t0005g0055 a0001c0001t0005g0075 a0001c0001t0005g0118 others(18): Show |
21 | HG00099.hp2 HG00280.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1291-400G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120313 | |||||||
| chr11:77120395 | A | G | 229 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(226): Show |
242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1291-318A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120395 | |||||||
| chr11:77120541 | T | C | 61 | a0001c0001t0003g0328 a0001c0001t0004g0002 a0001c0001t0004g0004 others(58): Show |
65 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1291-172T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120541 | |||||||
| chr11:77120576 | T | C | 229 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(226): Show |
242 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1291-137T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120576 | |||||||
| chr11:77120586 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1291-127G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120586 | |||||||
| chr11:77120649 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1291-64C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 9/12 | chr11 | 77120649 | |||||||
| chr11:77120965 | C | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1487+56C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77120965 | |||||||
| chr11:77121096 | G | A | 1 | a0001c0001t0011g0297 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1487+187G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121096 | |||||||
| chr11:77121164 | C | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0247 a0001c0001t0004g0291 others(3): Show |
7 | HG00642.hp2 HG00735.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1487+255C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121164 | |||||||
| chr11:77121326 | C | T | 1 | a0001c0001t0047g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1487+417C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121326 | |||||||
| chr11:77121337 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1487+428G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121337 | |||||||
| chr11:77121372 | A | C | 13 | a0001c0001t0006g0043 a0001c0001t0006g0226 a0001c0001t0006g0229 others(10): Show |
13 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1487+463A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121372 | |||||||
| chr11:77121388 | T | A | 1 | a0001c0001t0005g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1487+479T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121388 | |||||||
| chr11:77121400 | G | A | 6 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0001c0001t0016g0305 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487+491G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121400 | |||||||
| chr11:77121405 | G | A | 1 | a0001c0001t0037g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1487+496G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121405 | |||||||
| chr11:77121427 | A | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1488-507A>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121427 | |||||||
| chr11:77121474 | G | A | 2 | a0001c0001t0025g0242 a0001c0001t0058g0047 |
2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1488-460G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121474 | |||||||
| chr11:77121531 | C | T | 6 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0001c0001t0016g0305 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488-403C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121531 | |||||||
| chr11:77121673 | G | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(75): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1488-261G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121673 | |||||||
| chr11:77121766 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1488-168C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121766 | |||||||
| chr11:77121793 | G | C | 2 | a0001c0001t0024g0005 a0001c0001t0025g0110 |
3 | NA18940.hp2 NA19002.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1488-141G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 10/12 | chr11 | 77121793 | |||||||
| chr11:77122052 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.1603+3G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 11/12 | chr11 | 77122052 | |||||||
| chr11:77122154 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(80): Show |
88 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1603+105A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 11/12 | chr11 | 77122154 | |||||||
| chr11:77122292 | T | C | 153 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(150): Show |
161 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603+243T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 11/12 | chr11 | 77122292 | |||||||
| chr11:77122717 | G | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(83): Show |
splice_region_variant&intron_variant | LOW | c.1740+5G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122717 | |||||||
| chr11:77122735 | C | T | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1740+23C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122735 | |||||||
| chr11:77122773 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(76): Show |
84 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1740+61G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122773 | |||||||
| chr11:77122832 | G | A | 1 | a0003c0004t0002g0353 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1740+120G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122832 | |||||||
| chr11:77122892 | T | C | 3 | a0001c0001t0016g0244 a0001c0001t0016g0257 a0002c0003t0028g0334 |
3 | HG02647.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1740+180T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122892 | |||||||
| chr11:77122932 | G | C | 5 | a0001c0001t0003g0180 a0001c0001t0007g0241 a0001c0001t0047g0137 others(2): Show |
5 | HG00323.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+220G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77122932 | |||||||
| chr11:77123029 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1740+317G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123029 | |||||||
| chr11:77123107 | G | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1740+395G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123107 | |||||||
| chr11:77123128 | T | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1740+416T>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123128 | |||||||
| chr11:77123535 | G | A | 5 | a0001c0001t0015g0172 a0001c0001t0015g0341 a0001c0001t0052g0362 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1741-153G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123535 | |||||||
| chr11:77123570 | G | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(61): Show |
69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1741-118G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123570 | |||||||
| chr11:77123588 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0279 a0001c0001t0033g0225 |
3 | HG03130.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1741-100C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123588 | |||||||
| chr11:77123656 | C | T | 1 | a0001c0001t0046g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1741-32C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123656 | |||||||
| chr11:77123665 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0290 |
2 | HG00544.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1741-23C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123665 | |||||||
| chr11:77123666 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0011 others(80): Show |
88 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1741-22A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 12/12 | chr11 | 77123666 |