Item | Value |
---|---|
geneid | 1293 |
ensemblid | ENSG00000163359.17 |
hgncid | 2213 |
symbol | COL6A3 |
name | collagen type VI alpha 3 chain |
refseq_nuc | NM_004369.4 |
refseq_prot | NP_004360.2 |
ensembl_nuc | ENST00000295550.9 |
ensembl_prot | ENSP00000295550.4 |
mane_status | MANE Select |
chr | chr2 |
start | 237324018 |
end | 237414164 |
strand | - |
ver | v1.2 |
region | chr2:237324018-237414164 |
region5000 | chr2:237319018-237419164 |
regionname0 | COL6A3_chr2_237324018_237414164 |
regionname5000 | COL6A3_chr2_237319018_237419164 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 3177 | 62 | 14 | 12 | 24 | 2 | 10 | 18 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002 | 1/0 | 3177 | 53 | 1 | 16 | 21 | 0 | 14 | 16 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003 | 0/0 | 3177 | 34 | 14 | 6 | 11 | 0 | 3 | 9 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004 | 0/0 | 3177 | 30 | 2 | 1 | 21 | 0 | 6 | 16 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005 | 0/0 | 3177 | 19 | 9 | 5 | 1 | 1 | 3 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0006 | 0/0 | 3177 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0007 | 0/1 | 3176 | 7 | 1 | 2 | 2 | 1 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0008 | 0/0 | 3177 | 6 | 1 | 5 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009 | 0/0 | 3177 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0010 | 0/0 | 3177 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0011 | 0/0 | 3177 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0012 | 0/0 | 3177 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0013 | 0/0 | 3177 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0014 | 0/0 | 3177 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0015 | 0/0 | 3177 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0016 | 0/0 | 3177 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0017 | 0/0 | 3177 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0018 | 0/0 | 3177 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0019 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0020 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0021 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0022 | 0/0 | 3177 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0023 | 0/0 | 3177 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0024 | 0/0 | 3177 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0025 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0026 | 0/0 | 3177 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0027 | 0/0 | 3177 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0028 | 0/0 | 3177 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0029 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0030 | 0/0 | 3177 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0031 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0032 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0033 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0034 | 0/0 | 123 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0035 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0036 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0037 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0038 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0039 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0040 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0041 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0042 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0043 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0044 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0045 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0046 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0047 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0048 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0049 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0050 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0051 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0052 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0053 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0054 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0055 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0056 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0057 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0058 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0059 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0060 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0061 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0062 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0063 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0064 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0065 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0066 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0067 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0068 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0069 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0070 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0071 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 9534 | 39 | 1 | 8 | 17 | 0 | 12 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0002 | 0/0 | 9534 | 33 | 5 | 8 | 13 | 2 | 5 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0003 | 0/0 | 9534 | 11 | 0 | 0 | 8 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0004 | 0/0 | 9534 | 9 | 0 | 0 | 7 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0005 | 0/0 | 9534 | 9 | 0 | 2 | 4 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0006 | 0/0 | 9534 | 8 | 0 | 0 | 7 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0007 | 0/0 | 9534 | 7 | 0 | 0 | 7 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0008 | 0/0 | 9534 | 7 | 7 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0009 | 0/0 | 9534 | 6 | 0 | 5 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0010 | 0/0 | 9534 | 5 | 1 | 4 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0011 | 0/1 | 9531 | 5 | 1 | 2 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0012 | 0/0 | 9534 | 5 | 1 | 1 | 0 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0013 | 0/0 | 9534 | 4 | 0 | 0 | 4 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0014 | 0/0 | 9534 | 4 | 4 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0015 | 0/0 | 9534 | 4 | 0 | 1 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0016 | 0/0 | 9534 | 4 | 0 | 0 | 2 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0017 | 0/0 | 9534 | 4 | 0 | 3 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0018 | 0/0 | 9534 | 4 | 4 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0019 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0020 | 0/0 | 9534 | 3 | 0 | 2 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0021 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0022 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0023 | 0/0 | 9534 | 2 | 0 | 0 | 1 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0024 | 0/0 | 9534 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0025 | 0/0 | 9534 | 2 | 0 | 1 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0026 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0027 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0028 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0029 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0030 | 0/0 | 9531 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0031 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0032 | 0/0 | 9534 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0033 | 0/0 | 9534 | 2 | 1 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0034 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0035 | 0/0 | 9534 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0036 | 0/0 | 9534 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0037 | 0/0 | 9534 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0038 | 0/0 | 9534 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0039 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0040 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0041 | 0/0 | 9534 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0042 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0043 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0044 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0045 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0046 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0047 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0048 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0049 | 0/0 | 9531 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0050 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0051 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0052 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0053 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0054 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0055 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0056 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0057 | 0/0 | 9531 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0058 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0059 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0060 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0061 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0062 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0063 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0064 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0065 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0066 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0067 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0068 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0069 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0070 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0071 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0072 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0073 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0074 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0075 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0076 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0077 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0078 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0079 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0080 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0081 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0082 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0083 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0084 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0085 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0086 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0087 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0088 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0089 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0090 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0091 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0092 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0093 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0094 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0095 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0096 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0097 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0098 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0099 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0100 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0101 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0102 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0103 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0104 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0105 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0106 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0107 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0108 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0109 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0110 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0111 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0112 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0113 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0114 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0115 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0116 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0117 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0118 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0119 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0120 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0121 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0122 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0123 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0124 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0125 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0126 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0127 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0128 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0129 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0130 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0131 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0132 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0133 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0134 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0135 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0136 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0137 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0138 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0139 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0140 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0141 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
c0142 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 999 | 116 | 27 | 30 | 39 | 3 | 16 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0002 | 1/0 | 999 | 108 | 13 | 21 | 56 | 3 | 14 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0003 | 0/0 | 999 | 54 | 12 | 8 | 24 | 0 | 10 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0004 | 0/0 | 999 | 21 | 19 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0005 | 0/0 | 1000 | 13 | 13 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0006 | 0/0 | 999 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0007 | 0/0 | 999 | 2 | 0 | 1 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0008 | 0/0 | 1000 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0009 | 0/0 | 999 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0010 | 0/0 | 999 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0011 | 0/0 | 999 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
t0012 | 0/0 | 999 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0003 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0315 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 9534 | 33 | 5 | 8 | 13 | 2 | 5 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0004 | 0/0 | 9534 | 9 | 0 | 0 | 7 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0014 | 0/0 | 9534 | 4 | 4 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0037 | 0/0 | 9534 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0040 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0059 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0068 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0074 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0076 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0079 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0084 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0086 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0087 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0095 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0117 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0130 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0001c0134 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0001 | 1/0 | 9534 | 39 | 1 | 8 | 17 | 0 | 12 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0009 | 0/0 | 9534 | 6 | 0 | 5 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0022 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0092 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0106 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0108 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0109 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0002c0110 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0005 | 0/0 | 9534 | 9 | 0 | 2 | 4 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0015 | 0/0 | 9534 | 4 | 0 | 1 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0026 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0027 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0028 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0031 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0033 | 0/0 | 9534 | 2 | 1 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0039 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0075 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0080 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0082 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0089 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0093 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0105 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0118 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0121 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0003c0122 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0003 | 0/0 | 9534 | 11 | 0 | 0 | 8 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0006 | 0/0 | 9534 | 8 | 0 | 0 | 7 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0016 | 0/0 | 9534 | 4 | 0 | 0 | 2 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0071 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0072 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0102 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0113 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0119 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0120 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0004c0140 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0008 | 0/0 | 9534 | 7 | 7 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0012 | 0/0 | 9534 | 5 | 1 | 1 | 0 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0017 | 0/0 | 9534 | 4 | 0 | 3 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0090 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0101 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0005c0111 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0006c0007 | 0/0 | 9534 | 7 | 0 | 0 | 7 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0006c0064 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0006c0096 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0007c0011 | 0/1 | 9531 | 5 | 1 | 2 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0007c0030 | 0/0 | 9531 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0008c0010 | 0/0 | 9534 | 5 | 1 | 4 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0008c0094 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0009c0041 | 0/0 | 9534 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0009c0042 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0009c0124 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0009c0126 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0010c0018 | 0/0 | 9534 | 4 | 4 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0011c0069 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0011c0070 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0011c0088 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0011c0091 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0012c0013 | 0/0 | 9534 | 4 | 0 | 0 | 4 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0013c0034 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0013c0053 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0013c0097 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0014c0021 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0015c0036 | 0/0 | 9534 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0015c0085 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0016c0019 | 0/0 | 9534 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0017c0024 | 0/0 | 9534 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0017c0058 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0018c0020 | 0/0 | 9534 | 3 | 0 | 2 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0019c0044 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0020c0127 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0020c0129 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0021c0029 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0022c0078 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0022c0103 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0023c0032 | 0/0 | 9534 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0024c0038 | 0/0 | 9534 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0025c0114 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0025c0115 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0026c0035 | 0/0 | 9534 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0027c0023 | 0/0 | 9534 | 2 | 0 | 0 | 1 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0028c0025 | 0/0 | 9534 | 2 | 0 | 1 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0029c0043 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0030c0131 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0030c0132 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0031c0045 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0032c0142 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0033c0141 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0034c0046 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0035c0047 | 0/0 | 9534 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0036c0137 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0037c0051 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0038c0052 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0039c0128 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0040c0135 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0041c0136 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0042c0060 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0043c0061 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0044c0062 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0045c0067 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0046c0065 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0047c0066 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0048c0081 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0049c0104 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0050c0107 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0051c0083 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0052c0112 | 0/0 | 9534 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0053c0073 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0054c0077 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0055c0116 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0056c0063 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0057c0099 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0058c0098 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0059c0055 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0060c0054 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0061c0100 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0062c0056 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0063c0057 | 0/0 | 9531 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0064c0125 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0065c0123 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0066c0133 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0067c0050 | 0/0 | 9534 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0068c0049 | 0/0 | 9531 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0069c0048 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0070c0139 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 | |
a0071c0138 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 10532 | 9 | 3 | 3 | 2 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0002t0002 | 0/0 | 10532 | 14 | 0 | 5 | 4 | 2 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0002t0003 | 0/0 | 10532 | 7 | 1 | 0 | 5 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0002t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0002t0006 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0004t0001 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0004t0002 | 0/0 | 10532 | 7 | 0 | 0 | 5 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0014t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0014t0002 | 0/0 | 10532 | 3 | 3 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0037t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0037t0003 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0040t0001 | 0/0 | 10532 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0059t0004 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0068t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0074t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0076t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0079t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0084t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0086t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0087t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0095t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0117t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0130t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0001c0134t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0001t0001 | 0/0 | 10532 | 28 | 1 | 6 | 14 | 0 | 7 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0001t0002 | 1/0 | 10532 | 10 | 0 | 2 | 2 | 0 | 5 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0001t0009 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0009t0001 | 0/0 | 10532 | 4 | 0 | 3 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0009t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0009t0003 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0022t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0022t0002 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0092t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0106t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0108t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0109t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0002c0110t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0005t0001 | 0/0 | 10532 | 3 | 0 | 2 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0005t0002 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0005t0003 | 0/0 | 10532 | 3 | 0 | 0 | 2 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0005t0007 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0015t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0015t0003 | 0/0 | 10532 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0026t0001 | 0/0 | 10532 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0027t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0027t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0028t0004 | 0/0 | 10532 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0031t0004 | 0/0 | 10532 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0033t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0033t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0039t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0039t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0075t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0080t0005 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0082t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0089t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0093t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0105t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0118t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0121t0003 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0003c0122t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0003t0002 | 0/0 | 10532 | 5 | 0 | 0 | 5 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0003t0003 | 0/0 | 10532 | 6 | 0 | 0 | 3 | 0 | 3 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0006t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0006t0002 | 0/0 | 10532 | 4 | 0 | 0 | 4 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0006t0003 | 0/0 | 10532 | 3 | 0 | 0 | 3 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0016t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0016t0003 | 0/0 | 10532 | 3 | 0 | 0 | 1 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0071t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0072t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0102t0003 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0113t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0119t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0120t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0004c0140t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0008t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0008t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0008t0005 | 0/0 | 10533 | 5 | 5 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0012t0002 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0012t0003 | 0/0 | 10532 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0012t0004 | 0/0 | 10532 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0017t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0017t0003 | 0/0 | 10532 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0017t0007 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0090t0003 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0101t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0005c0111t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0006c0007t0001 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0006c0007t0002 | 0/0 | 10532 | 5 | 0 | 0 | 5 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0006c0064t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0006c0096t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0007c0011t0001 | 0/1 | 10529 | 5 | 1 | 2 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0007c0030t0001 | 0/0 | 10529 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0008c0010t0001 | 0/0 | 10532 | 4 | 0 | 4 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0008c0010t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0008c0094t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009c0041t0002 | 0/0 | 10532 | 2 | 1 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009c0042t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009c0042t0012 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009c0124t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0009c0126t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0010c0018t0003 | 0/0 | 10532 | 3 | 3 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0010c0018t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0011c0069t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0011c0070t0011 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0011c0088t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0011c0091t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0012c0013t0002 | 0/0 | 10532 | 4 | 0 | 0 | 4 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0013c0034t0005 | 0/0 | 10533 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0013c0053t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0013c0097t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0014c0021t0002 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0014c0021t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0015c0036t0001 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0015c0085t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0016c0019t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0016c0019t0002 | 0/0 | 10532 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0017c0024t0001 | 0/0 | 10532 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0017c0058t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0018c0020t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0018c0020t0003 | 0/0 | 10532 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0019c0044t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0019c0044t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0020c0127t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0020c0129t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0021c0029t0005 | 0/0 | 10533 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0022c0078t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0022c0103t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0023c0032t0001 | 0/0 | 10532 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0024c0038t0002 | 0/0 | 10532 | 2 | 0 | 0 | 0 | 0 | 2 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0025c0114t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0025c0115t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0026c0035t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0026c0035t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0027c0023t0001 | 0/0 | 10532 | 2 | 0 | 0 | 1 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0028c0025t0002 | 0/0 | 10532 | 2 | 0 | 1 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0029c0043t0001 | 0/0 | 10532 | 2 | 2 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0030c0131t0001 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0030c0132t0002 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0031c0045t0010 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0032c0142t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0033c0141t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0034c0046t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0035c0047t0002 | 0/0 | 10532 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0036c0137t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0037c0051t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0038c0052t0003 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0039c0128t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0040c0135t0008 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0041c0136t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0042c0060t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0043c0061t0001 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0044c0062t0005 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0045c0067t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0046c0065t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0047c0066t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0048c0081t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0049c0104t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0050c0107t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0051c0083t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0052c0112t0002 | 0/0 | 10532 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0053c0073t0008 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0054c0077t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0055c0116t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0056c0063t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0057c0099t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0058c0098t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0059c0055t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0060c0054t0004 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0061c0100t0002 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0062c0056t0002 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0063c0057t0002 | 0/0 | 10529 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0064c0125t0005 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0065c0123t0003 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0066c0133t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0067c0050t0001 | 0/0 | 10532 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0068c0049t0002 | 0/0 | 10529 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0069c0048t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0070c0139t0005 | 0/0 | 10533 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
a0071c0138t0001 | 0/0 | 10532 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | copy fasta | chr2 | 237319018 | 237419164 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0002t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0004t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0014t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0014t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0014t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0014t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0037t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0037t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0040t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0040t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0059t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0068t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0074t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0076t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0079t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0084t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0086t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0087t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0095t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0117t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0130t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0001c0134t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0002g0315 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0009t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0022t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0022t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0022t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0092t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0106t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0108t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0109t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0002c0110t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0005t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0015t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0015t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0015t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0015t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0026t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0026t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0027t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0027t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0028t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0028t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0031t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0031t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0033t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0033t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0039t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0039t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0075t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0080t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0082t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0089t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0093t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0105t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0118t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0121t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0003c0122t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0006t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0016t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0016t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0016t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0016t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0071t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0072t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0102t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0113t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0119t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0120t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0004c0140t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0008t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0012t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0012t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0012t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0012t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0012t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0017t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0017t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0017t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0017t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0090t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0101t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0005c0111t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0007t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0064t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0006c0096t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0011t0001g0003 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0011t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0011t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0011t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0030t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0007c0030t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0010t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0010t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0010t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0010t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0010t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0008c0094t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0041t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0041t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0042t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0042t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0124t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0009c0126t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0010c0018t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0010c0018t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0010c0018t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0010c0018t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0011c0069t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0011c0070t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0011c0088t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0011c0091t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0012c0013t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0012c0013t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0012c0013t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0012c0013t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0013c0034t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0013c0034t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0013c0053t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0013c0097t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0014c0021t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0014c0021t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0014c0021t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0015c0036t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0015c0036t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0015c0085t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0016c0019t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0016c0019t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0016c0019t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0017c0024t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0017c0024t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0017c0058t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0018c0020t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0018c0020t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0018c0020t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0019c0044t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0019c0044t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0020c0127t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0020c0129t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0021c0029t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0021c0029t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0022c0078t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0022c0103t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0023c0032t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0024c0038t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0024c0038t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0025c0114t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0025c0115t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0026c0035t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0026c0035t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0027c0023t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0027c0023t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0028c0025t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0028c0025t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0029c0043t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0029c0043t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0030c0131t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0030c0132t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0031c0045t0010g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0032c0142t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0033c0141t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0034c0046t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0035c0047t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0036c0137t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0037c0051t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0038c0052t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0039c0128t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0040c0135t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0041c0136t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0042c0060t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0043c0061t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0044c0062t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0045c0067t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0046c0065t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0047c0066t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0048c0081t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0049c0104t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0050c0107t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0051c0083t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0052c0112t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0053c0073t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0054c0077t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0055c0116t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0056c0063t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0057c0099t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0058c0098t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0059c0055t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0060c0054t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0061c0100t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0062c0056t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0063c0057t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0064c0125t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0065c0123t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0066c0133t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0067c0050t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0068c0049t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0069c0048t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0070c0139t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
a0071c0138t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0203 | EUR | GBR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00140 | hp2 | a0007 | c0011 | t0001 | g0291 | EUR | GBR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00408 | hp1 | a0006 | c0096 | t0002 | g0155 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00408 | hp2 | a0016 | c0019 | t0001 | g0216 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00438 | hp1 | a0001 | c0004 | t0002 | g0229 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00438 | hp2 | a0007 | c0030 | t0001 | g0245 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00558 | hp1 | a0004 | c0003 | t0003 | g0225 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00558 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0254 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00609 | hp2 | a0045 | c0067 | t0002 | g0288 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0268 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00639 | hp2 | a0002 | c0009 | t0001 | g0079 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00642 | hp1 | a0001 | c0084 | t0001 | g0195 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00642 | hp2 | a0003 | c0005 | t0001 | g0019 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00673 | hp1 | a0004 | c0016 | t0001 | g0242 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00673 | hp2 | a0004 | c0003 | t0002 | g0234 | EAS | CHS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00738 | hp1 | a0008 | c0010 | t0001 | g0089 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00738 | hp2 | a0002 | c0009 | t0003 | g0069 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00741 | hp1 | a0008 | c0010 | t0001 | g0293 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG00741 | hp2 | a0002 | c0009 | t0002 | g0223 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01071 | hp1 | a0002 | c0001 | t0001 | g0255 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01074 | hp1 | a0008 | c0010 | t0001 | g0218 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01074 | hp2 | a0002 | c0009 | t0001 | g0097 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01081 | hp1 | a0005 | c0012 | t0004 | g0144 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01081 | hp2 | a0026 | c0035 | t0002 | g0164 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01099 | hp1 | a0052 | c0112 | t0002 | g0143 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01106 | hp1 | a0002 | c0001 | t0002 | g0314 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01106 | hp2 | a0001 | c0059 | t0004 | g0222 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01109 | hp1 | a0002 | c0009 | t0001 | g0224 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01109 | hp2 | a0001 | c0130 | t0002 | g0237 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01167 | hp1 | a0018 | c0020 | t0003 | g0058 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01167 | hp2 | a0023 | c0032 | t0001 | g0001 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01169 | hp1 | a0023 | c0032 | t0001 | g0001 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0286 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0308 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01175 | hp2 | a0002 | c0001 | t0002 | g0294 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01192 | hp1 | a0002 | c0108 | t0001 | g0310 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01243 | hp1 | a0003 | c0082 | t0002 | g0197 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01243 | hp2 | a0007 | c0011 | t0001 | g0292 | AMR | PUR | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01255 | hp1 | a0008 | c0094 | t0001 | g0271 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01255 | hp2 | a0005 | c0090 | t0003 | g0122 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01256 | hp1 | a0001 | c0079 | t0002 | g0062 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01256 | hp2 | a0002 | c0109 | t0002 | g0140 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01261 | hp2 | a0002 | c0001 | t0001 | g0258 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01346 | hp1 | a0003 | c0089 | t0001 | g0116 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01346 | hp2 | a0003 | c0015 | t0001 | g0272 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01358 | hp1 | a0003 | c0121 | t0003 | g0191 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01358 | hp2 | a0005 | c0017 | t0007 | g0034 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01433 | hp1 | a0007 | c0011 | t0001 | g0309 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01433 | hp2 | a0005 | c0017 | t0003 | g0280 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0298 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01496 | hp2 | a0009 | c0041 | t0002 | g0303 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01516 | hp1 | a0005 | c0017 | t0001 | g0131 | EUR | IBS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01516 | hp2 | a0030 | c0132 | t0002 | g0283 | EUR | IBS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0281 | EUR | IBS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01517 | hp2 | a0030 | c0131 | t0001 | g0284 | EUR | IBS | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01884 | hp1 | a0011 | c0088 | t0003 | g0173 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01884 | hp2 | a0060 | c0054 | t0004 | g0167 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01928 | hp1 | a0047 | c0066 | t0002 | g0270 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01928 | hp2 | a0004 | c0102 | t0003 | g0028 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01934 | hp2 | a0017 | c0058 | t0002 | g0057 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01943 | hp1 | a0008 | c0010 | t0001 | g0217 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01943 | hp2 | a0018 | c0020 | t0003 | g0054 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01978 | hp1 | a0003 | c0005 | t0001 | g0018 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01981 | hp1 | a0002 | c0092 | t0002 | g0257 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01981 | hp2 | a0017 | c0024 | t0001 | g0055 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0085 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01993 | hp2 | a0005 | c0017 | t0003 | g0046 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02027 | hp2 | a0054 | c0077 | t0001 | g0087 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02056 | hp1 | a0015 | c0036 | t0001 | g0071 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02056 | hp2 | a0005 | c0101 | t0003 | g0238 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0045 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02071 | hp2 | a0003 | c0015 | t0003 | g0209 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02074 | hp1 | a0001 | c0002 | t0003 | g0161 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02074 | hp2 | a0004 | c0006 | t0002 | g0041 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02083 | hp1 | a0006 | c0007 | t0001 | g0273 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02083 | hp2 | a0003 | c0005 | t0003 | g0156 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02129 | hp2 | a0027 | c0023 | t0001 | g0124 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02132 | hp1 | a0004 | c0006 | t0003 | g0090 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02132 | hp2 | a0067 | c0050 | t0001 | g0277 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02135 | hp1 | a0001 | c0076 | t0003 | g0219 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02135 | hp2 | a0051 | c0083 | t0001 | g0141 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02145 | hp1 | a0003 | c0031 | t0004 | g0194 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02145 | hp2 | a0065 | c0123 | t0003 | g0109 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02148 | hp1 | a0028 | c0025 | t0002 | g0053 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02148 | hp2 | a0046 | c0065 | t0002 | g0275 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02165 | hp1 | a0014 | c0021 | t0003 | g0264 | EAS | CDX | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02165 | hp2 | a0001 | c0117 | t0001 | g0127 | EAS | CDX | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02257 | hp1 | a0041 | c0136 | t0001 | g0165 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02257 | hp2 | a0003 | c0028 | t0004 | g0184 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02258 | hp1 | a0011 | c0069 | t0002 | g0187 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02258 | hp2 | a0001 | c0074 | t0001 | g0169 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02280 | hp1 | a0009 | c0042 | t0004 | g0170 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02280 | hp2 | a0003 | c0039 | t0001 | g0176 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02293 | hp1 | a0017 | c0024 | t0001 | g0063 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02293 | hp2 | a0043 | c0061 | t0001 | g0260 | AMR | PEL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02451 | hp1 | a0005 | c0111 | t0003 | g0118 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02451 | hp2 | a0007 | c0011 | t0001 | g0003 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02523 | hp2 | a0050 | c0107 | t0002 | g0072 | EAS | KHV | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02572 | hp1 | a0003 | c0031 | t0004 | g0196 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02572 | hp2 | a0003 | c0033 | t0001 | g0174 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02602 | hp1 | a0001 | c0037 | t0001 | g0025 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0136 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02622 | hp1 | a0003 | c0027 | t0003 | g0119 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02622 | hp2 | a0003 | c0028 | t0004 | g0183 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02630 | hp1 | a0019 | c0044 | t0002 | g0066 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02630 | hp2 | a0005 | c0012 | t0004 | g0117 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02647 | hp1 | a0013 | c0034 | t0005 | g0102 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02647 | hp2 | a0009 | c0126 | t0004 | g0179 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02698 | hp1 | a0002 | c0110 | t0001 | g0076 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02698 | hp2 | a0002 | c0001 | t0002 | g0289 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02717 | hp1 | a0070 | c0139 | t0005 | g0202 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02717 | hp2 | a0026 | c0035 | t0001 | g0189 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02723 | hp1 | a0005 | c0008 | t0005 | g0083 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02723 | hp2 | a0001 | c0014 | t0002 | g0129 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02735 | hp1 | a0027 | c0023 | t0001 | g0125 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02735 | hp2 | a0005 | c0012 | t0002 | g0300 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02738 | hp1 | a0002 | c0001 | t0002 | g0313 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02738 | hp2 | a0035 | c0047 | t0002 | g0123 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02809 | hp1 | a0013 | c0097 | t0002 | g0107 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02809 | hp2 | a0039 | c0128 | t0004 | g0010 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02818 | hp1 | a0053 | c0073 | t0008 | g0304 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02818 | hp2 | a0005 | c0008 | t0005 | g0100 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02886 | hp1 | a0025 | c0115 | t0004 | g0120 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02886 | hp2 | a0001 | c0014 | t0002 | g0114 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02895 | hp1 | a0005 | c0008 | t0005 | g0180 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02895 | hp2 | a0013 | c0053 | t0004 | g0093 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02896 | hp1 | a0010 | c0018 | t0003 | g0106 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02896 | hp2 | a0005 | c0008 | t0005 | g0098 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02897 | hp1 | a0005 | c0008 | t0005 | g0181 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02897 | hp2 | a0010 | c0018 | t0003 | g0105 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02922 | hp1 | a0069 | c0048 | t0001 | g0051 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02922 | hp2 | a0029 | c0043 | t0001 | g0104 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02976 | hp1 | a0003 | c0026 | t0001 | g0182 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02976 | hp2 | a0025 | c0114 | t0001 | g0121 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03017 | hp1 | a0031 | c0045 | t0010 | g0007 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03017 | hp2 | a0004 | c0003 | t0003 | g0068 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03041 | hp1 | a0010 | c0018 | t0003 | g0052 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03041 | hp2 | a0057 | c0099 | t0004 | g0152 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03098 | hp1 | a0071 | c0138 | t0001 | g0166 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03098 | hp2 | a0020 | c0129 | t0001 | g0137 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03130 | hp1 | a0001 | c0068 | t0002 | g0138 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03130 | hp2 | a0004 | c0071 | t0004 | g0178 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03139 | hp1 | a0003 | c0080 | t0005 | g0099 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03139 | hp2 | a0064 | c0125 | t0005 | g0171 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03195 | hp1 | a0029 | c0043 | t0001 | g0108 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03195 | hp2 | a0004 | c0072 | t0001 | g0185 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03209 | hp1 | a0001 | c0087 | t0002 | g0148 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03209 | hp2 | a0040 | c0135 | t0008 | g0188 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03225 | hp1 | a0005 | c0008 | t0004 | g0133 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03239 | hp1 | a0001 | c0004 | t0002 | g0296 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03239 | hp2 | a0024 | c0038 | t0002 | g0111 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03453 | hp1 | a0001 | c0002 | t0004 | g0008 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03453 | hp2 | a0059 | c0055 | t0004 | g0162 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03486 | hp1 | a0021 | c0029 | t0005 | g0168 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03486 | hp2 | a0061 | c0100 | t0002 | g0126 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03492 | hp1 | a0002 | c0001 | t0002 | g0312 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03492 | hp2 | a0004 | c0003 | t0003 | g0075 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03516 | hp1 | a0003 | c0075 | t0001 | g0192 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03516 | hp2 | a0020 | c0127 | t0004 | g0211 | AFR | ESN | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03540 | hp1 | a0009 | c0042 | t0012 | g0172 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03540 | hp2 | a0013 | c0034 | t0005 | g0103 | AFR | GWD | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03579 | hp1 | a0001 | c0040 | t0001 | g0239 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03579 | hp2 | a0001 | c0014 | t0002 | g0200 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03654 | hp1 | a0002 | c0001 | t0001 | g0319 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03654 | hp2 | a0002 | c0001 | t0002 | g0295 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03669 | hp1 | a0003 | c0005 | t0001 | g0317 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03669 | hp2 | a0004 | c0006 | t0001 | g0094 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03688 | hp1 | a0018 | c0020 | t0001 | g0307 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03688 | hp2 | a0003 | c0005 | t0007 | g0023 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03704 | hp1 | a0004 | c0016 | t0003 | g0135 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03704 | hp2 | a0004 | c0016 | t0003 | g0095 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0040 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0316 | SAS | PJL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03831 | hp1 | a0001 | c0037 | t0003 | g0022 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0198 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0290 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03942 | hp1 | a0005 | c0012 | t0003 | g0142 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0050 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04115 | hp1 | a0005 | c0012 | t0003 | g0132 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04115 | hp2 | a0002 | c0001 | t0002 | g0311 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04184 | hp1 | a0002 | c0009 | t0001 | g0070 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0318 | SAS | BEB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04199 | hp2 | a0001 | c0134 | t0001 | g0011 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0088 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04204 | hp2 | a0004 | c0003 | t0003 | g0065 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04228 | hp1 | a0024 | c0038 | t0002 | g0110 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG04228 | hp2 | a0002 | c0001 | t0001 | g0276 | SAS | STU | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18522 | hp1 | a0009 | c0041 | t0002 | g0236 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18522 | hp2 | a0044 | c0062 | t0005 | g0190 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18747 | hp1 | a0006 | c0007 | t0001 | g0210 | EAS | CHB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0033 | EAS | CHB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18906 | hp2 | a0055 | c0116 | t0002 | g0177 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18939 | hp1 | a0006 | c0007 | t0002 | g0263 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18939 | hp2 | a0066 | c0133 | t0001 | g0015 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18941 | hp1 | a0003 | c0122 | t0002 | g0078 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18941 | hp2 | a0004 | c0003 | t0002 | g0208 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18942 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18942 | hp2 | a0007 | c0030 | t0001 | g0048 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18945 | hp1 | a0016 | c0019 | t0002 | g0212 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18945 | hp2 | a0012 | c0013 | t0002 | g0016 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18947 | hp1 | a0032 | c0142 | t0002 | g0232 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18947 | hp2 | a0001 | c0095 | t0002 | g0265 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18952 | hp1 | a0004 | c0140 | t0002 | g0205 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18952 | hp2 | a0033 | c0141 | t0002 | g0026 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18959 | hp1 | a0001 | c0004 | t0001 | g0153 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18959 | hp2 | a0016 | c0019 | t0002 | g0302 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18960 | hp2 | a0001 | c0004 | t0002 | g0230 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18964 | hp2 | a0012 | c0013 | t0002 | g0017 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18970 | hp1 | a0001 | c0004 | t0002 | g0235 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18970 | hp2 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18971 | hp1 | a0014 | c0021 | t0002 | g0282 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18971 | hp2 | a0002 | c0022 | t0002 | g0128 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18975 | hp1 | a0006 | c0007 | t0002 | g0215 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18975 | hp2 | a0006 | c0007 | t0002 | g0214 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18979 | hp1 | a0006 | c0007 | t0002 | g0285 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18981 | hp1 | a0003 | c0005 | t0003 | g0060 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18981 | hp2 | a0012 | c0013 | t0002 | g0014 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18983 | hp1 | a0004 | c0003 | t0002 | g0002 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18983 | hp2 | a0068 | c0049 | t0002 | g0279 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18984 | hp1 | a0004 | c0003 | t0003 | g0207 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18984 | hp2 | a0006 | c0064 | t0003 | g0047 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18986 | hp2 | a0003 | c0005 | t0002 | g0077 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18989 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18989 | hp2 | a0003 | c0005 | t0002 | g0080 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18995 | hp1 | a0004 | c0119 | t0002 | g0074 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18995 | hp2 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18998 | hp1 | a0001 | c0086 | t0003 | g0306 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18998 | hp2 | a0012 | c0013 | t0002 | g0049 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19000 | hp2 | a0004 | c0006 | t0002 | g0305 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19002 | hp1 | a0022 | c0103 | t0001 | g0233 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19002 | hp2 | a0037 | c0051 | t0002 | g0145 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0262 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19003 | hp2 | a0002 | c0022 | t0001 | g0027 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19004 | hp1 | a0004 | c0003 | t0003 | g0091 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19004 | hp2 | a0003 | c0015 | t0003 | g0199 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19005 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19005 | hp2 | a0001 | c0002 | t0006 | g0005 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19007 | hp1 | a0004 | c0003 | t0002 | g0256 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19007 | hp2 | a0003 | c0015 | t0003 | g0084 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19011 | hp1 | a0015 | c0085 | t0001 | g0037 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19030 | hp1 | a0009 | c0124 | t0003 | g0113 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19030 | hp2 | a0003 | c0027 | t0001 | g0149 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19043 | hp1 | a0011 | c0091 | t0003 | g0064 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19043 | hp2 | a0001 | c0014 | t0001 | g0147 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19054 | hp1 | a0042 | c0060 | t0001 | g0035 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19054 | hp2 | a0028 | c0025 | t0002 | g0213 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19055 | hp1 | a0002 | c0001 | t0009 | g0004 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19057 | hp1 | a0022 | c0078 | t0001 | g0247 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19057 | hp2 | a0001 | c0004 | t0002 | g0220 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19058 | hp1 | a0002 | c0106 | t0002 | g0231 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19058 | hp2 | a0006 | c0007 | t0002 | g0274 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19063 | hp1 | a0004 | c0006 | t0002 | g0299 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19063 | hp2 | a0063 | c0057 | t0002 | g0056 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19064 | hp2 | a0004 | c0120 | t0002 | g0024 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19068 | hp1 | a0004 | c0006 | t0002 | g0038 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19068 | hp2 | a0014 | c0021 | t0002 | g0266 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19079 | hp1 | a0004 | c0003 | t0002 | g0002 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19079 | hp2 | a0034 | c0046 | t0002 | g0253 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19080 | hp1 | a0003 | c0033 | t0003 | g0029 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19080 | hp2 | a0004 | c0113 | t0002 | g0226 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19081 | hp1 | a0001 | c0004 | t0002 | g0227 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19081 | hp2 | a0038 | c0052 | t0003 | g0082 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19083 | hp1 | a0015 | c0036 | t0001 | g0154 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19083 | hp2 | a0004 | c0006 | t0003 | g0278 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19087 | hp1 | a0003 | c0118 | t0002 | g0061 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19087 | hp2 | a0001 | c0002 | t0006 | g0006 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19088 | hp1 | a0002 | c0022 | t0002 | g0021 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19088 | hp2 | a0003 | c0093 | t0001 | g0250 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19089 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19089 | hp2 | a0062 | c0056 | t0002 | g0206 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19090 | hp2 | a0004 | c0016 | t0003 | g0134 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19240 | hp1 | a0058 | c0098 | t0001 | g0101 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA19240 | hp2 | a0003 | c0026 | t0001 | g0186 | AFR | YRI | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA20129 | hp1 | a0008 | c0010 | t0002 | g0042 | AFR | ASW | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA20129 | hp2 | a0021 | c0029 | t0005 | g0009 | AFR | ASW | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA20905 | hp1 | a0001 | c0004 | t0002 | g0067 | SAS | GIH | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA20905 | hp2 | a0003 | c0005 | t0003 | g0059 | SAS | GIH | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0259 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG01123 | hp2 | a0049 | c0104 | t0002 | g0020 | AMR | CLM | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02109 | hp1 | a0019 | c0044 | t0004 | g0221 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02109 | hp2 | a0011 | c0070 | t0011 | g0139 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02486 | hp1 | a0001 | c0040 | t0001 | g0130 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02486 | hp2 | a0003 | c0105 | t0001 | g0073 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02559 | hp1 | a0036 | c0137 | t0003 | g0081 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG02559 | hp2 | a0005 | c0008 | t0001 | g0086 | AFR | ACB | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03471 | hp1 | a0010 | c0018 | t0004 | g0112 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0151 | AFR | MSL | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG06807 | hp1 | a0003 | c0039 | t0003 | g0163 | AFR | USA | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
HG06807 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | USA | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18955 | hp1 | a0056 | c0063 | t0001 | g0044 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA18955 | hp2 | a0004 | c0006 | t0003 | g0013 | EAS | JPT | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA21309 | hp1 | a0048 | c0081 | t0002 | g0096 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | LWK | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
homoSapiens_chm13v2 | hp1 | a0007 | c0011 | t0001 | g0003 | REF | REF | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0002 | g0315 | REF | REF | COL6A3_chr2_237319018_237419164 | COL6A3 | chr2 | 237319018 | 237419164 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237334646 | T | C | 1 | a0051 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.9209A>G | p.Tyr3070Cys | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9451/10532 | 9209/9534 | 3070/3177 | chr2 | 237334646 | ||
chr2:237334649 | G | A | 27 | a0001a0006a0010others(24): Show | 112 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
missense_variant | MODERATE | c.9206C>T | p.Thr3069Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9448/10532 | 9206/9534 | 3069/3177 | chr2 | 237334649 | ||
chr2:237334707 | C | T | 2 | a0022a0038 | 3 | NA19002.hp1 NA19057.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.9148G>A | p.Ala3050Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9390/10532 | 9148/9534 | 3050/3177 | chr2 | 237334707 | ||
chr2:237334739 | G | A | 1 | a0034 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.9116C>T | p.Thr3039Met | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9358/10532 | 9116/9534 | 3039/3177 | chr2 | 237334739 | ||
chr2:237334821 | C | G | 62 | a0001a0003a0004others(59): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
missense_variant | MODERATE | c.9034G>C | p.Ala3012Pro | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9276/10532 | 9034/9534 | 3012/3177 | chr2 | 237334821 | ||
chr2:237334824 | T | C | 1 | a0050 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.9031A>G | p.Arg3011Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9273/10532 | 9031/9534 | 3011/3177 | chr2 | 237334824 | ||
chr2:237334838 | T | C | 1 | a0015 | 3 | HG02056.hp1 NA19011.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.9017A>G | p.Lys3006Arg | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9259/10532 | 9017/9534 | 3006/3177 | chr2 | 237334838 | ||
chr2:237334877 | C | T | 1 | a0046 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.8978G>A | p.Arg2993His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9220/10532 | 8978/9534 | 2993/3177 | chr2 | 237334877 | ||
chr2:237336138 | T | C | 4 | a0007a0052a0063others(1): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
missense_variant | MODERATE | c.8962A>G | p.Met2988Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9204/10532 | 8962/9534 | 2988/3177 | chr2 | 237336138 | ||
chr2:237336220 | TGCA | T | 3 | a0007a0063a0068 | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
disruptive_inframe_deletion | MODERATE | c.8877_8879delTGC | p.Ala2960del | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9121/10532 | 8877/9534 | 2959/3177 | chr2 | 237336220 | ||
chr2:237336278 | G | A | 2 | a0011a0071 | 5 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
missense_variant | MODERATE | c.8822C>T | p.Ala2941Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9064/10532 | 8822/9534 | 2941/3177 | chr2 | 237336278 | ||
chr2:237336320 | A | G | 50 | a0001a0003a0005others(47): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
missense_variant | MODERATE | c.8780T>C | p.Met2927Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9022/10532 | 8780/9534 | 2927/3177 | chr2 | 237336320 | ||
chr2:237336365 | G | A | 3 | a0014a0016a0056 | 7 | HG00408.hp2 HG02165.hp1 NA18945.hp1 others(4): Show |
missense_variant | MODERATE | c.8735C>T | p.Pro2912Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 8977/10532 | 8735/9534 | 2912/3177 | chr2 | 237336365 | ||
chr2:237336528 | C | T | 1 | a0052 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.8572G>A | p.Val2858Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 8814/10532 | 8572/9534 | 2858/3177 | chr2 | 237336528 | ||
chr2:237339091 | C | G | 1 | a0008 | 6 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(3): Show |
missense_variant | MODERATE | c.8491G>C | p.Asp2831His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/44 | 8733/10532 | 8491/9534 | 2831/3177 | chr2 | 237339091 | ||
chr2:237340458 | C | T | 1 | a0057 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.8458G>A | p.Val2820Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8700/10532 | 8458/9534 | 2820/3177 | chr2 | 237340458 | ||
chr2:237340988 | G | A | 1 | a0052 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.7928C>T | p.Ala2643Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8170/10532 | 7928/9534 | 2643/3177 | chr2 | 237340988 | ||
chr2:237341067 | C | T | 2 | a0053a0060 | 2 | HG01884.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.7849G>A | p.Asp2617Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8091/10532 | 7849/9534 | 2617/3177 | chr2 | 237341067 | ||
chr2:237342145 | A | G | 1 | a0064 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.7685T>C | p.Val2562Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/44 | 7927/10532 | 7685/9534 | 2562/3177 | chr2 | 237342145 | ||
chr2:237344373 | G | A | 3 | a0023a0046a0047 | 4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
missense_variant | MODERATE | c.7645C>T | p.Arg2549Trp | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7887/10532 | 7645/9534 | 2549/3177 | chr2 | 237344373 | ||
chr2:237344618 | G | A | 1 | a0036 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.7400C>T | p.Ser2467Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7642/10532 | 7400/9534 | 2467/3177 | chr2 | 237344618 | ||
chr2:237347829 | G | A | 1 | a0049 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.7007C>T | p.Pro2336Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/44 | 7249/10532 | 7007/9534 | 2336/3177 | chr2 | 237347829 | ||
chr2:237353378 | G | A | 9 | a0005a0013a0021others(6): Show | 32 | HG01081.hp1 HG01255.hp2 HG01358.hp2 others(29): Show |
missense_variant | MODERATE | c.6653C>T | p.Pro2218Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/44 | 6895/10532 | 6653/9534 | 2218/3177 | chr2 | 237353378 | ||
chr2:237363263 | G | A | 1 | a0024 | 2 | HG03239.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.6053C>T | p.Ala2018Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/44 | 6295/10532 | 6053/9534 | 2018/3177 | chr2 | 237363263 | ||
chr2:237363341 | A | G | 1 | a0054 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.5975T>C | p.Met1992Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/44 | 6217/10532 | 5975/9534 | 1992/3177 | chr2 | 237363341 | ||
chr2:237363392 | C | T | 1 | a0040 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.5924G>A | p.Arg1975His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/44 | 6166/10532 | 5924/9534 | 1975/3177 | chr2 | 237363392 | ||
chr2:237367128 | G | A | 2 | a0025a0055 | 3 | HG02886.hp1 HG02976.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.5059C>T | p.Pro1687Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/44 | 5301/10532 | 5059/9534 | 1687/3177 | chr2 | 237367128 | ||
chr2:237368568 | C | T | 5 | a0016a0027a0062others(2): Show | 8 | HG00408.hp2 HG02129.hp2 HG02735.hp1 others(5): Show |
missense_variant | MODERATE | c.4895G>A | p.Arg1632Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 5137/10532 | 4895/9534 | 1632/3177 | chr2 | 237368568 | ||
chr2:237368575 | G | A | 1 | a0061 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.4888C>T | p.Pro1630Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 5130/10532 | 4888/9534 | 1630/3177 | chr2 | 237368575 | ||
chr2:237368628 | G | A | 1 | a0031 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4835C>T | p.Ser1612Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 5077/10532 | 4835/9534 | 1612/3177 | chr2 | 237368628 | ||
chr2:237371800 | G | A | 1 | a0044 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.4217C>T | p.Thr1406Met | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4459/10532 | 4217/9534 | 1406/3177 | chr2 | 237371800 | ||
chr2:237371833 | C | T | 4 | a0006a0045a0046others(1): Show | 12 | HG00408.hp1 HG00609.hp2 HG01928.hp1 others(9): Show |
missense_variant | MODERATE | c.4184G>A | p.Arg1395Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4426/10532 | 4184/9534 | 1395/3177 | chr2 | 237371833 | ||
chr2:237371834 | G | A | 1 | a0029 | 2 | HG02922.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.4183C>T | p.Arg1395Trp | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4425/10532 | 4183/9534 | 1395/3177 | chr2 | 237371834 | ||
chr2:237372138 | A | C | 3 | a0012a0056a0066 | 6 | NA18939.hp2 NA18945.hp2 NA18955.hp1 others(3): Show |
missense_variant | MODERATE | c.3879T>G | p.Asp1293Glu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4121/10532 | 3879/9534 | 1293/3177 | chr2 | 237372138 | ||
chr2:237374645 | C | T | 1 | a0044 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3446G>A | p.Arg1149Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3688/10532 | 3446/9534 | 1149/3177 | chr2 | 237374645 | ||
chr2:237374829 | T | G | 20 | a0010a0013a0016others(17): Show | 35 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
missense_variant | MODERATE | c.3262A>C | p.Lys1088Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3504/10532 | 3262/9534 | 1088/3177 | chr2 | 237374829 | ||
chr2:237374900 | C | T | 1 | a0043 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.3191G>A | p.Arg1064Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3433/10532 | 3191/9534 | 1064/3177 | chr2 | 237374900 | ||
chr2:237376940 | C | T | 1 | a0042 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.2902G>A | p.Val968Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/44 | 3144/10532 | 2902/9534 | 968/3177 | chr2 | 237376940 | ||
chr2:237378645 | C | A | 7 | a0016a0017a0018others(4): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
missense_variant | MODERATE | c.2488G>T | p.Ala830Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/44 | 2730/10532 | 2488/9534 | 830/3177 | chr2 | 237378645 | ||
chr2:237378714 | C | T | 7 | a0016a0017a0018others(4): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
missense_variant | MODERATE | c.2419G>A | p.Ala807Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/44 | 2661/10532 | 2419/9534 | 807/3177 | chr2 | 237378714 | ||
chr2:237379157 | C | T | 4 | a0010a0040a0041others(1): Show | 7 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.1976G>A | p.Arg659His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/44 | 2218/10532 | 1976/9534 | 659/3177 | chr2 | 237379157 | ||
chr2:237381026 | C | A | 5 | a0009a0029a0036others(2): Show | 11 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
missense_variant | MODERATE | c.1786G>T | p.Ala596Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 2028/10532 | 1786/9534 | 596/3177 | chr2 | 237381026 | ||
chr2:237381199 | G | A | 3 | a0019a0020a0039 | 5 | HG02109.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.1613C>T | p.Thr538Met | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 1855/10532 | 1613/9534 | 538/3177 | chr2 | 237381199 | ||
chr2:237381334 | A | G | 1 | a0038 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.1478T>C | p.Val493Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 1720/10532 | 1478/9534 | 493/3177 | chr2 | 237381334 | ||
chr2:237387626 | G | A | 1 | a0030 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.1268C>T | p.Ala423Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1510/10532 | 1268/9534 | 423/3177 | chr2 | 237387626 | ||
chr2:237387630 | C | T | 1 | a0037 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1264G>A | p.Val422Met | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1506/10532 | 1264/9534 | 422/3177 | chr2 | 237387630 | ||
chr2:237387687 | G | A | 1 | a0066 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.1207C>T | p.Pro403Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1449/10532 | 1207/9534 | 403/3177 | chr2 | 237387687 | ||
chr2:237387936 | C | T | 1 | a0067 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.958G>A | p.Ala320Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1200/10532 | 958/9534 | 320/3177 | chr2 | 237387936 | ||
chr2:237388032 | C | T | 1 | a0068 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.862G>A | p.Asp288Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1104/10532 | 862/9534 | 288/3177 | chr2 | 237388032 | ||
chr2:237388055 | C | A | 1 | a0036 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.839G>T | p.Arg280Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1081/10532 | 839/9534 | 280/3177 | chr2 | 237388055 | ||
chr2:237388119 | C | T | 1 | a0069 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.775G>A | p.Ala259Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1017/10532 | 775/9534 | 259/3177 | chr2 | 237388119 | ||
chr2:237388164 | T | C | 2 | a0070a0071 | 2 | HG02717.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.730A>G | p.Ile244Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 972/10532 | 730/9534 | 244/3177 | chr2 | 237388164 | ||
chr2:237394589 | G | T | 1 | a0035 | 1 | HG02738.hp2 | missense_variant&splice_region_variant | MODERATE | c.707C>A | p.Thr236Lys | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/44 | 949/10532 | 707/9534 | 236/3177 | chr2 | 237394589 | ||
chr2:237394924 | G | T | 1 | a0034 | 1 | NA19079.hp2 | stop_gained | HIGH | c.372C>A | p.Tyr124* | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/44 | 614/10532 | 372/9534 | 124/3177 | chr2 | 237394924 | ||
chr2:237395004 | T | A | 2 | a0032a0033 | 2 | NA18947.hp1 NA18952.hp2 |
missense_variant | MODERATE | c.292A>T | p.Thr98Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/44 | 534/10532 | 292/9534 | 98/3177 | chr2 | 237395004 | ||
chr2:237396784 | C | T | 1 | a0031 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.34G>A | p.Val12Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/44 | 276/10532 | 34/9534 | 12/3177 | chr2 | 237396784 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237325642 | A | G | 2 | a0001c0134a0030c0131 | 2 | HG01517.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.9411T>C | p.Cys3137Cys | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/44 | 9653/10532 | 9411/9534 | 3137/3177 | chr2 | 237325642 | ||
chr2:237334642 | G | A | 14 | a0003c0005a0003c0015a0003c0027others(11): Show | 30 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(27): Show |
synonymous_variant | LOW | c.9213C>T | p.His3071His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9455/10532 | 9213/9534 | 3071/3177 | chr2 | 237334642 | ||
chr2:237334708 | G | A | 1 | a0001c0084 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.9147C>T | p.Leu3049Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9389/10532 | 9147/9534 | 3049/3177 | chr2 | 237334708 | ||
chr2:237334726 | G | A | 17 | a0003c0031a0003c0039a0003c0121others(14): Show | 30 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(27): Show |
synonymous_variant | LOW | c.9129C>T | p.Arg3043Arg | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9371/10532 | 9129/9534 | 3043/3177 | chr2 | 237334726 | ||
chr2:237334732 | C | T | 1 | a0002c0109 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.9123G>A | p.Thr3041Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9365/10532 | 9123/9534 | 3041/3177 | chr2 | 237334732 | ||
chr2:237334786 | G | A | 3 | a0003c0028a0003c0080a0025c0115 | 4 | HG02257.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.9069C>T | p.Thr3023Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/44 | 9311/10532 | 9069/9534 | 3023/3177 | chr2 | 237334786 | ||
chr2:237336280 | C | T | 4 | a0007c0011a0007c0030a0063c0057others(1): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.8820G>A | p.Thr2940Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9062/10532 | 8820/9534 | 2940/3177 | chr2 | 237336280 | ||
chr2:237336295 | C | T | 1 | a0002c0108 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.8805G>A | p.Ala2935Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 9047/10532 | 8805/9534 | 2935/3177 | chr2 | 237336295 | ||
chr2:237336355 | C | T | 1 | a0052c0112 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.8745G>A | p.Ala2915Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/44 | 8987/10532 | 8745/9534 | 2915/3177 | chr2 | 237336355 | ||
chr2:237340465 | T | C | 4 | a0007c0011a0007c0030a0063c0057others(1): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.8451A>G | p.Pro2817Pro | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8693/10532 | 8451/9534 | 2817/3177 | chr2 | 237340465 | ||
chr2:237340531 | G | A | 1 | a0001c0086 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.8385C>T | p.Phe2795Phe | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8627/10532 | 8385/9534 | 2795/3177 | chr2 | 237340531 | ||
chr2:237340570 | C | T | 1 | a0025c0114 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.8346G>A | p.Glu2782Glu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8588/10532 | 8346/9534 | 2782/3177 | chr2 | 237340570 | ||
chr2:237340771 | T | C | 6 | a0011c0069a0011c0070a0011c0088others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
synonymous_variant | LOW | c.8145A>G | p.Leu2715Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8387/10532 | 8145/9534 | 2715/3177 | chr2 | 237340771 | ||
chr2:237340906 | C | T | 2 | a0011c0069a0011c0091 | 2 | HG02258.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.8010G>A | p.Ala2670Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8252/10532 | 8010/9534 | 2670/3177 | chr2 | 237340906 | ||
chr2:237340909 | G | A | 1 | a0002c0110 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.8007C>T | p.His2669His | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8249/10532 | 8007/9534 | 2669/3177 | chr2 | 237340909 | ||
chr2:237340921 | T | G | 6 | a0011c0069a0011c0070a0011c0088others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
synonymous_variant | LOW | c.7995A>C | p.Ala2665Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8237/10532 | 7995/9534 | 2665/3177 | chr2 | 237340921 | ||
chr2:237340987 | C | T | 46 | a0001c0002a0001c0004a0001c0037others(43): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
synonymous_variant | LOW | c.7929G>A | p.Ala2643Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8171/10532 | 7929/9534 | 2643/3177 | chr2 | 237340987 | ||
chr2:237341074 | G | A | 4 | a0007c0011a0007c0030a0063c0057others(1): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.7842C>T | p.Ser2614Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8084/10532 | 7842/9534 | 2614/3177 | chr2 | 237341074 | ||
chr2:237341137 | G | A | 1 | a0005c0090 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.7779C>T | p.Ile2593Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/44 | 8021/10532 | 7779/9534 | 2593/3177 | chr2 | 237341137 | ||
chr2:237342128 | G | A | 1 | a0005c0101 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.7702C>T | p.Leu2568Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/44 | 7944/10532 | 7702/9534 | 2568/3177 | chr2 | 237342128 | ||
chr2:237344422 | C | T | 22 | a0004c0003a0004c0006a0004c0016others(19): Show | 50 | HG00558.hp1 HG00673.hp1 HG00673.hp2 others(47): Show |
synonymous_variant | LOW | c.7596G>A | p.Lys2532Lys | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7838/10532 | 7596/9534 | 2532/3177 | chr2 | 237344422 | ||
chr2:237344506 | G | A | 15 | a0003c0005a0003c0015a0003c0027others(12): Show | 32 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(29): Show |
synonymous_variant | LOW | c.7512C>T | p.Asn2504Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7754/10532 | 7512/9534 | 2504/3177 | chr2 | 237344506 | ||
chr2:237344509 | C | T | 3 | a0007c0030a0063c0057a0068c0049 | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
synonymous_variant | LOW | c.7509G>A | p.Arg2503Arg | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7751/10532 | 7509/9534 | 2503/3177 | chr2 | 237344509 | ||
chr2:237344659 | C | T | 1 | a0001c0076 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.7359G>A | p.Glu2453Glu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7601/10532 | 7359/9534 | 2453/3177 | chr2 | 237344659 | ||
chr2:237344689 | G | A | 16 | a0003c0031a0003c0039a0003c0121others(13): Show | 29 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(26): Show |
synonymous_variant | LOW | c.7329C>T | p.Ala2443Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/44 | 7571/10532 | 7329/9534 | 2443/3177 | chr2 | 237344689 | ||
chr2:237346509 | T | G | 6 | a0011c0069a0011c0070a0011c0088others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
synonymous_variant | LOW | c.7086A>C | p.Gly2362Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/44 | 7328/10532 | 7086/9534 | 2362/3177 | chr2 | 237346509 | ||
chr2:237347855 | T | C | 6 | a0011c0069a0011c0070a0011c0088others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
synonymous_variant | LOW | c.6981A>G | p.Glu2327Glu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/44 | 7223/10532 | 6981/9534 | 2327/3177 | chr2 | 237347855 | ||
chr2:237347864 | G | A | 2 | a0011c0070a0071c0138 | 2 | HG02109.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.6972C>T | p.Asn2324Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/44 | 7214/10532 | 6972/9534 | 2324/3177 | chr2 | 237347864 | ||
chr2:237348370 | G | A | 14 | a0003c0005a0003c0015a0003c0027others(11): Show | 31 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(28): Show |
synonymous_variant | LOW | c.6945C>T | p.Phe2315Phe | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/44 | 7187/10532 | 6945/9534 | 2315/3177 | chr2 | 237348370 | ||
chr2:237350171 | C | G | 82 | a0001c0002a0001c0004a0001c0014others(79): Show | 180 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
synonymous_variant | LOW | c.6855G>C | p.Gly2285Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/44 | 7097/10532 | 6855/9534 | 2285/3177 | chr2 | 237350171 | ||
chr2:237350201 | G | A | 1 | a0050c0107 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.6825C>T | p.Pro2275Pro | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/44 | 7067/10532 | 6825/9534 | 2275/3177 | chr2 | 237350201 | ||
chr2:237359074 | C | T | 60 | a0001c0004a0001c0014a0001c0040others(57): Show | 118 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
synonymous_variant | LOW | c.6369G>A | p.Leu2123Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 20/44 | 6611/10532 | 6369/9534 | 2123/3177 | chr2 | 237359074 | ||
chr2:237360133 | G | A | 1 | a0052c0112 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.6237C>T | p.Asn2079Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/44 | 6479/10532 | 6237/9534 | 2079/3177 | chr2 | 237360133 | ||
chr2:237365716 | G | A | 1 | a0004c0072 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.5820C>T | p.Ser1940Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/44 | 6062/10532 | 5820/9534 | 1940/3177 | chr2 | 237365716 | ||
chr2:237365824 | G | A | 1 | a0004c0113 | 1 | NA19080.hp2 | synonymous_variant | LOW | c.5712C>T | p.Asp1904Asp | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/44 | 5954/10532 | 5712/9534 | 1904/3177 | chr2 | 237365824 | ||
chr2:237366874 | G | C | 1 | a0011c0091 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.5313C>G | p.Val1771Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/44 | 5555/10532 | 5313/9534 | 1771/3177 | chr2 | 237366874 | ||
chr2:237367087 | C | T | 7 | a0001c0074a0003c0075a0009c0042others(4): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.5100G>A | p.Arg1700Arg | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/44 | 5342/10532 | 5100/9534 | 1700/3177 | chr2 | 237367087 | ||
chr2:237368780 | C | T | 1 | a0059c0055 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.4683G>A | p.Gln1561Gln | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 4925/10532 | 4683/9534 | 1561/3177 | chr2 | 237368780 | ||
chr2:237368930 | C | A | 46 | a0001c0004a0001c0037a0001c0040others(43): Show | 88 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
synonymous_variant | LOW | c.4533G>T | p.Gly1511Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 4775/10532 | 4533/9534 | 1511/3177 | chr2 | 237368930 | ||
chr2:237369152 | A | G | 80 | a0001c0004a0001c0037a0001c0040others(77): Show | 135 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(132): Show |
synonymous_variant | LOW | c.4311T>C | p.Ile1437Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/44 | 4553/10532 | 4311/9534 | 1437/3177 | chr2 | 237369152 | ||
chr2:237371970 | G | A | 2 | a0002c0092a0004c0119 | 2 | HG01981.hp1 NA18995.hp1 |
synonymous_variant | LOW | c.4047C>T | p.Asp1349Asp | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4289/10532 | 4047/9534 | 1349/3177 | chr2 | 237371970 | ||
chr2:237372012 | G | A | 2 | a0003c0039a0004c0120 | 3 | HG02280.hp2 HG06807.hp1 NA19064.hp2 |
synonymous_variant | LOW | c.4005C>T | p.Gly1335Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4247/10532 | 4005/9534 | 1335/3177 | chr2 | 237372012 | ||
chr2:237372186 | G | A | 1 | a0003c0093 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.3831C>T | p.Ser1277Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 4073/10532 | 3831/9534 | 1277/3177 | chr2 | 237372186 | ||
chr2:237372303 | G | A | 1 | a0008c0094 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.3714C>T | p.Ile1238Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/44 | 3956/10532 | 3714/9534 | 1238/3177 | chr2 | 237372303 | ||
chr2:237374671 | C | T | 1 | a0003c0039 | 2 | HG02280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.3420G>A | p.Thr1140Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3662/10532 | 3420/9534 | 1140/3177 | chr2 | 237374671 | ||
chr2:237374761 | G | A | 1 | a0001c0095 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.3330C>T | p.Ala1110Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3572/10532 | 3330/9534 | 1110/3177 | chr2 | 237374761 | ||
chr2:237374818 | G | A | 1 | a0006c0096 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.3273C>T | p.Val1091Val | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3515/10532 | 3273/9534 | 1091/3177 | chr2 | 237374818 | ||
chr2:237374962 | G | A | 39 | a0001c0004a0001c0037a0001c0059others(36): Show | 76 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
synonymous_variant | LOW | c.3129C>T | p.Gly1043Gly | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/44 | 3371/10532 | 3129/9534 | 1043/3177 | chr2 | 237374962 | ||
chr2:237376779 | T | C | 1 | a0003c0121 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.3063A>G | p.Pro1021Pro | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/44 | 3305/10532 | 3063/9534 | 1021/3177 | chr2 | 237376779 | ||
chr2:237376788 | G | A | 1 | a0003c0039 | 2 | HG02280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.3054C>T | p.Asn1018Asn | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/44 | 3296/10532 | 3054/9534 | 1018/3177 | chr2 | 237376788 | ||
chr2:237377034 | G | A | 1 | a0003c0122 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.2808C>T | p.Ile936Ile | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/44 | 3050/10532 | 2808/9534 | 936/3177 | chr2 | 237377034 | ||
chr2:237378670 | A | G | 1 | a0001c0059 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.2463T>C | p.Ser821Ser | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/44 | 2705/10532 | 2463/9534 | 821/3177 | chr2 | 237378670 | ||
chr2:237379219 | C | T | 7 | a0010c0018a0013c0053a0040c0135others(4): Show | 10 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(7): Show |
synonymous_variant | LOW | c.1914G>A | p.Arg638Arg | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/44 | 2156/10532 | 1914/9534 | 638/3177 | chr2 | 237379219 | ||
chr2:237381021 | G | A | 1 | a0001c0040 | 2 | HG02486.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.1791C>T | p.Phe597Phe | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 2033/10532 | 1791/9534 | 597/3177 | chr2 | 237381021 | ||
chr2:237381174 | G | A | 2 | a0070c0139a0071c0138 | 2 | HG02717.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.1638C>T | p.Ala546Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 1880/10532 | 1638/9534 | 546/3177 | chr2 | 237381174 | ||
chr2:237381423 | G | A | 1 | a0001c0130 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1389C>T | p.Ala463Ala | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/44 | 1631/10532 | 1389/9534 | 463/3177 | chr2 | 237381423 | ||
chr2:237387712 | G | A | 1 | a0001c0134 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1182C>T | p.Thr394Thr | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1424/10532 | 1182/9534 | 394/3177 | chr2 | 237387712 | ||
chr2:237388012 | G | A | 4 | a0010c0018a0040c0135a0041c0136others(1): Show | 7 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.882C>T | p.Phe294Phe | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/44 | 1124/10532 | 882/9534 | 294/3177 | chr2 | 237388012 | ||
chr2:237394818 | G | A | 1 | a0004c0140 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.478C>T | p.Leu160Leu | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/44 | 720/10532 | 478/9534 | 160/3177 | chr2 | 237394818 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237324107 | C | CA | 9 | a0003c0080t0005a0005c0008t0005a0013c0034t0005others(6): Show | 15 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*666dupT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 666 | chr2 | 237324107 | |||||
chr2:237324109 | C | A | 119 | a0001c0002t0001a0001c0002t0003a0001c0002t0004others(116): Show | 209 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*665G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 665 | chr2 | 237324109 | |||||
chr2:237324111 | A | C | 1 | a0011c0070t0011 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 663 | chr2 | 237324111 | |||||
chr2:237324168 | T | A | 33 | a0001c0002t0003a0001c0037t0003a0001c0076t0003others(30): Show | 57 | HG00558.hp1 HG00738.hp2 HG01167.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*606A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 606 | chr2 | 237324168 | |||||
chr2:237324723 | G | A | 2 | a0040c0135t0008a0053c0073t0008 | 2 | HG02818.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*51C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 51 | chr2 | 237324723 | |||||
chr2:237324767 | C | G | 54 | a0001c0002t0003a0001c0002t0004a0001c0037t0003others(51): Show | 81 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 44/44 | 7 | chr2 | 237324767 | |||||
chr2:237396820 | T | G | 1 | a0009c0042t0012 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/44 | 3 | chr2 | 237396820 | |||||
chr2:237414037 | C | T | 1 | a0031c0045t0010 | 1 | HG03017.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/44 | 17220 | chr2 | 237414037 | |||||
chr2:237414086 | A | C | 2 | a0001c0002t0006a0002c0001t0009 | 3 | NA19005.hp2 NA19055.hp1 NA19087.hp2 |
5_prime_UTR_variant | MODIFIER | c.-164T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/44 | 17269 | chr2 | 237414086 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237324840 | G | A | 78 | a0001c0002t0002g0012a0001c0002t0002g0039a0001c0002t0002g0043others(75): Show | 78 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.9494-26C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/43 | chr2 | 237324840 | ||||||
chr2:237324873 | A | G | 2 | a0005c0012t0004g0117a0010c0018t0004g0112 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.9494-59T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/43 | chr2 | 237324873 | ||||||
chr2:237324988 | C | T | 1 | a0011c0069t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9494-174G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/43 | chr2 | 237324988 | ||||||
chr2:237325022 | T | A | 14 | a0002c0001t0001g0316a0004c0006t0001g0094a0004c0016t0001g0242others(11): Show | 15 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.9494-208A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/43 | chr2 | 237325022 | ||||||
chr2:237325290 | A | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9493+270T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 43/43 | chr2 | 237325290 | ||||||
chr2:237325776 | G | A | 2 | a0002c0001t0001g0246a0003c0093t0001g0250 | 2 | NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.9329-52C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237325776 | ||||||
chr2:237326244 | A | AGT | 18 | a0001c0002t0001g0088a0001c0002t0001g0268a0001c0040t0001g0130others(15): Show | 18 | HG00558.hp2 HG00639.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.9329-522_9329-521d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | A | AGTGT | 26 | a0001c0002t0002g0012a0001c0004t0002g0229a0001c0004t0002g0230others(23): Show | 27 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.9329-524_9329-521d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | A | AGTGTGT | 49 | a0001c0002t0002g0039a0001c0002t0002g0204a0001c0002t0002g0318others(46): Show | 49 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.9329-526_9329-521d others(8): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | A | AGTGTGTG others(1): Show |
12 | a0001c0002t0002g0043a0001c0002t0002g0201a0001c0002t0002g0203others(9): Show | 12 | HG00140.hp1 HG01099.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.9329-528_9329-521d others(10): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | A | AGTGTGTG others(3): Show |
5 | a0001c0002t0002g0297a0001c0004t0002g0235a0003c0082t0002g0197others(2): Show | 5 | HG01243.hp1 HG02523.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.9329-530_9329-521d others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | A | AGTGTGTG others(5): Show |
1 | a0028c0025t0002g0213 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9329-532_9329-521d others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | AGT | A | 75 | a0001c0002t0003g0040a0001c0002t0003g0157a0001c0002t0003g0158others(72): Show | 75 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.9329-522_9329-521d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326244 | AGTGTGTG others(5): Show |
A | 15 | a0001c0037t0001g0025a0001c0134t0001g0011a0003c0005t0001g0018others(12): Show | 15 | HG00642.hp2 HG01346.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.9329-532_9329-521d others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326244 | ||||||
chr2:237326271 | G | A | 2 | a0003c0026t0001g0186a0069c0048t0001g0051 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.9329-547C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326271 | ||||||
chr2:237326410 | C | G | 26 | a0001c0002t0003g0157a0001c0002t0003g0158a0001c0002t0003g0159others(23): Show | 26 | HG00558.hp1 HG01167.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.9329-686G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326410 | ||||||
chr2:237326439 | C | A | 131 | a0001c0002t0001g0115a0001c0002t0003g0040a0001c0002t0003g0151others(128): Show | 132 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.9329-715G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326439 | ||||||
chr2:237326530 | G | A | 1 | a0001c0004t0002g0229 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9329-806C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326530 | ||||||
chr2:237326590 | A | T | 4 | a0002c0001t0001g0249a0002c0001t0001g0254a0002c0001t0001g0262others(1): Show | 4 | HG00408.hp2 HG00609.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.9329-866T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326590 | ||||||
chr2:237326668 | T | C | 1 | a0001c0076t0003g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.9329-944A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237326668 | ||||||
chr2:237327026 | C | A | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.9329-1302G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327026 | ||||||
chr2:237327027 | G | A | 1 | a0001c0037t0001g0025 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9329-1303C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327027 | ||||||
chr2:237327231 | C | T | 1 | a0049c0104t0002g0020 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.9329-1507G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327231 | ||||||
chr2:237327456 | T | C | 8 | a0001c0002t0003g0151a0003c0039t0003g0163a0010c0018t0003g0052others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.9329-1732A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327456 | ||||||
chr2:237327560 | C | T | 1 | a0040c0135t0008g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.9329-1836G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327560 | ||||||
chr2:237327592 | A | G | 56 | a0001c0059t0004g0222a0003c0005t0002g0077a0003c0005t0002g0080others(53): Show | 56 | HG01081.hp1 HG01106.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.9329-1868T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327592 | ||||||
chr2:237327610 | A | C | 51 | a0001c0059t0004g0222a0003c0005t0002g0077a0003c0005t0002g0080others(48): Show | 51 | HG01081.hp1 HG01106.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.9329-1886T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327610 | ||||||
chr2:237327616 | T | C | 48 | a0001c0059t0004g0222a0003c0005t0002g0077a0003c0005t0002g0080others(45): Show | 48 | HG01081.hp1 HG01106.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.9329-1892A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327616 | ||||||
chr2:237327620 | G | A | 51 | a0001c0059t0004g0222a0003c0005t0002g0077a0003c0005t0002g0080others(48): Show | 51 | HG01081.hp1 HG01106.hp2 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.9329-1896C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327620 | ||||||
chr2:237327657 | G | A | 48 | a0001c0059t0004g0222a0003c0005t0002g0077a0003c0005t0002g0080others(45): Show | 48 | HG01081.hp1 HG01106.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.9329-1933C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327657 | ||||||
chr2:237327696 | T | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.9329-1972A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327696 | ||||||
chr2:237327821 | G | A | 1 | a0003c0026t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.9329-2097C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327821 | ||||||
chr2:237327836 | C | CA | 9 | a0002c0001t0002g0313a0003c0105t0001g0073a0009c0042t0004g0170others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.9329-2113dupT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327836 | ||||||
chr2:237327851 | G | T | 1 | a0003c0005t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.9329-2127C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327851 | ||||||
chr2:237327911 | C | G | 1 | a0003c0082t0002g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9329-2187G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327911 | ||||||
chr2:237327930 | G | A | 1 | a0004c0016t0003g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.9329-2206C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237327930 | ||||||
chr2:237328031 | C | T | 6 | a0003c0105t0001g0073a0009c0042t0004g0170a0009c0042t0012g0172others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.9329-2307G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328031 | ||||||
chr2:237328059 | C | T | 1 | a0002c0092t0002g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.9329-2335G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328059 | ||||||
chr2:237328278 | T | C | 128 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(125): Show | 129 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.9329-2554A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328278 | ||||||
chr2:237328425 | G | A | 1 | a0014c0021t0002g0266 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.9329-2701C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328425 | ||||||
chr2:237328471 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9329-2747G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328471 | ||||||
chr2:237328572 | C | T | 1 | a0011c0070t0011g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9329-2848G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328572 | ||||||
chr2:237328573 | G | A | 7 | a0005c0008t0005g0083a0005c0008t0005g0098a0005c0008t0005g0100others(4): Show | 7 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.9329-2849C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328573 | ||||||
chr2:237328973 | G | A | 1 | a0003c0080t0005g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9329-3249C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237328973 | ||||||
chr2:237329020 | G | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.9329-3296C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329020 | ||||||
chr2:237329053 | CTTAATTT others(10): Show |
C | 1 | a0032c0142t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9329-3346_9329-333 others(21): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329053 | ||||||
chr2:237329076 | T | G | 118 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(115): Show | 119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.9329-3352A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329076 | ||||||
chr2:237329113 | A | T | 198 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(195): Show | 200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.9329-3389T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329113 | ||||||
chr2:237329161 | C | T | 118 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(115): Show | 119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.9329-3437G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329161 | ||||||
chr2:237329274 | C | T | 118 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(115): Show | 119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.9329-3550G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329274 | ||||||
chr2:237329470 | C | G | 1 | a0025c0114t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.9329-3746G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329470 | ||||||
chr2:237329674 | C | G | 2 | a0003c0026t0001g0182a0003c0026t0001g0186 | 2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.9328+3776G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329674 | ||||||
chr2:237329797 | T | C | 1 | a0041c0136t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.9328+3653A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329797 | ||||||
chr2:237329837 | A | C | 127 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(124): Show | 128 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.9328+3613T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329837 | ||||||
chr2:237329912 | C | A | 1 | a0032c0142t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9328+3538G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329912 | ||||||
chr2:237329948 | A | G | 3 | a0003c0089t0001g0116a0025c0114t0001g0121a0041c0136t0001g0165 | 3 | HG01346.hp1 HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.9328+3502T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237329948 | ||||||
chr2:237330001 | G | A | 208 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(205): Show | 210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.9328+3449C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330001 | ||||||
chr2:237330087 | C | T | 151 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(148): Show | 153 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.9328+3363G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330087 | ||||||
chr2:237330158 | C | A | 3 | a0008c0010t0001g0217a0008c0010t0001g0218a0008c0094t0001g0271 | 3 | HG01074.hp1 HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.9328+3292G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330158 | ||||||
chr2:237330230 | G | A | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.9328+3220C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330230 | ||||||
chr2:237330307 | G | A | 33 | a0001c0037t0003g0022a0004c0003t0002g0002a0004c0003t0002g0208others(30): Show | 34 | HG00558.hp1 HG00673.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.9328+3143C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330307 | ||||||
chr2:237330342 | A | G | 39 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(36): Show | 40 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.9328+3108T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330342 | ||||||
chr2:237330344 | G | C | 38 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(35): Show | 39 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.9328+3106C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330344 | ||||||
chr2:237330363 | G | T | 1 | a0003c0080t0005g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9328+3087C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330363 | ||||||
chr2:237330367 | C | T | 2 | a0003c0121t0003g0191a0005c0111t0003g0118 | 2 | HG01358.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.9328+3083G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330367 | ||||||
chr2:237330469 | G | A | 1 | a0003c0080t0005g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9328+2981C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330469 | ||||||
chr2:237330499 | A | T | 28 | a0002c0001t0001g0031a0002c0001t0001g0032a0002c0001t0001g0033others(25): Show | 28 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.9328+2951T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330499 | ||||||
chr2:237330546 | T | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.9328+2904A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330546 | ||||||
chr2:237330563 | G | A | 1 | a0003c0080t0005g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9328+2887C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330563 | ||||||
chr2:237330594 | T | C | 1 | a0002c0092t0002g0257 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.9328+2856A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330594 | ||||||
chr2:237330713 | G | A | 1 | a0002c0001t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.9328+2737C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330713 | ||||||
chr2:237330798 | C | T | 152 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(149): Show | 154 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.9328+2652G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330798 | ||||||
chr2:237330807 | A | G | 1 | a0003c0080t0005g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9328+2643T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237330807 | ||||||
chr2:237331012 | G | A | 2 | a0002c0001t0001g0031a0017c0058t0002g0057 | 2 | HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.9328+2438C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331012 | ||||||
chr2:237331414 | G | C | 4 | a0003c0028t0004g0183a0003c0028t0004g0184a0003c0080t0005g0099others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.9328+2036C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331414 | ||||||
chr2:237331562 | G | A | 1 | a0001c0134t0001g0011 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.9328+1888C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331562 | ||||||
chr2:237331724 | TA | T | 199 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(196): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.9328+1725delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331724 | ||||||
chr2:237331725 | A | T | 13 | a0002c0001t0002g0289a0002c0108t0001g0310a0004c0120t0002g0024others(10): Show | 14 | HG00140.hp2 HG00438.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.9328+1725T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331725 | ||||||
chr2:237331726 | A | T | 188 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.9328+1724T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331726 | ||||||
chr2:237331727 | A | T | 32 | a0001c0004t0002g0067a0003c0005t0001g0018a0003c0005t0001g0019others(29): Show | 32 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.9328+1723T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331727 | ||||||
chr2:237331728 | A | T | 1 | a0003c0005t0001g0317 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.9328+1722T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331728 | ||||||
chr2:237331953 | C | T | 2 | a0002c0001t0002g0312a0002c0001t0002g0313 | 2 | HG02738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.9328+1497G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331953 | ||||||
chr2:237331960 | C | T | 2 | a0003c0039t0003g0163a0036c0137t0003g0081 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.9328+1490G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237331960 | ||||||
chr2:237332043 | C | T | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.9328+1407G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332043 | ||||||
chr2:237332061 | C | CTACATAT others(3): Show |
1 | a0002c0001t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.9328+1388_9328+138 others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332061 | ||||||
chr2:237332063 | C | A | 1 | a0002c0001t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.9328+1387G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332063 | ||||||
chr2:237332065 | C | A | 2 | a0002c0001t0001g0316a0059c0055t0004g0162 | 2 | HG03453.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.9328+1385G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332065 | ||||||
chr2:237332067 | C | A | 2 | a0002c0001t0001g0316a0059c0055t0004g0162 | 2 | HG03453.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.9328+1383G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332067 | ||||||
chr2:237332070 | C | CATATATA others(1): Show |
6 | a0002c0001t0001g0030a0002c0001t0001g0244a0002c0001t0001g0254others(3): Show | 6 | HG00609.hp1 HG02630.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.9328+1372_9328+137 others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(3): Show |
5 | a0002c0001t0001g0198a0002c0001t0001g0319a0004c0016t0001g0242others(2): Show | 5 | HG00609.hp2 HG00673.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.9328+1370_9328+137 others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(5): Show |
6 | a0002c0001t0002g0314a0002c0009t0001g0070a0002c0109t0002g0140others(3): Show | 6 | HG01106.hp1 HG01256.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.9328+1368_9328+137 others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(7): Show |
9 | a0002c0001t0001g0262a0002c0001t0001g0276a0002c0001t0002g0241others(6): Show | 9 | HG00558.hp2 HG02257.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.9328+1366_9328+137 others(18): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(9): Show |
3 | a0002c0001t0001g0258a0002c0001t0001g0290a0002c0001t0002g0295 | 3 | HG01261.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.9328+1364_9328+137 others(20): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(11): Show |
5 | a0002c0001t0001g0249a0002c0001t0001g0259a0002c0001t0001g0298others(2): Show | 5 | HG01123.hp1 HG01496.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9328+1362_9328+137 others(22): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(13): Show |
2 | a0002c0001t0009g0004a0002c0022t0002g0128 | 2 | NA18971.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.9328+1360_9328+137 others(24): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(15): Show |
2 | a0002c0001t0001g0255a0002c0001t0002g0289 | 2 | HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.9328+1358_9328+137 others(26): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(17): Show |
1 | a0002c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.9328+1356_9328+137 others(28): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | CATATATA others(25): Show |
1 | a0002c0001t0002g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.9328+1348_9328+137 others(36): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | C | T | 2 | a0002c0001t0001g0316a0059c0055t0004g0162 | 2 | HG03453.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.9328+1380G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CAT | C | 4 | a0003c0080t0005g0099a0009c0042t0012g0172a0018c0020t0001g0307others(1): Show | 4 | HG02818.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.9328+1378_9328+137 others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(1): Show |
C | 4 | a0003c0027t0001g0149a0003c0033t0001g0174a0004c0003t0003g0068others(1): Show | 4 | HG02572.hp2 HG03017.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.9328+1372_9328+137 others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(3): Show |
C | 4 | a0003c0005t0001g0317a0004c0102t0003g0028a0032c0142t0002g0232others(1): Show | 4 | HG01928.hp2 HG03669.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.9328+1370_9328+137 others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(5): Show |
C | 11 | a0002c0001t0001g0031a0002c0001t0001g0085a0002c0001t0001g0246others(8): Show | 11 | HG00438.hp2 HG00639.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.9328+1368_9328+137 others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(7): Show |
C | 11 | a0002c0001t0001g0045a0002c0001t0001g0193a0002c0001t0002g0248others(8): Show | 12 | HG00140.hp2 HG01433.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.9328+1366_9328+137 others(18): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(9): Show |
C | 9 | a0002c0001t0001g0032a0002c0001t0001g0033a0002c0001t0001g0240others(6): Show | 9 | HG00673.hp2 HG00738.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.9328+1364_9328+137 others(20): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(19): Show |
C | 1 | a0005c0008t0004g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.9328+1354_9328+137 others(30): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(23): Show |
C | 32 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(29): Show | 32 | HG01081.hp1 HG01099.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.9328+1350_9328+137 others(34): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(25): Show |
C | 1 | a0002c0110t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.9328+1348_9328+137 others(36): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(27): Show |
C | 1 | a0002c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.9328+1346_9328+137 others(38): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332070 | CATATATA others(29): Show |
C | 2 | a0017c0024t0001g0055a0017c0024t0001g0063 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.9328+1344_9328+137 others(40): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332070 | ||||||
chr2:237332075 | A | ATATATAT others(16): Show |
1 | a0002c0001t0001g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9328+1352_9328+137 others(27): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332075 | ||||||
chr2:237332102 | TATATA | T | 5 | a0001c0002t0001g0092a0001c0004t0002g0229a0001c0004t0002g0230others(2): Show | 5 | HG00438.hp1 HG04199.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.9328+1343_9328+134 others(9): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332102 | ||||||
chr2:237332107 | A | ATAT | 3 | a0001c0002t0002g0203a0035c0047t0002g0123a0065c0123t0003g0109 | 3 | HG00140.hp1 HG02145.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.9328+1340_9328+134 others(7): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332107 | ||||||
chr2:237332111 | A | G | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.9328+1339T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332111 | ||||||
chr2:237332113 | A | G | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.9328+1337T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332113 | ||||||
chr2:237332115 | A | G | 4 | a0009c0042t0004g0170a0009c0042t0012g0172a0029c0043t0001g0108others(1): Show | 4 | HG02280.hp1 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.9328+1335T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332115 | ||||||
chr2:237332117 | A | ATATATAT others(19): Show |
1 | a0004c0119t0002g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(30): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(17): Show |
1 | a0003c0015t0003g0084 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(28): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(26): Show |
1 | a0001c0002t0003g0157 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(37): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(15): Show |
4 | a0003c0015t0003g0199a0003c0118t0002g0061a0003c0122t0002g0078others(1): Show | 4 | NA18941.hp1 NA19000.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(26): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(24): Show |
2 | a0001c0002t0002g0012a0006c0007t0002g0215 | 2 | NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(35): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(13): Show |
4 | a0003c0005t0002g0077a0003c0005t0002g0080a0004c0006t0002g0041others(1): Show | 4 | HG02074.hp2 HG03098.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(24): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(22): Show |
1 | a0030c0132t0002g0283 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(33): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(11): Show |
9 | a0003c0005t0003g0059a0003c0015t0003g0209a0004c0003t0002g0002others(6): Show | 10 | HG01943.hp1 HG02071.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(22): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(13): Show |
1 | a0004c0113t0002g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(24): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(20): Show |
10 | a0001c0002t0001g0088a0001c0002t0002g0043a0001c0002t0002g0201others(7): Show | 10 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(31): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(9): Show |
5 | a0001c0002t0002g0297a0003c0005t0003g0060a0024c0038t0002g0110others(2): Show | 5 | HG02735.hp1 HG04228.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(20): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(18): Show |
15 | a0001c0002t0001g0150a0001c0002t0003g0159a0001c0002t0006g0006others(12): Show | 15 | HG00408.hp1 HG00408.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(29): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(7): Show |
8 | a0001c0037t0003g0022a0003c0005t0003g0156a0003c0015t0001g0272others(5): Show | 8 | HG01167.hp1 HG01346.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(18): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(16): Show |
15 | a0001c0002t0001g0175a0001c0002t0002g0318a0001c0002t0003g0158others(12): Show | 16 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(27): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(5): Show |
12 | a0003c0005t0007g0023a0003c0033t0003g0029a0003c0093t0001g0250others(9): Show | 12 | HG00558.hp1 HG01074.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(14): Show |
13 | a0001c0002t0002g0039a0001c0002t0002g0267a0001c0002t0002g0286others(10): Show | 13 | HG01109.hp2 HG01169.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(25): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(3): Show |
9 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0028t0004g0183others(6): Show | 9 | HG00642.hp2 HG01978.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(5): Show |
1 | a0011c0070t0011g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(12): Show |
10 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0004t0001g0153others(7): Show | 10 | HG00639.hp1 HG01071.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(23): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(1): Show |
8 | a0003c0028t0004g0184a0004c0016t0003g0095a0008c0010t0001g0293others(5): Show | 8 | HG00741.hp1 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(55): Show |
1 | a0010c0018t0004g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.9328+1332_9328+133 others(66): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATAT others(10): Show |
6 | a0001c0002t0002g0146a0001c0002t0006g0005a0012c0013t0002g0014others(3): Show | 6 | HG01081.hp2 NA18981.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(21): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATATTA others(8): Show |
12 | a0001c0004t0002g0220a0001c0014t0001g0147a0001c0076t0003g0219others(9): Show | 12 | HG01256.hp1 HG01517.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(19): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATG | 3 | a0004c0003t0003g0091a0004c0006t0003g0013a0008c0094t0001g0271 | 3 | HG01255.hp1 NA18955.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(8): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATATTATA others(6): Show |
12 | a0001c0002t0001g0287a0001c0002t0002g0308a0001c0002t0003g0040others(9): Show | 12 | HG01175.hp1 HG01433.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(17): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | ATTATATA others(4): Show |
5 | a0001c0002t0001g0115a0005c0017t0007g0034a0006c0064t0003g0047others(2): Show | 5 | HG01123.hp2 HG01358.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.9328+1332_9328+133 others(15): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332117 | A | G | 76 | a0001c0002t0001g0036a0001c0002t0001g0092a0001c0002t0002g0203others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.9328+1333T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332117 | ||||||
chr2:237332180 | T | C | 207 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(204): Show | 209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.9328+1270A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332180 | ||||||
chr2:237332220 | C | T | 40 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(37): Show | 40 | HG00642.hp2 HG01346.hp1 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.9328+1230G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332220 | ||||||
chr2:237332486 | T | C | 1 | a0011c0088t0003g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.9328+964A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332486 | ||||||
chr2:237332688 | A | G | 2 | a0003c0031t0004g0194a0003c0031t0004g0196 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.9328+762T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332688 | ||||||
chr2:237332807 | C | T | 9 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(6): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.9328+643G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332807 | ||||||
chr2:237332925 | A | G | 1 | a0004c0006t0003g0278 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.9328+525T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332925 | ||||||
chr2:237332999 | C | T | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.9328+451G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237332999 | ||||||
chr2:237333119 | G | A | 1 | a0001c0002t0002g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.9328+331C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237333119 | ||||||
chr2:237333190 | T | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9328+260A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237333190 | ||||||
chr2:237333227 | T | C | 1 | a0001c0002t0006g0005 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.9328+223A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237333227 | ||||||
chr2:237333236 | A | C | 1 | a0001c0002t0006g0005 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.9328+214T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237333236 | ||||||
chr2:237333238 | T | G | 8 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(5): Show | 8 | HG00642.hp2 HG01346.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.9328+212A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 42/43 | chr2 | 237333238 | ||||||
chr2:237333714 | G | A | 1 | a0001c0002t0002g0012 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.9230-166C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333714 | ||||||
chr2:237333721 | A | G | 3 | a0005c0012t0002g0300a0005c0012t0003g0132a0005c0090t0003g0122 | 3 | HG01255.hp2 HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.9230-173T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333721 | ||||||
chr2:237333751 | G | A | 7 | a0001c0002t0001g0150a0001c0002t0001g0175a0001c0002t0004g0008others(4): Show | 7 | HG00642.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.9230-203C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333751 | ||||||
chr2:237333855 | C | A | 7 | a0003c0028t0004g0183a0003c0028t0004g0184a0003c0080t0005g0099others(4): Show | 7 | HG02257.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.9230-307G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333855 | ||||||
chr2:237333909 | G | A | 38 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(35): Show | 39 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.9230-361C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333909 | ||||||
chr2:237333978 | G | C | 1 | a0005c0012t0002g0300 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.9230-430C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237333978 | ||||||
chr2:237334101 | G | T | 1 | a0001c0117t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.9229+525C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334101 | ||||||
chr2:237334102 | C | T | 1 | a0001c0117t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.9229+524G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334102 | ||||||
chr2:237334194 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9229+432G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334194 | ||||||
chr2:237334291 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9229+335G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334291 | ||||||
chr2:237334327 | G | A | 1 | a0059c0055t0004g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.9229+299C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334327 | ||||||
chr2:237334381 | A | T | 31 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(28): Show | 31 | HG01081.hp1 HG01099.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.9229+245T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334381 | ||||||
chr2:237334502 | C | CTGT | 9 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(6): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.9229+121_9229+123d others(5): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334502 | ||||||
chr2:237334516 | T | C | 1 | a0003c0089t0001g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.9229+110A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 41/43 | chr2 | 237334516 | ||||||
chr2:237334908 | C | A | 1 | a0045c0067t0002g0288 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.8966-19G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237334908 | ||||||
chr2:237335013 | C | T | 10 | a0002c0001t0002g0289a0002c0001t0002g0295a0007c0011t0001g0003others(7): Show | 11 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.8966-124G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335013 | ||||||
chr2:237335088 | T | C | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8966-199A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335088 | ||||||
chr2:237335098 | T | C | 1 | a0011c0088t0003g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8966-209A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335098 | ||||||
chr2:237335207 | G | T | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.8966-318C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335207 | ||||||
chr2:237335210 | C | G | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.8966-321G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335210 | ||||||
chr2:237335210 | C | T | 4 | a0003c0028t0004g0183a0003c0028t0004g0184a0003c0080t0005g0099others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.8966-321G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335210 | ||||||
chr2:237335358 | C | T | 4 | a0002c0001t0001g0301a0002c0001t0009g0004a0045c0067t0002g0288others(1): Show | 4 | HG00609.hp2 NA18939.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8966-469G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335358 | ||||||
chr2:237335432 | C | A | 2 | a0008c0010t0001g0089a0008c0010t0001g0293 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.8966-543G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335432 | ||||||
chr2:237335541 | C | G | 28 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(25): Show | 28 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.8965+594G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335541 | ||||||
chr2:237335708 | G | C | 1 | a0001c0059t0004g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.8965+427C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335708 | ||||||
chr2:237335756 | T | G | 2 | a0001c0002t0002g0261a0006c0007t0002g0214 | 2 | NA18975.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.8965+379A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335756 | ||||||
chr2:237335833 | C | T | 9 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(6): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.8965+302G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335833 | ||||||
chr2:237335854 | T | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8965+281A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335854 | ||||||
chr2:237335883 | A | G | 9 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(6): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.8965+252T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335883 | ||||||
chr2:237335916 | G | C | 44 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(41): Show | 44 | HG00642.hp2 HG01346.hp1 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.8965+219C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335916 | ||||||
chr2:237335932 | T | C | 207 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(204): Show | 209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.8965+203A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237335932 | ||||||
chr2:237336067 | G | A | 1 | a0039c0128t0004g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8965+68C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237336067 | ||||||
chr2:237336073 | C | T | 4 | a0003c0028t0004g0183a0003c0028t0004g0184a0003c0080t0005g0099others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.8965+62G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 40/43 | chr2 | 237336073 | ||||||
chr2:237336590 | G | T | 2 | a0009c0041t0002g0236a0009c0041t0002g0303 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.8568-58C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237336590 | ||||||
chr2:237336610 | A | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-78T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237336610 | ||||||
chr2:237336843 | A | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-311T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237336843 | ||||||
chr2:237336932 | T | C | 1 | a0011c0091t0003g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.8568-400A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237336932 | ||||||
chr2:237336948 | C | T | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.8568-416G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237336948 | ||||||
chr2:237337224 | T | A | 2 | a0003c0033t0003g0029a0052c0112t0002g0143 | 2 | HG01099.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.8568-692A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337224 | ||||||
chr2:237337334 | G | A | 1 | a0017c0024t0001g0063 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.8568-802C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337334 | ||||||
chr2:237337440 | T | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-908A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337440 | ||||||
chr2:237337560 | T | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-1028A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337560 | ||||||
chr2:237337564 | C | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-1032G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337564 | ||||||
chr2:237337568 | A | G | 110 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.8568-1036T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337568 | ||||||
chr2:237337624 | G | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-1092C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337624 | ||||||
chr2:237337630 | A | C | 1 | a0006c0064t0003g0047 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.8568-1098T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337630 | ||||||
chr2:237337659 | G | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8568-1127C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337659 | ||||||
chr2:237337800 | G | A | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.8567+1215C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337800 | ||||||
chr2:237337820 | A | G | 30 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(27): Show | 30 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.8567+1195T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337820 | ||||||
chr2:237337821 | C | T | 10 | a0003c0089t0001g0116a0003c0105t0001g0073a0011c0069t0002g0187others(7): Show | 10 | HG01346.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.8567+1194G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337821 | ||||||
chr2:237337877 | A | AC | 58 | a0001c0014t0001g0147a0001c0014t0002g0114a0001c0014t0002g0129others(55): Show | 59 | HG00558.hp1 HG00673.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.8567+1137dupG | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337877 | ||||||
chr2:237337896 | A | G | 2 | a0009c0124t0003g0113a0009c0126t0004g0179 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8567+1119T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337896 | ||||||
chr2:237337975 | T | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8567+1040A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337975 | ||||||
chr2:237337977 | T | C | 9 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(6): Show | 10 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.8567+1038A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237337977 | ||||||
chr2:237338029 | C | T | 2 | a0009c0124t0003g0113a0009c0126t0004g0179 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8567+986G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338029 | ||||||
chr2:237338049 | T | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8567+966A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338049 | ||||||
chr2:237338568 | G | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8567+447C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338568 | ||||||
chr2:237338614 | A | G | 29 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(26): Show | 29 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.8567+401T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338614 | ||||||
chr2:237338678 | G | T | 2 | a0011c0070t0011g0139a0071c0138t0001g0166 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.8567+337C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338678 | ||||||
chr2:237338734 | G | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8567+281C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 39/43 | chr2 | 237338734 | ||||||
chr2:237339151 | G | A | 2 | a0017c0024t0001g0055a0017c0024t0001g0063 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.8465-34C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339151 | ||||||
chr2:237339160 | T | C | 4 | a0014c0021t0003g0264a0016c0019t0001g0216a0016c0019t0002g0212others(1): Show | 4 | HG00408.hp2 HG02165.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.8465-43A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339160 | ||||||
chr2:237339553 | A | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8465-436T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339553 | ||||||
chr2:237339742 | T | C | 3 | a0022c0078t0001g0247a0022c0103t0001g0233a0038c0052t0003g0082 | 3 | NA19002.hp1 NA19057.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.8465-625A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339742 | ||||||
chr2:237339845 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8464+607G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339845 | ||||||
chr2:237339854 | G | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.8464+598C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339854 | ||||||
chr2:237339960 | C | T | 3 | a0003c0027t0001g0149a0003c0033t0001g0174a0003c0075t0001g0192 | 3 | HG02572.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.8464+492G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237339960 | ||||||
chr2:237340052 | A | C | 1 | a0002c0001t0001g0255 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.8464+400T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340052 | ||||||
chr2:237340074 | G | A | 2 | a0002c0001t0002g0314a0052c0112t0002g0143 | 2 | HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.8464+378C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340074 | ||||||
chr2:237340128 | C | T | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.8464+324G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340128 | ||||||
chr2:237340210 | G | A | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.8464+242C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340210 | ||||||
chr2:237340224 | G | A | 1 | a0012c0013t0002g0017 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.8464+228C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340224 | ||||||
chr2:237340256 | A | T | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.8464+196T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 38/43 | chr2 | 237340256 | ||||||
chr2:237341274 | G | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7766-124C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341274 | ||||||
chr2:237341395 | T | C | 1 | a0001c0004t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7766-245A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341395 | ||||||
chr2:237341413 | G | A | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.7766-263C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341413 | ||||||
chr2:237341543 | T | TA | 45 | a0002c0001t0001g0193a0002c0001t0001g0240a0002c0001t0001g0243others(42): Show | 45 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.7766-394dupT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341543 | ||||||
chr2:237341543 | T | TAAAAAAA others(3): Show |
1 | a0011c0088t0003g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7766-403_7766-394d others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341543 | ||||||
chr2:237341543 | TA | T | 120 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(117): Show | 121 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.7766-394delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341543 | ||||||
chr2:237341543 | TAA | T | 15 | a0001c0002t0002g0043a0001c0002t0003g0159a0001c0079t0002g0062others(12): Show | 16 | HG00140.hp2 HG00438.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.7766-395_7766-394d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341543 | ||||||
chr2:237341572 | C | A | 2 | a0004c0006t0002g0299a0004c0140t0002g0205 | 2 | NA18952.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.7766-422G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341572 | ||||||
chr2:237341572 | C | G | 16 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(13): Show | 17 | HG00140.hp2 HG00438.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.7766-422G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341572 | ||||||
chr2:237341690 | C | T | 1 | a0008c0094t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7765+375G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341690 | ||||||
chr2:237341859 | C | T | 1 | a0001c0002t0002g0203 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7765+206G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341859 | ||||||
chr2:237341860 | G | A | 1 | a0049c0104t0002g0020 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.7765+205C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341860 | ||||||
chr2:237341901 | T | C | 1 | a0008c0010t0001g0217 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.7765+164A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341901 | ||||||
chr2:237341939 | C | T | 2 | a0003c0039t0003g0163a0036c0137t0003g0081 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7765+126G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341939 | ||||||
chr2:237341943 | G | C | 1 | a0008c0094t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.7765+122C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237341943 | ||||||
chr2:237342000 | C | G | 1 | a0041c0136t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7765+65G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 37/43 | chr2 | 237342000 | ||||||
chr2:237342196 | G | A | 7 | a0008c0010t0001g0089a0008c0010t0001g0217a0008c0010t0001g0218others(4): Show | 7 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.7669-35C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342196 | ||||||
chr2:237342392 | T | G | 51 | a0003c0028t0004g0183a0003c0028t0004g0184a0003c0031t0004g0194others(48): Show | 52 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.7669-231A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342392 | ||||||
chr2:237342395 | C | A | 2 | a0005c0017t0003g0046a0005c0017t0003g0280 | 2 | HG01433.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.7669-234G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342395 | ||||||
chr2:237342609 | T | G | 120 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(117): Show | 121 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.7669-448A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342609 | ||||||
chr2:237342611 | CAA | C | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.7669-452_7669-451d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342611 | ||||||
chr2:237342617 | G | C | 1 | a0001c0002t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7669-456C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342617 | ||||||
chr2:237342644 | C | T | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7669-483G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342644 | ||||||
chr2:237342690 | A | C | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.7669-529T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342690 | ||||||
chr2:237342708 | A | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7669-547T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342708 | ||||||
chr2:237342803 | T | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7669-642A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342803 | ||||||
chr2:237342983 | A | G | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7669-822T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237342983 | ||||||
chr2:237343039 | C | T | 1 | a0017c0024t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7669-878G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343039 | ||||||
chr2:237343217 | C | G | 1 | a0001c0095t0002g0265 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.7669-1056G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343217 | ||||||
chr2:237343221 | G | A | 1 | a0002c0009t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.7669-1060C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343221 | ||||||
chr2:237343333 | TA | T | 111 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(108): Show | 112 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.7668+1016delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343333 | ||||||
chr2:237343338 | A | G | 1 | a0003c0005t0003g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7668+1012T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343338 | ||||||
chr2:237343384 | G | A | 214 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(211): Show | 217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.7668+966C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343384 | ||||||
chr2:237343445 | G | A | 1 | a0004c0003t0002g0002 | 2 | NA18983.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.7668+905C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343445 | ||||||
chr2:237343451 | G | T | 7 | a0001c0002t0001g0150a0001c0002t0001g0175a0001c0002t0004g0008others(4): Show | 7 | HG00642.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7668+899C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343451 | ||||||
chr2:237343512 | CTCAAAAA others(29): Show |
C | 2 | a0006c0007t0002g0215a0033c0141t0002g0026 | 2 | NA18952.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.7668+802_7668+837d others(38): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343512 | ||||||
chr2:237343512 | CTCAAAAA others(30): Show |
C | 4 | a0006c0007t0002g0285a0023c0032t0001g0001a0046c0065t0002g0275others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+801_7668+837d others(39): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343512 | ||||||
chr2:237343514 | CAAAAAAA others(3): Show |
C | 2 | a0002c0109t0002g0140a0032c0142t0002g0232 | 2 | HG01256.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.7668+826_7668+835d others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(4): Show |
C | 8 | a0002c0001t0001g0031a0002c0001t0001g0240a0002c0001t0002g0311others(5): Show | 8 | HG01109.hp1 HG01928.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.7668+825_7668+835d others(13): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(5): Show |
C | 15 | a0002c0001t0001g0033a0002c0001t0001g0085a0002c0001t0001g0136others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.7668+824_7668+835d others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(6): Show |
C | 2 | a0002c0001t0001g0252a0002c0092t0002g0257 | 2 | HG01981.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.7668+823_7668+835d others(15): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(7): Show |
C | 3 | a0002c0001t0002g0241a0002c0022t0002g0021a0002c0022t0002g0128 | 3 | HG00558.hp2 NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.7668+822_7668+835d others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(8): Show |
C | 3 | a0011c0091t0003g0064a0034c0046t0002g0253a0052c0112t0002g0143 | 3 | HG01099.hp1 NA19043.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.7668+821_7668+835d others(17): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(9): Show |
C | 3 | a0002c0001t0001g0243a0011c0070t0011g0139a0071c0138t0001g0166 | 3 | HG02027.hp1 HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7668+820_7668+835d others(18): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(10): Show |
C | 1 | a0011c0069t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7668+819_7668+835d others(19): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(15): Show |
C | 1 | a0002c0001t0009g0004 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.7668+814_7668+835d others(24): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(16): Show |
C | 2 | a0002c0001t0001g0301a0002c0106t0002g0231 | 2 | NA18954.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.7668+813_7668+835d others(25): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(17): Show |
C | 4 | a0002c0001t0001g0045a0002c0001t0001g0193a0002c0001t0001g0244others(1): Show | 4 | HG02071.hp1 NA18970.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.7668+812_7668+835d others(26): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(18): Show |
C | 6 | a0002c0001t0001g0198a0002c0001t0001g0246a0002c0001t0001g0249others(3): Show | 6 | HG03831.hp2 NA18986.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.7668+811_7668+835d others(27): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(19): Show |
C | 2 | a0002c0001t0001g0255a0008c0010t0001g0218 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.7668+810_7668+835d others(28): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(20): Show |
C | 5 | a0002c0001t0001g0254a0002c0001t0001g0258a0008c0010t0001g0293others(2): Show | 5 | HG00609.hp1 HG00741.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.7668+809_7668+835d others(29): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(21): Show |
C | 5 | a0008c0010t0001g0089a0008c0010t0001g0217a0008c0010t0002g0042others(2): Show | 5 | HG00738.hp1 HG01255.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+808_7668+835d others(30): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(22): Show |
C | 4 | a0001c0014t0002g0114a0001c0014t0002g0200a0004c0006t0001g0094others(1): Show | 4 | HG02886.hp2 HG03579.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.7668+807_7668+835d others(31): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(23): Show |
C | 19 | a0001c0014t0002g0129a0001c0068t0002g0138a0001c0087t0002g0148others(16): Show | 19 | HG00673.hp1 HG00673.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.7668+806_7668+835d others(32): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(24): Show |
C | 31 | a0001c0014t0001g0147a0002c0009t0001g0079a0004c0003t0002g0002others(28): Show | 32 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.7668+805_7668+835d others(33): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(25): Show |
C | 10 | a0002c0001t0001g0030a0002c0001t0001g0032a0007c0011t0001g0003others(7): Show | 11 | HG01433.hp1 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.7668+804_7668+835d others(34): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(26): Show |
C | 2 | a0011c0088t0003g0173a0067c0050t0001g0277 | 2 | HG01884.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.7668+803_7668+835d others(35): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(28): Show |
C | 3 | a0001c0004t0002g0229a0002c0009t0001g0097a0003c0105t0001g0073 | 3 | HG00438.hp1 HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.7668+801_7668+835d others(37): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(29): Show |
C | 37 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0002g0201others(34): Show | 37 | HG00408.hp1 HG00408.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.7668+800_7668+835d others(38): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(30): Show |
C | 66 | a0001c0002t0001g0036a0001c0002t0001g0115a0001c0002t0001g0150others(63): Show | 66 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.7668+799_7668+835d others(39): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(31): Show |
C | 5 | a0001c0002t0003g0158a0001c0079t0002g0062a0010c0018t0003g0105others(2): Show | 5 | HG00609.hp2 HG01256.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+798_7668+835d others(40): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(32): Show |
C | 5 | a0002c0001t0001g0276a0003c0028t0004g0183a0003c0028t0004g0184others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+797_7668+835d others(41): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(33): Show |
C | 5 | a0005c0101t0003g0238a0009c0124t0003g0113a0009c0126t0004g0179others(2): Show | 5 | HG02056.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+796_7668+835d others(42): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(34): Show |
C | 23 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(20): Show | 23 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.7668+795_7668+835d others(43): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343514 | CAAAAAAA others(35): Show |
C | 2 | a0005c0008t0005g0098a0005c0111t0003g0118 | 2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.7668+794_7668+835d others(44): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343514 | ||||||
chr2:237343523 | AAAAAAAA others(47): Show |
A | 1 | a0040c0135t0008g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7668+773_7668+826d others(56): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343523 | ||||||
chr2:237343537 | AAAAAAAA others(33): Show |
A | 24 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0002g0077others(21): Show | 24 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.7668+773_7668+812d others(42): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343537 | ||||||
chr2:237343538 | AAAAAAAA others(32): Show |
A | 7 | a0003c0005t0001g0317a0003c0005t0007g0023a0003c0027t0001g0149others(4): Show | 7 | HG02293.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.7668+773_7668+811d others(41): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343538 | ||||||
chr2:237343540 | AAAAAAAA others(30): Show |
A | 1 | a0001c0004t0002g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.7668+773_7668+809d others(39): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343540 | ||||||
chr2:237343550 | A | C | 2 | a0006c0007t0002g0215a0033c0141t0002g0026 | 2 | NA18952.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.7668+800T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343550 | ||||||
chr2:237343551 | A | C | 4 | a0006c0007t0002g0285a0023c0032t0001g0001a0046c0065t0002g0275others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.7668+799T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343551 | ||||||
chr2:237343560 | A | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.7668+790T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343560 | ||||||
chr2:237343561 | A | C | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.7668+789T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343561 | ||||||
chr2:237343562 | A | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7668+788T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343562 | ||||||
chr2:237343564 | A | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.7668+786T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343564 | ||||||
chr2:237343567 | A | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7668+783T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343567 | ||||||
chr2:237343575 | A | C | 26 | a0002c0001t0001g0031a0002c0001t0001g0032a0002c0001t0001g0033others(23): Show | 26 | HG00639.hp2 HG00738.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.7668+775T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343575 | ||||||
chr2:237343576 | A | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7668+774T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343576 | ||||||
chr2:237343591 | A | G | 1 | a0020c0129t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7668+759T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343591 | ||||||
chr2:237343614 | G | A | 1 | a0019c0044t0002g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7668+736C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343614 | ||||||
chr2:237343630 | G | A | 110 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.7668+720C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343630 | ||||||
chr2:237343670 | C | T | 1 | a0001c0002t0006g0005 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7668+680G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343670 | ||||||
chr2:237343754 | T | A | 8 | a0007c0011t0001g0003a0007c0011t0001g0291a0007c0011t0001g0292others(5): Show | 9 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.7668+596A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237343754 | ||||||
chr2:237344053 | C | T | 1 | a0001c0059t0004g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7668+297G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344053 | ||||||
chr2:237344153 | T | C | 1 | a0020c0127t0004g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7668+197A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344153 | ||||||
chr2:237344240 | G | A | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.7668+110C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344240 | ||||||
chr2:237344255 | G | C | 3 | a0011c0069t0002g0187a0011c0088t0003g0173a0011c0091t0003g0064 | 3 | HG01884.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7668+95C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344255 | ||||||
chr2:237344255 | G | T | 2 | a0011c0070t0011g0139a0071c0138t0001g0166 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7668+95C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344255 | ||||||
chr2:237344282 | C | T | 1 | a0011c0091t0003g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7668+68G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344282 | ||||||
chr2:237344329 | C | G | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7668+21G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 36/43 | chr2 | 237344329 | ||||||
chr2:237344875 | C | T | 30 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(27): Show | 30 | HG01081.hp1 HG01099.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.7175-32G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 35/43 | chr2 | 237344875 | ||||||
chr2:237344996 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7163-44G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 34/43 | chr2 | 237344996 | ||||||
chr2:237345010 | C | T | 2 | a0011c0069t0002g0187a0011c0091t0003g0064 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7162+48G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 34/43 | chr2 | 237345010 | ||||||
chr2:237345124 | G | C | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.7126-30C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 33/43 | chr2 | 237345124 | ||||||
chr2:237345263 | G | A | 2 | a0003c0039t0003g0163a0036c0137t0003g0081 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7093-50C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345263 | ||||||
chr2:237345279 | G | T | 1 | a0005c0012t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7093-66C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345279 | ||||||
chr2:237345287 | A | G | 31 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(28): Show | 31 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.7093-74T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345287 | ||||||
chr2:237345381 | A | T | 1 | a0022c0103t0001g0233 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.7093-168T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345381 | ||||||
chr2:237345414 | G | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7093-201C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345414 | ||||||
chr2:237345456 | G | C | 8 | a0004c0072t0001g0185a0009c0126t0004g0179a0019c0044t0002g0066others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.7093-243C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345456 | ||||||
chr2:237345475 | ATGTAAAG others(14): Show |
A | 26 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(23): Show | 26 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.7093-283_7093-263d others(23): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345475 | ||||||
chr2:237345502 | C | T | 3 | a0003c0005t0001g0317a0027c0023t0001g0124a0027c0023t0001g0125 | 3 | HG02129.hp2 HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.7093-289G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345502 | ||||||
chr2:237345514 | T | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7093-301A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345514 | ||||||
chr2:237345543 | G | A | 1 | a0004c0120t0002g0024 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.7093-330C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345543 | ||||||
chr2:237345607 | G | A | 2 | a0003c0039t0003g0163a0036c0137t0003g0081 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7093-394C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345607 | ||||||
chr2:237345661 | G | A | 29 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.7093-448C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345661 | ||||||
chr2:237345876 | G | C | 1 | a0016c0019t0002g0302 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.7092+627C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237345876 | ||||||
chr2:237346199 | C | T | 2 | a0027c0023t0001g0124a0027c0023t0001g0125 | 2 | HG02129.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.7092+304G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237346199 | ||||||
chr2:237346226 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7092+277G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237346226 | ||||||
chr2:237346477 | C | T | 67 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(64): Show | 67 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.7092+26G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 32/43 | chr2 | 237346477 | ||||||
chr2:237346642 | G | A | 29 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.7030-77C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237346642 | ||||||
chr2:237346665 | GACTCCAT others(18): Show |
G | 2 | a0026c0035t0002g0164a0039c0128t0004g0010 | 2 | HG01081.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.7030-125_7030-101d others(27): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237346665 | ||||||
chr2:237346710 | G | T | 1 | a0001c0002t0001g0092 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.7030-145C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237346710 | ||||||
chr2:237346952 | A | G | 1 | a0051c0083t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.7030-387T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237346952 | ||||||
chr2:237347043 | C | A | 224 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(221): Show | 226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.7030-478G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347043 | ||||||
chr2:237347197 | C | T | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7029+610G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347197 | ||||||
chr2:237347228 | T | C | 2 | a0003c0089t0001g0116a0025c0114t0001g0121 | 2 | HG01346.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7029+579A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347228 | ||||||
chr2:237347231 | C | T | 2 | a0003c0089t0001g0116a0025c0114t0001g0121 | 2 | HG01346.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7029+576G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347231 | ||||||
chr2:237347243 | C | CT | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7029+563_7029+564i others(3): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347243 | ||||||
chr2:237347244 | C | A | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7029+563G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347244 | ||||||
chr2:237347289 | T | TCA | 11 | a0001c0002t0001g0088a0001c0004t0002g0067a0003c0005t0002g0077others(8): Show | 11 | HG00438.hp2 HG01099.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7029+516_7029+517d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347289 | ||||||
chr2:237347358 | G | A | 29 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.7029+449C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347358 | ||||||
chr2:237347405 | C | T | 1 | a0001c0037t0001g0025 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7029+402G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347405 | ||||||
chr2:237347467 | C | T | 7 | a0001c0002t0002g0203a0003c0082t0002g0197a0003c0089t0001g0116others(4): Show | 7 | HG00140.hp1 HG01243.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.7029+340G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347467 | ||||||
chr2:237347478 | G | A | 1 | a0004c0113t0002g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7029+329C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347478 | ||||||
chr2:237347528 | C | T | 61 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(58): Show | 61 | HG00642.hp2 HG01081.hp1 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.7029+279G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347528 | ||||||
chr2:237347529 | G | A | 4 | a0004c0003t0002g0208a0004c0006t0002g0299a0004c0120t0002g0024others(1): Show | 4 | NA18941.hp2 NA18952.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.7029+278C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347529 | ||||||
chr2:237347536 | C | T | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7029+271G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347536 | ||||||
chr2:237347546 | C | T | 1 | a0011c0069t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7029+261G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347546 | ||||||
chr2:237347551 | C | T | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.7029+256G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 31/43 | chr2 | 237347551 | ||||||
chr2:237347925 | A | C | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.6967-56T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237347925 | ||||||
chr2:237347929 | T | C | 6 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(3): Show | 6 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.6967-60A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237347929 | ||||||
chr2:237347931 | C | T | 1 | a0019c0044t0004g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6967-62G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237347931 | ||||||
chr2:237348182 | G | A | 26 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(23): Show | 26 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.6966+167C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237348182 | ||||||
chr2:237348242 | AGT | A | 29 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.6966+105_6966+106d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237348242 | ||||||
chr2:237348263 | G | GA | 26 | a0003c0031t0004g0194a0003c0031t0004g0196a0003c0039t0001g0176others(23): Show | 26 | HG01081.hp1 HG01255.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.6966+85_6966+86ins others(1): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 30/43 | chr2 | 237348263 | ||||||
chr2:237348484 | C | A | 70 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(67): Show | 70 | HG00438.hp2 HG00642.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.6931-100G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 29/43 | chr2 | 237348484 | ||||||
chr2:237348570 | C | G | 32 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(29): Show | 32 | HG00642.hp2 HG01346.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.6930+43G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 29/43 | chr2 | 237348570 | ||||||
chr2:237348585 | G | A | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.6930+28C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 29/43 | chr2 | 237348585 | ||||||
chr2:237348710 | A | G | 61 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(58): Show | 61 | HG00642.hp2 HG01081.hp1 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.6880-47T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348710 | ||||||
chr2:237348721 | C | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.6880-58G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348721 | ||||||
chr2:237348722 | G | A | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.6880-59C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348722 | ||||||
chr2:237348875 | C | T | 3 | a0003c0105t0001g0073a0029c0043t0001g0104a0029c0043t0001g0108 | 3 | HG02486.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.6880-212G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348875 | ||||||
chr2:237348891 | T | C | 8 | a0011c0069t0002g0187a0011c0070t0011g0139a0011c0088t0003g0173others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.6880-228A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348891 | ||||||
chr2:237348993 | G | A | 2 | a0001c0002t0001g0092a0001c0002t0006g0006 | 2 | NA18960.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.6880-330C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237348993 | ||||||
chr2:237349098 | C | A | 1 | a0010c0018t0004g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6880-435G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349098 | ||||||
chr2:237349130 | C | G | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.6880-467G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349130 | ||||||
chr2:237349174 | G | C | 5 | a0003c0089t0001g0116a0003c0105t0001g0073a0025c0114t0001g0121others(2): Show | 5 | HG01346.hp1 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.6880-511C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349174 | ||||||
chr2:237349252 | C | T | 9 | a0004c0072t0001g0185a0009c0126t0004g0179a0019c0044t0002g0066others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.6880-589G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349252 | ||||||
chr2:237349253 | G | T | 75 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(72): Show | 75 | HG00438.hp2 HG00642.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.6880-590C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349253 | ||||||
chr2:237349452 | C | A | 1 | a0006c0007t0001g0210 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6879+695G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349452 | ||||||
chr2:237349602 | ATTTC | A | 110 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.6879+541_6879+544d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349602 | ||||||
chr2:237349623 | G | A | 3 | a0009c0124t0003g0113a0011c0091t0003g0064a0038c0052t0003g0082 | 3 | NA19030.hp1 NA19043.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.6879+524C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349623 | ||||||
chr2:237349637 | C | T | 242 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(239): Show | 244 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.6879+510G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349637 | ||||||
chr2:237349653 | G | T | 1 | a0003c0005t0003g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6879+494C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349653 | ||||||
chr2:237349897 | C | A | 2 | a0019c0044t0002g0066a0019c0044t0004g0221 | 2 | HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.6879+250G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237349897 | ||||||
chr2:237350114 | G | A | 10 | a0002c0001t0001g0198a0002c0001t0001g0244a0002c0001t0001g0249others(7): Show | 10 | HG00609.hp1 HG00609.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.6879+33C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 28/43 | chr2 | 237350114 | ||||||
chr2:237350318 | C | T | 1 | a0009c0124t0003g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6817-109G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350318 | ||||||
chr2:237350473 | C | T | 8 | a0009c0041t0002g0236a0009c0041t0002g0303a0011c0069t0002g0187others(5): Show | 8 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.6817-264G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350473 | ||||||
chr2:237350480 | C | T | 1 | a0016c0019t0002g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6817-271G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350480 | ||||||
chr2:237350567 | A | G | 4 | a0005c0017t0001g0131a0005c0017t0003g0046a0005c0017t0003g0280others(1): Show | 4 | HG01358.hp2 HG01433.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6817-358T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350567 | ||||||
chr2:237350610 | T | C | 3 | a0001c0002t0001g0036a0001c0002t0002g0297a0028c0025t0002g0213 | 3 | NA19054.hp2 NA19055.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.6817-401A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350610 | ||||||
chr2:237350622 | G | A | 1 | a0001c0002t0002g0146 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6817-413C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350622 | ||||||
chr2:237350727 | C | T | 1 | a0003c0005t0007g0023 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6816+403G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350727 | ||||||
chr2:237350733 | G | A | 4 | a0007c0030t0001g0048a0007c0030t0001g0245a0063c0057t0002g0056others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.6816+397C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350733 | ||||||
chr2:237350744 | A | G | 33 | a0003c0005t0001g0018a0003c0005t0001g0019a0003c0005t0001g0317others(30): Show | 33 | HG00642.hp2 HG01346.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.6816+386T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350744 | ||||||
chr2:237350778 | A | G | 5 | a0004c0003t0003g0091a0004c0003t0003g0207a0004c0003t0003g0225others(2): Show | 5 | HG00558.hp1 HG03704.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.6816+352T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350778 | ||||||
chr2:237350822 | G | T | 1 | a0004c0016t0003g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6816+308C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350822 | ||||||
chr2:237350858 | A | C | 1 | a0011c0069t0002g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6816+272T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350858 | ||||||
chr2:237350939 | G | T | 1 | a0040c0135t0008g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6816+191C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350939 | ||||||
chr2:237350991 | C | T | 1 | a0004c0006t0002g0305 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.6816+139G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350991 | ||||||
chr2:237350993 | C | T | 1 | a0002c0001t0002g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6816+137G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237350993 | ||||||
chr2:237351032 | G | A | 109 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(106): Show | 110 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.6816+98C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 27/43 | chr2 | 237351032 | ||||||
chr2:237351280 | A | C | 1 | a0025c0115t0004g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6754-88T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351280 | ||||||
chr2:237351433 | C | T | 1 | a0001c0004t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6754-241G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351433 | ||||||
chr2:237351493 | G | T | 25 | a0003c0039t0003g0163a0004c0071t0004g0178a0005c0008t0004g0133others(22): Show | 25 | HG01081.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.6754-301C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351493 | ||||||
chr2:237351638 | G | A | 1 | a0071c0138t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6754-446C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351638 | ||||||
chr2:237351638 | G | C | 182 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(179): Show | 184 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.6754-446C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351638 | ||||||
chr2:237351738 | A | G | 3 | a0001c0004t0002g0229a0001c0004t0002g0230a0001c0004t0002g0235 | 3 | HG00438.hp1 NA18960.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.6754-546T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351738 | ||||||
chr2:237351747 | T | G | 2 | a0001c0074t0001g0169a0058c0098t0001g0101 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.6754-555A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351747 | ||||||
chr2:237351805 | A | G | 114 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(111): Show | 115 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.6754-613T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351805 | ||||||
chr2:237351967 | C | A | 236 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(233): Show | 238 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.6753+555G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351967 | ||||||
chr2:237351987 | C | T | 1 | a0001c0002t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6753+535G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351987 | ||||||
chr2:237351996 | G | A | 2 | a0024c0038t0002g0110a0024c0038t0002g0111 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.6753+526C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237351996 | ||||||
chr2:237352058 | T | A | 178 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(175): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.6753+464A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352058 | ||||||
chr2:237352154 | A | G | 4 | a0009c0124t0003g0113a0011c0070t0011g0139a0063c0057t0002g0056others(1): Show | 4 | HG02109.hp2 NA18983.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.6753+368T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352154 | ||||||
chr2:237352157 | C | T | 1 | a0009c0124t0003g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6753+365G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352157 | ||||||
chr2:237352186 | G | T | 170 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(167): Show | 173 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.6753+336C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352186 | ||||||
chr2:237352343 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6753+179A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352343 | ||||||
chr2:237352420 | G | C | 1 | a0055c0116t0002g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6753+102C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352420 | ||||||
chr2:237352469 | G | A | 174 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(171): Show | 177 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.6753+53C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352469 | ||||||
chr2:237352470 | C | A | 174 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(171): Show | 177 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.6753+52G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352470 | ||||||
chr2:237352496 | G | T | 1 | a0001c0014t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6753+26C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 26/43 | chr2 | 237352496 | ||||||
chr2:237352699 | C | T | 5 | a0001c0002t0002g0281a0007c0011t0001g0309a0008c0010t0001g0217others(2): Show | 5 | HG01074.hp1 HG01433.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.6691-115G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237352699 | ||||||
chr2:237352866 | C | A | 66 | a0001c0004t0002g0067a0003c0005t0001g0018a0003c0005t0001g0019others(63): Show | 66 | HG00438.hp2 HG00642.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.6691-282G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237352866 | ||||||
chr2:237352942 | T | C | 256 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(253): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.6691-358A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237352942 | ||||||
chr2:237353101 | T | C | 173 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(170): Show | 176 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.6690+240A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353101 | ||||||
chr2:237353103 | T | G | 173 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(170): Show | 176 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.6690+238A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353103 | ||||||
chr2:237353164 | A | C | 1 | a0001c0074t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6690+177T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353164 | ||||||
chr2:237353207 | T | C | 68 | a0001c0004t0002g0067a0003c0005t0001g0018a0003c0005t0001g0019others(65): Show | 68 | HG00438.hp2 HG00642.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.6690+134A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353207 | ||||||
chr2:237353298 | G | T | 1 | a0001c0002t0002g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.6690+43C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353298 | ||||||
chr2:237353302 | A | G | 6 | a0021c0029t0005g0168a0029c0043t0001g0104a0029c0043t0001g0108others(3): Show | 6 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.6690+39T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 25/43 | chr2 | 237353302 | ||||||
chr2:237353611 | C | T | 33 | a0001c0004t0002g0067a0003c0005t0001g0018a0003c0005t0001g0019others(30): Show | 33 | HG00438.hp2 HG00642.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.6628-208G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353611 | ||||||
chr2:237353636 | G | A | 9 | a0001c0014t0002g0114a0001c0014t0002g0129a0001c0014t0002g0200others(6): Show | 9 | HG01081.hp2 HG01358.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.6628-233C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353636 | ||||||
chr2:237353748 | G | A | 1 | a0003c0093t0001g0250 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.6628-345C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353748 | ||||||
chr2:237353782 | C | A | 1 | a0001c0004t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.6628-379G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353782 | ||||||
chr2:237353878 | C | A | 4 | a0021c0029t0005g0168a0029c0043t0001g0104a0029c0043t0001g0108others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.6628-475G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353878 | ||||||
chr2:237353990 | T | C | 59 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0227others(56): Show | 61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.6628-587A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237353990 | ||||||
chr2:237354011 | A | AT | 24 | a0001c0074t0001g0169a0002c0001t0001g0244a0002c0001t0002g0289others(21): Show | 25 | HG00140.hp2 HG00558.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.6628-609dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354011 | ||||||
chr2:237354011 | AT | A | 10 | a0001c0014t0002g0114a0001c0014t0002g0129a0001c0014t0002g0200others(7): Show | 10 | HG01358.hp1 HG02723.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.6628-609delA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354011 | ||||||
chr2:237354024 | T | C | 4 | a0003c0005t0002g0077a0003c0005t0002g0080a0003c0118t0002g0061others(1): Show | 4 | NA18941.hp1 NA18986.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.6628-621A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354024 | ||||||
chr2:237354098 | G | A | 2 | a0001c0002t0001g0092a0001c0002t0006g0006 | 2 | NA18960.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.6628-695C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354098 | ||||||
chr2:237354147 | A | G | 252 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(249): Show | 255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.6628-744T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354147 | ||||||
chr2:237354260 | C | T | 1 | a0038c0052t0003g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6627+639G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354260 | ||||||
chr2:237354319 | A | AT | 113 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(110): Show | 114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.6627+579dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354319 | ||||||
chr2:237354339 | A | C | 128 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(125): Show | 130 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.6627+560T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354339 | ||||||
chr2:237354362 | A | G | 2 | a0029c0043t0001g0104a0029c0043t0001g0108 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.6627+537T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354362 | ||||||
chr2:237354363 | C | T | 2 | a0025c0114t0001g0121a0025c0115t0004g0120 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6627+536G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354363 | ||||||
chr2:237354513 | C | T | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6627+386G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354513 | ||||||
chr2:237354656 | C | A | 33 | a0001c0004t0002g0067a0003c0005t0001g0018a0003c0005t0001g0019others(30): Show | 33 | HG00438.hp2 HG00642.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.6627+243G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354656 | ||||||
chr2:237354853 | T | G | 1 | a0009c0124t0003g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6627+46A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 24/43 | chr2 | 237354853 | ||||||
chr2:237354950 | T | A | 4 | a0002c0001t0001g0136a0002c0001t0001g0290a0002c0001t0001g0316others(1): Show | 4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.6592-16A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237354950 | ||||||
chr2:237354960 | TG | T | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6592-27delC | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237354960 | ||||||
chr2:237355146 | G | A | 1 | a0001c0002t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6592-212C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355146 | ||||||
chr2:237355253 | C | A | 2 | a0003c0039t0003g0163a0036c0137t0003g0081 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6592-319G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355253 | ||||||
chr2:237355341 | C | T | 2 | a0029c0043t0001g0104a0029c0043t0001g0108 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.6592-407G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355341 | ||||||
chr2:237355421 | T | C | 93 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(90): Show | 94 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.6592-487A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355421 | ||||||
chr2:237355467 | G | A | 27 | a0004c0071t0004g0178a0005c0008t0001g0086a0005c0008t0004g0133others(24): Show | 27 | HG01081.hp1 HG01255.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.6592-533C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355467 | ||||||
chr2:237355482 | C | A | 46 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0227others(43): Show | 47 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.6592-548G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355482 | ||||||
chr2:237355530 | G | A | 1 | a0001c0002t0002g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6592-596C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355530 | ||||||
chr2:237355539 | C | A | 3 | a0011c0070t0011g0139a0063c0057t0002g0056a0068c0049t0002g0279 | 3 | HG02109.hp2 NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6592-605G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355539 | ||||||
chr2:237355580 | A | G | 121 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(118): Show | 122 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.6592-646T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355580 | ||||||
chr2:237355621 | G | A | 1 | a0004c0006t0003g0013 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.6592-687C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355621 | ||||||
chr2:237355753 | C | T | 46 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0227others(43): Show | 47 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.6592-819G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355753 | ||||||
chr2:237355798 | C | T | 1 | a0071c0138t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6592-864G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355798 | ||||||
chr2:237355866 | C | T | 2 | a0009c0041t0002g0236a0009c0041t0002g0303 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.6592-932G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355866 | ||||||
chr2:237355920 | G | A | 1 | a0040c0135t0008g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6592-986C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237355920 | ||||||
chr2:237356044 | G | T | 1 | a0011c0070t0011g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6592-1110C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356044 | ||||||
chr2:237356107 | C | T | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6592-1173G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356107 | ||||||
chr2:237356242 | A | G | 2 | a0063c0057t0002g0056a0068c0049t0002g0279 | 2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6591+1096T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356242 | ||||||
chr2:237356319 | T | C | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6591+1019A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356319 | ||||||
chr2:237356409 | A | C | 52 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0227others(49): Show | 54 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.6591+929T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356409 | ||||||
chr2:237356435 | C | G | 4 | a0009c0124t0003g0113a0009c0126t0004g0179a0063c0057t0002g0056others(1): Show | 4 | HG02647.hp2 NA18983.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.6591+903G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356435 | ||||||
chr2:237356464 | A | G | 1 | a0016c0019t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6591+874T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356464 | ||||||
chr2:237356530 | C | G | 12 | a0003c0026t0001g0182a0003c0026t0001g0186a0004c0072t0001g0185others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6591+808G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356530 | ||||||
chr2:237356587 | C | A | 4 | a0001c0004t0002g0229a0001c0004t0002g0230a0001c0004t0002g0235others(1): Show | 4 | HG00438.hp1 NA18960.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.6591+751G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356587 | ||||||
chr2:237356625 | T | C | 1 | a0058c0098t0001g0101 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6591+713A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356625 | ||||||
chr2:237356745 | T | C | 6 | a0003c0075t0001g0192a0009c0124t0003g0113a0009c0126t0004g0179others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6591+593A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356745 | ||||||
chr2:237356837 | C | G | 2 | a0063c0057t0002g0056a0068c0049t0002g0279 | 2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6591+501G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356837 | ||||||
chr2:237356888 | C | T | 111 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(108): Show | 112 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.6591+450G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356888 | ||||||
chr2:237356993 | T | C | 1 | a0011c0091t0003g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6591+345A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237356993 | ||||||
chr2:237357018 | A | C | 73 | a0001c0002t0002g0203a0001c0004t0001g0153a0001c0004t0001g0228others(70): Show | 75 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.6591+320T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237357018 | ||||||
chr2:237357033 | A | T | 1 | a0002c0001t0009g0004 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.6591+305T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237357033 | ||||||
chr2:237357036 | T | G | 1 | a0002c0001t0009g0004 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.6591+302A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237357036 | ||||||
chr2:237357039 | G | T | 1 | a0002c0001t0009g0004 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.6591+299C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237357039 | ||||||
chr2:237357041 | C | T | 189 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(186): Show | 192 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.6591+297G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 23/43 | chr2 | 237357041 | ||||||
chr2:237357475 | A | C | 9 | a0009c0042t0004g0170a0009c0042t0012g0172a0011c0069t0002g0187others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.6538-84T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357475 | ||||||
chr2:237357503 | C | T | 39 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0200others(36): Show | 39 | HG00438.hp2 HG00642.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.6538-112G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357503 | ||||||
chr2:237357605 | G | C | 102 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(99): Show | 103 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.6537+212C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357605 | ||||||
chr2:237357660 | C | T | 2 | a0053c0073t0008g0304a0060c0054t0004g0167 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6537+157G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357660 | ||||||
chr2:237357724 | G | A | 1 | a0055c0116t0002g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6537+93C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357724 | ||||||
chr2:237357754 | G | A | 1 | a0003c0075t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6537+63C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 22/43 | chr2 | 237357754 | ||||||
chr2:237357990 | G | A | 82 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(79): Show | 83 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.6472-108C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237357990 | ||||||
chr2:237358058 | G | A | 8 | a0003c0075t0001g0192a0010c0018t0003g0052a0010c0018t0003g0105others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.6472-176C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237358058 | ||||||
chr2:237358139 | T | C | 2 | a0020c0127t0004g0211a0061c0100t0002g0126 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6472-257A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237358139 | ||||||
chr2:237358198 | T | G | 2 | a0063c0057t0002g0056a0068c0049t0002g0279 | 2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6472-316A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237358198 | ||||||
chr2:237358415 | G | A | 162 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(159): Show | 163 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.6471+106C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237358415 | ||||||
chr2:237358432 | C | A | 1 | a0004c0003t0002g0208 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6471+89G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 21/43 | chr2 | 237358432 | ||||||
chr2:237358779 | T | C | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6409-196A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 20/43 | chr2 | 237358779 | ||||||
chr2:237358944 | G | A | 27 | a0003c0026t0001g0182a0003c0026t0001g0186a0003c0039t0001g0176others(24): Show | 27 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.6408+91C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 20/43 | chr2 | 237358944 | ||||||
chr2:237358991 | T | C | 2 | a0009c0126t0004g0179a0026c0035t0002g0164 | 2 | HG01081.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.6408+44A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 20/43 | chr2 | 237358991 | ||||||
chr2:237359268 | G | A | 1 | a0002c0009t0003g0069 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6310-18C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 18/43 | chr2 | 237359268 | ||||||
chr2:237359554 | G | A | 1 | a0002c0001t0001g0254 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.6283-166C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/43 | chr2 | 237359554 | ||||||
chr2:237359779 | C | T | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6282+309G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/43 | chr2 | 237359779 | ||||||
chr2:237359811 | A | C | 140 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(137): Show | 141 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.6282+277T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/43 | chr2 | 237359811 | ||||||
chr2:237359945 | C | T | 2 | a0026c0035t0002g0164a0057c0099t0004g0152 | 2 | HG01081.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6282+143G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/43 | chr2 | 237359945 | ||||||
chr2:237360038 | G | A | 9 | a0005c0012t0003g0142a0005c0012t0004g0144a0010c0018t0003g0105others(6): Show | 9 | HG01081.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.6282+50C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 17/43 | chr2 | 237360038 | ||||||
chr2:237360162 | G | A | 1 | a0021c0029t0005g0168 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.6211-3C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360162 | ||||||
chr2:237360288 | C | T | 1 | a0041c0136t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6211-129G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360288 | ||||||
chr2:237360302 | G | A | 1 | a0004c0003t0003g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.6211-143C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360302 | ||||||
chr2:237360323 | G | T | 1 | a0065c0123t0003g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6211-164C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360323 | ||||||
chr2:237360464 | G | A | 1 | a0002c0001t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6211-305C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360464 | ||||||
chr2:237360476 | C | T | 2 | a0025c0114t0001g0121a0025c0115t0004g0120 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6211-317G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360476 | ||||||
chr2:237360477 | G | A | 125 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(122): Show | 126 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.6211-318C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360477 | ||||||
chr2:237360511 | C | T | 1 | a0048c0081t0002g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6211-352G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360511 | ||||||
chr2:237360558 | T | C | 4 | a0003c0028t0004g0183a0003c0028t0004g0184a0041c0136t0001g0165others(1): Show | 4 | HG02257.hp1 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6211-399A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360558 | ||||||
chr2:237360664 | C | A | 2 | a0019c0044t0002g0066a0019c0044t0004g0221 | 2 | HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.6210+457G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360664 | ||||||
chr2:237360754 | C | T | 1 | a0001c0002t0002g0286 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6210+367G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360754 | ||||||
chr2:237360786 | C | T | 5 | a0016c0019t0002g0212a0016c0019t0002g0302a0062c0056t0002g0206others(2): Show | 5 | NA18945.hp1 NA18959.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.6210+335G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360786 | ||||||
chr2:237360949 | A | G | 13 | a0001c0074t0001g0169a0003c0075t0001g0192a0005c0012t0003g0142others(10): Show | 13 | HG01081.hp1 HG02258.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.6210+172T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 16/43 | chr2 | 237360949 | ||||||
chr2:237361190 | C | T | 5 | a0001c0074t0001g0169a0003c0075t0001g0192a0009c0124t0003g0113others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.6157-16G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361190 | ||||||
chr2:237361228 | C | G | 67 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0114others(64): Show | 67 | HG00438.hp2 HG00642.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.6157-54G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361228 | ||||||
chr2:237361475 | T | G | 1 | a0040c0135t0008g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6156+264A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361475 | ||||||
chr2:237361508 | C | A | 1 | a0008c0010t0001g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.6156+231G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361508 | ||||||
chr2:237361685 | T | C | 7 | a0001c0074t0001g0169a0003c0075t0001g0192a0013c0034t0005g0102others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.6156+54A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361685 | ||||||
chr2:237361735 | G | A | 3 | a0005c0012t0002g0300a0005c0012t0003g0132a0005c0090t0003g0122 | 3 | HG01255.hp2 HG02735.hp2 HG04115.hp1 |
splice_region_variant&intron_variant | LOW | c.6156+4C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 15/43 | chr2 | 237361735 | ||||||
chr2:237361837 | G | A | 1 | a0002c0001t0001g0050 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.6064-6C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237361837 | ||||||
chr2:237361876 | C | A | 4 | a0001c0004t0002g0229a0001c0004t0002g0230a0001c0004t0002g0235others(1): Show | 4 | HG00438.hp1 NA18960.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.6064-45G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237361876 | ||||||
chr2:237361898 | G | A | 2 | a0063c0057t0002g0056a0068c0049t0002g0279 | 2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6064-67C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237361898 | ||||||
chr2:237361902 | T | C | 58 | a0001c0002t0002g0012a0001c0004t0001g0153a0001c0004t0001g0228others(55): Show | 59 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.6064-71A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237361902 | ||||||
chr2:237362001 | C | G | 5 | a0016c0019t0002g0212a0016c0019t0002g0302a0062c0056t0002g0206others(2): Show | 5 | NA18945.hp1 NA18959.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.6064-170G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362001 | ||||||
chr2:237362027 | C | T | 1 | a0002c0001t0001g0244 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.6064-196G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362027 | ||||||
chr2:237362042 | T | C | 4 | a0013c0034t0005g0102a0013c0034t0005g0103a0036c0137t0003g0081others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.6064-211A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362042 | ||||||
chr2:237362083 | A | G | 74 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0114others(71): Show | 74 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.6064-252T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362083 | ||||||
chr2:237362195 | C | G | 1 | a0057c0099t0004g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6064-364G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362195 | ||||||
chr2:237362251 | C | A | 50 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0114others(47): Show | 50 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.6064-420G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362251 | ||||||
chr2:237362470 | A | T | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6064-639T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362470 | ||||||
chr2:237362471 | T | A | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6064-640A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362471 | ||||||
chr2:237362472 | G | T | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6064-641C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362472 | ||||||
chr2:237362473 | G | T | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6064-642C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362473 | ||||||
chr2:237362586 | A | G | 74 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0114others(71): Show | 74 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.6063+667T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362586 | ||||||
chr2:237362600 | T | C | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6063+653A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362600 | ||||||
chr2:237362620 | A | G | 1 | a0022c0103t0001g0233 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.6063+633T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362620 | ||||||
chr2:237362641 | A | C | 59 | a0001c0004t0002g0067a0001c0014t0001g0147a0001c0014t0002g0114others(56): Show | 59 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.6063+612T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362641 | ||||||
chr2:237362647 | C | T | 1 | a0033c0141t0002g0026 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.6063+606G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362647 | ||||||
chr2:237362679 | C | T | 2 | a0008c0010t0001g0217a0008c0010t0001g0218 | 2 | HG01074.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.6063+574G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362679 | ||||||
chr2:237362842 | C | T | 1 | a0002c0110t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6063+411G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362842 | ||||||
chr2:237362913 | T | G | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6063+340A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362913 | ||||||
chr2:237362972 | C | T | 1 | a0002c0001t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6063+281G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237362972 | ||||||
chr2:237363010 | C | T | 18 | a0001c0014t0001g0147a0001c0068t0002g0138a0001c0084t0001g0195others(15): Show | 18 | HG00642.hp1 HG01081.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.6063+243G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237363010 | ||||||
chr2:237363077 | A | T | 1 | a0012c0013t0002g0014 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6063+176T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237363077 | ||||||
chr2:237363093 | G | A | 4 | a0021c0029t0005g0168a0029c0043t0001g0104a0029c0043t0001g0108others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.6063+160C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237363093 | ||||||
chr2:237363143 | GC | G | 190 | a0001c0002t0001g0088a0001c0002t0001g0150a0001c0002t0001g0175others(187): Show | 193 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.6063+109delG | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237363143 | ||||||
chr2:237363239 | T | TA | 35 | a0001c0014t0002g0200a0001c0040t0001g0130a0001c0040t0001g0239others(32): Show | 35 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.6063+13dupT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 14/43 | chr2 | 237363239 | ||||||
chr2:237363691 | C | T | 5 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(2): Show | 5 | HG00642.hp1 HG01081.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.5918-293G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237363691 | ||||||
chr2:237363692 | G | A | 1 | a0071c0138t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5918-294C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237363692 | ||||||
chr2:237363781 | T | C | 1 | a0005c0101t0003g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5918-383A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237363781 | ||||||
chr2:237363786 | A | C | 1 | a0002c0001t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5918-388T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237363786 | ||||||
chr2:237364022 | T | G | 1 | a0002c0108t0001g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5917+328A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364022 | ||||||
chr2:237364076 | T | A | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5917+274A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364076 | ||||||
chr2:237364213 | C | T | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5917+137G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364213 | ||||||
chr2:237364241 | C | T | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5917+109G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364241 | ||||||
chr2:237364258 | G | A | 7 | a0001c0004t0002g0296a0016c0019t0001g0216a0016c0019t0002g0212others(4): Show | 7 | HG00408.hp2 HG02129.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.5917+92C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364258 | ||||||
chr2:237364322 | C | G | 11 | a0003c0026t0001g0182a0003c0026t0001g0186a0003c0027t0001g0149others(8): Show | 11 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5917+28G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364322 | ||||||
chr2:237364323 | T | C | 2 | a0036c0137t0003g0081a0065c0123t0003g0109 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.5917+27A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 13/43 | chr2 | 237364323 | ||||||
chr2:237364531 | C | T | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5839-103G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364531 | ||||||
chr2:237364793 | TTGTGTGT others(15): Show |
T | 74 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(71): Show | 75 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.5839-387_5839-366d others(24): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364793 | ||||||
chr2:237364839 | G | C | 7 | a0001c0002t0002g0146a0012c0013t0002g0014a0012c0013t0002g0016others(4): Show | 7 | NA18945.hp2 NA18955.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.5839-411C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364839 | ||||||
chr2:237364865 | G | GTGTGTGC others(67): Show |
1 | a0001c0002t0001g0269 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.5839-511_5839-438d others(76): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364865 | ||||||
chr2:237364892 | C | T | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5839-464G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364892 | ||||||
chr2:237364901 | G | A | 72 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(69): Show | 73 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.5839-473C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364901 | ||||||
chr2:237364910 | C | T | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5839-482G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237364910 | ||||||
chr2:237365046 | A | C | 8 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(5): Show | 8 | HG00408.hp2 HG02129.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.5839-618T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365046 | ||||||
chr2:237365104 | G | A | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5838+594C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365104 | ||||||
chr2:237365225 | G | A | 1 | a0003c0093t0001g0250 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5838+473C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365225 | ||||||
chr2:237365286 | C | T | 24 | a0003c0026t0001g0182a0003c0026t0001g0186a0003c0027t0001g0149others(21): Show | 24 | HG01358.hp1 HG01496.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.5838+412G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365286 | ||||||
chr2:237365328 | A | G | 1 | a0002c0009t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5838+370T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365328 | ||||||
chr2:237365417 | G | A | 1 | a0009c0126t0004g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5838+281C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365417 | ||||||
chr2:237365686 | G | T | 2 | a0012c0013t0002g0014a0056c0063t0001g0044 | 2 | NA18955.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.5838+12C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 12/43 | chr2 | 237365686 | ||||||
chr2:237366052 | C | T | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5501-17G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366052 | ||||||
chr2:237366185 | C | A | 74 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(71): Show | 75 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.5501-150G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366185 | ||||||
chr2:237366342 | A | G | 1 | a0004c0003t0002g0208 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5501-307T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366342 | ||||||
chr2:237366356 | A | C | 2 | a0010c0018t0003g0105a0010c0018t0003g0106 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5501-321T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366356 | ||||||
chr2:237366456 | A | C | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5500+231T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366456 | ||||||
chr2:237366589 | G | A | 5 | a0005c0012t0003g0132a0005c0017t0001g0131a0005c0017t0003g0046others(2): Show | 5 | HG01255.hp2 HG01358.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.5500+98C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366589 | ||||||
chr2:237366616 | G | A | 3 | a0025c0114t0001g0121a0025c0115t0004g0120a0055c0116t0002g0177 | 3 | HG02886.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5500+71C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366616 | ||||||
chr2:237366665 | A | C | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.5500+22T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 11/43 | chr2 | 237366665 | ||||||
chr2:237367310 | A | T | 1 | a0002c0001t0001g0244 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4901-24T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367310 | ||||||
chr2:237367541 | C | T | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4901-255G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367541 | ||||||
chr2:237367578 | G | A | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4901-292C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367578 | ||||||
chr2:237367634 | T | C | 8 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(5): Show | 8 | HG00408.hp2 HG02129.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.4901-348A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367634 | ||||||
chr2:237367692 | A | G | 102 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(99): Show | 103 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.4901-406T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367692 | ||||||
chr2:237367742 | A | G | 102 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(99): Show | 103 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.4901-456T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367742 | ||||||
chr2:237367871 | C | T | 15 | a0001c0040t0001g0130a0001c0040t0001g0239a0001c0074t0001g0169others(12): Show | 15 | HG01081.hp2 HG01884.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4901-585G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237367871 | ||||||
chr2:237368019 | T | G | 74 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(71): Show | 75 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.4900+544A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368019 | ||||||
chr2:237368022 | C | T | 13 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0124t0003g0113others(10): Show | 13 | HG01496.hp2 HG02257.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.4900+541G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368022 | ||||||
chr2:237368202 | A | G | 75 | a0001c0002t0002g0261a0001c0004t0001g0153a0001c0004t0001g0228others(72): Show | 76 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4900+361T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368202 | ||||||
chr2:237368211 | A | G | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4900+352T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368211 | ||||||
chr2:237368218 | C | A | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4900+345G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368218 | ||||||
chr2:237368554 | G | A | 2 | a0014c0021t0002g0266a0014c0021t0002g0282 | 2 | NA18971.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4900+9C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 10/43 | chr2 | 237368554 | ||||||
chr2:237369288 | G | C | 1 | a0001c0002t0001g0269 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4286-111C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369288 | ||||||
chr2:237369375 | A | C | 3 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0227 | 3 | NA18959.hp1 NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4286-198T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369375 | ||||||
chr2:237369438 | G | T | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4286-261C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369438 | ||||||
chr2:237369439 | T | C | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4286-262A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369439 | ||||||
chr2:237369490 | T | G | 21 | a0001c0040t0001g0130a0001c0040t0001g0239a0001c0074t0001g0169others(18): Show | 21 | HG00408.hp2 HG01081.hp2 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.4286-313A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369490 | ||||||
chr2:237369493 | G | T | 1 | a0001c0002t0003g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4286-316C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369493 | ||||||
chr2:237369499 | G | A | 94 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(91): Show | 95 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.4286-322C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369499 | ||||||
chr2:237369712 | C | T | 1 | a0013c0053t0004g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4286-535G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369712 | ||||||
chr2:237369861 | A | G | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4286-684T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237369861 | ||||||
chr2:237370026 | A | T | 1 | a0001c0002t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4286-849T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370026 | ||||||
chr2:237370027 | T | A | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4286-850A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370027 | ||||||
chr2:237370175 | C | T | 1 | a0038c0052t0003g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4286-998G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370175 | ||||||
chr2:237370199 | G | A | 1 | a0054c0077t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4286-1022C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370199 | ||||||
chr2:237370206 | T | A | 1 | a0003c0031t0004g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4286-1029A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370206 | ||||||
chr2:237370240 | A | AT | 12 | a0001c0095t0002g0265a0002c0001t0001g0198a0002c0001t0001g0243others(9): Show | 12 | HG01884.hp2 HG02027.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.4286-1064dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370240 | ||||||
chr2:237370240 | AT | A | 6 | a0002c0001t0001g0246a0007c0030t0001g0048a0016c0019t0002g0302others(3): Show | 6 | HG03453.hp2 HG03486.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.4286-1064delA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370240 | ||||||
chr2:237370375 | A | G | 1 | a0004c0140t0002g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4286-1198T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370375 | ||||||
chr2:237370387 | T | C | 1 | a0004c0003t0003g0225 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4286-1210A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370387 | ||||||
chr2:237370399 | C | T | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4286-1222G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370399 | ||||||
chr2:237370428 | G | T | 1 | a0055c0116t0002g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4286-1251C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370428 | ||||||
chr2:237370449 | G | A | 1 | a0004c0006t0002g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4286-1272C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370449 | ||||||
chr2:237370488 | C | T | 5 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0124t0003g0113others(2): Show | 5 | HG01496.hp2 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4285+1244G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370488 | ||||||
chr2:237370489 | G | A | 2 | a0044c0062t0005g0190a0059c0055t0004g0162 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4285+1243C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370489 | ||||||
chr2:237370515 | G | T | 1 | a0005c0017t0003g0280 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4285+1217C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370515 | ||||||
chr2:237370516 | C | T | 2 | a0001c0002t0002g0039a0001c0002t0003g0040 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4285+1216G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370516 | ||||||
chr2:237370782 | G | A | 1 | a0011c0091t0003g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4285+950C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370782 | ||||||
chr2:237370819 | T | C | 90 | a0001c0002t0006g0005a0001c0004t0001g0153a0001c0004t0001g0228others(87): Show | 91 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.4285+913A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237370819 | ||||||
chr2:237371028 | C | T | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4285+704G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371028 | ||||||
chr2:237371197 | C | T | 1 | a0002c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4285+535G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371197 | ||||||
chr2:237371249 | C | T | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4285+483G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371249 | ||||||
chr2:237371389 | G | T | 1 | a0004c0016t0003g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4285+343C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371389 | ||||||
chr2:237371715 | C | T | 8 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(5): Show | 8 | HG00408.hp2 HG02129.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.4285+17G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371715 | ||||||
chr2:237371723 | C | T | 5 | a0017c0024t0001g0055a0017c0024t0001g0063a0018c0020t0003g0054others(2): Show | 5 | HG01167.hp1 HG01943.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.4285+9G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 9/43 | chr2 | 237371723 | ||||||
chr2:237372444 | A | G | 4 | a0003c0039t0001g0176a0003c0039t0003g0163a0036c0137t0003g0081others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3680-107T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372444 | ||||||
chr2:237372562 | T | A | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3680-225A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372562 | ||||||
chr2:237372562 | T | G | 8 | a0004c0102t0003g0028a0016c0019t0002g0302a0017c0024t0001g0055others(5): Show | 8 | HG01167.hp1 HG01928.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.3680-225A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372562 | ||||||
chr2:237372567 | A | G | 2 | a0036c0137t0003g0081a0065c0123t0003g0109 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.3680-230T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372567 | ||||||
chr2:237372598 | G | A | 1 | a0002c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3680-261C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372598 | ||||||
chr2:237372609 | T | C | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3680-272A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372609 | ||||||
chr2:237372774 | T | C | 1 | a0001c0002t0002g0012 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3680-437A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372774 | ||||||
chr2:237372821 | G | A | 1 | a0003c0015t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3680-484C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372821 | ||||||
chr2:237372972 | G | A | 11 | a0003c0026t0001g0182a0003c0026t0001g0186a0003c0027t0001g0149others(8): Show | 11 | HG01358.hp1 HG01981.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3680-635C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237372972 | ||||||
chr2:237373073 | C | T | 3 | a0002c0001t0001g0243a0002c0001t0001g0244a0003c0033t0003g0029 | 3 | HG02027.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3680-736G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373073 | ||||||
chr2:237373076 | A | T | 2 | a0010c0018t0003g0052a0010c0018t0004g0112 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3680-739T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373076 | ||||||
chr2:237373114 | C | T | 3 | a0002c0009t0001g0224a0002c0009t0003g0069a0002c0108t0001g0310 | 3 | HG00738.hp2 HG01109.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3680-777G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373114 | ||||||
chr2:237373146 | T | C | 1 | a0001c0014t0002g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3680-809A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373146 | ||||||
chr2:237373185 | C | T | 13 | a0016c0019t0001g0216a0016c0019t0002g0212a0017c0024t0001g0055others(10): Show | 13 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.3680-848G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373185 | ||||||
chr2:237373209 | C | T | 1 | a0005c0012t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3680-872G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373209 | ||||||
chr2:237373299 | C | T | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3680-962G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373299 | ||||||
chr2:237373482 | C | A | 2 | a0002c0001t0001g0262a0014c0021t0003g0264 | 2 | HG02165.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3679+930G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373482 | ||||||
chr2:237373485 | G | A | 43 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0042t0004g0170others(40): Show | 43 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.3679+927C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373485 | ||||||
chr2:237373609 | C | T | 1 | a0043c0061t0001g0260 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3679+803G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373609 | ||||||
chr2:237373678 | G | A | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3679+734C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373678 | ||||||
chr2:237373693 | G | A | 1 | a0003c0015t0003g0209 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3679+719C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373693 | ||||||
chr2:237373703 | AC | A | 18 | a0010c0018t0003g0052a0010c0018t0003g0105a0010c0018t0003g0106others(15): Show | 18 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3679+708delG | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373703 | ||||||
chr2:237373713 | C | A | 18 | a0010c0018t0003g0052a0010c0018t0003g0105a0010c0018t0003g0106others(15): Show | 18 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3679+699G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373713 | ||||||
chr2:237373813 | G | T | 1 | a0005c0017t0003g0046 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3679+599C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373813 | ||||||
chr2:237373901 | T | G | 1 | a0002c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3679+511A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237373901 | ||||||
chr2:237374011 | A | C | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3679+401T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237374011 | ||||||
chr2:237374057 | T | G | 142 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(139): Show | 143 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.3679+355A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237374057 | ||||||
chr2:237374072 | G | A | 23 | a0013c0034t0005g0102a0013c0034t0005g0103a0013c0097t0002g0107others(20): Show | 23 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.3679+340C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237374072 | ||||||
chr2:237374174 | C | T | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3679+238G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 8/43 | chr2 | 237374174 | ||||||
chr2:237375036 | C | T | 6 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0124t0003g0113others(3): Show | 6 | HG01496.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3071-16G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375036 | ||||||
chr2:237375129 | C | T | 2 | a0070c0139t0005g0202a0071c0138t0001g0166 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3071-109G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375129 | ||||||
chr2:237375306 | A | G | 9 | a0001c0002t0001g0115a0001c0002t0002g0039a0001c0002t0002g0203others(6): Show | 9 | HG00140.hp1 HG01169.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3071-286T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375306 | ||||||
chr2:237375419 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.3071-399G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375419 | ||||||
chr2:237375464 | A | G | 144 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(141): Show | 145 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.3071-444T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375464 | ||||||
chr2:237375573 | G | A | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3071-553C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375573 | ||||||
chr2:237375710 | T | C | 1 | a0001c0004t0001g0228 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3071-690A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375710 | ||||||
chr2:237375791 | C | T | 1 | a0003c0027t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3071-771G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375791 | ||||||
chr2:237375833 | G | A | 9 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3071-813C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375833 | ||||||
chr2:237375839 | G | A | 106 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(103): Show | 107 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.3071-819C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375839 | ||||||
chr2:237375878 | G | A | 95 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(92): Show | 96 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.3071-858C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375878 | ||||||
chr2:237375943 | T | A | 1 | a0005c0017t0003g0280 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3070+829A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237375943 | ||||||
chr2:237376063 | T | C | 1 | a0001c0014t0002g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3070+709A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376063 | ||||||
chr2:237376075 | A | G | 87 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(84): Show | 88 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.3070+697T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376075 | ||||||
chr2:237376104 | G | A | 11 | a0010c0018t0003g0052a0010c0018t0003g0105a0010c0018t0003g0106others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.3070+668C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376104 | ||||||
chr2:237376139 | C | T | 17 | a0001c0014t0002g0129a0001c0074t0001g0169a0003c0026t0001g0182others(14): Show | 17 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.3070+633G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376139 | ||||||
chr2:237376322 | T | G | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3070+450A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376322 | ||||||
chr2:237376327 | A | G | 146 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(143): Show | 147 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.3070+445T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376327 | ||||||
chr2:237376476 | T | A | 2 | a0002c0001t0001g0255a0002c0001t0001g0258 | 2 | HG01071.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.3070+296A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376476 | ||||||
chr2:237376500 | A | G | 4 | a0001c0068t0002g0138a0011c0070t0011g0139a0021c0029t0005g0168others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3070+272T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376500 | ||||||
chr2:237376517 | A | G | 2 | a0001c0068t0002g0138a0011c0070t0011g0139 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3070+255T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 7/43 | chr2 | 237376517 | ||||||
chr2:237377455 | A | G | 5 | a0002c0009t0001g0079a0002c0009t0001g0097a0002c0009t0003g0069others(2): Show | 5 | HG00639.hp2 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2498-111T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377455 | ||||||
chr2:237377575 | A | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2498-231T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377575 | ||||||
chr2:237377589 | A | G | 1 | a0004c0071t0004g0178 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2498-245T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377589 | ||||||
chr2:237377624 | G | A | 1 | a0001c0037t0001g0025 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2498-280C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377624 | ||||||
chr2:237377646 | G | A | 3 | a0003c0026t0001g0182a0003c0026t0001g0186a0011c0069t0002g0187 | 3 | HG02258.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2498-302C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377646 | ||||||
chr2:237377748 | GA | G | 93 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(90): Show | 94 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2498-405delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377748 | ||||||
chr2:237377759 | G | T | 1 | a0041c0136t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2498-415C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377759 | ||||||
chr2:237377931 | C | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2498-587G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377931 | ||||||
chr2:237377970 | T | C | 130 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(127): Show | 131 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2498-626A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237377970 | ||||||
chr2:237378175 | C | T | 4 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2497+461G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237378175 | ||||||
chr2:237378244 | A | G | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2497+392T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237378244 | ||||||
chr2:237378251 | C | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2497+385G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237378251 | ||||||
chr2:237378261 | G | A | 2 | a0005c0111t0003g0118a0013c0097t0002g0107 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2497+375C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 6/43 | chr2 | 237378261 | ||||||
chr2:237379291 | C | T | 2 | a0029c0043t0001g0104a0029c0043t0001g0108 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1898-56G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379291 | ||||||
chr2:237379309 | G | A | 1 | a0013c0053t0004g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1898-74C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379309 | ||||||
chr2:237379344 | T | G | 4 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898-109A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379344 | ||||||
chr2:237379363 | C | T | 1 | a0021c0029t0005g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1898-128G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379363 | ||||||
chr2:237379714 | T | C | 2 | a0029c0043t0001g0104a0029c0043t0001g0108 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1898-479A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379714 | ||||||
chr2:237379753 | T | C | 1 | a0004c0006t0001g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1898-518A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379753 | ||||||
chr2:237379877 | C | T | 1 | a0003c0015t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1898-642G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237379877 | ||||||
chr2:237380025 | C | T | 1 | a0004c0102t0003g0028 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1898-790G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380025 | ||||||
chr2:237380124 | A | AAGAG | 146 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(143): Show | 147 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1897+787_1897+790d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380124 | ||||||
chr2:237380221 | G | A | 1 | a0069c0048t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1897+694C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380221 | ||||||
chr2:237380227 | G | A | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1897+688C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380227 | ||||||
chr2:237380465 | G | C | 9 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1897+450C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380465 | ||||||
chr2:237380537 | G | T | 1 | a0001c0004t0002g0296 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1897+378C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380537 | ||||||
chr2:237380752 | G | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1897+163C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380752 | ||||||
chr2:237380756 | C | A | 1 | a0026c0035t0001g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1897+159G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 5/43 | chr2 | 237380756 | ||||||
chr2:237381516 | T | C | 10 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0042t0004g0170others(7): Show | 10 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-17A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381516 | ||||||
chr2:237381541 | C | T | 1 | a0026c0035t0001g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1313-42G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381541 | ||||||
chr2:237381570 | A | G | 4 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-71T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381570 | ||||||
chr2:237381802 | A | G | 11 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1313-303T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381802 | ||||||
chr2:237381912 | C | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1313-413G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381912 | ||||||
chr2:237381980 | T | C | 1 | a0021c0029t0005g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1313-481A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237381980 | ||||||
chr2:237382006 | C | T | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1313-507G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382006 | ||||||
chr2:237382068 | G | A | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1313-569C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382068 | ||||||
chr2:237382250 | G | C | 11 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(8): Show | 11 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1313-751C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382250 | ||||||
chr2:237382336 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1313-837A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382336 | ||||||
chr2:237382527 | T | C | 36 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(33): Show | 36 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1313-1028A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382527 | ||||||
chr2:237382562 | C | T | 1 | a0001c0079t0002g0062 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1313-1063G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382562 | ||||||
chr2:237382684 | G | A | 1 | a0004c0071t0004g0178 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1313-1185C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382684 | ||||||
chr2:237382821 | T | C | 1 | a0038c0052t0003g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1313-1322A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382821 | ||||||
chr2:237382891 | G | A | 1 | a0001c0059t0004g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1313-1392C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382891 | ||||||
chr2:237382919 | T | C | 1 | a0001c0002t0002g0012 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1313-1420A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382919 | ||||||
chr2:237382938 | C | T | 3 | a0009c0042t0004g0170a0009c0042t0012g0172a0064c0125t0005g0171 | 3 | HG02280.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1313-1439G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237382938 | ||||||
chr2:237383171 | G | A | 2 | a0070c0139t0005g0202a0071c0138t0001g0166 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1313-1672C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383171 | ||||||
chr2:237383284 | G | A | 2 | a0002c0001t0002g0311a0004c0016t0003g0135 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1313-1785C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383284 | ||||||
chr2:237383308 | C | T | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1313-1809G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383308 | ||||||
chr2:237383324 | T | C | 1 | a0002c0009t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1313-1825A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383324 | ||||||
chr2:237383538 | T | C | 2 | a0001c0068t0002g0138a0011c0070t0011g0139 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1313-2039A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383538 | ||||||
chr2:237383555 | G | A | 1 | a0038c0052t0003g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1313-2056C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383555 | ||||||
chr2:237383585 | C | A | 1 | a0001c0002t0003g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1313-2086G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383585 | ||||||
chr2:237383990 | G | A | 4 | a0001c0004t0002g0229a0001c0004t0002g0230a0001c0004t0002g0235others(1): Show | 4 | HG00438.hp1 NA18960.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-2491C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237383990 | ||||||
chr2:237384125 | C | A | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1313-2626G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384125 | ||||||
chr2:237384180 | C | G | 4 | a0001c0002t0001g0175a0003c0033t0001g0174a0005c0012t0004g0117others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-2681G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384180 | ||||||
chr2:237384297 | A | T | 1 | a0016c0019t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1313-2798T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384297 | ||||||
chr2:237384393 | A | G | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1313-2894T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384393 | ||||||
chr2:237384875 | A | G | 2 | a0027c0023t0001g0124a0027c0023t0001g0125 | 2 | HG02129.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1312+2707T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384875 | ||||||
chr2:237384945 | C | A | 2 | a0003c0005t0002g0077a0003c0122t0002g0078 | 2 | NA18941.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1312+2637G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384945 | ||||||
chr2:237384968 | T | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+2614A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237384968 | ||||||
chr2:237385047 | C | T | 2 | a0001c0068t0002g0138a0011c0070t0011g0139 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1312+2535G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385047 | ||||||
chr2:237385258 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+2324A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385258 | ||||||
chr2:237385391 | G | C | 2 | a0001c0040t0001g0130a0001c0040t0001g0239 | 2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1312+2191C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385391 | ||||||
chr2:237385561 | C | G | 3 | a0001c0004t0002g0220a0002c0009t0001g0224a0002c0108t0001g0310 | 3 | HG01109.hp1 HG01192.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1312+2021G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385561 | ||||||
chr2:237385587 | C | T | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312+1995G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385587 | ||||||
chr2:237385613 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1969T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385613 | ||||||
chr2:237385781 | T | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1801A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385781 | ||||||
chr2:237385791 | T | C | 141 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(138): Show | 142 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1312+1791A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385791 | ||||||
chr2:237385926 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1656T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385926 | ||||||
chr2:237385961 | A | G | 36 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(33): Show | 36 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1312+1621T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237385961 | ||||||
chr2:237386012 | C | T | 4 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+1570G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386012 | ||||||
chr2:237386036 | T | C | 2 | a0020c0127t0004g0211a0020c0129t0001g0137 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1312+1546A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386036 | ||||||
chr2:237386041 | T | A | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1541A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386041 | ||||||
chr2:237386058 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1524G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386058 | ||||||
chr2:237386153 | T | G | 36 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(33): Show | 36 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1312+1429A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386153 | ||||||
chr2:237386157 | A | C | 7 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(4): Show | 7 | HG01081.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+1425T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386157 | ||||||
chr2:237386197 | G | A | 12 | a0009c0042t0004g0170a0009c0042t0012g0172a0013c0034t0005g0102others(9): Show | 12 | HG01081.hp2 HG02280.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1312+1385C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386197 | ||||||
chr2:237386354 | G | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1312+1228C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386354 | ||||||
chr2:237386358 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1224A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386358 | ||||||
chr2:237386501 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1081T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386501 | ||||||
chr2:237386503 | C | T | 9 | a0005c0012t0003g0132a0005c0017t0001g0131a0005c0017t0003g0046others(6): Show | 9 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1312+1079G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386503 | ||||||
chr2:237386539 | G | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+1043C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386539 | ||||||
chr2:237386734 | C | G | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1312+848G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386734 | ||||||
chr2:237386907 | G | GT | 11 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312+674dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386907 | ||||||
chr2:237386967 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+615A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237386967 | ||||||
chr2:237387020 | A | T | 1 | a0001c0076t0003g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1312+562T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387020 | ||||||
chr2:237387042 | A | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+540T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387042 | ||||||
chr2:237387058 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+524T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387058 | ||||||
chr2:237387192 | T | C | 2 | a0040c0135t0008g0188a0069c0048t0001g0051 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1312+390A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387192 | ||||||
chr2:237387208 | A | G | 143 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(140): Show | 144 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1312+374T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387208 | ||||||
chr2:237387288 | C | T | 3 | a0025c0114t0001g0121a0025c0115t0004g0120a0055c0116t0002g0177 | 3 | HG02886.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1312+294G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387288 | ||||||
chr2:237387322 | G | T | 1 | a0013c0053t0004g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1312+260C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387322 | ||||||
chr2:237387364 | T | C | 2 | a0001c0040t0001g0130a0001c0040t0001g0239 | 2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1312+218A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387364 | ||||||
chr2:237387489 | G | A | 1 | a0001c0002t0001g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1312+93C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 4/43 | chr2 | 237387489 | ||||||
chr2:237388469 | G | C | 3 | a0009c0126t0004g0179a0029c0043t0001g0104a0029c0043t0001g0108 | 3 | HG02647.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.710-285C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388469 | ||||||
chr2:237388684 | C | T | 5 | a0001c0002t0001g0150a0001c0002t0004g0008a0001c0014t0002g0114others(2): Show | 5 | HG01346.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.710-500G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388684 | ||||||
chr2:237388691 | G | T | 2 | a0002c0022t0002g0021a0002c0022t0002g0128 | 2 | NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.710-507C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388691 | ||||||
chr2:237388799 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-615A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388799 | ||||||
chr2:237388849 | G | A | 1 | a0001c0117t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.710-665C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388849 | ||||||
chr2:237388890 | C | G | 1 | a0021c0029t0005g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.710-706G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388890 | ||||||
chr2:237388948 | A | G | 1 | a0070c0139t0005g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.710-764T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237388948 | ||||||
chr2:237389212 | A | C | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.710-1028T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237389212 | ||||||
chr2:237389299 | A | G | 2 | a0004c0003t0003g0068a0004c0003t0003g0075 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.710-1115T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237389299 | ||||||
chr2:237389442 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-1258T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237389442 | ||||||
chr2:237389565 | A | G | 1 | a0001c0004t0002g0296 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.710-1381T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237389565 | ||||||
chr2:237389713 | C | T | 1 | a0058c0098t0001g0101 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.710-1529G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237389713 | ||||||
chr2:237390036 | A | T | 2 | a0001c0002t0002g0043a0005c0017t0003g0280 | 2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.710-1852T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390036 | ||||||
chr2:237390091 | C | T | 1 | a0003c0005t0001g0317 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.710-1907G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390091 | ||||||
chr2:237390186 | C | T | 3 | a0001c0074t0001g0169a0003c0075t0001g0192a0053c0073t0008g0304 | 3 | HG02258.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.710-2002G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390186 | ||||||
chr2:237390260 | A | C | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.710-2076T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390260 | ||||||
chr2:237390306 | G | A | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-2122C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390306 | ||||||
chr2:237390349 | G | A | 2 | a0014c0021t0002g0266a0014c0021t0002g0282 | 2 | NA18971.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.710-2165C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390349 | ||||||
chr2:237390378 | T | C | 3 | a0001c0002t0003g0151a0002c0001t0001g0255a0002c0001t0001g0258 | 3 | HG01071.hp1 HG01261.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.710-2194A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390378 | ||||||
chr2:237390479 | C | T | 12 | a0001c0014t0002g0129a0003c0026t0001g0182a0003c0026t0001g0186others(9): Show | 12 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.710-2295G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390479 | ||||||
chr2:237390546 | G | A | 73 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(70): Show | 74 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.710-2362C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390546 | ||||||
chr2:237390551 | G | GT | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-2368dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390551 | ||||||
chr2:237390587 | G | A | 140 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(137): Show | 141 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.710-2403C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390587 | ||||||
chr2:237390643 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-2459A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390643 | ||||||
chr2:237390775 | T | G | 26 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(23): Show | 26 | HG00408.hp2 HG01167.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-2591A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390775 | ||||||
chr2:237390894 | A | G | 2 | a0036c0137t0003g0081a0065c0123t0003g0109 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.710-2710T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390894 | ||||||
chr2:237390988 | G | A | 11 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.710-2804C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237390988 | ||||||
chr2:237391199 | G | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-3015C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391199 | ||||||
chr2:237391215 | C | T | 36 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(33): Show | 36 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.710-3031G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391215 | ||||||
chr2:237391504 | C | CTGTT | 31 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0002g0012others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.709+3079_709+3082d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391504 | ||||||
chr2:237391504 | CTGTT | C | 74 | a0001c0002t0001g0092a0001c0002t0001g0268a0001c0002t0001g0269others(71): Show | 75 | HG00558.hp2 HG00639.hp1 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.709+3079_709+3082d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391504 | ||||||
chr2:237391504 | CTGTTTGT others(1): Show |
C | 72 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(69): Show | 73 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.709+3075_709+3082d others(10): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391504 | ||||||
chr2:237391504 | CTGTTTGT others(5): Show |
C | 5 | a0003c0005t0001g0018a0013c0097t0002g0107a0025c0114t0001g0121others(2): Show | 5 | HG01978.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+3071_709+3082d others(14): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391504 | ||||||
chr2:237391504 | CTGTTTGT others(9): Show |
C | 12 | a0003c0005t0007g0023a0009c0126t0004g0179a0010c0018t0003g0052others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.709+3067_709+3082d others(18): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391504 | ||||||
chr2:237391554 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+3033G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391554 | ||||||
chr2:237391771 | C | T | 1 | a0042c0060t0001g0035 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.709+2816G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391771 | ||||||
chr2:237391850 | G | C | 1 | a0033c0141t0002g0026 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.709+2737C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391850 | ||||||
chr2:237391907 | G | C | 26 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(23): Show | 26 | HG00408.hp2 HG01167.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.709+2680C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391907 | ||||||
chr2:237391918 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+2669T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237391918 | ||||||
chr2:237392147 | C | T | 1 | a0001c0079t0002g0062 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.709+2440G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392147 | ||||||
chr2:237392209 | A | G | 2 | a0027c0023t0001g0124a0027c0023t0001g0125 | 2 | HG02129.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.709+2378T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392209 | ||||||
chr2:237392376 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+2211G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392376 | ||||||
chr2:237392411 | C | T | 2 | a0004c0003t0003g0068a0004c0003t0003g0075 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.709+2176G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392411 | ||||||
chr2:237392541 | G | A | 242 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(239): Show | 244 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.709+2046C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392541 | ||||||
chr2:237392722 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+1865T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392722 | ||||||
chr2:237392751 | G | A | 7 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(4): Show | 7 | HG01081.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.709+1836C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392751 | ||||||
chr2:237392817 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+1770G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392817 | ||||||
chr2:237392848 | C | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+1739G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392848 | ||||||
chr2:237392909 | G | A | 1 | a0005c0111t0003g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.709+1678C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237392909 | ||||||
chr2:237393018 | C | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.709+1569G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393018 | ||||||
chr2:237393052 | A | C | 10 | a0013c0034t0005g0102a0013c0034t0005g0103a0013c0097t0002g0107others(7): Show | 10 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.709+1535T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393052 | ||||||
chr2:237393300 | C | A | 2 | a0036c0137t0003g0081a0065c0123t0003g0109 | 2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.709+1287G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393300 | ||||||
chr2:237393569 | C | A | 5 | a0001c0014t0002g0129a0003c0027t0001g0149a0003c0027t0003g0119others(2): Show | 5 | HG01358.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.709+1018G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393569 | ||||||
chr2:237393616 | A | T | 4 | a0001c0014t0001g0147a0001c0084t0001g0195a0003c0031t0004g0194others(1): Show | 4 | HG00642.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.709+971T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393616 | ||||||
chr2:237393670 | C | T | 9 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.709+917G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393670 | ||||||
chr2:237393698 | T | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+889A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393698 | ||||||
chr2:237393904 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+683G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237393904 | ||||||
chr2:237394063 | G | T | 1 | a0004c0006t0002g0305 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.709+524C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394063 | ||||||
chr2:237394178 | G | A | 2 | a0029c0043t0001g0104a0029c0043t0001g0108 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.709+409C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394178 | ||||||
chr2:237394365 | A | T | 1 | a0002c0001t0002g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.709+222T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394365 | ||||||
chr2:237394381 | A | G | 1 | a0068c0049t0002g0279 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.709+206T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394381 | ||||||
chr2:237394491 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.709+96T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394491 | ||||||
chr2:237394495 | G | A | 3 | a0004c0003t0002g0208a0004c0120t0002g0024a0004c0140t0002g0205 | 3 | NA18941.hp2 NA18952.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.709+92C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 3/43 | chr2 | 237394495 | ||||||
chr2:237395263 | A | G | 143 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(140): Show | 144 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.92-59T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395263 | ||||||
chr2:237395275 | C | T | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-71G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395275 | ||||||
chr2:237395303 | G | T | 17 | a0001c0014t0002g0129a0001c0074t0001g0169a0003c0026t0001g0182others(14): Show | 17 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.92-99C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395303 | ||||||
chr2:237395474 | A | G | 1 | a0019c0044t0004g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.92-270T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395474 | ||||||
chr2:237395475 | C | G | 1 | a0004c0016t0003g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.92-271G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395475 | ||||||
chr2:237395621 | C | T | 15 | a0001c0014t0002g0129a0001c0074t0001g0169a0003c0026t0001g0182others(12): Show | 15 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.92-417G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395621 | ||||||
chr2:237395637 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-433T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395637 | ||||||
chr2:237395745 | T | A | 11 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(8): Show | 11 | HG01884.hp2 HG02257.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-541A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395745 | ||||||
chr2:237395851 | A | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92-647T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395851 | ||||||
chr2:237395876 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-672T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395876 | ||||||
chr2:237395923 | T | C | 1 | a0003c0118t0002g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.92-719A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237395923 | ||||||
chr2:237396011 | G | A | 3 | a0003c0026t0001g0182a0003c0026t0001g0186a0011c0069t0002g0187 | 3 | HG02258.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.91+716C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396011 | ||||||
chr2:237396084 | G | A | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+643C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396084 | ||||||
chr2:237396375 | A | G | 12 | a0001c0014t0002g0129a0003c0026t0001g0182a0003c0026t0001g0186others(9): Show | 12 | HG01358.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.91+352T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396375 | ||||||
chr2:237396478 | C | G | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.91+249G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396478 | ||||||
chr2:237396533 | G | T | 9 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+194C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396533 | ||||||
chr2:237396568 | C | T | 242 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(239): Show | 244 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.91+159G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396568 | ||||||
chr2:237396581 | G | A | 2 | a0030c0131t0001g0284a0030c0132t0002g0283 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.91+146C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396581 | ||||||
chr2:237396625 | T | C | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+102A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396625 | ||||||
chr2:237396712 | G | A | 2 | a0004c0006t0003g0013a0012c0013t0002g0014 | 2 | NA18955.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.91+15C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 2/43 | chr2 | 237396712 | ||||||
chr2:237396930 | G | A | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-30-83C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237396930 | ||||||
chr2:237397017 | T | TGATA | 111 | a0001c0002t0001g0036a0001c0002t0001g0268a0001c0002t0001g0269others(108): Show | 113 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-30-174_-30-171dup others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397017 | ||||||
chr2:237397017 | T | TGATAGAT others(1): Show |
121 | a0001c0002t0001g0150a0001c0002t0001g0287a0001c0002t0002g0039others(118): Show | 122 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.-30-178_-30-171dup others(8): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397017 | ||||||
chr2:237397017 | T | TGATAGAT others(5): Show |
51 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0115others(48): Show | 51 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-30-182_-30-171dup others(12): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397017 | ||||||
chr2:237397017 | T | TGATAGAT others(9): Show |
12 | a0001c0002t0002g0286a0001c0002t0004g0008a0002c0009t0002g0223others(9): Show | 12 | HG00609.hp2 HG00741.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-186_-30-171dup others(16): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397017 | ||||||
chr2:237397017 | TGATA | T | 6 | a0001c0004t0002g0220a0002c0001t0001g0243a0002c0001t0002g0312others(3): Show | 6 | HG02027.hp1 HG02132.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-174_-30-171del others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397017 | ||||||
chr2:237397058 | A | G | 1 | a0002c0001t0002g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-30-211T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397058 | ||||||
chr2:237397060 | A | T | 1 | a0002c0001t0002g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-30-213T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397060 | ||||||
chr2:237397082 | C | T | 141 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(138): Show | 142 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-30-235G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397082 | ||||||
chr2:237397139 | A | AGAAGG | 37 | a0003c0039t0001g0176a0003c0039t0003g0163a0009c0126t0004g0179others(34): Show | 37 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.-30-297_-30-293dup others(5): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397139 | ||||||
chr2:237397144 | GGAAGGGA others(3): Show |
G | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-307_-30-298del others(10): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397144 | ||||||
chr2:237397186 | TAAGGGAA others(48): Show |
T | 1 | a0002c0001t0001g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-30-394_-30-340del others(55): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397186 | ||||||
chr2:237397245 | G | A | 9 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-398C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397245 | ||||||
chr2:237397401 | A | G | 39 | a0003c0039t0001g0176a0003c0039t0003g0163a0009c0126t0004g0179others(36): Show | 39 | HG00408.hp2 HG01081.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-30-554T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397401 | ||||||
chr2:237397406 | G | GGAGAGAA others(13): Show |
1 | a0004c0003t0003g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-30-579_-30-560dup others(20): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397406 | ||||||
chr2:237397730 | A | T | 3 | a0007c0030t0001g0048a0007c0030t0001g0245a0023c0032t0001g0001 | 4 | HG00438.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-883T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237397730 | ||||||
chr2:237398022 | T | C | 1 | a0059c0055t0004g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-30-1175A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398022 | ||||||
chr2:237398037 | C | G | 5 | a0001c0059t0004g0222a0002c0009t0002g0223a0003c0005t0001g0018others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-1190G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398037 | ||||||
chr2:237398146 | A | G | 1 | a0052c0112t0002g0143 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-30-1299T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398146 | ||||||
chr2:237398213 | T | A | 5 | a0001c0014t0002g0129a0003c0027t0001g0149a0003c0027t0003g0119others(2): Show | 5 | HG01358.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-1366A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398213 | ||||||
chr2:237398219 | T | C | 39 | a0003c0039t0001g0176a0003c0039t0003g0163a0009c0126t0004g0179others(36): Show | 39 | HG00408.hp2 HG01081.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-30-1372A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398219 | ||||||
chr2:237398295 | C | T | 3 | a0002c0001t0001g0243a0002c0001t0001g0244a0003c0033t0003g0029 | 3 | HG02027.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-30-1448G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398295 | ||||||
chr2:237398311 | G | A | 2 | a0002c0001t0001g0259a0002c0001t0001g0298 | 2 | HG01123.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-30-1464C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398311 | ||||||
chr2:237398490 | T | G | 1 | a0044c0062t0005g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-1643A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398490 | ||||||
chr2:237398563 | A | G | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-1716T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398563 | ||||||
chr2:237398597 | A | G | 1 | a0003c0082t0002g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-30-1750T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398597 | ||||||
chr2:237398598 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-30-1751C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398598 | ||||||
chr2:237398699 | C | T | 1 | a0026c0035t0002g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-30-1852G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398699 | ||||||
chr2:237398775 | G | T | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-1928C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398775 | ||||||
chr2:237398843 | T | A | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-1996A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237398843 | ||||||
chr2:237399061 | T | A | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-2214A>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399061 | ||||||
chr2:237399144 | A | G | 1 | a0002c0001t0009g0004 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-30-2297T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399144 | ||||||
chr2:237399156 | C | T | 1 | a0001c0014t0002g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-30-2309G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399156 | ||||||
chr2:237399523 | G | A | 1 | a0041c0136t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30-2676C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399523 | ||||||
chr2:237399587 | G | A | 8 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-2740C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399587 | ||||||
chr2:237399868 | G | A | 7 | a0013c0034t0005g0102a0013c0034t0005g0103a0026c0035t0001g0189others(4): Show | 7 | HG01081.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30-3021C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399868 | ||||||
chr2:237399963 | C | T | 2 | a0019c0044t0002g0066a0019c0044t0004g0221 | 2 | HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-30-3116G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237399963 | ||||||
chr2:237400027 | C | T | 8 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-3180G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400027 | ||||||
chr2:237400232 | A | T | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-3385T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400232 | ||||||
chr2:237400233 | T | C | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-3386A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400233 | ||||||
chr2:237400234 | C | A | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-3387G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400234 | ||||||
chr2:237400371 | A | G | 1 | a0001c0004t0002g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-30-3524T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400371 | ||||||
chr2:237400496 | A | T | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-3649T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400496 | ||||||
chr2:237400642 | A | G | 1 | a0020c0127t0004g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30-3795T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400642 | ||||||
chr2:237400712 | C | T | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-30-3865G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400712 | ||||||
chr2:237400848 | A | T | 1 | a0009c0042t0012g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30-4001T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237400848 | ||||||
chr2:237401069 | G | A | 1 | a0001c0014t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30-4222C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401069 | ||||||
chr2:237401239 | G | A | 91 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(88): Show | 92 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-30-4392C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401239 | ||||||
chr2:237401492 | A | C | 1 | a0028c0025t0002g0053 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-30-4645T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401492 | ||||||
chr2:237401563 | C | T | 1 | a0003c0005t0003g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-30-4716G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401563 | ||||||
chr2:237401575 | C | A | 1 | a0009c0126t0004g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30-4728G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401575 | ||||||
chr2:237401690 | A | AT | 9 | a0001c0002t0002g0146a0002c0001t0002g0241a0004c0006t0003g0013others(6): Show | 9 | HG00558.hp2 NA18939.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-4844dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401690 | ||||||
chr2:237401690 | AT | A | 79 | a0001c0002t0001g0287a0001c0004t0001g0153a0001c0004t0001g0228others(76): Show | 80 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-30-4844delA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401690 | ||||||
chr2:237401716 | C | A | 38 | a0003c0039t0001g0176a0003c0039t0003g0163a0009c0126t0004g0179others(35): Show | 38 | HG00408.hp2 HG01081.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30-4869G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401716 | ||||||
chr2:237401792 | C | T | 1 | a0001c0004t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-30-4945G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401792 | ||||||
chr2:237401964 | C | T | 2 | a0001c0076t0003g0219a0038c0052t0003g0082 | 2 | HG02135.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-30-5117G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401964 | ||||||
chr2:237401980 | C | T | 1 | a0007c0030t0001g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-30-5133G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237401980 | ||||||
chr2:237402233 | G | A | 1 | a0006c0007t0002g0215 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-30-5386C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402233 | ||||||
chr2:237402655 | T | C | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-5808A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402655 | ||||||
chr2:237402765 | G | A | 10 | a0009c0041t0002g0236a0009c0041t0002g0303a0009c0042t0004g0170others(7): Show | 10 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-5918C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402765 | ||||||
chr2:237402787 | G | C | 1 | a0001c0130t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30-5940C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402787 | ||||||
chr2:237402856 | C | T | 3 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167 | 3 | HG01884.hp2 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-30-6009G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402856 | ||||||
chr2:237402936 | G | A | 1 | a0045c0067t0002g0288 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-30-6089C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402936 | ||||||
chr2:237402969 | C | T | 142 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(139): Show | 142 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-30-6122G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237402969 | ||||||
chr2:237403001 | G | A | 14 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(11): Show | 14 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30-6154C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403001 | ||||||
chr2:237403027 | T | C | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-6180A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403027 | ||||||
chr2:237403097 | T | C | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-6250A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403097 | ||||||
chr2:237403238 | A | G | 1 | a0004c0016t0001g0242 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-30-6391T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403238 | ||||||
chr2:237403631 | C | G | 317 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(314): Show | 320 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-30-6784G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403631 | ||||||
chr2:237403681 | T | C | 4 | a0013c0053t0004g0093a0059c0055t0004g0162a0060c0054t0004g0167others(1): Show | 4 | HG01884.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-6834A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403681 | ||||||
chr2:237403699 | T | G | 1 | a0071c0138t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-30-6852A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403699 | ||||||
chr2:237403867 | C | T | 1 | a0002c0001t0002g0241 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-30-7020G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403867 | ||||||
chr2:237403968 | TA | T | 6 | a0001c0014t0002g0200a0001c0040t0001g0130a0001c0040t0001g0239others(3): Show | 6 | HG02486.hp1 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-7122delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403968 | ||||||
chr2:237403975 | A | T | 1 | a0071c0138t0001g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-30-7128T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237403975 | ||||||
chr2:237404298 | G | C | 8 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-7451C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237404298 | ||||||
chr2:237404453 | A | C | 1 | a0003c0026t0001g0182 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-30-7606T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237404453 | ||||||
chr2:237404522 | G | A | 2 | a0016c0019t0002g0302a0028c0025t0002g0213 | 2 | NA18959.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-30-7675C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237404522 | ||||||
chr2:237404553 | A | G | 36 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(33): Show | 36 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.-30-7706T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237404553 | ||||||
chr2:237404909 | A | C | 1 | a0021c0029t0005g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30-8062T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237404909 | ||||||
chr2:237405027 | TTATCCAG others(4): Show |
T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-8191_-30-8181d others(13): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405027 | ||||||
chr2:237405133 | G | A | 1 | a0002c0001t0002g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-30-8286C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405133 | ||||||
chr2:237405178 | C | A | 4 | a0002c0001t0001g0136a0002c0001t0001g0290a0002c0001t0001g0316others(1): Show | 4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-8331G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405178 | ||||||
chr2:237405179 | T | G | 4 | a0002c0001t0001g0136a0002c0001t0001g0290a0002c0001t0001g0316others(1): Show | 4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-8332A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405179 | ||||||
chr2:237405240 | G | A | 2 | a0001c0068t0002g0138a0011c0070t0011g0139 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-30-8393C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405240 | ||||||
chr2:237405355 | T | TA | 4 | a0007c0011t0001g0291a0007c0011t0001g0292a0008c0010t0001g0089others(1): Show | 4 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-8509dupT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405355 | ||||||
chr2:237405434 | A | C | 15 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(12): Show | 15 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+8519T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405434 | ||||||
chr2:237405684 | C | G | 142 | a0001c0004t0001g0153a0001c0004t0001g0228a0001c0004t0002g0067others(139): Show | 143 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-31+8269G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405684 | ||||||
chr2:237405770 | G | A | 14 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(11): Show | 14 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+8183C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405770 | ||||||
chr2:237405985 | A | G | 1 | a0004c0003t0003g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-31+7968T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237405985 | ||||||
chr2:237406058 | C | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+7895G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406058 | ||||||
chr2:237406082 | C | A | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+7871G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406082 | ||||||
chr2:237406133 | C | T | 34 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(31): Show | 34 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.-31+7820G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406133 | ||||||
chr2:237406256 | T | G | 1 | a0021c0029t0005g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31+7697A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406256 | ||||||
chr2:237406277 | A | G | 1 | a0011c0091t0003g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-31+7676T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406277 | ||||||
chr2:237406393 | C | T | 2 | a0001c0068t0002g0138a0011c0070t0011g0139 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-31+7560G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406393 | ||||||
chr2:237406478 | G | A | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+7475C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406478 | ||||||
chr2:237406511 | G | A | 2 | a0002c0001t0002g0294a0013c0097t0002g0107 | 2 | HG01175.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-31+7442C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406511 | ||||||
chr2:237406522 | C | T | 14 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(11): Show | 14 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+7431G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406522 | ||||||
chr2:237406553 | T | C | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+7400A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406553 | ||||||
chr2:237406611 | C | T | 14 | a0016c0019t0001g0216a0016c0019t0002g0212a0016c0019t0002g0302others(11): Show | 14 | HG00408.hp2 HG01167.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+7342G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406611 | ||||||
chr2:237406612 | G | A | 21 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(18): Show | 21 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+7341C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406612 | ||||||
chr2:237406658 | C | T | 35 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(32): Show | 35 | HG00408.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-31+7295G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406658 | ||||||
chr2:237406692 | C | T | 3 | a0007c0011t0001g0309a0008c0010t0001g0217a0008c0010t0001g0218 | 3 | HG01074.hp1 HG01433.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-31+7261G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406692 | ||||||
chr2:237406739 | G | C | 1 | a0016c0019t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-31+7214C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406739 | ||||||
chr2:237406832 | C | T | 1 | a0013c0097t0002g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+7121G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406832 | ||||||
chr2:237406907 | C | CT | 34 | a0001c0002t0002g0308a0001c0074t0001g0169a0001c0079t0002g0062others(31): Show | 34 | HG00408.hp2 HG01167.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.-31+7045dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406907 | ||||||
chr2:237406907 | C | CTT | 11 | a0001c0068t0002g0138a0003c0039t0001g0176a0003c0039t0003g0163others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+7044_-31+7045d others(4): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406907 | ||||||
chr2:237406907 | C | CTTT | 10 | a0009c0126t0004g0179a0010c0018t0003g0052a0010c0018t0003g0105others(7): Show | 10 | HG02647.hp1 HG02647.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+7043_-31+7045d others(5): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406907 | ||||||
chr2:237406959 | G | T | 2 | a0005c0008t0005g0180a0005c0008t0005g0181 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-31+6994C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237406959 | ||||||
chr2:237407071 | G | A | 1 | a0002c0001t0002g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-31+6882C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407071 | ||||||
chr2:237407281 | G | C | 1 | a0001c0002t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-31+6672C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407281 | ||||||
chr2:237407366 | G | A | 26 | a0001c0002t0002g0146a0001c0014t0001g0147a0001c0084t0001g0195others(23): Show | 26 | HG00642.hp1 HG01081.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-31+6587C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407366 | ||||||
chr2:237407450 | A | G | 6 | a0001c0002t0003g0157a0001c0002t0003g0158a0001c0002t0003g0159others(3): Show | 6 | HG02074.hp1 HG02083.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+6503T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407450 | ||||||
chr2:237407494 | C | T | 25 | a0001c0002t0002g0146a0001c0002t0002g0297a0001c0014t0001g0147others(22): Show | 25 | HG00642.hp1 HG01081.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-31+6459G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407494 | ||||||
chr2:237407637 | G | C | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-31+6316C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407637 | ||||||
chr2:237407734 | C | T | 1 | a0004c0140t0002g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-31+6219G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407734 | ||||||
chr2:237407739 | C | T | 13 | a0001c0002t0002g0146a0001c0014t0001g0147a0001c0087t0002g0148others(10): Show | 13 | HG01081.hp1 HG01099.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6214G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237407739 | ||||||
chr2:237408008 | C | G | 1 | a0001c0002t0002g0012 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-31+5945G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408008 | ||||||
chr2:237408190 | TA | T | 9 | a0010c0018t0003g0105a0010c0018t0003g0106a0013c0034t0005g0102others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+5762delT | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408190 | ||||||
chr2:237408197 | T | C | 2 | a0003c0039t0001g0176a0003c0039t0003g0163 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-31+5756A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408197 | ||||||
chr2:237408267 | G | A | 1 | a0020c0129t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31+5686C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408267 | ||||||
chr2:237408310 | T | C | 129 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0287others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-31+5643A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408310 | ||||||
chr2:237408347 | C | T | 2 | a0006c0064t0003g0047a0007c0030t0001g0048 | 2 | NA18942.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-31+5606G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408347 | ||||||
chr2:237408366 | C | T | 7 | a0001c0004t0001g0153a0003c0015t0003g0209a0004c0003t0002g0208others(4): Show | 7 | HG00408.hp1 HG02071.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+5587G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408366 | ||||||
chr2:237408432 | C | G | 4 | a0001c0086t0003g0306a0004c0140t0002g0205a0016c0019t0002g0302others(1): Show | 4 | NA18952.hp1 NA18959.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+5521G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408432 | ||||||
chr2:237408438 | G | A | 1 | a0002c0109t0002g0140 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-31+5515C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408438 | ||||||
chr2:237408477 | C | T | 3 | a0001c0002t0002g0203a0001c0002t0002g0204a0003c0082t0002g0197 | 3 | HG00140.hp1 HG01243.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-31+5476G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408477 | ||||||
chr2:237408603 | G | A | 1 | a0055c0116t0002g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-31+5350C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408603 | ||||||
chr2:237408738 | T | C | 1 | a0001c0087t0002g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-31+5215A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408738 | ||||||
chr2:237408750 | A | T | 306 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(303): Show | 309 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-31+5203T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408750 | ||||||
chr2:237408844 | G | T | 1 | a0035c0047t0002g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-31+5109C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408844 | ||||||
chr2:237408979 | C | T | 1 | a0009c0126t0004g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-31+4974G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237408979 | ||||||
chr2:237409080 | G | A | 1 | a0001c0004t0002g0296 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-31+4873C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409080 | ||||||
chr2:237409152 | C | T | 2 | a0004c0006t0001g0094a0004c0016t0003g0095 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-31+4801G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409152 | ||||||
chr2:237409177 | G | C | 2 | a0024c0038t0002g0110a0024c0038t0002g0111 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-31+4776C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409177 | ||||||
chr2:237409179 | A | C | 171 | a0001c0002t0001g0175a0001c0002t0001g0268a0001c0002t0001g0269others(168): Show | 173 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-31+4774T>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409179 | ||||||
chr2:237409241 | G | A | 1 | a0016c0019t0002g0302 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-31+4712C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409241 | ||||||
chr2:237409287 | CTTTT | C | 9 | a0003c0026t0001g0182a0003c0026t0001g0186a0003c0028t0004g0183others(6): Show | 9 | HG02257.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+4662_-31+4665d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409287 | ||||||
chr2:237409304 | T | C | 17 | a0001c0002t0001g0115a0001c0014t0002g0114a0003c0026t0001g0182others(14): Show | 17 | HG01346.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31+4649A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409304 | ||||||
chr2:237409329 | G | A | 1 | a0004c0003t0003g0091 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-31+4624C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409329 | ||||||
chr2:237409406 | A | T | 108 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(105): Show | 109 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.-31+4547T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409406 | ||||||
chr2:237409416 | A | G | 128 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0287others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-31+4537T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409416 | ||||||
chr2:237409528 | G | GT | 11 | a0001c0002t0001g0150a0001c0002t0002g0146a0001c0002t0003g0151others(8): Show | 11 | HG01081.hp1 HG01099.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+4424dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409528 | ||||||
chr2:237409533 | T | TTTTG | 14 | a0003c0121t0003g0191a0010c0018t0003g0105a0010c0018t0003g0106others(11): Show | 14 | HG01358.hp1 HG02145.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+4416_-31+4419d others(6): Show |
COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409533 | ||||||
chr2:237409537 | G | T | 2 | a0005c0090t0003g0122a0026c0035t0002g0164 | 2 | HG01081.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-31+4416C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409537 | ||||||
chr2:237409672 | G | A | 97 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(94): Show | 98 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.-31+4281C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409672 | ||||||
chr2:237409714 | G | A | 2 | a0001c0002t0002g0318a0003c0005t0001g0317 | 2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-31+4239C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409714 | ||||||
chr2:237409727 | G | A | 1 | a0005c0017t0003g0046 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-31+4226C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409727 | ||||||
chr2:237409730 | C | G | 1 | a0005c0012t0004g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-31+4223G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409730 | ||||||
chr2:237409851 | C | T | 1 | a0001c0134t0001g0011 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-31+4102G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237409851 | ||||||
chr2:237410167 | C | G | 4 | a0001c0068t0002g0138a0011c0070t0011g0139a0025c0114t0001g0121others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+3786G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410167 | ||||||
chr2:237410238 | G | A | 1 | a0057c0099t0004g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-31+3715C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410238 | ||||||
chr2:237410300 | C | CT | 45 | a0001c0002t0001g0036a0001c0002t0002g0012a0001c0002t0002g0039others(42): Show | 46 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.-31+3652dupA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410300 | ||||||
chr2:237410300 | CT | C | 15 | a0001c0002t0001g0092a0001c0002t0001g0150a0001c0002t0002g0297others(12): Show | 15 | HG01496.hp1 HG02109.hp2 HG02735.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+3652delA | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410300 | ||||||
chr2:237410343 | G | A | 188 | a0001c0002t0001g0115a0001c0002t0001g0175a0001c0002t0001g0268others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-31+3610C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410343 | ||||||
chr2:237410429 | G | A | 1 | a0009c0041t0002g0303 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-31+3524C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410429 | ||||||
chr2:237410482 | T | G | 2 | a0004c0006t0001g0094a0004c0016t0003g0095 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-31+3471A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410482 | ||||||
chr2:237410524 | C | G | 1 | a0039c0128t0004g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31+3429G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410524 | ||||||
chr2:237410538 | C | G | 1 | a0003c0015t0003g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-31+3415G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410538 | ||||||
chr2:237410615 | C | A | 8 | a0010c0018t0003g0105a0010c0018t0003g0106a0013c0034t0005g0102others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-31+3338G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410615 | ||||||
chr2:237410791 | T | G | 1 | a0002c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-31+3162A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237410791 | ||||||
chr2:237411069 | G | A | 127 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0287others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-31+2884C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411069 | ||||||
chr2:237411174 | C | T | 3 | a0013c0034t0005g0102a0013c0034t0005g0103a0058c0098t0001g0101 | 3 | HG02647.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-31+2779G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411174 | ||||||
chr2:237411175 | C | T | 1 | a0003c0082t0002g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-31+2778G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411175 | ||||||
chr2:237411226 | A | G | 1 | a0039c0128t0004g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-31+2727T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411226 | ||||||
chr2:237411359 | T | G | 1 | a0002c0109t0002g0140 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-31+2594A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411359 | ||||||
chr2:237411395 | C | T | 3 | a0001c0084t0001g0195a0003c0031t0004g0194a0003c0031t0004g0196 | 3 | HG00642.hp1 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-31+2558G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411395 | ||||||
chr2:237411396 | G | A | 1 | a0053c0073t0008g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-31+2557C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411396 | ||||||
chr2:237411535 | C | T | 1 | a0002c0001t0001g0193 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-31+2418G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411535 | ||||||
chr2:237411633 | G | A | 1 | a0051c0083t0001g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-31+2320C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411633 | ||||||
chr2:237411679 | G | C | 1 | a0048c0081t0002g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+2274C>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411679 | ||||||
chr2:237411728 | T | G | 128 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0287others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-31+2225A>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411728 | ||||||
chr2:237411754 | G | A | 1 | a0004c0006t0002g0305 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-31+2199C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411754 | ||||||
chr2:237411837 | T | C | 1 | a0003c0075t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-31+2116A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411837 | ||||||
chr2:237411894 | A | T | 11 | a0001c0002t0001g0150a0001c0002t0002g0146a0001c0002t0003g0151others(8): Show | 11 | HG01081.hp1 HG01099.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+2059T>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237411894 | ||||||
chr2:237412137 | C | G | 307 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(304): Show | 310 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.-31+1816G>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412137 | ||||||
chr2:237412290 | G | A | 1 | a0057c0099t0004g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-31+1663C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412290 | ||||||
chr2:237412338 | G | A | 5 | a0001c0002t0001g0115a0001c0014t0002g0114a0003c0089t0001g0116others(2): Show | 5 | HG01346.hp1 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+1615C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412338 | ||||||
chr2:237412435 | A | G | 2 | a0001c0002t0004g0008a0021c0029t0005g0009 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-31+1518T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412435 | ||||||
chr2:237412569 | C | A | 128 | a0001c0002t0001g0268a0001c0002t0001g0269a0001c0002t0001g0287others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-31+1384G>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412569 | ||||||
chr2:237412623 | C | T | 1 | a0059c0055t0004g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-31+1330G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412623 | ||||||
chr2:237412674 | T | C | 306 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(303): Show | 309 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-31+1279A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412674 | ||||||
chr2:237412764 | C | T | 6 | a0001c0002t0003g0157a0001c0002t0003g0158a0001c0002t0003g0159others(3): Show | 6 | HG02074.hp1 HG02083.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+1189G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412764 | ||||||
chr2:237412806 | T | C | 1 | a0002c0009t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-31+1147A>G | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412806 | ||||||
chr2:237412814 | G | T | 1 | a0005c0012t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-31+1139C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412814 | ||||||
chr2:237412847 | C | T | 3 | a0001c0004t0001g0153a0006c0096t0002g0155a0015c0036t0001g0154 | 3 | HG00408.hp1 NA18959.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-31+1106G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412847 | ||||||
chr2:237412851 | G | A | 109 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(106): Show | 110 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-31+1102C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412851 | ||||||
chr2:237412880 | G | A | 1 | a0001c0086t0003g0306 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-31+1073C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412880 | ||||||
chr2:237412947 | G | A | 159 | a0001c0002t0001g0175a0001c0002t0001g0268a0001c0002t0001g0269others(156): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-31+1006C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237412947 | ||||||
chr2:237413033 | C | T | 294 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.-31+920G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413033 | ||||||
chr2:237413044 | G | T | 95 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(92): Show | 96 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.-31+909C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413044 | ||||||
chr2:237413196 | G | A | 7 | a0001c0002t0001g0115a0001c0014t0002g0114a0003c0089t0001g0116others(4): Show | 7 | HG01346.hp1 HG02886.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+757C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413196 | ||||||
chr2:237413376 | G | A | 9 | a0010c0018t0003g0105a0010c0018t0003g0106a0013c0034t0005g0102others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+577C>T | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413376 | ||||||
chr2:237413389 | G | T | 7 | a0001c0002t0001g0115a0001c0014t0002g0114a0003c0089t0001g0116others(4): Show | 7 | HG01346.hp1 HG02886.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+564C>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413389 | ||||||
chr2:237413514 | C | T | 9 | a0010c0018t0003g0105a0010c0018t0003g0106a0013c0034t0005g0102others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+439G>A | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413514 | ||||||
chr2:237413936 | A | G | 95 | a0001c0002t0001g0036a0001c0002t0001g0088a0001c0002t0001g0092others(92): Show | 96 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.-31+17T>C | COL6A3 | ENSG00000163359.17 | transcript | ENST00000295550.9 | protein_coding | 1/43 | chr2 | 237413936 |