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 | copy fasta | chr11 | 77061971 | 77131155 |
a0002 | 0/0 | 640 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003 | 0/0 | 640 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0004 | 0/0 | 640 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0005 | 0/0 | 640 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0006 | 0/0 | 640 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0007 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0008 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0009 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0010 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0011 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0012 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0013 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1923 | 335 | 63 | 69 | 150 | 10 | 41 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0002 | 0/0 | 1923 | 13 | 13 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0003 | 0/0 | 1923 | 8 | 7 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0004 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0005 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0006 | 0/0 | 1923 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0007 | 0/0 | 1923 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0008 | 0/0 | 1923 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0009 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0010 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0012 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0013 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0014 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0015 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0016 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0017 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0018 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0019 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0020 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0021 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
c0022 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2445 | 96 | 12 | 23 | 38 | 3 | 18 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0002 | 0/0 | 2437 | 59 | 8 | 6 | 38 | 1 | 6 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0003 | 0/0 | 2445 | 47 | 5 | 8 | 28 | 0 | 6 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0004 | 0/0 | 2445 | 18 | 0 | 4 | 11 | 0 | 3 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0005 | 0/0 | 2445 | 15 | 4 | 6 | 0 | 4 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0006 | 0/0 | 2437 | 13 | 10 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0007 | 0/0 | 2447 | 13 | 8 | 3 | 0 | 0 | 2 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0008 | 0/0 | 2447 | 10 | 0 | 0 | 10 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0009 | 0/0 | 2449 | 10 | 0 | 2 | 8 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0010 | 0/0 | 2449 | 8 | 0 | 1 | 6 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0011 | 0/0 | 2447 | 8 | 4 | 4 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0012 | 0/0 | 2449 | 6 | 6 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0013 | 0/0 | 2445 | 6 | 0 | 5 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0014 | 0/0 | 2447 | 5 | 5 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0015 | 0/0 | 2441 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0016 | 0/0 | 2443 | 4 | 2 | 0 | 1 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0017 | 0/0 | 2439 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0018 | 0/0 | 2447 | 3 | 0 | 0 | 2 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0019 | 0/0 | 2445 | 3 | 2 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0020 | 0/0 | 2453 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0021 | 0/0 | 2457 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0022 | 0/0 | 2447 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0023 | 0/0 | 2445 | 2 | 0 | 0 | 1 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0024 | 0/0 | 2449 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0025 | 0/0 | 2453 | 2 | 0 | 1 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0026 | 0/0 | 2445 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0027 | 0/0 | 2451 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0028 | 0/0 | 2445 | 2 | 1 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0029 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0030 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0031 | 0/0 | 2445 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0032 | 0/0 | 2445 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0033 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0034 | 0/0 | 2445 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0035 | 0/0 | 2445 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0036 | 0/0 | 2451 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0037 | 0/0 | 2445 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0038 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0039 | 0/0 | 2473 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0040 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0041 | 0/0 | 2455 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0042 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0043 | 0/0 | 2461 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0044 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0045 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0046 | 0/0 | 2449 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0047 | 0/0 | 2447 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0048 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0049 | 0/0 | 2447 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0050 | 0/0 | 2439 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0051 | 0/0 | 2447 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0052 | 0/0 | 2441 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0053 | 0/0 | 2445 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0054 | 0/0 | 2445 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0055 | 0/0 | 2447 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0056 | 0/0 | 2449 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0057 | 0/0 | 2449 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
t0058 | 0/0 | 2453 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1923 | 335 | 63 | 69 | 150 | 10 | 41 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002 | 0/0 | 1923 | 13 | 13 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0007 | 0/0 | 1923 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0012 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0015 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0019 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0020 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003 | 0/0 | 1923 | 8 | 7 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0021 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003c0004 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003c0009 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0004c0005 | 0/0 | 1923 | 3 | 0 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0005c0006 | 0/0 | 1923 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0006c0008 | 0/0 | 1923 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0007c0010 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0008c0013 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0009c0014 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0010c0018 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0011c0016 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0012c0017 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0013c0022 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | 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 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0002 | 0/0 | 4359 | 54 | 5 | 6 | 36 | 1 | 6 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0003 | 0/0 | 4367 | 43 | 3 | 7 | 28 | 0 | 5 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0004 | 0/0 | 4367 | 16 | 0 | 4 | 9 | 0 | 3 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0005 | 0/0 | 4367 | 15 | 4 | 6 | 0 | 4 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0006 | 0/0 | 4359 | 11 | 8 | 0 | 3 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0007 | 0/0 | 4369 | 11 | 7 | 2 | 0 | 0 | 2 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0008 | 0/0 | 4369 | 10 | 0 | 0 | 10 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0009 | 0/0 | 4371 | 10 | 0 | 2 | 8 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0010 | 0/0 | 4371 | 8 | 0 | 1 | 6 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0011 | 0/0 | 4369 | 5 | 2 | 3 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0012 | 0/0 | 4371 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0013 | 0/0 | 4367 | 4 | 0 | 3 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0014 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0015 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0016 | 0/0 | 4365 | 3 | 2 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0017 | 0/0 | 4361 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0018 | 0/0 | 4369 | 3 | 0 | 0 | 2 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0019 | 0/0 | 4367 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0020 | 0/0 | 4375 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0022 | 0/0 | 4369 | 2 | 2 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0023 | 0/0 | 4367 | 2 | 0 | 0 | 1 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0024 | 0/0 | 4371 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0025 | 0/0 | 4375 | 2 | 0 | 1 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0027 | 0/0 | 4373 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0028 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0029 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0030 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0032 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0033 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0034 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0035 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0036 | 0/0 | 4373 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0037 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0038 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0039 | 0/0 | 4395 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0041 | 0/0 | 4377 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0042 | 0/0 | 4377 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0043 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0045 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0046 | 0/0 | 4371 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0047 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0048 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0049 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0051 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0052 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0053 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0054 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0055 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0056 | 0/0 | 4371 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0057 | 0/0 | 4371 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0001t0058 | 0/0 | 4375 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0006 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0012 | 0/0 | 4371 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0014 | 0/0 | 4369 | 4 | 4 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0015 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0002t0050 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0007t0026 | 0/0 | 4367 | 2 | 0 | 0 | 0 | 2 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0011t0031 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0012t0013 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0015t0003 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0019t0044 | 0/0 | 4385 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0001c0020t0002 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0001 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0006 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0007 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0011 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0015 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0017 | 0/0 | 4361 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0003t0028 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0002c0021t0019 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003c0004t0002 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003c0004t0021 | 0/0 | 4379 | 3 | 3 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0003c0009t0029 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0004c0005t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0004c0005t0004 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0004c0005t0040 | 0/0 | 4375 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0005c0006t0011 | 0/0 | 4369 | 2 | 1 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0006c0008t0003 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0007c0010t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0008c0013t0013 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0009c0014t0002 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0010c0018t0004 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0011c0016t0001 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0012c0017t0016 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | chr11 | 77061971 | 77131155 |
a0013c0022t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | copy fasta | 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 |
a0001c0001t0001g0026 | 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 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0102 | 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 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0147 | 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 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0328 | 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 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0336 | 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 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0002 | 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 |
a0001c0001t0002g0012 | 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 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0062 | 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 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0207 | 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 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0236 | 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 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0013 | 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 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0086 | 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 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0003g0339 | 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 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 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 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0172 | 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 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0005g0345 | 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 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0006g0343 | 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 |
a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0246 | 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 |
a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0007g0330 | 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 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0008g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0028 | 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 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0070 | 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 |
a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0010g0030 | 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 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0010g0263 | 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 |
a0001c0001t0010g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0010g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0010g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0011g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0011g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0012g0353 | 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 |
a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0014g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0016g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0016g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0016g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0018g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0018g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0018g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0019g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0019g0187 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0020g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0020g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0022g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0022g0271 | 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 |
a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0024g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0025g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0027g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0027g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0028g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0029g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0030g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0032g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0033g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0034g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0035g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0036g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0037g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0038g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0039g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0041g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0042g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0043g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0045g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0046g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0047g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0048g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0049g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0051g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0052g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0053g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0054g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0055g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0056g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0057g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0001t0058g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0002g0210 | 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 |
a0001c0002t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0002t0050g0361 | 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 |
a0001c0011t0031g0231 | 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 |
a0001c0015t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0019t0044g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0001c0020t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0003t0001g0211 | 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 |
a0002c0003t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0003t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0003t0015g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0003t0017g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0003t0028g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0002c0021t0019g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0003c0004t0002g0354 | 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 |
a0003c0004t0021g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0003c0009t0029g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0004c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0004c0005t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0004c0005t0040g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0005c0006t0011g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0005c0006t0011g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0006c0008t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0007c0010t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0008c0013t0013g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0009c0014t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0010c0018t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0011c0016t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0012c0017t0016g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
a0013c0022t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0114 | EUR | GBR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0340 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00323 | hp1 | a0001 | c0001 | t0047 | g0139 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0303 | EUR | FIN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0337 | 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 | g0137 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00423 | hp2 | a0001 | c0001 | t0008 | g0344 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00438 | hp2 | a0001 | c0001 | t0023 | g0140 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0086 | 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 | g0029 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00609 | hp2 | a0001 | c0001 | t0009 | g0069 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0148 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00639 | hp2 | a0002 | c0003 | t0007 | g0297 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | CHS | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | 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 | g0136 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00741 | hp1 | a0001 | c0001 | t0035 | g0304 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0263 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01071 | hp2 | a0001 | c0001 | t0039 | g0159 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01074 | hp1 | a0001 | c0001 | t0034 | g0321 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0233 | 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 | g0355 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01099 | hp1 | a0008 | c0013 | t0013 | g0050 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0268 | 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 | g0075 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0187 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0345 | AMR | PUR | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01255 | hp1 | a0001 | c0001 | t0011 | g0296 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0287 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0076 | 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 | g0061 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0062 | 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 | g0283 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01358 | hp2 | a0001 | c0015 | t0003 | g0315 | 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 | g0266 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01496 | hp1 | a0001 | c0001 | t0041 | g0320 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0293 | 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 | g0341 | 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 | g0211 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01884 | hp2 | a0001 | c0001 | t0029 | g0362 | 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 | g0195 | 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 | g0115 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01943 | hp1 | a0001 | c0001 | t0055 | g0059 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01943 | hp2 | a0001 | c0001 | t0009 | g0045 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01952 | hp1 | a0001 | c0001 | t0058 | g0049 | 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 | g0295 | 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 | g0154 | 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 | g0306 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02004 | hp2 | a0001 | c0001 | t0057 | g0055 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02015 | hp2 | a0001 | c0001 | t0042 | g0190 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0057 | 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 | a0013 | c0022 | t0003 | g0177 | 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 | g0168 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02056 | hp2 | a0004 | c0005 | t0001 | g0241 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | 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 | g0202 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0242 | 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 | g0071 | 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 | g0087 | 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 | g0109 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0058 | 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 | g0070 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02165 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | CDX | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02258 | hp1 | a0005 | c0006 | t0011 | g0357 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0163 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02273 | hp1 | a0001 | c0001 | t0056 | g0046 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02280 | hp1 | a0002 | c0003 | t0017 | g0199 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02280 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0294 | AMR | PEL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02300 | hp2 | a0001 | c0001 | t0025 | g0247 | 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 | g0326 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02523 | hp2 | a0001 | c0001 | t0008 | g0142 | EAS | KHV | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0239 | 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 | g0270 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0174 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02615 | hp2 | a0001 | c0001 | t0046 | g0182 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02630 | hp1 | a0002 | c0003 | t0011 | g0234 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02647 | hp1 | a0001 | c0002 | t0014 | g0184 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02647 | hp2 | a0002 | c0003 | t0028 | g0335 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02717 | hp1 | a0001 | c0002 | t0012 | g0185 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02717 | hp2 | a0001 | c0001 | t0051 | g0364 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02723 | hp1 | a0002 | c0003 | t0015 | g0197 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02723 | hp2 | a0001 | c0019 | t0044 | g0228 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0246 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0347 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02738 | hp2 | a0006 | c0008 | t0003 | g0019 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02809 | hp2 | a0001 | c0001 | t0052 | g0363 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02818 | hp1 | a0002 | c0021 | t0019 | g0198 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02818 | hp2 | a0001 | c0001 | t0017 | g0232 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02886 | hp2 | a0001 | c0002 | t0014 | g0221 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02895 | hp1 | a0001 | c0002 | t0007 | g0208 | 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 | g0276 | 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 | g0350 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02922 | hp2 | a0001 | c0001 | t0022 | g0223 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02965 | hp1 | a0001 | c0002 | t0012 | g0194 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0277 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0175 | 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 | g0237 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02976 | hp2 | a0003 | c0009 | t0029 | g0360 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0339 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0176 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03098 | hp2 | a0001 | c0001 | t0020 | g0164 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03130 | hp1 | a0001 | c0001 | t0033 | g0226 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03139 | hp1 | a0001 | c0001 | t0022 | g0271 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03195 | hp1 | a0001 | c0001 | t0043 | g0098 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03209 | hp1 | a0003 | c0004 | t0021 | g0235 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03225 | hp1 | a0001 | c0011 | t0031 | g0231 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0275 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0280 | 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 | g0354 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0298 | 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 | g0307 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0141 | 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 | g0214 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ESN | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0229 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0188 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0243 | AFR | MSL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0167 | 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 | g0126 | SAS | PJL | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0085 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0336 | 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 | g0348 | 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 | g0119 | 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 | g0352 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0274 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0284 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG03942 | hp2 | a0001 | c0001 | t0038 | g0132 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | BEB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18522 | hp1 | a0001 | c0002 | t0012 | g0179 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0343 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0255 | AFR | YRI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0338 | 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 | g0004 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0118 | 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 | g0291 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18948 | hp1 | a0001 | c0001 | t0027 | g0135 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0053 | 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 | g0269 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0244 | 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 | g0313 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18959 | hp2 | a0001 | c0001 | t0032 | g0079 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18963 | hp2 | a0001 | c0001 | t0008 | g0205 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0103 | 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 | g0162 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18965 | hp2 | a0012 | c0017 | t0016 | g0121 | 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 | g0155 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0112 | 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 | g0130 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18973 | hp1 | a0001 | c0001 | t0054 | g0309 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0144 | 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 | g0147 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18980 | hp2 | a0004 | c0005 | t0040 | g0068 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18983 | hp1 | a0001 | c0001 | t0010 | g0281 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0131 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18986 | hp2 | a0001 | c0001 | t0018 | g0056 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0282 | 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 | g0156 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0286 | 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 | g0044 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0319 | 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 | g0116 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19002 | hp2 | a0001 | c0001 | t0025 | g0111 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0318 | 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 | g0245 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0173 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19043 | hp1 | a0001 | c0001 | t0017 | g0101 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19057 | hp2 | a0001 | c0001 | t0028 | g0170 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19068 | hp2 | a0009 | c0014 | t0002 | g0204 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19074 | hp2 | a0001 | c0001 | t0009 | g0279 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19076 | hp1 | a0010 | c0018 | t0004 | g0107 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19079 | hp1 | a0001 | c0001 | t0010 | g0305 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19079 | hp2 | a0001 | c0020 | t0002 | g0285 | 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 | g0004 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0301 | 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 | g0149 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19085 | hp2 | a0007 | c0010 | t0001 | g0312 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0289 | 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 | g0134 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0097 | 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 | g0323 | AFR | ASW | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20129 | hp2 | a0001 | c0002 | t0014 | g0209 | AFR | ASW | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0054 | EUR | TSI | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20905 | hp1 | a0001 | c0001 | t0013 | g0027 | SAS | GIH | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20905 | hp2 | a0001 | c0001 | t0018 | g0120 | SAS | GIH | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01123 | hp1 | a0001 | c0001 | t0037 | g0110 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0330 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0342 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0353 | AFR | ACB | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG02559 | hp1 | a0011 | 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 | g0351 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0166 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA18955 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20300 | hp1 | a0001 | c0001 | t0048 | g0267 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA20300 | hp2 | a0001 | c0002 | t0050 | g0361 | AFR | USA | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | LWK | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | CAPN5_chr11_77061971_77131155 | CAPN5 | chr11 | 77061971 | 77131155 |
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 | a0002a0013 | 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 | a0006 | 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 | a0003a0013 | 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 | a0007 | 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 | a0008 | 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 | a0009 | 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 | a0010 | 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 | a0012 | 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 | a0011 | 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 |
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 | a0001c0002a0002c0021 | 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 |
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 | a0001c0001t0013a0001c0001t0055a0001c0001t0056others(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 | a0001c0001t0053a0001c0001t0054 | 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 | a0001c0001t0029a0001c0001t0051a0001c0001t0052others(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 | a0001c0001t0014a0001c0002t0014 | 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 | a0001c0001t0016a0001c0001t0028a0002c0003t0028others(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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(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 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(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 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(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 | a0001c0001t0015a0001c0001t0052a0001c0002t0015others(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 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(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 | a0001c0001t0009a0001c0001t0010a0001c0001t0012others(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 | a0001c0001t0027a0001c0001t0036 | 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 | a0001c0001t0025a0001c0001t0058a0004c0005t0040 | 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 | a0001c0001t0041a0001c0001t0042 | 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 | a0001c0001t0016a0001c0001t0038a0001c0001t0045others(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 | a0001c0001t0015a0001c0001t0052a0001c0002t0015others(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 | a0001c0001t0017a0001c0002t0050a0002c0003t0017 | 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 | a0001c0001t0002a0001c0001t0006a0001c0001t0029others(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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(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 | a0001c0001t0041a0001c0001t0043a0001c0019t0044others(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 | a0001c0001t0019a0002c0021t0019 | 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 |
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 | a0001c0001t0001g0016a0001c0007t0026g0017a0001c0007t0026g0018 | 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 | a0001c0001t0001g0014a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0168a0001c0001t0001g0359a0001c0001t0002g0167 | 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 | a0001c0001t0001g0168a0001c0001t0002g0167a0006c0008t0003g0019 | 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 | a0001c0001t0001g0168a0001c0001t0002g0167a0006c0008t0003g0019 | 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 | a0001c0001t0005g0169 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0028g0170 | 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 | 167 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0102others(164): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): 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 | a0001c0001t0001g0358 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | 211 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(208): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0035others(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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0258others(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 | a0001c0001t0001g0168a0001c0001t0001g0244a0001c0001t0001g0249others(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 |
31 | a0001c0001t0001g0160a0001c0001t0001g0222a0001c0001t0001g0224others(28): Show | 31 | HG00544.hp1 HG00639.hp2 HG01167.hp1 others(28): 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 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0152others(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 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0125others(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 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0116others(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 | a0001c0001t0001g0108a0001c0001t0001g0180a0001c0001t0003g0109others(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 | a0001c0001t0001g0175a0001c0001t0002g0105a0001c0001t0002g0106others(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 | a0001c0001t0003g0104 | 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 | a0001c0001t0002g0171a0001c0001t0003g0103 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0102 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | ||||||
chr11:77067712
|
T | TG | 364 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(361): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-36+619dupG | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 77067712 | |||||
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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0005g0169 | 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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0002g0024a0001c0001t0002g0037 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0168others(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 | a0001c0002t0014g0221a0001c0019t0044g0228 | 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 | a0001c0001t0022g0271a0001c0001t0048g0267a0002c0003t0028g0335 | 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 | a0001c0001t0007g0262a0001c0001t0010g0263 | 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 | a0001c0001t0017g0101 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0017g0101 | 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 | a0001c0001t0001g0100a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0006g0227a0001c0001t0017g0232a0001c0001t0033g0226others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0168others(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 | a0001c0001t0003g0123 | 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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0225others(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 | a0001c0001t0004g0334 | 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 | a0002c0003t0002g0356a0005c0006t0011g0357 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0008g0149 | 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 | a0001c0001t0001g0249 | 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 | 71 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(68): Show | 73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): 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 | a0001c0001t0001g0282a0001c0001t0010g0281 | 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 | a0001c0001t0001g0186a0001c0001t0005g0172 | 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 | 211 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(208): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-36+2835T>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069929 | ||||||
chr11:77069957
|
A | G | 278 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(275): Show | 287 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-36+2863A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069957 | ||||||
chr11:77069960
|
A | G | 278 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(275): Show | 287 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-36+2866A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77069960 | ||||||
chr11:77069961
|
A | C | 278 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(275): Show | 287 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(284): 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 | a0001c0001t0001g0358 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0002g0333 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0175a0001c0001t0001g0186a0001c0001t0001g0215others(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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | 72 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-36+3648A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77070742 | ||||||
chr11:77070747
|
A | G | 184 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(181): Show | 192 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(189): 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 | a0001c0001t0022g0223 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0002t0014g0221a0001c0019t0044g0228 | 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 | a0001c0001t0006g0280 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | 71 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(68): Show | 73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-36+3976C>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77071070 | ||||||
chr11:77071332
|
A | G | 265 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(262): Show | 274 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(271): 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0168others(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 | 72 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0300 | 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 | a0011c0016t0001g0036 | 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 | a0001c0019t0044g0228 | 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 | a0001c0001t0001g0100a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0003g0095a0001c0001t0003g0096 | 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 | a0001c0001t0001g0222a0001c0002t0002g0210a0001c0002t0003g0213others(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 | a0001c0001t0003g0150 | 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 | a0001c0001t0029g0362a0001c0001t0051g0364a0001c0001t0052g0363others(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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0001g0100a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0002g0236 | 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 | a0001c0001t0001g0224 | 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 | 71 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(68): Show | 73 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(70): 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 | a0001c0001t0003g0270 | 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 | a0001c0001t0002g0011a0001c0001t0045g0351a0005c0006t0011g0355 | 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 | a0002c0003t0028g0335 | 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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239others(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 | a0001c0001t0011g0148a0001c0001t0039g0159 | 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 | a0001c0001t0007g0284 | 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 | a0005c0006t0011g0355 | 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 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0003g0040 | 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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0022g0271a0001c0001t0048g0267a0002c0003t0028g0335 | 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 | a0001c0001t0003g0181a0001c0001t0046g0182 | 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 | a0001c0001t0001g0035a0001c0001t0003g0023 | 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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0168others(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 | a0001c0020t0002g0285 | 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 | a0001c0001t0017g0232 | 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 | 265 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(262): Show | 274 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.-36+6888A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77073982 | ||||||
chr11:77074046
|
C | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(212): Show | 224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-36+6952C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77074046 | ||||||
chr11:77074148
|
G | A | 265 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(262): Show | 274 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(271): 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 | a0001c0001t0001g0014a0001c0001t0001g0165a0001c0001t0001g0168others(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 | a0001c0001t0001g0332 | 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 | a0001c0002t0014g0209 | 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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239others(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 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0001t0003g0144others(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 | a0001c0001t0001g0143a0001c0001t0037g0110 | 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 | 203 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0102others(200): Show | 211 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(208): 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 | 278 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(275): Show | 287 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-36+7949C>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77075043 | ||||||
chr11:77075054
|
G | C | 265 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(262): Show | 274 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(271): 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 | a0001c0001t0001g0217a0001c0001t0002g0178a0001c0001t0002g0216 | 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 | 276 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0100others(273): Show | 285 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(282): 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 | a0001c0001t0002g0011a0001c0001t0045g0351a0005c0006t0011g0355 | 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 | a0001c0001t0002g0011a0001c0001t0045g0351a0005c0006t0011g0355 | 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 | a0001c0001t0007g0097a0001c0001t0043g0098 | 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 | a0001c0001t0001g0186a0001c0001t0001g0215a0001c0001t0005g0172others(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 | a0001c0001t0001g0336a0001c0001t0002g0302 | 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 | a0001c0001t0005g0119a0001c0001t0018g0120 | 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 | a0001c0001t0001g0331 | 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 | a0002c0003t0002g0356a0005c0006t0011g0357 | 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 | a0013c0022t0003g0177 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0186others(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 | a0001c0001t0001g0222a0001c0002t0002g0210a0001c0002t0003g0213others(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 | a0001c0001t0006g0043a0002c0003t0006g0042 | 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 | a0001c0001t0003g0181a0001c0001t0046g0182 | 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 | a0001c0002t0012g0179 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | a0001c0001t0001g0151a0001c0001t0001g0152 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0022g0271a0001c0001t0048g0267 | 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 | a0001c0001t0001g0222a0001c0002t0002g0210a0001c0002t0003g0213others(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 | a0001c0001t0001g0222 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35-7436A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077416 | ||||||
chr11:77077453
|
C | A | 364 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(361): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-35-7399C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77077453 | ||||||
chr11:77077457
|
G | T | 1 | a0001c0001t0006g0240 | 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 | a0001c0001t0002g0337 | 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 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239 | 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 | a0001c0001t0003g0268 | 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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | a0003c0009t0029g0360 | 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 | a0001c0001t0001g0358 | 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 | a0001c0001t0003g0270a0003c0004t0021g0009a0003c0004t0021g0235 | 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 | a0005c0006t0011g0355 | 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 | a0001c0001t0001g0222a0001c0002t0002g0210a0001c0002t0003g0213others(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 | 167 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(164): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): 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 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0165others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0042g0190 | 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 | a0001c0001t0005g0345 | 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 | a0001c0001t0001g0016a0001c0007t0026g0017a0001c0007t0026g0018 | 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 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | a0001c0001t0006g0237a0003c0004t0021g0009a0003c0004t0021g0235 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0003g0181a0001c0001t0006g0237a0001c0001t0046g0182others(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 | 278 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(275): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): 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 | a0001c0001t0001g0006a0001c0001t0001g0090 | 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 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0001g0258others(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 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0039others(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 | a0001c0001t0001g0222a0001c0001t0001g0300a0001c0001t0002g0010others(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 | 70 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0108others(67): Show | 72 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(69): 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 | a0001c0001t0001g0102a0001c0001t0001g0117a0001c0001t0001g0134others(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 | a0001c0001t0001g0141a0001c0001t0008g0142 | 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 | a0001c0001t0004g0272a0001c0001t0006g0043a0001c0001t0012g0229others(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 | a0001c0001t0002g0011a0001c0001t0002g0236a0001c0001t0002g0238others(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 | a0005c0006t0011g0355 | 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 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0180others(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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239others(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 | a0001c0001t0002g0011a0001c0001t0002g0236a0001c0001t0002g0238others(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 | a0001c0001t0019g0187 | 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 | a0001c0002t0012g0194 | 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 | 76 | a0001c0001t0001g0007a0001c0001t0001g0100a0001c0001t0001g0102others(73): Show | 78 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-35-3603G>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081249 | ||||||
chr11:77081385
|
C | A | 168 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(165): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): 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 | a0001c0001t0002g0011a0001c0001t0002g0236a0001c0001t0002g0238others(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 | a0001c0001t0002g0011a0001c0001t0002g0236a0001c0001t0002g0238others(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 | a0002c0003t0028g0335 | 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 | a0001c0001t0001g0134a0001c0001t0027g0135 | 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 | 280 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(277): Show | 291 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-35-2876A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081976 | ||||||
chr11:77081979
|
C | A | 226 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(223): Show | 235 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-35-2873C>A | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 1/12 | chr11 | 77081979 | ||||||
chr11:77081984
|
A | G | 227 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0039others(224): Show | 236 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(233): 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 | a0001c0001t0001g0249a0001c0001t0003g0181a0001c0001t0006g0237others(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 | a0001c0001t0002g0239 | 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 | a0001c0001t0001g0175a0001c0001t0011g0176 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0003g0150 | 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 | a0005c0006t0011g0355 | 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 | a0001c0001t0001g0244a0001c0001t0001g0258a0001c0001t0001g0260others(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 | a0001c0001t0005g0169 | 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 | a0001c0001t0009g0202 | 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 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0165others(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 | a0001c0001t0006g0230 | 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 | a0001c0001t0029g0362a0001c0001t0052g0363 | 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 | a0001c0001t0048g0267 | 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 |
65 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0108others(62): Show | 66 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(63): 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 | a0001c0001t0012g0353a0003c0004t0002g0354 | 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 | a0001c0001t0001g0352 | 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 | a0001c0001t0004g0248 | 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 | a0001c0001t0006g0240a0001c0001t0007g0008a0002c0003t0001g0211 | 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 | 158 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0035others(155): 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 | a0001c0001t0001g0286a0001c0001t0027g0135 | 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 | 113 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0033others(110): 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 | a0001c0001t0001g0100a0001c0001t0007g0097a0001c0001t0011g0298others(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 | a0001c0002t0050g0361 | 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 | a0001c0001t0001g0066 | 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 | a0009c0014t0002g0204 | 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 | a0001c0001t0004g0274a0001c0001t0005g0169 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0003g0193 | 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0002g0303a0001c0001t0005g0054 | 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 | a0001c0001t0002g0302 | 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 | 234 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(231): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0349a0001c0001t0001g0358a0001c0001t0002g0037others(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 | a0001c0001t0020g0163a0001c0001t0020g0164a0001c0001t0020g0166 | 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 | a0001c0002t0014g0184 | 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 | a0002c0003t0007g0297 | 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 | a0001c0001t0014g0275a0001c0002t0007g0208 | 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 | a0001c0001t0006g0227a0001c0001t0012g0200a0001c0001t0012g0353others(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 | a0001c0001t0045g0351 | 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0002t0014g0221 | 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 | a0001c0001t0023g0140 | 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 | a0001c0001t0006g0227a0001c0001t0012g0200a0001c0001t0012g0353others(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 | a0001c0001t0001g0115 | 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 | 316 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(313): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): 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 | a0001c0001t0001g0175a0001c0001t0001g0278a0001c0001t0007g0277others(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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0006g0227a0001c0001t0012g0200a0001c0001t0012g0353others(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 | 110 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(107): 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 | 311 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(308): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0006g0227a0001c0001t0012g0200a0001c0001t0012g0353others(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 | 316 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(313): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.165+3587A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77088638 | ||||||
chr11:77088665
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(96): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(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 | a0001c0001t0004g0274 | 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 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0186others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(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 | a0001c0001t0046g0182 | 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 | a0001c0001t0003g0052 | 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 | a0001c0001t0048g0267a0001c0011t0031g0231 | 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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | a0001c0001t0005g0169a0001c0002t0014g0221 | 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 | a0001c0001t0005g0169a0001c0002t0014g0221 | 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 | a0001c0001t0005g0169a0001c0002t0014g0221 | 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 | a0001c0001t0005g0169a0001c0002t0014g0221 | 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 | a0001c0001t0005g0169a0001c0002t0014g0221 | 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 | a0001c0001t0007g0008a0001c0001t0020g0163a0001c0001t0020g0164others(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 | a0001c0001t0001g0041a0001c0001t0001g0147 | 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 | a0001c0001t0046g0182 | 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0052g0363 | 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 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0165others(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 | a0001c0001t0011g0148 | 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 | 106 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.166-2746G>T | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77090936 | ||||||
chr11:77091069
|
C | T | 106 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(103): Show | 114 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(111): 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 | a0001c0001t0035g0304 | 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 | a0001c0001t0001g0143 | 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 | 33 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0080others(30): Show | 36 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.166-2291G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77091391 | ||||||
chr11:77091428
|
T | C | 33 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0080others(30): Show | 36 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(33): 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 | a0012c0017t0016g0121 | 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 | a0001c0001t0010g0305 | 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 | a0001c0002t0012g0179a0001c0002t0012g0185 | 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 | a0001c0001t0022g0271 | 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 | a0001c0001t0001g0066a0001c0001t0001g0100a0001c0001t0001g0186others(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 | a0001c0002t0014g0221 | 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 | a0001c0011t0031g0231 | 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 | a0001c0001t0005g0169 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0008g0156 | 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 | a0001c0001t0017g0232 | 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 | a0001c0001t0001g0175a0001c0001t0001g0278a0001c0019t0044g0228others(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 | a0001c0001t0007g0277a0001c0001t0007g0330 | 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 | 33 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0080others(30): Show | 36 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.166-1417A>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092265 | ||||||
chr11:77092282
|
A | G | 110 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(107): Show | 118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.166-1400A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 2/12 | chr11 | 77092282 | ||||||
chr11:77092402
|
G | T | 43 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(40): 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 | a0001c0001t0005g0341 | 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 | 234 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(231): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): 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 | a0006c0008t0003g0019 | 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 | a0001c0001t0001g0048a0001c0001t0001g0102a0001c0001t0002g0118others(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 | a0001c0001t0001g0276a0001c0001t0022g0223a0001c0001t0022g0271others(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 | 224 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0075others(221): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): 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 | a0001c0001t0001g0222a0001c0001t0011g0176a0001c0001t0012g0229others(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 | a0001c0001t0022g0223a0001c0001t0022g0271a0001c0002t0002g0210others(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 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0141others(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 | a0001c0001t0006g0227a0001c0001t0033g0226 | 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 | a0001c0001t0003g0063a0001c0001t0003g0087a0001c0001t0003g0192 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0006g0230 | 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 | a0003c0004t0021g0009a0003c0004t0021g0235 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0064others(74): Show | 79 | HG00423.hp2 HG00639.hp2 HG00673.hp2 others(76): 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 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0005g0067others(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 | a0001c0001t0001g0336 | 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 | a0001c0001t0015g0173a0001c0002t0015g0350 | 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 | a0001c0001t0001g0301a0001c0001t0001g0332 | 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 | a0001c0001t0001g0215a0001c0001t0002g0314a0005c0006t0011g0357 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0175a0001c0001t0001g0278a0001c0001t0002g0011others(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 | a0001c0001t0051g0364 | 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 | a0001c0001t0001g0276a0001c0001t0017g0101a0001c0001t0017g0232others(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 | a0001c0001t0006g0240a0001c0002t0003g0213a0001c0002t0006g0212 | 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 | a0001c0001t0007g0008a0001c0001t0046g0182 | 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 | a0001c0001t0008g0128a0001c0001t0008g0156 | 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 | a0001c0001t0001g0078a0001c0001t0002g0303a0001c0001t0004g0003others(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 | a0001c0001t0002g0012 | 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 | a0001c0001t0006g0280 | 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 | 235 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(232): 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 | a0001c0001t0017g0101a0001c0001t0017g0232a0001c0002t0050g0361others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0006g0230 | 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 | a0001c0001t0003g0023a0002c0003t0007g0297 | 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 | a0001c0001t0010g0030a0001c0001t0010g0034a0004c0005t0001g0241 | 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 | a0001c0001t0001g0122a0001c0001t0008g0131a0001c0001t0008g0149others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0002g0011a0001c0019t0044g0228a0005c0006t0011g0355others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0009g0028 | 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 | a0001c0001t0048g0267 | 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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0017g0101 | 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 | a0001c0001t0001g0276a0001c0001t0005g0196a0001c0001t0020g0163others(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 | a0001c0011t0031g0231 | 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 | a0001c0001t0048g0267 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0276a0001c0001t0005g0196a0001c0001t0020g0163others(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 | a0001c0001t0001g0100a0001c0001t0001g0186a0001c0001t0001g0215others(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 | a0001c0001t0001g0100a0001c0001t0001g0186a0001c0001t0001g0215others(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 | a0001c0001t0001g0072 | 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 | 236 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(233): 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0078a0001c0001t0011g0298 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0273 | 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 | a0001c0001t0003g0063a0001c0001t0003g0087 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0002g0118a0001c0001t0002g0138a0001c0001t0002g0216 | 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 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0117others(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 | a0001c0001t0002g0002a0001c0001t0002g0020a0001c0001t0002g0062others(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 | a0001c0001t0001g0041a0001c0001t0001g0261a0001c0001t0001g0359others(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 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0225others(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 | 22 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0004g0003others(19): 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 | 22 | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0001g0091others(19): Show | 24 | HG00738.hp2 HG01081.hp1 HG01099.hp1 others(21): 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | 52 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(49): 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 | 52 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(49): 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 | 236 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(233): 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 | a0001c0001t0001g0286a0001c0001t0001g0328a0001c0001t0027g0135 | 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 | 53 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(50): 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 | a0001c0001t0043g0098a0001c0002t0003g0213a0001c0002t0006g0212 | 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0037g0110 | 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0001g0336 | 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0012g0353 | 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 |
185 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(182): 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 | a0001c0001t0001g0077a0001c0001t0007g0284a0001c0001t0048g0267others(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 | a0001c0001t0032g0079 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0005g0169 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0003g0060 | 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 | a0006c0008t0003g0019 | 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 | a0001c0001t0011g0296 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0002g0218a0001c0001t0002g0292a0001c0001t0003g0021others(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 | a0001c0001t0003g0270 | 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0032g0079 | 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 | a0001c0001t0002g0292a0001c0001t0003g0021a0001c0001t0003g0052others(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 | 67 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(64): 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 | a0001c0001t0002g0218a0001c0001t0003g0313a0001c0001t0003g0329others(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 | a0001c0001t0002g0218a0001c0001t0003g0313a0001c0001t0003g0329others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | 47 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(44): 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 | 236 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(233): 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 | 48 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(45): 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 | a0001c0001t0003g0313a0001c0001t0003g0329a0001c0001t0003g0339others(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 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0152others(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 | a0001c0001t0003g0313a0001c0001t0003g0329a0001c0001t0003g0339others(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 | 65 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(62): 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 | a0001c0001t0010g0281a0001c0001t0010g0291 | 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 | a0001c0001t0003g0329a0001c0001t0004g0274 | 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 | a0013c0022t0003g0177 | 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 | a0001c0001t0003g0313a0001c0001t0003g0329a0001c0001t0004g0274others(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 | a0001c0001t0003g0313a0001c0001t0007g0262a0001c0001t0010g0263others(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 | a0001c0001t0056g0046 | 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 | a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0008g0142 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0261others(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 | a0001c0002t0007g0208 | 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 | 48 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0004g0003others(45): 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 | a0001c0002t0007g0208 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | 116 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(113): 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0007g0008a0001c0001t0048g0267 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0004c0005t0001g0241 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239others(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 | a0001c0001t0011g0233a0002c0003t0011g0234 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0008g0142a0001c0001t0009g0081a0001c0001t0011g0233others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0002g0088a0001c0001t0002g0218a0001c0001t0009g0081 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0010g0263 | 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 | a0001c0002t0003g0213a0001c0002t0006g0212 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0002g0254 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0011t0031g0231 | 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 | a0001c0001t0017g0101a0001c0001t0017g0232a0001c0002t0050g0361others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0352a0001c0001t0023g0093 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0004g0274 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0005g0054 | 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 | a0001c0011t0031g0231 | 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 |
246 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(243): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0008g0259 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0300a0001c0001t0001g0325a0001c0001t0003g0095others(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 | a0008c0013t0013g0050 | 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 | a0006c0008t0003g0019 | 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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239others(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 | a0001c0001t0001g0066a0001c0001t0003g0145a0001c0001t0003g0153 | 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 | a0001c0001t0019g0187 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0001g0080 | 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 | |||||
chr11:77098724
|
A | G | 364 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(361): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.297+4911A>G | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098724 | ||||||
chr11:77098728
|
G | C | 363 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(360): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.297+4915G>C | CAPN5 | ENSG00000149260.18 | transcript | ENST00000648180.1 | protein_coding | 3/12 | chr11 | 77098728 | ||||||
chr11:77098728
|
G | GCTGACCC others(220): Show |
1 | a0001c0001t0003g0104 | 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 | a0001c0001t0001g0039a0001c0001t0001g0125a0001c0001t0020g0163 | 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 | a0001c0001t0007g0008a0001c0001t0048g0267 | 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 | a0001c0001t0005g0169 | 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 | a0001c0001t0005g0119a0004c0005t0004g0029 | 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 | a0001c0001t0005g0196a0001c0001t0007g0246a0001c0001t0045g0351 | 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 | a0001c0001t0022g0271 | 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 | a0001c0001t0005g0196a0001c0001t0007g0246a0001c0001t0011g0298others(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 | a0003c0004t0002g0354 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0005g0196a0001c0001t0007g0246a0001c0001t0045g0351 | 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 | a0003c0004t0002g0354 | 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 | a0003c0004t0002g0354 | 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 | a0001c0002t0007g0208 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0005g0196a0001c0001t0007g0246a0001c0001t0045g0351others(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 | a0001c0001t0005g0196a0001c0001t0007g0246a0001c0001t0045g0351others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0012g0353 | 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 | a0001c0001t0007g0246 | 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 | a0001c0001t0007g0246 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0001t0014g0275a0001c0002t0014g0221 | 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 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0013g0001others(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 | 52 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(49): 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 | a0001c0001t0007g0246a0001c0001t0047g0139 | 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 | a0001c0001t0048g0267 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0001g0358a0001c0001t0002g0292a0001c0001t0003g0013others(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 | a0001c0001t0003g0023a0002c0003t0007g0297 | 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 | a0001c0001t0001g0126a0001c0001t0001g0152a0001c0001t0001g0261others(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 | a0001c0001t0006g0043a0001c0001t0006g0183a0001c0001t0006g0206others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0020g0163a0001c0001t0020g0164a0001c0001t0020g0166 | 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 | 53 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(50): 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 | a0001c0001t0002g0167a0001c0001t0002g0218a0001c0001t0002g0302 | 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 | a0001c0001t0049g0114 | 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 | a0001c0001t0002g0265a0001c0020t0002g0285 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351a0001c0002t0007g0208 | 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 | 236 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(233): 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 | a0001c0001t0048g0267 | 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 | a0001c0001t0048g0267 | 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 | a0001c0001t0002g0167a0001c0001t0002g0218 | 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 | a0003c0009t0029g0360 | 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 | a0001c0001t0024g0004a0001c0001t0025g0111 | 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 | a0001c0001t0046g0182 | 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 | 50 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(47): 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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0046g0182 | 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0020g0163a0001c0001t0020g0164a0001c0001t0020g0166 | 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 | a0001c0001t0001g0358a0001c0001t0002g0292a0001c0001t0003g0013others(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 | a0001c0001t0007g0283 | 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 | a0001c0001t0001g0336 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0046g0182 | 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 | 83 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(80): 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 | a0001c0001t0001g0336 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0100a0001c0001t0001g0175a0001c0001t0001g0186others(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 | 25 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0004g0003others(22): 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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0005c0006t0011g0355 | 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 | a0001c0001t0002g0011a0001c0019t0044g0228a0005c0006t0011g0355others(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 | 8 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 10 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(7): 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0017g0101a0001c0001t0017g0232a0001c0002t0050g0361others(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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0046g0182 | 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 | a0001c0001t0019g0174 | 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 | a0001c0001t0006g0227a0001c0001t0006g0280a0001c0001t0033g0226 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0003c0004t0002g0354 | 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 | 51 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(48): 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 | a0001c0001t0001g0352 | 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 | a0001c0001t0005g0054a0001c0001t0005g0067a0001c0001t0005g0119others(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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0002g0238 | 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 | a0001c0001t0002g0178 | 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 | a0005c0006t0011g0355 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0020t0002g0285 | 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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0003g0124 | 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 | a0001c0001t0002g0292a0001c0001t0003g0052a0001c0001t0003g0095others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0048g0267 | 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 | a0001c0001t0002g0191 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0002g0011a0001c0001t0046g0182a0001c0019t0044g0228others(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 | a0001c0001t0006g0227 | 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 | a0001c0001t0005g0054a0001c0001t0005g0067a0001c0001t0005g0119others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0002g0011a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0043g0098 | 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 | a0001c0001t0003g0181a0001c0001t0007g0246a0001c0001t0011g0176others(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 | a0012c0017t0016g0121 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0046g0182 | 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 | a0001c0011t0031g0231 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0002t0007g0208 | 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 | a0001c0001t0055g0059 | 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 | a0001c0001t0006g0183a0001c0001t0006g0206a0001c0001t0006g0219 | 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0004g0137 | 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 | a0001c0001t0007g0246a0001c0001t0047g0139 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0048g0267 | 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 | 355 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(352): Show | 372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): 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 | a0001c0001t0046g0182 | 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 | a0001c0011t0031g0231 | 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 | a0001c0001t0001g0336 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0002g0273 | 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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0003g0245a0001c0001t0003g0256 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0002t0002g0210 | 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 | a0001c0001t0001g0100a0001c0001t0001g0175a0001c0001t0001g0186others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | 231 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(228): 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 | a0001c0001t0001g0244 | 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 | a0004c0005t0040g0068 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0005g0294 | 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 | 232 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(229): 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 | a0001c0001t0005g0293 | 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 | a0001c0001t0009g0057 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0011g0233 | 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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0002g0011a0001c0001t0046g0182a0001c0019t0044g0228others(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 | a0001c0001t0002g0011a0001c0019t0044g0228a0005c0006t0011g0355others(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 | a0001c0001t0003g0087 | 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 | a0001c0001t0003g0087 | 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 | 52 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(49): 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 | a0001c0001t0001g0225a0001c0001t0001g0358a0001c0001t0002g0024others(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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0001g0358a0001c0001t0002g0011a0001c0001t0011g0298others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0001t0006g0043a0001c0001t0006g0183a0001c0001t0006g0206others(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 | a0001c0001t0001g0358 | 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 | a0001c0019t0044g0228 | 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 | a0001c0001t0001g0358a0001c0001t0002g0011a0001c0001t0011g0298others(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 | a0001c0001t0017g0101a0001c0001t0017g0232a0001c0002t0050g0361others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0358a0001c0001t0002g0011a0001c0001t0011g0298others(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 | a0001c0002t0007g0208 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0039g0159 | 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 | a0001c0001t0002g0254 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0001t0002g0011a0001c0001t0046g0182a0001c0019t0044g0228others(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 | a0001c0001t0014g0275a0001c0002t0014g0221 | 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0009g0069a0001c0001t0009g0070 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0005g0054a0001c0001t0005g0067a0001c0001t0005g0119others(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 | 52 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(49): 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 | a0001c0001t0001g0358a0001c0001t0011g0298a0001c0001t0012g0200others(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 | a0003c0004t0021g0009a0003c0004t0021g0235 | 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 | a0001c0001t0008g0344 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0003g0104 | 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 | a0001c0001t0001g0324 | 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 | a0001c0001t0001g0258a0001c0001t0054g0309 | 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 |
230 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(227): 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 | a0001c0001t0001g0258a0001c0001t0007g0008a0001c0001t0007g0277others(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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0004g0295 | 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 | a0001c0001t0001g0358 | 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 | a0001c0001t0002g0011a0001c0019t0044g0228a0005c0006t0011g0355others(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 | a0001c0001t0003g0104a0001c0001t0003g0193 | 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 | a0001c0001t0006g0227 | 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 | 51 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(48): 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 | a0001c0001t0002g0011a0001c0001t0007g0008a0001c0001t0007g0277others(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 | a0001c0001t0002g0236a0001c0001t0002g0238a0001c0001t0002g0239 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0001t0002g0292a0001c0001t0003g0013a0001c0001t0003g0015others(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 | a0001c0001t0027g0162 | 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 | a0001c0001t0001g0175a0001c0001t0001g0278a0002c0003t0001g0211 | 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 | a0001c0001t0001g0225a0001c0001t0002g0002a0001c0001t0002g0010others(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 | a0001c0011t0031g0231 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0260others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0011g0148 | 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 | a0005c0006t0011g0355a0005c0006t0011g0357 | 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 | a0001c0001t0038g0132 | 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 | 154 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(151): 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 | a0001c0001t0024g0004a0001c0001t0025g0111 | 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 | 146 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0075others(143): 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 | a0001c0011t0031g0231 | 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 | a0001c0001t0015g0173 | 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 | a0001c0001t0007g0008a0001c0001t0007g0277a0001c0001t0007g0330others(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 | a0001c0001t0009g0028a0001c0001t0009g0279 | 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 | a0001c0001t0002g0011a0001c0019t0044g0228 | 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 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0225others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | 59 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(56): 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 | a0001c0001t0003g0250 | 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 | a0001c0001t0001g0336 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0007g0097 | 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 | a0001c0001t0003g0109 | 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 | a0001c0001t0024g0004a0001c0001t0025g0111 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0019t0044g0228 | 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 | a0001c0001t0006g0230a0001c0001t0006g0338 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255a0001c0001t0016g0307others(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 | a0001c0001t0016g0243a0001c0001t0016g0255a0001c0001t0016g0307others(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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0008g0344 | 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 | 60 | a0001c0001t0003g0329a0001c0001t0004g0003a0001c0001t0004g0005others(57): 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0043g0098 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0003g0323a0001c0001t0007g0283a0001c0015t0003g0315 | 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 | a0001c0001t0005g0196a0001c0001t0045g0351 | 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 | a0001c0001t0003g0347 | 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 | a0007c0010t0001g0312 | 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 | a0001c0019t0044g0228 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255a0001c0001t0016g0307others(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 | a0001c0001t0048g0267 | 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0003g0181a0001c0001t0007g0246a0001c0001t0047g0139others(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 | a0001c0001t0005g0054a0001c0001t0005g0067a0001c0001t0005g0119others(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 | 230 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(227): 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 | 62 | a0001c0001t0003g0329a0001c0001t0004g0003a0001c0001t0004g0005others(59): 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 | 230 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(227): 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 | a0001c0001t0003g0087 | 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 | a0001c0001t0002g0167 | 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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0011g0298 | 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 | a0001c0001t0004g0003a0001c0001t0004g0248a0001c0001t0004g0295others(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 | a0001c0001t0047g0139 | 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 | a0001c0001t0002g0105 | 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 | a0001c0001t0006g0043a0001c0001t0006g0227a0001c0001t0006g0230others(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 | a0001c0001t0005g0172 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255a0001c0001t0016g0307others(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 | a0001c0001t0037g0110 | 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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0025g0247a0001c0001t0058g0049 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255a0001c0001t0016g0307others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0024g0004a0001c0001t0025g0111 | 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 | a0003c0004t0002g0354 | 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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0003c0004t0002g0354 | 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 | a0001c0001t0016g0243a0001c0001t0016g0255a0002c0003t0028g0335 | 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 | a0001c0001t0003g0181a0001c0001t0007g0246a0001c0001t0047g0139others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0015g0173a0001c0001t0015g0342a0001c0001t0052g0363others(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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 | a0001c0001t0006g0227a0001c0001t0006g0280a0001c0001t0033g0226 | 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 | a0001c0001t0046g0182 | 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 | a0001c0001t0002g0207a0001c0001t0002g0292 | 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 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(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 |