Item | Value |
---|---|
geneid | 11322 |
ensemblid | ENSG00000141524.19 |
hgncid | 18021 |
symbol | TMC6 |
name | transmembrane channel like 6 |
refseq_nuc | NM_001127198.5 |
refseq_prot | NP_001120670.1 |
ensembl_nuc | ENST00000590602.6 |
ensembl_prot | ENSP00000465261.1 |
mane_status | MANE Select |
chr | chr17 |
start | 78107397 |
end | 78128755 |
strand | - |
ver | v1.2 |
region | chr17:78107397-78128755 |
region5000 | chr17:78102397-78133755 |
regionname0 | TMC6_chr17_78107397_78128755 |
regionname5000 | TMC6_chr17_78102397_78133755 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 805 | 185 | 32 | 41 | 72 | 11 | 27 | 50 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002 | 0/0 | 805 | 69 | 20 | 21 | 13 | 4 | 11 | 8 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003 | 0/0 | 805 | 69 | 3 | 15 | 47 | 1 | 3 | 42 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004 | 0/0 | 805 | 46 | 16 | 3 | 24 | 1 | 2 | 20 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005 | 0/0 | 805 | 42 | 10 | 2 | 27 | 0 | 3 | 21 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006 | 0/0 | 805 | 8 | 0 | 0 | 7 | 0 | 1 | 6 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0007 | 0/0 | 805 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0008 | 0/0 | 805 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0009 | 0/0 | 805 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0010 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0011 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0012 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0013 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0014 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0015 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0016 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0017 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0018 | 0/0 | 805 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0019 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0020 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0021 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0022 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0023 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2418 | 144 | 30 | 31 | 52 | 8 | 21 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0002 | 0/0 | 2418 | 66 | 20 | 19 | 12 | 4 | 11 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0003 | 0/0 | 2418 | 63 | 3 | 15 | 42 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0004 | 0/0 | 2418 | 40 | 8 | 2 | 27 | 0 | 3 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0005 | 0/0 | 2418 | 37 | 1 | 10 | 17 | 3 | 6 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0006 | 0/0 | 2418 | 35 | 14 | 2 | 16 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0007 | 0/0 | 2418 | 6 | 6 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0008 | 0/0 | 2418 | 6 | 0 | 0 | 5 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0009 | 0/0 | 2418 | 5 | 0 | 0 | 4 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0010 | 0/0 | 2418 | 4 | 0 | 0 | 4 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0011 | 0/0 | 2418 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0012 | 0/0 | 2418 | 3 | 2 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0013 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0014 | 0/0 | 2418 | 2 | 0 | 1 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0015 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0016 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0017 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0018 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0019 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0021 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0022 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0023 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0024 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0025 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0026 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0027 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0028 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0029 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0030 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0031 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0032 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0033 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0034 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0035 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0036 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
c0037 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 5970 | 120 | 6 | 30 | 57 | 10 | 16 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0002 | 0/0 | 5971 | 65 | 18 | 15 | 19 | 4 | 9 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0003 | 0/0 | 5970 | 57 | 4 | 15 | 31 | 1 | 6 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0004 | 0/0 | 6108 | 23 | 4 | 0 | 15 | 0 | 4 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0005 | 0/0 | 5985 | 20 | 1 | 2 | 17 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0006 | 0/0 | 5971 | 9 | 1 | 2 | 4 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0007 | 0/0 | 6095 | 9 | 9 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0008 | 0/0 | 5986 | 6 | 2 | 0 | 4 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0009 | 0/0 | 5971 | 6 | 6 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0010 | 0/0 | 6109 | 5 | 4 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0011 | 0/0 | 6108 | 5 | 3 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0012 | 0/0 | 5985 | 5 | 1 | 0 | 4 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0013 | 0/0 | 6096 | 4 | 4 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0014 | 0/0 | 5970 | 4 | 0 | 0 | 4 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0015 | 0/0 | 5970 | 4 | 4 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0016 | 0/0 | 6094 | 4 | 0 | 2 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0017 | 0/0 | 6108 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0018 | 0/0 | 5970 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0019 | 0/0 | 5986 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0020 | 0/0 | 5971 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0021 | 0/0 | 5969 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0022 | 0/0 | 6108 | 3 | 0 | 3 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0023 | 0/0 | 5970 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0024 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0025 | 0/0 | 5986 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0026 | 0/0 | 6095 | 2 | 0 | 0 | 1 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0027 | 0/0 | 6134 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0028 | 0/0 | 5985 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0029 | 0/0 | 5970 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0030 | 0/0 | 5986 | 2 | 1 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0031 | 0/0 | 5970 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0032 | 0/0 | 6095 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0033 | 0/0 | 5970 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0034 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0035 | 0/0 | 5986 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0036 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0037 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0038 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0039 | 0/1 | 6183 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0040 | 0/0 | 6109 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0041 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0042 | 0/0 | 6095 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0043 | 0/0 | 6094 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0044 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0045 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0046 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0047 | 0/0 | 5971 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0048 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0049 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0050 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0051 | 0/0 | 5971 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0052 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0053 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0054 | 0/0 | 5971 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0055 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0056 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0057 | 0/0 | 5985 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0058 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0059 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0060 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0061 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0062 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0063 | 0/0 | 6182 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0064 | 0/0 | 6094 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0065 | 0/0 | 6093 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0066 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0067 | 0/0 | 6094 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0068 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0069 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0070 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0071 | 0/0 | 5970 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0072 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0073 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0074 | 0/0 | 5970 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0075 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0076 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0077 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0078 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0079 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0080 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0081 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0082 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0083 | 0/0 | 6094 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0084 | 0/0 | 5970 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0085 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0086 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0087 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0088 | 0/0 | 6094 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0089 | 0/0 | 5970 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
t0090 | 0/0 | 5970 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0398 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0416 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0417 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0418 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0420 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0421 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0423 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0424 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0425 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0426 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0427 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0428 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0429 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0430 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0431 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0432 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0433 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0434 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
g0435 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2418 | 144 | 30 | 31 | 52 | 8 | 21 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0001c0005 | 0/0 | 2418 | 37 | 1 | 10 | 17 | 3 | 6 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0001c0017 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0001c0033 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0001c0035 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0002c0002 | 0/0 | 2418 | 66 | 20 | 19 | 12 | 4 | 11 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0002c0014 | 0/0 | 2418 | 2 | 0 | 1 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0002c0023 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0003c0003 | 0/0 | 2418 | 63 | 3 | 15 | 42 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0003c0009 | 0/0 | 2418 | 5 | 0 | 0 | 4 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0003c0037 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0004c0006 | 0/0 | 2418 | 35 | 14 | 2 | 16 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0004c0010 | 0/0 | 2418 | 4 | 0 | 0 | 4 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0004c0011 | 0/0 | 2418 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0004c0012 | 0/0 | 2418 | 3 | 2 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0004c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0005c0004 | 0/0 | 2418 | 40 | 8 | 2 | 27 | 0 | 3 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0005c0018 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0006c0008 | 0/0 | 2418 | 6 | 0 | 0 | 5 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0006c0016 | 0/0 | 2418 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0007c0007 | 0/0 | 2418 | 6 | 6 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0008c0013 | 0/0 | 2418 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0009c0015 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0010c0019 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0011c0022 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0012c0021 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0013c0024 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0014c0036 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0015c0025 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0016c0034 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0017c0032 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0018c0027 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0019c0028 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0020c0029 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0021c0030 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0022c0031 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 | |
a0023c0026 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8387 | 55 | 3 | 19 | 14 | 7 | 11 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0002 | 0/0 | 8388 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0003 | 0/0 | 8387 | 14 | 0 | 3 | 8 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0004 | 0/0 | 8525 | 13 | 2 | 0 | 9 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0005 | 0/0 | 8402 | 8 | 1 | 1 | 6 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0007 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0008 | 0/0 | 8403 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0009 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0011 | 0/0 | 8525 | 5 | 3 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0012 | 0/0 | 8402 | 3 | 1 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0013 | 0/0 | 8513 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0015 | 0/0 | 8387 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0016 | 0/0 | 8511 | 2 | 0 | 0 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0017 | 0/0 | 8525 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0018 | 0/0 | 8387 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0020 | 0/0 | 8388 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0022 | 0/0 | 8525 | 3 | 0 | 3 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0023 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0030 | 0/0 | 8403 | 2 | 1 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0032 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0033 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0035 | 0/0 | 8403 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0039 | 0/1 | 8600 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0055 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0056 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0063 | 0/0 | 8599 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0064 | 0/0 | 8511 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0066 | 0/0 | 8525 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0068 | 0/0 | 8526 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0073 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0074 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0076 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0077 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0078 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0080 | 0/0 | 8387 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0083 | 0/0 | 8511 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0084 | 0/0 | 8387 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0001t0088 | 0/0 | 8511 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0001 | 0/0 | 8387 | 6 | 0 | 1 | 1 | 2 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0003 | 0/0 | 8387 | 14 | 1 | 5 | 6 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0004 | 0/0 | 8525 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0005 | 0/0 | 8402 | 3 | 0 | 1 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0012 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0014 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0016 | 0/0 | 8511 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0028 | 0/0 | 8402 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0057 | 0/0 | 8402 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0059 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0060 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0070 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0071 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0072 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0079 | 0/0 | 8387 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0005t0081 | 0/0 | 8387 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0017t0001 | 0/0 | 8387 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0033t0004 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0001c0035t0001 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0002 | 0/0 | 8388 | 35 | 8 | 12 | 6 | 3 | 6 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0006 | 0/0 | 8388 | 5 | 0 | 2 | 1 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0007 | 0/0 | 8512 | 4 | 4 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0008 | 0/0 | 8403 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0009 | 0/0 | 8388 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0010 | 0/0 | 8526 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0012 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0013 | 0/0 | 8513 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0015 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0023 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0025 | 0/0 | 8403 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0026 | 0/0 | 8512 | 2 | 0 | 0 | 1 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0034 | 0/0 | 8403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0036 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0038 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0044 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0048 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0049 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0050 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0052 | 0/0 | 8364 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0054 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0002t0069 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0014t0001 | 0/0 | 8387 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0014t0005 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0002c0023t0002 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0001 | 0/0 | 8387 | 33 | 2 | 9 | 20 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0003 | 0/0 | 8387 | 14 | 0 | 5 | 9 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0004 | 0/0 | 8525 | 5 | 0 | 0 | 5 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0005 | 0/0 | 8402 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0016 | 0/0 | 8511 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0029 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0031 | 0/0 | 8387 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0062 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0065 | 0/0 | 8510 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0086 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0003t0089 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0009t0001 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0009t0014 | 0/0 | 8387 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0009t0061 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0003c0037t0001 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0001 | 0/0 | 8387 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0002 | 0/0 | 8388 | 13 | 0 | 2 | 8 | 1 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0003 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0006 | 0/0 | 8388 | 3 | 1 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0007 | 0/0 | 8512 | 4 | 4 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0008 | 0/0 | 8403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0009 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0010 | 0/0 | 8526 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0013 | 0/0 | 8513 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0019 | 0/0 | 8403 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0024 | 0/0 | 8388 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0043 | 0/0 | 8511 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0006t0047 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0010t0001 | 0/0 | 8387 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0010t0075 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0011t0002 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0011t0008 | 0/0 | 8403 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0012t0010 | 0/0 | 8526 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0012t0040 | 0/0 | 8526 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0012t0041 | 0/0 | 8526 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0004c0020t0008 | 0/0 | 8403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0001 | 0/0 | 8387 | 12 | 1 | 0 | 11 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0003 | 0/0 | 8387 | 14 | 3 | 2 | 7 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0004 | 0/0 | 8525 | 2 | 0 | 0 | 1 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0005 | 0/0 | 8402 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0021 | 0/0 | 8386 | 3 | 0 | 0 | 3 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0033 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0058 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0067 | 0/0 | 8511 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0082 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0087 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0004t0090 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0005c0018t0027 | 0/0 | 8551 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0008t0002 | 0/0 | 8388 | 2 | 0 | 0 | 2 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0008t0006 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0008t0045 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0008t0046 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0008t0051 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0016t0002 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0006c0016t0037 | 0/0 | 8403 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0007c0007t0002 | 0/0 | 8388 | 3 | 3 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0007c0007t0009 | 0/0 | 8388 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0007c0007t0042 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0008c0013t0002 | 0/0 | 8388 | 2 | 2 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0008c0013t0032 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0009c0015t0002 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0009c0015t0010 | 0/0 | 8526 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0010c0019t0002 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0011c0022t0002 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0012c0021t0002 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0013c0024t0005 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0014c0036t0029 | 0/0 | 8429 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0015c0025t0001 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0016c0034t0001 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0017c0032t0053 | 0/0 | 8443 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0018c0027t0001 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0019c0028t0002 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0020c0029t0005 | 0/0 | 8402 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0021c0030t0085 | 0/0 | 9267 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0022c0031t0004 | 0/0 | 8525 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
a0023c0026t0023 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | copy fasta | chr17 | 78102397 | 78133755 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0416 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0417 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0418 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0428 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0430 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0432 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0001g0433 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0429 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0434 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0003g0435 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0011g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0011g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0011g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0012g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0012g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0015g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0016g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0016g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0017g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0018g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0020g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0022g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0022g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0022g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0023g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0030g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0030g0431 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0032g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0033g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0035g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0039g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0055g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0056g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0063g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0064g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0066g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0068g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0073g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0074g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0076g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0077g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0078g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0080g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0083g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0084g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0001t0088g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0003g0421 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0012g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0014g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0016g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0028g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0028g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0057g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0059g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0060g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0070g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0071g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0072g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0079g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0005t0081g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0017t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0017t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0033t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0001c0035t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0012g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0025g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0026g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0026g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0034g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0036g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0038g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0044g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0048g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0049g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0050g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0052g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0054g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0002t0069g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0014t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0014t0005g0420 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0002c0023t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0001g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0003g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0004g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0004g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0005g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0016g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0029g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0031g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0031g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0062g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0065g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0086g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0003t0089g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0009t0001g0398 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0009t0014g0424 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0009t0014g0425 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0009t0014g0426 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0009t0061g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0003c0037t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0019g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0019g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0043g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0006t0047g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0010t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0010t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0010t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0010t0075g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0011t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0011t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0011t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0012t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0012t0040g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0012t0041g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0004c0020t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0005g0427 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0021g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0021g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0021g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0033g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0058g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0067g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0082g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0087g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0004t0090g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0018t0027g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0005c0018t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0045g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0046g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0008t0051g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0016t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0006c0016t0037g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0007c0007t0042g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0008c0013t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0008c0013t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0008c0013t0032g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0009c0015t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0009c0015t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0010c0019t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0011c0022t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0012c0021t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0013c0024t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0014c0036t0029g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0015c0025t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0016c0034t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0017c0032t0053g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0018c0027t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0019c0028t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0020c0029t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0021c0030t0085g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0022c0031t0004g0423 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
a0023c0026t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0239 | EUR | GBR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0417 | EUR | GBR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0240 | EUR | GBR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0133 | EUR | GBR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | FIN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0435 | EUR | FIN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | FIN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00323 | hp2 | a0003 | c0003 | t0065 | g0364 | EUR | FIN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0374 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00423 | hp1 | a0005 | c0004 | t0001 | g0208 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00544 | hp1 | a0003 | c0003 | t0003 | g0368 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00597 | hp1 | a0005 | c0004 | t0004 | g0201 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00621 | hp2 | a0004 | c0006 | t0003 | g0234 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00639 | hp1 | a0002 | c0002 | t0048 | g0105 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0383 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0434 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | CHS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0124 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00733 | hp2 | a0001 | c0005 | t0003 | g0319 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00735 | hp1 | a0001 | c0005 | t0003 | g0001 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0430 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0355 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00738 | hp2 | a0001 | c0005 | t0079 | g0307 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0349 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG00741 | hp2 | a0001 | c0005 | t0081 | g0312 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01069 | hp1 | a0001 | c0005 | t0003 | g0306 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01069 | hp2 | a0005 | c0004 | t0003 | g0003 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01070 | hp1 | a0004 | c0012 | t0040 | g0033 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01070 | hp2 | a0002 | c0002 | t0025 | g0002 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01071 | hp1 | a0005 | c0004 | t0003 | g0003 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01071 | hp2 | a0002 | c0002 | t0025 | g0002 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01074 | hp2 | a0004 | c0006 | t0002 | g0052 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01081 | hp2 | a0003 | c0003 | t0003 | g0351 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01099 | hp1 | a0002 | c0002 | t0006 | g0098 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01099 | hp2 | a0001 | c0001 | t0011 | g0288 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01106 | hp2 | a0002 | c0002 | t0006 | g0071 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0372 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01109 | hp2 | a0001 | c0001 | t0080 | g0338 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01167 | hp1 | a0001 | c0005 | t0003 | g0001 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0416 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01168 | hp2 | a0002 | c0002 | t0054 | g0122 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01169 | hp1 | a0001 | c0005 | t0003 | g0001 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01175 | hp1 | a0001 | c0005 | t0001 | g0242 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01175 | hp2 | a0002 | c0023 | t0002 | g0140 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01192 | hp2 | a0004 | c0006 | t0002 | g0053 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01243 | hp1 | a0001 | c0001 | t0084 | g0345 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01255 | hp2 | a0001 | c0005 | t0005 | g0305 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0418 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0433 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0290 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0415 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0429 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0323 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01433 | hp1 | a0002 | c0014 | t0001 | g0228 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01433 | hp2 | a0001 | c0001 | t0030 | g0341 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0117 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0120 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01884 | hp1 | a0005 | c0004 | t0003 | g0203 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01884 | hp2 | a0004 | c0006 | t0019 | g0026 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01891 | hp1 | a0004 | c0012 | t0041 | g0031 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01891 | hp2 | a0005 | c0004 | t0082 | g0195 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01928 | hp1 | a0003 | c0003 | t0003 | g0362 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0428 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01934 | hp2 | a0003 | c0003 | t0003 | g0193 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01943 | hp2 | a0001 | c0005 | t0016 | g0181 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01952 | hp2 | a0001 | c0001 | t0022 | g0266 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0094 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01978 | hp2 | a0003 | c0003 | t0001 | g0382 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01981 | hp1 | a0001 | c0001 | t0022 | g0265 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0365 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01993 | hp2 | a0001 | c0001 | t0022 | g0180 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0432 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02004 | hp2 | a0003 | c0003 | t0001 | g0371 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02015 | hp1 | a0001 | c0001 | t0056 | g0158 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02015 | hp2 | a0004 | c0020 | t0008 | g0058 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02027 | hp1 | a0003 | c0003 | t0031 | g0360 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02027 | hp2 | a0005 | c0004 | t0033 | g0197 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02040 | hp1 | a0016 | c0034 | t0001 | g0205 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02040 | hp2 | a0005 | c0004 | t0005 | g0218 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0160 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02056 | hp1 | a0004 | c0006 | t0047 | g0044 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0013 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02071 | hp1 | a0004 | c0010 | t0001 | g0231 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02071 | hp2 | a0001 | c0017 | t0001 | g0293 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02074 | hp1 | a0011 | c0022 | t0002 | g0139 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02074 | hp2 | a0005 | c0004 | t0001 | g0206 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0407 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02080 | hp2 | a0001 | c0005 | t0028 | g0169 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02129 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02129 | hp2 | a0002 | c0002 | t0010 | g0136 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02132 | hp1 | a0013 | c0024 | t0005 | g0194 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02135 | hp1 | a0001 | c0001 | t0012 | g0292 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02135 | hp2 | a0005 | c0004 | t0001 | g0217 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02145 | hp2 | a0001 | c0001 | t0020 | g0085 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0377 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02148 | hp2 | a0003 | c0003 | t0003 | g0386 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02155 | hp1 | a0001 | c0001 | t0076 | g0295 | EAS | CDX | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02155 | hp2 | a0002 | c0002 | t0026 | g0101 | EAS | CDX | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02165 | hp1 | a0002 | c0002 | t0034 | g0115 | EAS | CDX | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02257 | hp1 | a0012 | c0021 | t0002 | g0066 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02257 | hp2 | a0001 | c0001 | t0055 | g0192 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0076 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02258 | hp2 | a0007 | c0007 | t0042 | g0064 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02273 | hp2 | a0003 | c0003 | t0003 | g0402 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02280 | hp2 | a0002 | c0002 | t0013 | g0059 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0373 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02293 | hp2 | a0002 | c0002 | t0038 | g0123 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02451 | hp2 | a0002 | c0002 | t0023 | g0237 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02523 | hp1 | a0001 | c0001 | t0012 | g0163 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02523 | hp2 | a0006 | c0016 | t0037 | g0141 | EAS | KHV | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02602 | hp1 | a0005 | c0004 | t0004 | g0209 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02602 | hp2 | a0001 | c0001 | t0074 | g0156 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02615 | hp1 | a0002 | c0002 | t0015 | g0236 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02615 | hp2 | a0001 | c0001 | t0064 | g0275 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02622 | hp1 | a0005 | c0018 | t0027 | g0018 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02622 | hp2 | a0005 | c0004 | t0067 | g0210 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02630 | hp1 | a0004 | c0006 | t0013 | g0040 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02630 | hp2 | a0023 | c0026 | t0023 | g0248 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02647 | hp2 | a0001 | c0001 | t0035 | g0086 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02683 | hp2 | a0004 | c0006 | t0002 | g0051 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02698 | hp2 | a0001 | c0005 | t0001 | g0241 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0081 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0268 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0350 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02735 | hp1 | a0001 | c0005 | t0003 | g0245 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02735 | hp2 | a0002 | c0002 | t0006 | g0113 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0324 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0280 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0079 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02809 | hp2 | a0001 | c0001 | t0032 | g0276 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02818 | hp1 | a0004 | c0006 | t0010 | g0037 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02818 | hp2 | a0005 | c0004 | t0090 | g0226 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0084 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02895 | hp1 | a0005 | c0004 | t0003 | g0204 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0089 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02896 | hp1 | a0002 | c0002 | t0007 | g0131 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02922 | hp1 | a0002 | c0002 | t0007 | g0107 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02922 | hp2 | a0017 | c0032 | t0053 | g0091 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02965 | hp1 | a0008 | c0013 | t0002 | g0029 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02965 | hp2 | a0007 | c0007 | t0009 | g0063 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02970 | hp1 | a0001 | c0001 | t0073 | g0282 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02976 | hp1 | a0009 | c0015 | t0002 | g0112 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02976 | hp2 | a0002 | c0002 | t0007 | g0110 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03017 | hp2 | a0002 | c0002 | t0049 | g0074 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03041 | hp1 | a0004 | c0006 | t0007 | g0036 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03041 | hp2 | a0004 | c0006 | t0009 | g0038 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03098 | hp1 | a0005 | c0004 | t0087 | g0191 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0289 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03130 | hp1 | a0005 | c0004 | t0001 | g0220 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03130 | hp2 | a0022 | c0031 | t0004 | g0423 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03139 | hp1 | a0004 | c0006 | t0019 | g0025 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03139 | hp2 | a0007 | c0007 | t0009 | g0065 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03195 | hp1 | a0002 | c0002 | t0008 | g0106 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03195 | hp2 | a0009 | c0015 | t0010 | g0111 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03209 | hp1 | a0005 | c0018 | t0027 | g0017 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03225 | hp1 | a0001 | c0001 | t0020 | g0088 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03225 | hp2 | a0002 | c0002 | t0069 | g0422 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03453 | hp1 | a0002 | c0002 | t0052 | g0130 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03486 | hp1 | a0004 | c0006 | t0024 | g0027 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0285 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03490 | hp2 | a0001 | c0005 | t0003 | g0244 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03491 | hp1 | a0001 | c0001 | t0088 | g0336 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03491 | hp2 | a0005 | c0004 | t0003 | g0004 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03492 | hp2 | a0005 | c0004 | t0003 | g0004 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0274 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03516 | hp2 | a0004 | c0006 | t0007 | g0032 | AFR | ESN | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03540 | hp2 | a0008 | c0013 | t0032 | g0179 | AFR | GWD | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03579 | hp1 | a0001 | c0001 | t0013 | g0083 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03579 | hp2 | a0001 | c0033 | t0004 | g0347 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0403 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03688 | hp2 | a0002 | c0002 | t0050 | g0132 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03704 | hp2 | a0010 | c0019 | t0002 | g0069 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03710 | hp1 | a0001 | c0005 | t0001 | g0342 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0352 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03831 | hp2 | a0006 | c0008 | t0051 | g0143 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03834 | hp1 | a0002 | c0002 | t0044 | g0103 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03834 | hp2 | a0001 | c0005 | t0004 | g0310 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0339 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04115 | hp1 | a0001 | c0001 | t0063 | g0178 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04115 | hp2 | a0001 | c0005 | t0071 | g0182 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04184 | hp2 | a0002 | c0002 | t0006 | g0114 | SAS | BEB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04199 | hp1 | a0004 | c0006 | t0002 | g0047 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0099 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04228 | hp1 | a0003 | c0009 | t0001 | g0398 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0343 | SAS | STU | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18522 | hp1 | a0002 | c0002 | t0007 | g0108 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18522 | hp2 | a0004 | c0006 | t0010 | g0057 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18612 | hp1 | a0001 | c0001 | t0078 | g0346 | EAS | CHB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | CHB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0397 | EAS | CHB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | CHB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18906 | hp1 | a0002 | c0002 | t0009 | g0129 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18906 | hp2 | a0004 | c0006 | t0007 | g0035 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18939 | hp1 | a0004 | c0006 | t0002 | g0019 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18939 | hp2 | a0001 | c0005 | t0005 | g0308 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18943 | hp2 | a0001 | c0005 | t0003 | g0189 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18944 | hp1 | a0005 | c0004 | t0003 | g0199 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18944 | hp2 | a0005 | c0004 | t0001 | g0219 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0409 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18946 | hp1 | a0005 | c0004 | t0021 | g0221 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18946 | hp2 | a0004 | c0006 | t0006 | g0041 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18947 | hp1 | a0003 | c0003 | t0001 | g0385 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0405 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18948 | hp1 | a0004 | c0006 | t0002 | g0043 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18948 | hp2 | a0001 | c0005 | t0003 | g0421 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18950 | hp1 | a0004 | c0010 | t0001 | g0229 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18950 | hp2 | a0006 | c0008 | t0002 | g0148 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18951 | hp1 | a0004 | c0006 | t0002 | g0042 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18951 | hp2 | a0005 | c0004 | t0005 | g0213 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0390 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18952 | hp2 | a0001 | c0005 | t0059 | g0173 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18953 | hp1 | a0004 | c0006 | t0002 | g0021 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18954 | hp1 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18954 | hp2 | a0005 | c0004 | t0003 | g0196 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18956 | hp1 | a0005 | c0004 | t0003 | g0200 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0410 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18957 | hp1 | a0005 | c0004 | t0001 | g0216 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18959 | hp1 | a0006 | c0008 | t0002 | g0147 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18959 | hp2 | a0003 | c0009 | t0014 | g0425 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18960 | hp1 | a0003 | c0003 | t0005 | g0384 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18960 | hp2 | a0015 | c0025 | t0001 | g0247 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18962 | hp1 | a0005 | c0004 | t0001 | g0152 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18965 | hp1 | a0006 | c0008 | t0006 | g0144 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18966 | hp1 | a0003 | c0003 | t0003 | g0413 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18966 | hp2 | a0020 | c0029 | t0005 | g0301 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18968 | hp1 | a0001 | c0005 | t0003 | g0183 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18968 | hp2 | a0004 | c0006 | t0043 | g0048 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18969 | hp1 | a0003 | c0003 | t0029 | g0391 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18969 | hp2 | a0001 | c0005 | t0012 | g0309 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0387 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18971 | hp1 | a0005 | c0004 | t0021 | g0211 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18973 | hp1 | a0003 | c0009 | t0014 | g0426 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18975 | hp2 | a0002 | c0002 | t0012 | g0419 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18977 | hp1 | a0005 | c0004 | t0001 | g0223 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18977 | hp2 | a0001 | c0005 | t0003 | g0187 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18978 | hp1 | a0003 | c0009 | t0061 | g0395 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0406 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18979 | hp1 | a0004 | c0010 | t0075 | g0232 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18979 | hp2 | a0001 | c0001 | t0033 | g0164 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18981 | hp1 | a0003 | c0003 | t0004 | g0380 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0367 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18982 | hp2 | a0002 | c0002 | t0006 | g0126 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18983 | hp1 | a0004 | c0011 | t0008 | g0151 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18983 | hp2 | a0005 | c0004 | t0003 | g0227 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18985 | hp1 | a0001 | c0001 | t0068 | g0253 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18988 | hp1 | a0001 | c0005 | t0003 | g0188 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18988 | hp2 | a0001 | c0005 | t0005 | g0184 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18989 | hp1 | a0014 | c0036 | t0029 | g0412 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18989 | hp2 | a0003 | c0003 | t0003 | g0404 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0411 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18990 | hp2 | a0006 | c0008 | t0045 | g0145 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18991 | hp2 | a0001 | c0001 | t0017 | g0014 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0358 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18992 | hp2 | a0004 | c0006 | t0001 | g0233 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18994 | hp1 | a0003 | c0003 | t0031 | g0359 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18995 | hp1 | a0002 | c0002 | t0036 | g0102 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18998 | hp1 | a0004 | c0006 | t0002 | g0049 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA18998 | hp2 | a0003 | c0003 | t0004 | g0400 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19000 | hp1 | a0001 | c0005 | t0060 | g0190 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19000 | hp2 | a0005 | c0004 | t0001 | g0214 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0375 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19002 | hp2 | a0006 | c0008 | t0046 | g0146 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0414 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19003 | hp2 | a0001 | c0005 | t0014 | g0313 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0376 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19005 | hp1 | a0005 | c0004 | t0058 | g0224 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19005 | hp2 | a0003 | c0003 | t0001 | g0361 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19007 | hp2 | a0003 | c0003 | t0004 | g0357 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0408 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19009 | hp2 | a0001 | c0005 | t0003 | g0186 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19010 | hp2 | a0004 | c0006 | t0001 | g0235 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19011 | hp1 | a0001 | c0005 | t0028 | g0170 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0287 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19030 | hp2 | a0007 | c0007 | t0002 | g0061 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19043 | hp1 | a0002 | c0002 | t0009 | g0128 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19043 | hp2 | a0021 | c0030 | t0085 | g0283 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19056 | hp1 | a0006 | c0016 | t0002 | g0142 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0392 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19057 | hp1 | a0001 | c0005 | t0001 | g0315 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19057 | hp2 | a0002 | c0014 | t0005 | g0420 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19059 | hp1 | a0001 | c0001 | t0018 | g0012 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19059 | hp2 | a0003 | c0037 | t0001 | g0363 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19060 | hp2 | a0003 | c0003 | t0086 | g0381 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0388 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19062 | hp2 | a0003 | c0003 | t0004 | g0366 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19063 | hp1 | a0005 | c0004 | t0003 | g0222 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19063 | hp2 | a0003 | c0003 | t0089 | g0393 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19064 | hp1 | a0001 | c0001 | t0066 | g0259 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19064 | hp2 | a0001 | c0035 | t0001 | g0348 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19065 | hp1 | a0001 | c0005 | t0070 | g0185 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19065 | hp2 | a0004 | c0006 | t0008 | g0055 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19066 | hp1 | a0005 | c0004 | t0001 | g0212 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19066 | hp2 | a0003 | c0009 | t0014 | g0424 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19067 | hp1 | a0003 | c0003 | t0005 | g0354 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19067 | hp2 | a0004 | c0006 | t0002 | g0050 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19068 | hp1 | a0003 | c0003 | t0001 | g0378 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19068 | hp2 | a0004 | c0010 | t0001 | g0230 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19070 | hp1 | a0003 | c0003 | t0003 | g0394 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19070 | hp2 | a0005 | c0004 | t0021 | g0225 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0369 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19074 | hp2 | a0003 | c0003 | t0003 | g0389 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19077 | hp1 | a0004 | c0006 | t0006 | g0046 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19077 | hp2 | a0003 | c0003 | t0005 | g0370 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19079 | hp1 | a0005 | c0004 | t0001 | g0215 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19079 | hp2 | a0004 | c0011 | t0008 | g0023 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19080 | hp1 | a0003 | c0003 | t0004 | g0396 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19080 | hp2 | a0001 | c0001 | t0077 | g0257 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19081 | hp1 | a0004 | c0011 | t0002 | g0022 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19081 | hp2 | a0005 | c0004 | t0005 | g0427 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19084 | hp1 | a0001 | c0017 | t0001 | g0294 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0353 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19085 | hp2 | a0005 | c0004 | t0001 | g0153 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19086 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19088 | hp1 | a0004 | c0006 | t0002 | g0020 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0399 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19090 | hp1 | a0005 | c0004 | t0003 | g0207 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19090 | hp2 | a0001 | c0005 | t0072 | g0299 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19091 | hp1 | a0005 | c0004 | t0003 | g0198 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19091 | hp2 | a0004 | c0006 | t0002 | g0045 | EAS | JPT | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19240 | hp1 | a0004 | c0012 | t0010 | g0034 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA19240 | hp2 | a0005 | c0004 | t0003 | g0202 | AFR | YRI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20129 | hp1 | a0019 | c0028 | t0002 | g0082 | AFR | ASW | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20129 | hp2 | a0001 | c0001 | t0030 | g0431 | AFR | ASW | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20752 | hp1 | a0001 | c0005 | t0057 | g0311 | EUR | TSI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20752 | hp2 | a0018 | c0027 | t0001 | g0246 | EUR | TSI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20805 | hp1 | a0004 | c0006 | t0002 | g0056 | EUR | TSI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20805 | hp2 | a0002 | c0002 | t0026 | g0119 | EUR | TSI | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20905 | hp1 | a0001 | c0001 | t0083 | g0314 | SAS | GIH | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | GIH | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01123 | hp1 | a0003 | c0003 | t0016 | g0401 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02109 | hp1 | a0004 | c0006 | t0006 | g0054 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02109 | hp2 | a0004 | c0006 | t0024 | g0028 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02486 | hp1 | a0004 | c0006 | t0007 | g0039 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0356 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02559 | hp1 | a0007 | c0007 | t0002 | g0062 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0149 | AFR | ACB | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0286 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG03471 | hp2 | a0001 | c0001 | t0013 | g0087 | AFR | MSL | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG06807 | hp1 | a0001 | c0005 | t0003 | g0243 | AFR | USA | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
HG06807 | hp2 | a0008 | c0013 | t0002 | g0030 | AFR | USA | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20300 | hp1 | a0004 | c0006 | t0019 | g0024 | AFR | USA | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA20300 | hp2 | a0003 | c0003 | t0062 | g0379 | AFR | USA | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA21309 | hp1 | a0001 | c0001 | t0015 | g0273 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
NA21309 | hp2 | a0007 | c0007 | t0002 | g0060 | AFR | LWK | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0039 | g0090 | REF | REF | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | TMC6_chr17_78102397_78133755 | TMC6 | chr17 | 78102397 | 78133755 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:78113182 | G | A | 1 | a0019 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2384C>T | p.Pro795Leu | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2602/8387 | 2384/2418 | 795/805 | chr17 | 78113182 | ||
chr17:78113553 | C | A | 1 | a0020 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.2349G>T | p.Arg783Ser | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/20 | 2567/8387 | 2349/2418 | 783/805 | chr17 | 78113553 | ||
chr17:78113573 | T | TCTCGTAG others(35): Show |
1 | a0014 | 1 | NA18989.hp1 | conservative_inframe_insertion | MODERATE | c.2287_2328dupGACAAA others(36): Show |
p.Glu776_Arg777insAs others(40): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/20 | 2546/8387 | 2328/2418 | 776/805 | chr17 | 78113573 | ||
chr17:78119360 | C | T | 1 | a0018 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1748G>A | p.Arg583Gln | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/20 | 1966/8387 | 1748/2418 | 583/805 | chr17 | 78119360 | ||
chr17:78120716 | C | T | 1 | a0016 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1652G>A | p.Arg551Gln | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/20 | 1870/8387 | 1652/2418 | 551/805 | chr17 | 78120716 | ||
chr17:78120777 | G | A | 1 | a0011 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1591C>T | p.Arg531Cys | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/20 | 1809/8387 | 1591/2418 | 531/805 | chr17 | 78120777 | ||
chr17:78121077 | G | A | 1 | a0009 | 2 | HG02976.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.1471C>T | p.Arg491Cys | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/20 | 1689/8387 | 1471/2418 | 491/805 | chr17 | 78121077 | ||
chr17:78121605 | G | A | 1 | a0021 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1334C>T | p.Ala445Val | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/20 | 1552/8387 | 1334/2418 | 445/805 | chr17 | 78121605 | ||
chr17:78121663 | C | T | 1 | a0012 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1276G>A | p.Gly426Arg | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/20 | 1494/8387 | 1276/2418 | 426/805 | chr17 | 78121663 | ||
chr17:78122693 | G | A | 1 | a0022 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1139C>T | p.Ala380Val | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/20 | 1357/8387 | 1139/2418 | 380/805 | chr17 | 78122693 | ||
chr17:78123996 | C | A | 1 | a0017 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1075G>T | p.Val359Leu | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/20 | 1293/8387 | 1075/2418 | 359/805 | chr17 | 78123996 | ||
chr17:78124556 | C | T | 1 | a0007 | 6 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
missense_variant | MODERATE | c.859G>A | p.Val287Ile | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/20 | 1077/8387 | 859/2418 | 287/805 | chr17 | 78124556 | ||
chr17:78124577 | C | T | 1 | a0023 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.838G>A | p.Ala280Thr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/20 | 1056/8387 | 838/2418 | 280/805 | chr17 | 78124577 | ||
chr17:78124711 | T | C | 1 | a0006 | 8 | HG02523.hp2 HG03831.hp2 NA18950.hp2 others(5): Show |
missense_variant | MODERATE | c.704A>G | p.Lys235Arg | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/20 | 922/8387 | 704/2418 | 235/805 | chr17 | 78124711 | ||
chr17:78124912 | G | A | 1 | a0008 | 3 | HG02965.hp1 HG03540.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.610C>T | p.Arg204Trp | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 7/20 | 828/8387 | 610/2418 | 204/805 | chr17 | 78124912 | ||
chr17:78124923 | G | A | 4 | a0005a0008a0013others(1): Show | 47 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(44): Show |
missense_variant | MODERATE | c.599C>T | p.Ser200Phe | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 7/20 | 817/8387 | 599/2418 | 200/805 | chr17 | 78124923 | ||
chr17:78124950 | C | T | 2 | a0004a0015 | 47 | HG00621.hp2 HG01070.hp1 HG01074.hp2 others(44): Show |
missense_variant | MODERATE | c.572G>A | p.Gly191Asp | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 7/20 | 790/8387 | 572/2418 | 191/805 | chr17 | 78124950 | ||
chr17:78125237 | G | A | 2 | a0003a0014 | 70 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
missense_variant | MODERATE | c.457C>T | p.Leu153Phe | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 6/20 | 675/8387 | 457/2418 | 153/805 | chr17 | 78125237 | ||
chr17:78125765 | A | T | 1 | a0013 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.391T>A | p.Tyr131Asn | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/20 | 609/8387 | 391/2418 | 131/805 | chr17 | 78125765 | ||
chr17:78125783 | A | G | 8 | a0002a0004a0006others(5): Show | 134 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(131): Show |
missense_variant | MODERATE | c.373T>C | p.Trp125Arg | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/20 | 591/8387 | 373/2418 | 125/805 | chr17 | 78125783 | ||
chr17:78126777 | C | T | 1 | a0010 | 1 | HG03704.hp2 | missense_variant&splice_region_variant | MODERATE | c.56G>A | p.Gly19Asp | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 2/20 | 274/8387 | 56/2418 | 19/805 | chr17 | 78126777 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:78117272 | G | A | 1 | a0003c0037 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.2274C>T | p.Ser758Ser | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/20 | 2492/8387 | 2274/2418 | 758/805 | chr17 | 78117272 | ||
chr17:78117593 | G | A | 1 | a0015c0025 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.2073C>T | p.Tyr691Tyr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 17/20 | 2291/8387 | 2073/2418 | 691/805 | chr17 | 78117593 | ||
chr17:78117599 | G | A | 1 | a0001c0017 | 2 | HG02071.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.2067C>T | p.Thr689Thr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 17/20 | 2285/8387 | 2067/2418 | 689/805 | chr17 | 78117599 | ||
chr17:78117873 | G | A | 6 | a0001c0005a0001c0035a0002c0014others(3): Show | 50 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(47): Show |
synonymous_variant | LOW | c.1950C>T | p.Thr650Thr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 16/20 | 2168/8387 | 1950/2418 | 650/805 | chr17 | 78117873 | ||
chr17:78119016 | G | A | 1 | a0021c0030 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1842C>T | p.Pro614Pro | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/20 | 2060/8387 | 1842/2418 | 614/805 | chr17 | 78119016 | ||
chr17:78121066 | G | A | 1 | a0004c0012 | 3 | HG01070.hp1 HG01891.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1482C>T | p.Ala494Ala | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/20 | 1700/8387 | 1482/2418 | 494/805 | chr17 | 78121066 | ||
chr17:78121595 | G | A | 1 | a0002c0023 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1344C>T | p.Cys448Cys | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/20 | 1562/8387 | 1344/2418 | 448/805 | chr17 | 78121595 | ||
chr17:78122686 | G | A | 1 | a0004c0020 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1146C>T | p.Thr382Thr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/20 | 1364/8387 | 1146/2418 | 382/805 | chr17 | 78122686 | ||
chr17:78124102 | C | T | 1 | a0004c0010 | 4 | HG02071.hp1 NA18950.hp1 NA18979.hp1 others(1): Show |
synonymous_variant | LOW | c.969G>A | p.Leu323Leu | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/20 | 1187/8387 | 969/2418 | 323/805 | chr17 | 78124102 | ||
chr17:78124150 | G | A | 1 | a0001c0033 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.921C>T | p.Tyr307Tyr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/20 | 1139/8387 | 921/2418 | 307/805 | chr17 | 78124150 | ||
chr17:78125181 | G | A | 1 | a0001c0035 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.513C>T | p.Ser171Ser | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 6/20 | 731/8387 | 513/2418 | 171/805 | chr17 | 78125181 | ||
chr17:78125763 | G | A | 1 | a0005c0018 | 2 | HG02622.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.393C>T | p.Tyr131Tyr | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/20 | 611/8387 | 393/2418 | 131/805 | chr17 | 78125763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:78107582 | C | T | 30 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(27): Show | 56 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5566G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5566 | chr17 | 78107582 | |||||
chr17:78107603 | G | C | 25 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(22): Show | 51 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*5545C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5545 | chr17 | 78107603 | |||||
chr17:78107679 | G | A | 1 | a0001c0001t0066 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5469C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5469 | chr17 | 78107679 | |||||
chr17:78107778 | C | T | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5370G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5370 | chr17 | 78107778 | |||||
chr17:78107835 | T | C | 1 | a0001c0001t0076 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5313A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5313 | chr17 | 78107835 | |||||
chr17:78107958 | G | A | 1 | a0002c0002t0048 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5190C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5190 | chr17 | 78107958 | |||||
chr17:78108035 | C | T | 5 | a0001c0001t0016a0001c0001t0088a0001c0005t0016others(2): Show | 7 | HG01123.hp1 HG01943.hp2 HG02155.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5113G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5113 | chr17 | 78108035 | |||||
chr17:78108125 | C | T | 2 | a0001c0005t0028a0002c0002t0034 | 3 | HG02080.hp2 HG02165.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5023G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5023 | chr17 | 78108125 | |||||
chr17:78108148 | T | A | 1 | a0002c0002t0049 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5000A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 5000 | chr17 | 78108148 | |||||
chr17:78108257 | C | T | 1 | a0001c0005t0057 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4891G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4891 | chr17 | 78108257 | |||||
chr17:78108292 | T | C | 2 | a0001c0001t0020a0005c0004t0087 | 4 | HG02145.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4856A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4856 | chr17 | 78108292 | |||||
chr17:78108459 | G | A | 2 | a0001c0001t0088a0005c0018t0027 | 3 | HG02622.hp1 HG03209.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4689C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4689 | chr17 | 78108459 | |||||
chr17:78108492 | CTG | C | 22 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(19): Show | 48 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4654_*4655delCA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4654 | chr17 | 78108492 | |||||
chr17:78108562 | C | G | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4586G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4586 | chr17 | 78108562 | |||||
chr17:78108698 | C | G | 1 | a0004c0012t0040 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4450G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4450 | chr17 | 78108698 | |||||
chr17:78108778 | G | A | 1 | a0001c0001t0077 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4370C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4370 | chr17 | 78108778 | |||||
chr17:78108910 | G | A | 1 | a0005c0004t0058 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4238C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4238 | chr17 | 78108910 | |||||
chr17:78108950 | T | TCTTCCGA others(8): Show |
20 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(17): Show | 46 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4197_*4198insCTCG others(11): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4197 | chr17 | 78108950 | |||||
chr17:78108998 | G | T | 1 | a0001c0001t0039 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4150C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4150 | chr17 | 78108998 | |||||
chr17:78109090 | G | A | 1 | a0007c0007t0042 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4058C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4058 | chr17 | 78109090 | |||||
chr17:78109127 | T | C | 5 | a0001c0001t0007a0002c0002t0007a0002c0002t0052others(2): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4021A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 4021 | chr17 | 78109127 | |||||
chr17:78109225 | G | C | 1 | a0001c0001t0083 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3923C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3923 | chr17 | 78109225 | |||||
chr17:78109299 | C | T | 1 | a0003c0003t0062 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3849G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3849 | chr17 | 78109299 | |||||
chr17:78109313 | G | A | 1 | a0001c0005t0060 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3835C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3835 | chr17 | 78109313 | |||||
chr17:78109365 | C | T | 1 | a0004c0010t0075 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3783G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3783 | chr17 | 78109365 | |||||
chr17:78109366 | G | C | 1 | a0002c0002t0050 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3782C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3782 | chr17 | 78109366 | |||||
chr17:78109623 | C | T | 1 | a0001c0001t0022 | 3 | HG01952.hp2 HG01981.hp1 HG01993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3525G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3525 | chr17 | 78109623 | |||||
chr17:78109650 | C | T | 25 | a0001c0001t0005a0001c0001t0008a0001c0001t0012others(22): Show | 45 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3498G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3498 | chr17 | 78109650 | |||||
chr17:78109673 | G | A | 25 | a0001c0001t0005a0001c0001t0008a0001c0001t0012others(22): Show | 45 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3475C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3475 | chr17 | 78109673 | |||||
chr17:78109772 | A | G | 1 | a0001c0001t0074 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3376T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3376 | chr17 | 78109772 | |||||
chr17:78110026 | G | A | 2 | a0001c0001t0015a0002c0002t0015 | 4 | HG02615.hp1 HG02723.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3122C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3122 | chr17 | 78110026 | |||||
chr17:78110046 | A | C | 3 | a0001c0001t0015a0001c0001t0073a0002c0002t0015 | 5 | HG02615.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3102T>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3102 | chr17 | 78110046 | |||||
chr17:78110069 | GA | G | 5 | a0001c0001t0064a0005c0004t0021a0005c0018t0027others(2): Show | 8 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3078delT | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 3078 | chr17 | 78110069 | |||||
chr17:78110227 | C | T | 27 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(24): Show | 54 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2921G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2921 | chr17 | 78110227 | |||||
chr17:78110280 | G | A | 7 | a0001c0001t0009a0001c0001t0023a0002c0002t0009others(4): Show | 9 | HG02451.hp2 HG02630.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2868C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2868 | chr17 | 78110280 | |||||
chr17:78110342 | C | G | 3 | a0001c0005t0072a0006c0008t0045a0006c0008t0046 | 3 | NA18990.hp2 NA19002.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2806G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2806 | chr17 | 78110342 | |||||
chr17:78110366 | A | G | 1 | a0001c0001t0064 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2782T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2782 | chr17 | 78110366 | |||||
chr17:78110599 | C | T | 1 | a0007c0007t0042 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2549 | chr17 | 78110599 | |||||
chr17:78110628 | C | T | 1 | a0001c0001t0056 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2520G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2520 | chr17 | 78110628 | |||||
chr17:78110649 | GA | G | 36 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(33): Show | 64 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2498delT | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2498 | chr17 | 78110649 | |||||
chr17:78110746 | G | C | 1 | a0003c0009t0061 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2402C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2402 | chr17 | 78110746 | |||||
chr17:78110854 | A | G | 6 | a0001c0001t0016a0001c0001t0083a0001c0001t0088others(3): Show | 8 | HG01123.hp1 HG01943.hp2 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2294T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2294 | chr17 | 78110854 | |||||
chr17:78110932 | A | C | 1 | a0001c0005t0071 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2216T>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2216 | chr17 | 78110932 | |||||
chr17:78110942 | C | CAGAGACA others(9): Show |
67 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(64): Show | 123 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2205_*2206insTATT others(12): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2205 | chr17 | 78110942 | |||||
chr17:78110942 | C | CGGAGACA others(9): Show |
1 | a0001c0001t0030 | 2 | HG01433.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2205_*2206insTATT others(12): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2205 | chr17 | 78110942 | |||||
chr17:78110988 | G | A | 2 | a0017c0032t0053a0021c0030t0085 | 2 | HG02922.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2160C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2160 | chr17 | 78110988 | |||||
chr17:78110990 | G | A | 2 | a0001c0001t0078a0006c0008t0051 | 2 | HG03831.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2158C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2158 | chr17 | 78110990 | |||||
chr17:78111005 | T | C | 1 | a0001c0005t0079 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2143A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2143 | chr17 | 78111005 | |||||
chr17:78111053 | C | G | 1 | a0001c0005t0070 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 2095 | chr17 | 78111053 | |||||
chr17:78111151 | C | T | 1 | a0003c0003t0031 | 2 | HG02027.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1997 | chr17 | 78111151 | |||||
chr17:78111159 | C | G | 2 | a0004c0012t0040a0004c0012t0041 | 2 | HG01070.hp1 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1989G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1989 | chr17 | 78111159 | |||||
chr17:78111312 | A | G | 38 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(35): Show | 68 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1836T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1836 | chr17 | 78111312 | |||||
chr17:78111491 | G | A | 3 | a0001c0005t0014a0003c0003t0089a0003c0009t0014 | 5 | NA18959.hp2 NA18973.hp1 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1657C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1657 | chr17 | 78111491 | |||||
chr17:78111495 | C | T | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1653G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1653 | chr17 | 78111495 | |||||
chr17:78111715 | G | A | 1 | a0001c0001t0080 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1433C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1433 | chr17 | 78111715 | |||||
chr17:78111801 | G | A | 1 | a0001c0005t0081 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1347 | chr17 | 78111801 | |||||
chr17:78111909 | A | G | 1 | a0002c0002t0069 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1239T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1239 | chr17 | 78111909 | |||||
chr17:78111931 | A | ATGACGGG others(103): Show |
1 | a0001c0001t0068 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1216_*1217insGCCT others(106): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1216 | chr17 | 78111931 | |||||
chr17:78111931 | A | ATGACGGG others(102): Show |
35 | a0001c0001t0004a0001c0001t0007a0001c0001t0011others(32): Show | 70 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1216_*1217insGCCT others(105): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1216 | chr17 | 78111931 | |||||
chr17:78111931 | A | ATGACGGG others(844): Show |
1 | a0021c0030t0085 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1216_*1217insGCCT others(847): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1216 | chr17 | 78111931 | |||||
chr17:78111931 | A | ATGACGGG others(176): Show |
2 | a0001c0001t0039a0001c0001t0063 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1216_*1217insGCCT others(179): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1216 | chr17 | 78111931 | |||||
chr17:78111931 | A | ATGACGGG others(141): Show |
1 | a0005c0018t0027 | 2 | HG02622.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1216_*1217insGCCT others(144): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1216 | chr17 | 78111931 | |||||
chr17:78111944 | CCCCGCAG others(32): Show |
C | 1 | a0002c0002t0052 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165_*1203delAACC others(35): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1165 | chr17 | 78111944 | |||||
chr17:78111948 | G | A | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1200 | chr17 | 78111948 | |||||
chr17:78111963 | T | A | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1185 | chr17 | 78111963 | |||||
chr17:78111966 | G | A | 1 | a0005c0004t0082 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1182C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1182 | chr17 | 78111966 | |||||
chr17:78111970 | A | C | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178T>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1178 | chr17 | 78111970 | |||||
chr17:78111983 | T | C | 8 | a0001c0001t0016a0001c0001t0083a0001c0001t0088others(5): Show | 11 | HG01123.hp1 HG01943.hp2 HG02155.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1165A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1165 | chr17 | 78111983 | |||||
chr17:78111987 | G | A | 7 | a0001c0001t0013a0001c0001t0032a0002c0002t0013others(4): Show | 8 | HG02280.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1161C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1161 | chr17 | 78111987 | |||||
chr17:78111991 | G | A | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1157C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1157 | chr17 | 78111991 | |||||
chr17:78112002 | A | T | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1146T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1146 | chr17 | 78112002 | |||||
chr17:78112004 | G | A | 1 | a0001c0005t0059 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1144 | chr17 | 78112004 | |||||
chr17:78112005 | C | A | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1143 | chr17 | 78112005 | |||||
chr17:78112022 | A | G | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1126T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1126 | chr17 | 78112022 | |||||
chr17:78112026 | A | G | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1122 | chr17 | 78112026 | |||||
chr17:78112057 | C | T | 1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1091G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1091 | chr17 | 78112057 | |||||
chr17:78112079 | C | CTGACGGG others(32): Show |
1 | a0017c0032t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1068_*1069insTGAC others(35): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1068 | chr17 | 78112079 | |||||
chr17:78112113 | A | G | 1 | a0005c0018t0027 | 2 | HG02622.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1035 | chr17 | 78112113 | |||||
chr17:78112116 | C | A | 1 | a0005c0018t0027 | 2 | HG02622.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1032G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1032 | chr17 | 78112116 | |||||
chr17:78112124 | C | A | 2 | a0002c0002t0038a0003c0003t0062 | 2 | HG02293.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1024G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1024 | chr17 | 78112124 | |||||
chr17:78112132 | T | C | 1 | a0005c0018t0027 | 2 | HG02622.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1016A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 1016 | chr17 | 78112132 | |||||
chr17:78112207 | G | C | 1 | a0001c0001t0084 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*941C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 941 | chr17 | 78112207 | |||||
chr17:78112299 | G | C | 1 | a0001c0001t0035 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 849 | chr17 | 78112299 | |||||
chr17:78112346 | G | A | 1 | a0021c0030t0085 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 802 | chr17 | 78112346 | |||||
chr17:78112437 | G | A | 7 | a0001c0001t0009a0001c0001t0023a0002c0002t0009others(4): Show | 9 | HG02451.hp2 HG02630.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 711 | chr17 | 78112437 | |||||
chr17:78112448 | C | G | 1 | a0001c0001t0030 | 2 | HG01433.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*700G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 700 | chr17 | 78112448 | |||||
chr17:78112480 | G | A | 1 | a0003c0003t0086 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 668 | chr17 | 78112480 | |||||
chr17:78112531 | A | G | 5 | a0001c0001t0013a0001c0001t0032a0002c0002t0013others(2): Show | 6 | HG02280.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 617 | chr17 | 78112531 | |||||
chr17:78112556 | C | T | 22 | a0001c0001t0003a0001c0001t0012a0001c0001t0030others(19): Show | 88 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*592G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 592 | chr17 | 78112556 | |||||
chr17:78112658 | G | A | 1 | a0005c0004t0087 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 490 | chr17 | 78112658 | |||||
chr17:78112720 | G | C | 1 | a0002c0002t0054 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 428 | chr17 | 78112720 | |||||
chr17:78112779 | C | T | 3 | a0002c0002t0036a0003c0003t0029a0014c0036t0029 | 3 | NA18969.hp1 NA18989.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*369G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 369 | chr17 | 78112779 | |||||
chr17:78112784 | G | A | 1 | a0001c0001t0088 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 364 | chr17 | 78112784 | |||||
chr17:78112868 | G | A | 1 | a0003c0003t0089 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 280 | chr17 | 78112868 | |||||
chr17:78112904 | C | T | 1 | a0001c0001t0011 | 5 | HG01099.hp2 HG01261.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*244G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 244 | chr17 | 78112904 | |||||
chr17:78112972 | T | A | 1 | a0005c0004t0090 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 176 | chr17 | 78112972 | |||||
chr17:78112992 | C | T | 20 | a0001c0001t0005a0001c0001t0008a0001c0001t0035others(17): Show | 37 | HG01255.hp2 HG01361.hp1 HG01884.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*156G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 20/20 | 156 | chr17 | 78112992 | |||||
chr17:78126873 | C | T | 2 | a0004c0006t0019a0004c0006t0024 | 5 | HG01884.hp2 HG02109.hp2 HG03139.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-41G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 2/20 | 41 | chr17 | 78126873 | |||||
chr17:78126887 | G | T | 1 | a0001c0001t0055 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 2/20 | 55 | chr17 | 78126887 | |||||
chr17:78128729 | A | AG | 63 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(60): Show | 139 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(136): Show |
5_prime_UTR_variant | MODIFIER | c.-193dupC | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/20 | 1898 | chr17 | 78128729 | |||||
chr17:78128754 | C | T | 2 | a0001c0001t0017a0001c0001t0018 | 6 | HG02056.hp2 HG02129.hp1 NA18954.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-217G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/20 | 1922 | chr17 | 78128754 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:78113215 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG02698.hp1 | splice_region_variant&intron_variant | LOW | c.2355-4G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113215 | ||||||
chr17:78113252 | C | T | 1 | a0007c0007t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2355-41G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113252 | ||||||
chr17:78113277 | G | A | 108 | a0001c0001t0004g0161a0001c0001t0004g0249a0001c0001t0004g0250others(105): Show | 108 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.2355-66C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113277 | ||||||
chr17:78113328 | G | A | 8 | a0003c0003t0003g0367a0003c0003t0003g0368a0003c0003t0003g0369others(5): Show | 8 | HG00544.hp1 NA18946.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.2355-117C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113328 | ||||||
chr17:78113421 | T | G | 1 | a0005c0004t0001g0220 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2354+127A>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113421 | ||||||
chr17:78113435 | C | T | 1 | a0003c0003t0003g0351 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2354+113G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 19/19 | chr17 | 78113435 | ||||||
chr17:78113661 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2278-37A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113661 | ||||||
chr17:78113686 | T | C | 6 | a0001c0001t0013g0083a0001c0001t0013g0087a0001c0001t0032g0276others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2278-62A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113686 | ||||||
chr17:78113793 | A | T | 5 | a0001c0005t0014g0313a0003c0003t0089g0393a0003c0009t0014g0424others(2): Show | 5 | NA18959.hp2 NA18973.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2278-169T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113793 | ||||||
chr17:78113813 | C | T | 1 | a0001c0001t0005g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2278-189G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113813 | ||||||
chr17:78113818 | G | T | 2 | a0001c0001t0078g0346a0006c0008t0051g0143 | 2 | HG03831.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2278-194C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113818 | ||||||
chr17:78113922 | C | T | 3 | a0001c0001t0004g0161a0001c0001t0017g0009a0001c0001t0017g0013 | 3 | HG00558.hp2 HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2278-298G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78113922 | ||||||
chr17:78114024 | C | T | 1 | a0001c0017t0001g0293 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2278-400G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114024 | ||||||
chr17:78114135 | G | GC | 7 | a0001c0005t0003g0183a0001c0005t0003g0186a0001c0005t0003g0187others(4): Show | 7 | NA18943.hp2 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2278-512dupG | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114135 | ||||||
chr17:78114177 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2278-553G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114177 | ||||||
chr17:78114280 | TGACACTC others(24): Show |
T | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-687_2278-657d others(33): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114280 | ||||||
chr17:78114307 | C | A | 2 | a0002c0002t0002g0120a0010c0019t0002g0069 | 2 | HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2278-683G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114307 | ||||||
chr17:78114384 | T | G | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-760A>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114384 | ||||||
chr17:78114387 | A | T | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-763T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114387 | ||||||
chr17:78114404 | T | G | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-780A>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114404 | ||||||
chr17:78114419 | G | A | 3 | a0001c0001t0020g0084a0001c0001t0020g0085a0001c0001t0020g0088 | 3 | HG02145.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2278-795C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114419 | ||||||
chr17:78114422 | A | T | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-798T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114422 | ||||||
chr17:78114433 | T | G | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-809A>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114433 | ||||||
chr17:78114437 | A | G | 87 | a0001c0001t0001g0005a0001c0001t0003g0154a0001c0001t0003g0316others(84): Show | 89 | HG00544.hp1 HG00558.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.2278-813T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114437 | ||||||
chr17:78114454 | A | T | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-830T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114454 | ||||||
chr17:78114462 | G | A | 42 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2278-838C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114462 | ||||||
chr17:78114474 | G | T | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-850C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114474 | ||||||
chr17:78114508 | A | G | 1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2278-884T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114508 | ||||||
chr17:78114569 | A | G | 1 | a0003c0003t0004g0396 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2278-945T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114569 | ||||||
chr17:78114620 | A | C | 1 | a0003c0003t0001g0406 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2278-996T>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114620 | ||||||
chr17:78114822 | C | T | 1 | a0001c0001t0064g0275 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2278-1198G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114822 | ||||||
chr17:78114858 | G | A | 1 | a0002c0002t0006g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2278-1234C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114858 | ||||||
chr17:78114928 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2278-1304C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114928 | ||||||
chr17:78114957 | C | T | 1 | a0002c0002t0049g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2278-1333G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78114957 | ||||||
chr17:78115042 | T | TCTACAGC others(14): Show |
1 | a0002c0002t0069g0422 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2278-1439_2278-141 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115042 | ||||||
chr17:78115067 | C | T | 1 | a0004c0010t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2278-1443G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115067 | ||||||
chr17:78115122 | C | G | 39 | a0001c0001t0004g0252a0001c0001t0004g0281a0001c0001t0009g0016others(36): Show | 39 | HG01070.hp1 HG01099.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2278-1498G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115122 | ||||||
chr17:78115170 | A | G | 69 | a0001c0001t0002g0150a0001c0001t0003g0168a0001c0001t0004g0161others(66): Show | 70 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.2278-1546T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115170 | ||||||
chr17:78115198 | C | A | 1 | a0001c0005t0079g0307 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2278-1574G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115198 | ||||||
chr17:78115256 | G | A | 1 | a0002c0002t0050g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2278-1632C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115256 | ||||||
chr17:78115287 | C | T | 1 | a0001c0005t0005g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2278-1663G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115287 | ||||||
chr17:78115303 | A | G | 32 | a0001c0001t0008g0089a0001c0001t0009g0016a0001c0001t0013g0083others(29): Show | 32 | HG00639.hp1 HG01884.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.2278-1679T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115303 | ||||||
chr17:78115385 | A | G | 1 | a0001c0005t0071g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2278-1761T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115385 | ||||||
chr17:78115418 | G | C | 21 | a0001c0001t0011g0286a0001c0001t0011g0287a0001c0001t0011g0288others(18): Show | 21 | HG00639.hp1 HG01099.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2278-1794C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115418 | ||||||
chr17:78115436 | G | A | 1 | a0004c0006t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2278-1812C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115436 | ||||||
chr17:78115479 | A | G | 266 | a0001c0001t0001g0155a0001c0001t0001g0159a0001c0001t0001g0165others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2277+1790T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115479 | ||||||
chr17:78115493 | G | C | 1 | a0006c0008t0051g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2277+1776C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115493 | ||||||
chr17:78115515 | G | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0176a0001c0001t0001g0277others(74): Show | 78 | HG00140.hp2 HG01069.hp1 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.2277+1754C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115515 | ||||||
chr17:78115548 | G | A | 3 | a0003c0009t0001g0398a0005c0004t0003g0199a0005c0004t0003g0200 | 3 | HG04228.hp1 NA18944.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2277+1721C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115548 | ||||||
chr17:78115593 | A | T | 13 | a0001c0001t0008g0089a0001c0001t0013g0083a0001c0001t0013g0087others(10): Show | 13 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2277+1676T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115593 | ||||||
chr17:78115614 | G | C | 1 | a0002c0002t0049g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2277+1655C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(14): Show |
5 | a0001c0001t0001g0007a0001c0001t0030g0341a0002c0002t0002g0135others(2): Show | 6 | HG01433.hp2 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277+1634_2277+165 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(161): Show |
1 | a0005c0018t0027g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(56): Show |
1 | a0004c0006t0003g0234 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(350): Show |
1 | a0004c0006t0002g0042 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(119): Show |
1 | a0001c0005t0003g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(35): Show |
5 | a0001c0001t0003g0166a0001c0005t0014g0313a0002c0002t0006g0071others(2): Show | 5 | HG01106.hp2 HG02083.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.2277+1613_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(56): Show |
1 | a0001c0001t0063g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(77): Show |
1 | a0002c0002t0002g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(77): Show |
1 | a0005c0004t0001g0153 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(560): Show |
1 | a0004c0006t0002g0050 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(434): Show |
1 | a0001c0005t0003g0319 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(445): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGAGCG others(602): Show |
1 | a0001c0001t0004g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(613): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(14): Show |
2 | a0002c0002t0002g0068a0004c0006t0047g0044 | 2 | HG02056.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2277+1654_2277+165 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(560): Show |
1 | a0002c0002t0002g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(329): Show |
1 | a0002c0002t0007g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(35): Show |
1 | a0001c0001t0001g0432 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(77): Show |
1 | a0023c0026t0023g0248 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(56): Show |
1 | a0002c0002t0007g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(392): Show |
1 | a0004c0006t0006g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(245): Show |
1 | a0005c0004t0003g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(119): Show |
1 | a0002c0002t0050g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(161): Show |
1 | a0002c0002t0007g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(224): Show |
1 | a0005c0004t0087g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(287): Show |
1 | a0002c0002t0052g0130 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | G | GAGGGGCG others(434): Show |
1 | a0005c0004t0067g0210 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2277+1654_2277+165 others(445): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(14): Show |
G | 1 | a0007c0007t0042g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2277+1634_2277+165 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(35): Show |
G | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | NA18964.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2277+1613_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(77): Show |
G | 1 | a0004c0006t0007g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2277+1571_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(98): Show |
G | 2 | a0001c0001t0073g0282a0005c0004t0082g0195 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2277+1550_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(119): Show |
G | 1 | a0002c0002t0009g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2277+1529_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(161): Show |
G | 1 | a0002c0002t0007g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2277+1487_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115614 | GAGGAGCG others(245): Show |
G | 2 | a0005c0018t0027g0018a0007c0007t0002g0061 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2277+1403_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115614 | ||||||
chr17:78115618 | A | AGCGAAGG others(56): Show |
1 | a0001c0005t0003g0421 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(455): Show |
1 | a0016c0034t0001g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(35): Show |
2 | a0004c0006t0043g0048a0008c0013t0002g0030 | 2 | HG06807.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2277+1650_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(77): Show |
1 | a0003c0003t0001g0365 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(98): Show |
1 | a0001c0001t0005g0304 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(224): Show |
1 | a0004c0006t0002g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(14): Show |
10 | a0001c0001t0003g0260a0001c0001t0033g0164a0001c0001t0084g0345others(7): Show | 10 | HG00597.hp2 HG01123.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2277+1630_2277+165 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(434): Show |
1 | a0001c0001t0004g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(445): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(371): Show |
1 | a0001c0001t0001g0278 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(182): Show |
1 | a0001c0001t0001g0317 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(623): Show |
1 | a0003c0003t0001g0350 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(634): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(455): Show |
1 | a0001c0001t0001g0331 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(98): Show |
1 | a0002c0002t0023g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(182): Show |
1 | a0004c0006t0002g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(140): Show |
1 | a0003c0003t0004g0396 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(392): Show |
1 | a0004c0006t0019g0024 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(161): Show |
1 | a0001c0001t0004g0249 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(203): Show |
1 | a0001c0001t0002g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(224): Show |
1 | a0005c0004t0003g0203 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(308): Show |
1 | a0004c0006t0001g0233 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(308): Show |
1 | a0004c0006t0019g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(371): Show |
1 | a0004c0006t0002g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(205): Show |
1 | a0001c0001t0001g0433 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(216): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(35): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0329a0001c0001t0009g0016others(2): Show | 6 | HG02735.hp2 HG02896.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277+1609_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(854): Show |
1 | a0003c0003t0001g0356 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(865): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(812): Show |
1 | a0001c0001t0018g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(823): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(287): Show |
1 | a0001c0001t0003g0318 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(161): Show |
1 | a0002c0002t0002g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(224): Show |
1 | a0004c0006t0002g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(56): Show |
8 | a0001c0001t0015g0268a0002c0002t0002g0100a0002c0002t0006g0114others(5): Show | 8 | HG00738.hp1 HG02145.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.2277+1588_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(266): Show |
1 | a0002c0002t0044g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(623): Show |
1 | a0001c0001t0001g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(634): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(203): Show |
1 | a0001c0033t0004g0347 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(959): Show |
1 | a0003c0003t0001g0390 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(970): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(413): Show |
1 | a0004c0006t0002g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(266): Show |
1 | a0002c0002t0002g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(308): Show |
1 | a0001c0001t0001g0334 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(77): Show |
6 | a0001c0001t0001g0175a0001c0001t0066g0259a0001c0005t0012g0309others(3): Show | 6 | HG01070.hp1 HG01109.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2277+1567_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(602): Show |
1 | a0001c0001t0001g0430 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(613): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(602): Show |
1 | a0005c0004t0003g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(613): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(371): Show |
1 | a0001c0001t0001g0165 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(1820): Show |
1 | a0003c0003t0001g0387 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(1831): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(392): Show |
1 | a0004c0006t0019g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(245): Show |
1 | a0001c0001t0012g0292 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(287): Show |
1 | a0002c0002t0006g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(1757): Show |
1 | a0001c0001t0001g0416 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(1768): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(352): Show |
1 | a0001c0001t0001g0428 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(363): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(224): Show |
1 | a0001c0001t0077g0257 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(392): Show |
1 | a0002c0002t0038g0123 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(455): Show |
1 | a0020c0029t0005g0301 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(308): Show |
1 | a0004c0006t0009g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(98): Show |
4 | a0001c0001t0004g0258a0003c0003t0031g0360a0004c0006t0002g0056others(1): Show | 4 | HG02027.hp1 HG03486.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2277+1546_2277+165 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(560): Show |
1 | a0001c0001t0078g0346 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(140): Show |
1 | a0001c0001t0015g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(161): Show |
1 | a0006c0016t0037g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(119): Show |
5 | a0001c0001t0001g0328a0001c0001t0012g0163a0001c0001t0074g0156others(2): Show | 5 | HG01123.hp2 HG02523.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.2277+1525_2277+165 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(161): Show |
1 | a0002c0002t0002g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(518): Show |
1 | a0002c0002t0002g0124 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(529): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(140): Show |
4 | a0002c0002t0002g0093a0003c0003t0001g0371a0004c0006t0002g0053others(1): Show | 4 | HG01106.hp1 HG01192.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2277+1504_2277+165 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(413): Show |
1 | a0001c0005t0028g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(182): Show |
1 | a0004c0010t0075g0232 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(287): Show |
1 | a0003c0003t0003g0402 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(161): Show |
4 | a0001c0001t0001g0159a0001c0001t0017g0013a0003c0003t0001g0392others(1): Show | 4 | HG02056.hp2 HG02602.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2277+1483_2277+165 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(182): Show |
8 | a0001c0001t0001g0174a0001c0001t0001g0267a0001c0001t0001g0270others(5): Show | 9 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.2277+1462_2277+165 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(329): Show |
1 | a0003c0009t0061g0395 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(266): Show |
1 | a0001c0001t0018g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(287): Show |
1 | a0001c0001t0005g0302 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(203): Show |
1 | a0003c0003t0031g0359 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2277+1441_2277+165 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(877): Show |
1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(888): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(224): Show |
4 | a0001c0001t0003g0264a0004c0011t0002g0022a0005c0004t0005g0427others(1): Show | 4 | HG01952.hp1 NA18971.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2277+1420_2277+165 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(245): Show |
2 | a0001c0001t0001g0155a0001c0001t0076g0295 | 2 | HG02155.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2277+1399_2277+165 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(266): Show |
2 | a0001c0001t0001g0238a0003c0037t0001g0363 | 2 | HG01346.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.2277+1378_2277+165 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(392): Show |
1 | a0002c0002t0006g0126 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(287): Show |
1 | a0001c0001t0018g0012 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2277+1357_2277+165 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(497): Show |
1 | a0005c0004t0003g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2277+1650_2277+165 others(508): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(308): Show |
3 | a0001c0005t0001g0315a0003c0003t0001g0349a0003c0003t0062g0379 | 3 | HG00741.hp1 NA19057.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2277+1336_2277+165 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(329): Show |
1 | a0001c0001t0017g0014 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(350): Show |
7 | a0001c0001t0003g0154a0001c0001t0004g0161a0002c0002t0002g0076others(4): Show | 7 | HG00558.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+1650_2277+165 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(1148): Show |
1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(1159): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(371): Show |
1 | a0004c0010t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(392): Show |
2 | a0001c0005t0081g0312a0005c0004t0090g0226 | 2 | HG00741.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2277+1650_2277+165 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(413): Show |
3 | a0003c0003t0001g0408a0004c0006t0007g0036a0007c0007t0002g0062 | 3 | HG02559.hp1 HG03041.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2277+1650_2277+165 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(434): Show |
1 | a0003c0003t0001g0358 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(445): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(455): Show |
1 | a0001c0001t0004g0256 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(476): Show |
1 | a0001c0001t0056g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(487): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(581): Show |
1 | a0001c0001t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(592): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(539): Show |
1 | a0001c0001t0001g0325 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(550): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(623): Show |
1 | a0003c0003t0003g0394 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(634): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(686): Show |
1 | a0005c0004t0003g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(697): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(791): Show |
1 | a0004c0006t0002g0021 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(802): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(812): Show |
1 | a0004c0006t0007g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(823): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(959): Show |
1 | a0005c0004t0001g0206 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(970): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(917): Show |
1 | a0001c0005t0059g0173 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(928): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(1421): Show |
1 | a0001c0005t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(1432): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(1568): Show |
1 | a0004c0011t0008g0023 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(1579): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(329): Show |
1 | a0002c0002t0002g0095 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | AGCGAAGG others(665): Show |
1 | a0002c0002t0002g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2277+1650_2277+165 others(676): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | G | 29 | a0001c0001t0001g0171a0001c0001t0001g0432a0001c0001t0003g0339others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.2277+1651T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | A | GGCGAAGG others(119): Show |
1 | a0019c0028t0002g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2277+1651_2277+165 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(14): Show |
A | 11 | a0001c0005t0003g0183a0001c0005t0005g0308a0001c0005t0016g0181others(8): Show | 11 | HG00597.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2277+1630_2277+165 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(35): Show |
A | 6 | a0001c0001t0001g0298a0001c0001t0001g0330a0001c0001t0055g0192others(3): Show | 6 | HG00673.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277+1609_2277+165 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(56): Show |
A | 7 | a0001c0001t0015g0274a0001c0035t0001g0348a0003c0003t0001g0409others(4): Show | 7 | HG02109.hp2 HG02148.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+1588_2277+165 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(77): Show |
A | 7 | a0001c0001t0001g0263a0001c0001t0004g0261a0001c0001t0005g0297others(4): Show | 7 | HG01891.hp1 HG02071.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+1567_2277+165 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(98): Show |
A | 7 | a0001c0001t0001g0284a0001c0001t0001g0415a0001c0001t0004g0281others(4): Show | 7 | HG01346.hp1 HG01361.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2277+1546_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(119): Show |
A | 7 | a0001c0001t0005g0177a0001c0001t0016g0280a0001c0001t0022g0265others(4): Show | 7 | HG01981.hp1 HG02083.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+1525_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(140): Show |
A | 2 | a0001c0001t0003g0435a0006c0008t0051g0143 | 2 | HG00280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2277+1504_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(161): Show |
A | 4 | a0001c0001t0030g0431a0002c0002t0008g0106a0002c0002t0036g0102others(1): Show | 4 | HG03195.hp1 NA18995.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2277+1483_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(182): Show |
A | 2 | a0003c0003t0003g0362a0007c0007t0009g0065 | 2 | HG01928.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2277+1462_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(203): Show |
A | 1 | a0001c0001t0022g0180 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2277+1441_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(224): Show |
A | 3 | a0001c0001t0013g0083a0005c0004t0003g0200a0008c0013t0032g0179 | 3 | HG03540.hp2 HG03579.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2277+1420_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115618 | AGCGAAGG others(245): Show |
A | 7 | a0001c0001t0008g0089a0001c0001t0013g0087a0001c0001t0032g0276others(4): Show | 7 | HG00140.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+1399_2277+165 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115618 | ||||||
chr17:78115624 | G | C | 1 | a0003c0003t0001g0406 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2277+1645C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115624 | ||||||
chr17:78115633 | C | CACAGGGG others(497): Show |
1 | a0004c0006t0002g0019 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2277+1635_2277+163 others(508): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115633 | ||||||
chr17:78115639 | G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0333a0001c0001t0004g0251others(8): Show | 12 | HG00408.hp2 HG00673.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.2277+1630C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(14): Show |
9 | a0001c0001t0001g0172a0001c0001t0004g0250a0001c0001t0080g0338others(6): Show | 9 | HG00423.hp2 HG01109.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2277+1629_2277+163 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(980): Show |
1 | a0003c0003t0001g0353 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(991): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(224): Show |
1 | a0003c0003t0001g0399 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(245): Show |
1 | a0001c0005t0001g0241 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(518): Show |
1 | a0001c0005t0003g0001 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2277+1629_2277+163 others(529): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(1400): Show |
1 | a0001c0001t0003g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(1411): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(560): Show |
1 | a0001c0001t0003g0271 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(35): Show |
3 | a0001c0001t0004g0272a0002c0002t0069g0422a0005c0004t0033g0197 | 3 | HG02027.hp2 HG03225.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2277+1629_2277+163 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(98): Show |
1 | a0003c0003t0003g0351 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(245): Show |
1 | a0001c0001t0003g0429 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(98): Show |
1 | a0001c0005t0004g0310 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(329): Show |
1 | a0003c0003t0065g0364 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(392): Show |
1 | a0001c0001t0088g0336 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(308): Show |
1 | a0002c0002t0002g0079 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(413): Show |
1 | a0001c0001t0083g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115639 | G | GGCGAAGG others(539): Show |
1 | a0001c0001t0001g0320 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2277+1629_2277+163 others(550): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115639 | ||||||
chr17:78115641 | C | CGAAGGGA others(14): Show |
1 | a0002c0002t0002g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2277+1627_2277+162 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115641 | ||||||
chr17:78115656 | CAGGGGCG others(183): Show |
C | 1 | a0005c0004t0001g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2277+1423_2277+161 others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115656 | ||||||
chr17:78115660 | G | A | 11 | a0001c0001t0004g0300a0001c0001t0022g0266a0001c0001t0063g0178others(8): Show | 11 | HG00673.hp1 HG01175.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.2277+1609C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(14): Show |
9 | a0001c0001t0003g0339a0001c0001t0017g0009a0001c0005t0060g0190others(6): Show | 9 | HG00408.hp1 HG01192.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.2277+1608_2277+160 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(142): Show |
1 | a0001c0001t0001g0006 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2277+1608_2277+160 others(153): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(455): Show |
1 | a0003c0009t0001g0398 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(287): Show |
1 | a0005c0004t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(371): Show |
1 | a0002c0002t0002g0127 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(77): Show |
1 | a0001c0001t0011g0290 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(644): Show |
1 | a0008c0013t0002g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(655): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(833): Show |
1 | a0002c0002t0002g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(844): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(203): Show |
1 | a0004c0006t0007g0032 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(413): Show |
1 | a0001c0001t0011g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(224): Show |
1 | a0001c0005t0028g0170 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(56): Show |
1 | a0002c0002t0002g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(161): Show |
1 | a0001c0001t0001g0007 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2277+1608_2277+160 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(308): Show |
1 | a0003c0003t0005g0354 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(287): Show |
1 | a0011c0022t0002g0139 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(581): Show |
1 | a0001c0005t0001g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(592): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(665): Show |
1 | a0003c0003t0003g0369 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(676): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(1064): Show |
1 | a0003c0003t0001g0407 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(1075): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115660 | G | GGCGAAGG others(560): Show |
1 | a0002c0002t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2277+1608_2277+160 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115660 | ||||||
chr17:78115662 | C | CGAAGGGA others(224): Show |
1 | a0002c0002t0002g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2277+1606_2277+160 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115662 | ||||||
chr17:78115681 | G | A | 15 | a0001c0001t0003g0166a0001c0001t0003g0434a0001c0001t0004g0300others(12): Show | 15 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2277+1588C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | AGCGAAGG others(14): Show |
1 | a0002c0002t0002g0127 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2277+1588_2277+158 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(14): Show |
8 | a0001c0001t0003g0316a0001c0001t0011g0288a0001c0001t0012g0160others(5): Show | 8 | HG01099.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2277+1587_2277+158 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(35): Show |
1 | a0001c0001t0003g0168 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(203): Show |
1 | a0001c0001t0005g0167 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(833): Show |
1 | a0003c0003t0001g0383 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(844): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(35): Show |
2 | a0001c0005t0001g0239a0003c0003t0003g0389 | 2 | HG00099.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2277+1587_2277+158 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(56): Show |
1 | a0001c0001t0001g0333 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(182): Show |
1 | a0001c0001t0080g0338 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(56): Show |
1 | a0002c0002t0012g0419 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(350): Show |
1 | a0004c0006t0010g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(917): Show |
1 | a0001c0001t0005g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(928): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115681 | G | GGCGAAGG others(1274): Show |
1 | a0005c0004t0003g0204 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2277+1587_2277+158 others(1285): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115681 | ||||||
chr17:78115684 | G | A | 1 | a0001c0001t0004g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2277+1585C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115684 | ||||||
chr17:78115702 | G | A | 9 | a0001c0001t0003g0434a0001c0001t0004g0300a0001c0001t0005g0167others(6): Show | 9 | HG00639.hp1 HG00642.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.2277+1567C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(14): Show |
2 | a0001c0001t0020g0084a0001c0001t0020g0088 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2277+1566_2277+156 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(728): Show |
1 | a0003c0003t0003g0367 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(739): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(56): Show |
1 | a0001c0005t0072g0299 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(329): Show |
1 | a0001c0005t0071g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(560): Show |
1 | a0001c0005t0070g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(35): Show |
3 | a0002c0002t0002g0075a0003c0003t0001g0399a0016c0034t0001g0205 | 3 | HG01257.hp2 HG02040.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2277+1566_2277+156 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(560): Show |
1 | a0002c0014t0001g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(182): Show |
1 | a0013c0024t0005g0194 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(560): Show |
1 | a0004c0006t0002g0020 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(560): Show |
1 | a0005c0004t0005g0218 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(140): Show |
1 | a0001c0001t0003g0291 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(266): Show |
1 | a0005c0004t0001g0220 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(854): Show |
1 | a0001c0005t0003g0244 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(865): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(413): Show |
1 | a0004c0006t0010g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115702 | G | GGCGAAGG others(686): Show |
1 | a0002c0002t0002g0135 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2277+1566_2277+156 others(697): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115702 | ||||||
chr17:78115723 | G | A | 22 | a0001c0001t0004g0272a0001c0001t0011g0290a0001c0001t0023g0285others(19): Show | 23 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2277+1546C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(14): Show |
4 | a0001c0005t0072g0299a0002c0002t0013g0059a0003c0003t0005g0384others(1): Show | 4 | HG02280.hp2 HG03209.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2277+1545_2277+154 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(119): Show |
1 | a0001c0001t0011g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(203): Show |
1 | a0001c0001t0020g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(245): Show |
1 | a0002c0002t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(1190): Show |
1 | a0003c0003t0003g0368 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(1201): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(35): Show |
1 | a0010c0019t0002g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(77): Show |
1 | a0003c0003t0001g0410 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(77): Show |
1 | a0001c0001t0003g0316 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(161): Show |
2 | a0001c0001t0020g0084a0001c0001t0020g0088 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2277+1545_2277+154 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(182): Show |
1 | a0003c0009t0014g0426 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(1337): Show |
1 | a0001c0005t0003g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(1348): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(77): Show |
1 | a0001c0005t0003g0188 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(392): Show |
1 | a0006c0016t0002g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(770): Show |
1 | a0003c0003t0003g0374 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(781): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(392): Show |
1 | a0004c0006t0006g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(455): Show |
1 | a0003c0003t0001g0403 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(466): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115723 | G | GGCGAAGG others(226): Show |
1 | a0001c0001t0012g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2277+1545_2277+154 others(237): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115723 | ||||||
chr17:78115744 | G | A | 11 | a0001c0001t0001g0317a0001c0001t0001g0331a0001c0001t0003g0168others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2277+1525C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAACG others(392): Show |
1 | a0003c0003t0001g0406 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(14): Show |
2 | a0001c0001t0003g0429a0002c0002t0002g0072 | 2 | HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2277+1524_2277+152 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(119): Show |
1 | a0003c0009t0014g0425 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(35): Show |
2 | a0001c0001t0001g0171a0001c0005t0060g0190 | 2 | NA19000.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2277+1524_2277+152 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(182): Show |
1 | a0003c0009t0014g0424 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(392): Show |
1 | a0002c0002t0026g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(119): Show |
1 | a0003c0003t0001g0385 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(2240): Show |
1 | a0010c0019t0002g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(2251): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(161): Show |
1 | a0003c0003t0001g0361 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(161): Show |
2 | a0001c0001t0001g0172a0001c0001t0017g0009 | 2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2277+1524_2277+152 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(919): Show |
1 | a0002c0002t0010g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(930): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(266): Show |
1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2277+1524_2277+152 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115744 | G | GGCGAAGG others(1106): Show |
1 | a0001c0001t0004g0252 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2277+1524_2277+152 others(1117): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115744 | ||||||
chr17:78115747 | G | GAAGGGAG others(854): Show |
1 | a0001c0005t0005g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2277+1521_2277+152 others(865): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115747 | ||||||
chr17:78115759 | C | T | 1 | a0002c0002t0048g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2277+1510G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115759 | ||||||
chr17:78115765 | G | A | 19 | a0001c0001t0001g0317a0001c0001t0003g0318a0001c0001t0004g0300others(16): Show | 19 | HG00140.hp1 HG00673.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.2277+1504C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(14): Show |
2 | a0001c0001t0003g0434a0002c0002t0002g0109 | 2 | HG00642.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2277+1503_2277+150 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(539): Show |
1 | a0003c0003t0001g0375 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(550): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(161): Show |
1 | a0001c0005t0014g0313 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(413): Show |
1 | a0001c0001t0004g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(203): Show |
1 | a0005c0004t0001g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(214): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(917): Show |
1 | a0004c0006t0043g0048 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(928): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(287): Show |
1 | a0001c0001t0002g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(602): Show |
1 | a0005c0004t0033g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(613): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(518): Show |
1 | a0001c0001t0005g0303 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(529): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(854): Show |
1 | a0004c0006t0003g0234 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(865): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(182): Show |
1 | a0002c0002t0002g0099 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(770): Show |
1 | a0005c0004t0001g0215 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(781): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(245): Show |
1 | a0001c0001t0001g0337 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(329): Show |
1 | a0002c0002t0006g0071 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115765 | G | GGCGAAGG others(1400): Show |
1 | a0002c0023t0002g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2277+1503_2277+150 others(1411): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115765 | ||||||
chr17:78115772 | G | A | 1 | a0002c0002t0015g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2277+1497C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115772 | ||||||
chr17:78115786 | G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0171a0001c0001t0001g0317others(19): Show | 23 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2277+1483C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(266): Show |
1 | a0002c0002t0002g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(35): Show |
1 | a0001c0001t0011g0286 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(98): Show |
1 | a0003c0003t0001g0405 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(109): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(140): Show |
1 | a0001c0001t0003g0168 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(707): Show |
1 | a0002c0002t0002g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(718): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(119): Show |
1 | a0001c0001t0064g0275 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(266): Show |
1 | a0001c0001t0001g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(161): Show |
1 | a0001c0005t0003g0421 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(172): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115786 | G | GGCGAAGG others(539): Show |
1 | a0001c0001t0003g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2277+1482_2277+148 others(550): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115786 | ||||||
chr17:78115807 | G | A | 17 | a0001c0001t0001g0279a0001c0001t0003g0318a0001c0001t0003g0339others(14): Show | 17 | HG00323.hp2 HG00673.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2277+1462C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(14): Show |
5 | a0001c0001t0001g0296a0001c0001t0001g0333a0001c0001t0004g0324others(2): Show | 5 | HG01358.hp1 HG02300.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2277+1461_2277+146 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(119): Show |
1 | a0002c0002t0026g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(413): Show |
1 | a0003c0003t0089g0393 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(35): Show |
2 | a0001c0001t0005g0167a0007c0007t0002g0060 | 2 | NA18991.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2277+1461_2277+146 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(140): Show |
1 | a0004c0020t0008g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(728): Show |
1 | a0001c0005t0057g0311 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(739): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(119): Show |
1 | a0003c0003t0001g0388 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115807 | G | GGCGAAGG others(371): Show |
1 | a0002c0002t0002g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2277+1461_2277+146 others(382): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115807 | ||||||
chr17:78115828 | G | A | 19 | a0001c0001t0001g0263a0001c0001t0003g0435a0001c0001t0004g0300others(16): Show | 19 | HG00280.hp2 HG00673.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2277+1441C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(14): Show |
2 | a0002c0002t0044g0103a0004c0006t0002g0043 | 2 | HG03834.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2277+1440_2277+144 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(35): Show |
1 | a0005c0004t0003g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(224): Show |
1 | a0002c0002t0002g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(707): Show |
1 | a0003c0003t0001g0397 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(718): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(1148): Show |
1 | a0003c0003t0004g0380 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(1159): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(56): Show |
1 | a0001c0001t0004g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(67): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(1442): Show |
1 | a0002c0002t0002g0120 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(1453): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(350): Show |
1 | a0001c0001t0003g0339 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(938): Show |
1 | a0005c0004t0001g0219 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(949): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(938): Show |
1 | a0001c0001t0001g0340 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(949): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(392): Show |
1 | a0001c0001t0001g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(1001): Show |
1 | a0004c0006t0006g0041 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(1012): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(308): Show |
1 | a0002c0002t0002g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(319): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(476): Show |
1 | a0003c0003t0001g0352 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(487): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115828 | G | GGCGAAGG others(644): Show |
1 | a0001c0001t0068g0253 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2277+1440_2277+144 others(655): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115828 | ||||||
chr17:78115841 | G | A | 1 | a0001c0001t0022g0266 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2277+1428C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115841 | ||||||
chr17:78115846 | A | AGGGGCGA others(895): Show |
1 | a0003c0003t0003g0413 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2277+1422_2277+142 others(906): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115846 | ||||||
chr17:78115847 | G | GGGGCGAA others(621): Show |
1 | a0004c0006t0001g0235 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2277+1421_2277+142 others(632): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115847 | ||||||
chr17:78115849 | G | A | 22 | a0001c0001t0004g0250a0001c0001t0004g0300a0001c0001t0011g0287others(19): Show | 25 | HG00140.hp1 HG00423.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2277+1420C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | AGCGAAGG others(1001): Show |
1 | a0002c0002t0002g0075 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2277+1420_2277+142 others(1012): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(14): Show |
2 | a0001c0005t0001g0241a0001c0005t0003g0187 | 2 | HG02698.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2277+1419_2277+142 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(35): Show |
1 | a0001c0001t0004g0251 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(665): Show |
1 | a0001c0005t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(676): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(1400): Show |
1 | a0002c0002t0054g0122 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(1411): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(392): Show |
1 | a0004c0012t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(403): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(140): Show |
1 | a0002c0002t0009g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(245): Show |
1 | a0003c0003t0001g0376 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(77): Show |
1 | a0005c0018t0027g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(182): Show |
1 | a0001c0005t0001g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(193): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(329): Show |
1 | a0001c0001t0001g0332 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(140): Show |
1 | a0002c0002t0049g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(151): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(266): Show |
1 | a0002c0002t0069g0422 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(224): Show |
1 | a0001c0001t0016g0343 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(235): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115849 | G | GGCGAAGG others(329): Show |
1 | a0001c0005t0005g0305 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2277+1419_2277+142 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115849 | ||||||
chr17:78115870 | G | A | 20 | a0001c0001t0003g0168a0001c0001t0003g0316a0001c0001t0005g0162others(17): Show | 21 | HG01069.hp2 HG01071.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.2277+1399C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | AGCGAAGG others(959): Show |
1 | a0003c0003t0003g0351 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2277+1399_2277+140 others(970): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(14): Show |
2 | a0002c0002t0002g0092a0003c0003t0065g0364 | 2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2277+1398_2277+139 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(539): Show |
1 | a0001c0001t0001g0321 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(550): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(560): Show |
1 | a0004c0010t0001g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(571): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(350): Show |
1 | a0002c0002t0013g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(266): Show |
1 | a0001c0017t0001g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(1211): Show |
1 | a0001c0001t0001g0296 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(1222): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(980): Show |
1 | a0012c0021t0002g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(991): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115870 | G | GGCGAAGG others(728): Show |
1 | a0002c0002t0048g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2277+1398_2277+139 others(739): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115870 | ||||||
chr17:78115879 | A | AGTGGGCA others(563): Show |
1 | a0002c0002t0002g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2277+1389_2277+139 others(574): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115879 | ||||||
chr17:78115891 | G | A | 9 | a0001c0001t0001g0340a0001c0001t0003g0168a0001c0001t0003g0435others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.2277+1378C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | AGCGAAGG others(728): Show |
1 | a0007c0007t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2277+1378_2277+137 others(739): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(14): Show |
2 | a0003c0003t0001g0406a0004c0006t0006g0054 | 2 | HG02109.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2277+1377_2277+137 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(245): Show |
1 | a0002c0002t0002g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(256): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(1358): Show |
1 | a0005c0004t0001g0214 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(1369): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(77): Show |
1 | a0001c0001t0011g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(88): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(350): Show |
1 | a0001c0001t0003g0316 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(287): Show |
1 | a0004c0006t0047g0044 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(298): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(602): Show |
1 | a0003c0003t0003g0389 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(613): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115891 | G | GGCGAAGG others(791): Show |
1 | a0001c0005t0079g0307 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2277+1377_2277+137 others(802): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115891 | ||||||
chr17:78115912 | G | A | 12 | a0001c0001t0008g0089a0001c0001t0013g0083a0001c0001t0013g0087others(9): Show | 12 | HG02080.hp1 HG02630.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2277+1357C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(14): Show |
4 | a0001c0001t0001g0171a0001c0001t0011g0287a0001c0001t0011g0288others(1): Show | 4 | HG01099.hp2 NA18969.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2277+1356_2277+135 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(266): Show |
1 | a0001c0001t0011g0290 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(277): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(329): Show |
1 | a0001c0001t0011g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(340): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(35): Show |
1 | a0001c0001t0007g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(119): Show |
1 | a0001c0001t0011g0286 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(130): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(350): Show |
1 | a0004c0011t0008g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(361): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115912 | G | GGCGAAGG others(728): Show |
1 | a0014c0036t0029g0412 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2277+1356_2277+135 others(739): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115912 | ||||||
chr17:78115915 | G | A | 1 | a0003c0003t0001g0407 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2277+1354C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115915 | ||||||
chr17:78115915 | G | GAAGGGAG others(14): Show |
1 | a0004c0006t0006g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2277+1353_2277+135 others(25): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115915 | ||||||
chr17:78115915 | G | GAAGGGAG others(35): Show |
1 | a0004c0006t0002g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2277+1353_2277+135 others(46): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115915 | ||||||
chr17:78115915 | G | GAAGGGAG others(413): Show |
1 | a0005c0004t0001g0152 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2277+1353_2277+135 others(424): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115915 | ||||||
chr17:78115944 | G | A | 1 | a0002c0002t0006g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2277+1325C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115944 | ||||||
chr17:78115976 | G | A | 9 | a0001c0001t0008g0089a0001c0001t0013g0083a0001c0001t0013g0087others(6): Show | 9 | HG02258.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2277+1293C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115976 | ||||||
chr17:78115987 | C | T | 80 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0001g0284others(77): Show | 80 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.2277+1282G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78115987 | ||||||
chr17:78116052 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2277+1217G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116052 | ||||||
chr17:78116074 | A | T | 45 | a0001c0001t0001g0172a0001c0001t0001g0317a0001c0001t0003g0168others(42): Show | 47 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2277+1195T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116074 | ||||||
chr17:78116097 | C | A | 4 | a0001c0001t0001g0277a0001c0001t0004g0324a0001c0005t0016g0181others(1): Show | 4 | HG01943.hp2 HG02738.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2277+1172G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116097 | ||||||
chr17:78116142 | G | A | 170 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0172others(167): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.2277+1127C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116142 | ||||||
chr17:78116172 | T | C | 42 | a0001c0001t0001g0263a0001c0001t0001g0279a0001c0001t0003g0260others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2277+1097A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116172 | ||||||
chr17:78116195 | T | C | 1 | a0005c0004t0003g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2277+1074A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116195 | ||||||
chr17:78116276 | C | CT | 142 | a0001c0001t0001g0263a0001c0001t0001g0267a0001c0001t0001g0278others(139): Show | 144 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.2277+992dupA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116276 | ||||||
chr17:78116276 | CT | C | 10 | a0001c0001t0009g0016a0003c0003t0001g0392a0004c0006t0002g0042others(7): Show | 10 | HG02074.hp2 HG02258.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2277+992delA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116276 | ||||||
chr17:78116318 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2277+951G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116318 | ||||||
chr17:78116330 | G | A | 2 | a0001c0001t0001g0007a0003c0003t0001g0352 | 3 | HG01515.hp1 HG01517.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2277+939C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116330 | ||||||
chr17:78116378 | A | G | 1 | a0012c0021t0002g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2277+891T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116378 | ||||||
chr17:78116407 | G | C | 1 | a0001c0001t0004g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2277+862C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116407 | ||||||
chr17:78116493 | G | A | 25 | a0001c0001t0001g0263a0001c0001t0003g0260a0001c0001t0003g0264others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2277+776C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116493 | ||||||
chr17:78116539 | T | A | 21 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0430others(18): Show | 21 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2277+730A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116539 | ||||||
chr17:78116614 | G | C | 2 | a0004c0012t0040g0033a0004c0012t0041g0031 | 2 | HG01070.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2277+655C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116614 | ||||||
chr17:78116671 | A | G | 273 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0159others(270): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2277+598T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116671 | ||||||
chr17:78116718 | G | A | 1 | a0012c0021t0002g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2277+551C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116718 | ||||||
chr17:78116760 | C | G | 6 | a0007c0007t0002g0060a0007c0007t0002g0061a0007c0007t0002g0062others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2277+509G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116760 | ||||||
chr17:78116884 | A | G | 78 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0254others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.2277+385T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116884 | ||||||
chr17:78116950 | T | C | 7 | a0001c0005t0003g0183a0001c0005t0003g0186a0001c0005t0003g0187others(4): Show | 7 | NA18943.hp2 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277+319A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78116950 | ||||||
chr17:78117058 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2277+211G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78117058 | ||||||
chr17:78117074 | A | G | 3 | a0004c0006t0002g0019a0004c0006t0002g0020a0004c0006t0002g0021 | 3 | NA18939.hp1 NA18953.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2277+195T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78117074 | ||||||
chr17:78117187 | T | G | 1 | a0002c0002t0002g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2277+82A>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78117187 | ||||||
chr17:78117205 | G | A | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2277+64C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78117205 | ||||||
chr17:78117210 | G | A | 3 | a0001c0001t0004g0252a0004c0012t0040g0033a0004c0012t0041g0031 | 3 | HG01070.hp1 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2277+59C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 18/19 | chr17 | 78117210 | ||||||
chr17:78117396 | C | T | 3 | a0005c0004t0090g0226a0005c0018t0027g0017a0005c0018t0027g0018 | 3 | HG02622.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2199-49G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 17/19 | chr17 | 78117396 | ||||||
chr17:78117710 | G | A | 1 | a0003c0003t0089g0393 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2022-66C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 16/19 | chr17 | 78117710 | ||||||
chr17:78117757 | C | A | 6 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0077others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2021+45G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 16/19 | chr17 | 78117757 | ||||||
chr17:78117791 | G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0428a0002c0002t0023g0237 | 4 | HG01257.hp1 HG01258.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+11C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 16/19 | chr17 | 78117791 | ||||||
chr17:78117953 | G | A | 1 | a0003c0003t0065g0364 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1888-18C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78117953 | ||||||
chr17:78118020 | G | A | 20 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0430others(17): Show | 20 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1888-85C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118020 | ||||||
chr17:78118154 | C | T | 1 | a0001c0001t0073g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1888-219G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118154 | ||||||
chr17:78118158 | G | C | 7 | a0001c0005t0001g0315a0001c0005t0003g0421a0003c0009t0014g0424others(4): Show | 7 | NA18948.hp2 NA18959.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1888-223C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118158 | ||||||
chr17:78118277 | C | A | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1888-342G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118277 | ||||||
chr17:78118473 | G | A | 3 | a0001c0001t0003g0269a0001c0001t0003g0271a0001c0001t0004g0272 | 3 | HG00558.hp1 NA18612.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1887+498C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118473 | ||||||
chr17:78118480 | T | C | 302 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0238others(299): Show | 305 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.1887+491A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118480 | ||||||
chr17:78118513 | G | A | 1 | a0003c0003t0001g0365 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1887+458C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118513 | ||||||
chr17:78118557 | A | AAAAAT | 301 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0238others(298): Show | 304 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.1887+409_1887+413d others(7): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118557 | ||||||
chr17:78118578 | G | A | 6 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0077others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887+393C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118578 | ||||||
chr17:78118711 | C | T | 3 | a0003c0003t0003g0367a0003c0003t0003g0368a0003c0003t0003g0369 | 3 | HG00544.hp1 NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1887+260G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118711 | ||||||
chr17:78118723 | A | G | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1887+248T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118723 | ||||||
chr17:78118773 | A | G | 302 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0238others(299): Show | 305 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.1887+198T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118773 | ||||||
chr17:78118774 | G | C | 1 | a0004c0006t0002g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1887+197C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118774 | ||||||
chr17:78118810 | G | A | 1 | a0003c0003t0003g0394 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1887+161C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118810 | ||||||
chr17:78118860 | C | T | 199 | a0001c0001t0001g0238a0001c0001t0001g0254a0001c0001t0001g0255others(196): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1887+111G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118860 | ||||||
chr17:78118882 | C | G | 302 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0238others(299): Show | 305 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.1887+89G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118882 | ||||||
chr17:78118894 | G | T | 302 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0238others(299): Show | 305 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.1887+77C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118894 | ||||||
chr17:78118902 | C | T | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1887+69G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118902 | ||||||
chr17:78118910 | T | C | 2 | a0005c0004t0001g0208a0005c0004t0058g0224 | 2 | HG00423.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1887+61A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 15/19 | chr17 | 78118910 | ||||||
chr17:78119053 | A | AG | 8 | a0001c0001t0001g0317a0001c0001t0017g0014a0001c0001t0068g0253others(5): Show | 8 | HG00423.hp1 NA18985.hp1 NA18985.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1812-8dupC | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119053 | ||||||
chr17:78119100 | A | T | 199 | a0001c0001t0001g0238a0001c0001t0001g0254a0001c0001t0001g0255others(196): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1812-54T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119100 | ||||||
chr17:78119126 | G | A | 1 | a0002c0002t0002g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1812-80C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119126 | ||||||
chr17:78119127 | G | T | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1812-81C>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119127 | ||||||
chr17:78119220 | G | A | 48 | a0001c0001t0001g0008a0001c0001t0001g0172a0001c0001t0001g0277others(45): Show | 51 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1811+77C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119220 | ||||||
chr17:78119242 | G | C | 2 | a0002c0002t0002g0093a0002c0002t0048g0105 | 2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1811+55C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119242 | ||||||
chr17:78119245 | A | G | 1 | a0001c0001t0018g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1811+52T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119245 | ||||||
chr17:78119272 | T | C | 355 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0171others(352): Show | 361 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.1811+25A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 14/19 | chr17 | 78119272 | ||||||
chr17:78119397 | CT | C | 75 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0298others(72): Show | 75 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.1716-6delA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119397 | ||||||
chr17:78119410 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1716-18C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119410 | ||||||
chr17:78119503 | T | C | 5 | a0002c0002t0013g0059a0002c0002t0015g0236a0004c0006t0010g0057others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716-111A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119503 | ||||||
chr17:78119535 | C | T | 2 | a0002c0002t0009g0128a0002c0002t0009g0129 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1716-143G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119535 | ||||||
chr17:78119601 | C | T | 1 | a0004c0006t0010g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716-209G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119601 | ||||||
chr17:78119603 | G | C | 4 | a0002c0002t0013g0059a0002c0002t0015g0236a0004c0006t0010g0057others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-211C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119603 | ||||||
chr17:78119645 | T | C | 1 | a0001c0005t0003g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1716-253A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119645 | ||||||
chr17:78119646 | C | T | 1 | a0001c0005t0003g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1716-254G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119646 | ||||||
chr17:78119701 | C | T | 4 | a0002c0002t0007g0131a0002c0002t0009g0128a0002c0002t0009g0129others(1): Show | 4 | HG02896.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716-309G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119701 | ||||||
chr17:78119705 | G | A | 1 | a0004c0006t0010g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716-313C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119705 | ||||||
chr17:78119708 | C | T | 1 | a0001c0001t0017g0009 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1716-316G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119708 | ||||||
chr17:78119871 | C | T | 1 | a0004c0006t0010g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1716-479G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119871 | ||||||
chr17:78119927 | C | T | 4 | a0002c0002t0013g0059a0002c0002t0015g0236a0004c0006t0010g0057others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-535G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119927 | ||||||
chr17:78119936 | C | A | 165 | a0001c0001t0001g0238a0001c0001t0001g0254a0001c0001t0001g0255others(162): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1716-544G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119936 | ||||||
chr17:78119954 | T | A | 1 | a0001c0001t0083g0314 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1716-562A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78119954 | ||||||
chr17:78120072 | T | C | 207 | a0001c0001t0001g0172a0001c0001t0001g0238a0001c0001t0001g0254others(204): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1715+581A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120072 | ||||||
chr17:78120147 | C | T | 1 | a0004c0006t0002g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1715+506G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120147 | ||||||
chr17:78120152 | C | CT | 14 | a0001c0001t0001g0322a0001c0001t0003g0154a0001c0001t0004g0161others(11): Show | 14 | HG00558.hp2 HG01192.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1715+500dupA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120152 | CT | C | 84 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0172others(81): Show | 85 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1715+500delA | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120152 | CTT | C | 7 | a0001c0001t0068g0253a0001c0005t0072g0299a0002c0002t0002g0093others(4): Show | 7 | HG01106.hp1 HG01433.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1715+499_1715+500d others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120152 | CTTT | C | 170 | a0001c0001t0001g0238a0001c0001t0001g0254a0001c0001t0001g0255others(167): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1715+498_1715+500d others(5): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120152 | CTTTT | C | 7 | a0001c0001t0001g0270a0001c0005t0001g0315a0002c0002t0007g0110others(4): Show | 7 | HG01516.hp2 HG02976.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.1715+497_1715+500d others(6): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120152 | CTTTTTTT others(4): Show |
C | 1 | a0018c0027t0001g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1715+490_1715+500d others(13): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120152 | ||||||
chr17:78120203 | G | A | 2 | a0001c0001t0073g0282a0002c0002t0023g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1715+450C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120203 | ||||||
chr17:78120262 | C | T | 1 | a0001c0001t0012g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1715+391G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120262 | ||||||
chr17:78120309 | G | A | 1 | a0005c0004t0090g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1715+344C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120309 | ||||||
chr17:78120316 | C | T | 4 | a0002c0002t0013g0059a0002c0002t0015g0236a0008c0013t0002g0030others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715+337G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120316 | ||||||
chr17:78120348 | C | T | 4 | a0002c0002t0013g0059a0002c0002t0015g0236a0008c0013t0002g0030others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715+305G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120348 | ||||||
chr17:78120415 | C | T | 30 | a0001c0001t0001g0321a0001c0001t0012g0292a0001c0001t0076g0295others(27): Show | 30 | HG00621.hp2 HG01074.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.1715+238G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120415 | ||||||
chr17:78120584 | CTCCCGGC others(6): Show |
C | 46 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(43): Show | 49 | HG00140.hp2 HG00408.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1715+56_1715+68del others(13): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 13/19 | chr17 | 78120584 | ||||||
chr17:78120836 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.1536-4G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/19 | chr17 | 78120836 | ||||||
chr17:78120907 | G | A | 1 | a0003c0003t0001g0411 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1536-75C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/19 | chr17 | 78120907 | ||||||
chr17:78120920 | C | T | 7 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0077others(4): Show | 7 | HG01243.hp2 HG01257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536-88G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/19 | chr17 | 78120920 | ||||||
chr17:78120951 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1535+62G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 12/19 | chr17 | 78120951 | ||||||
chr17:78121234 | G | A | 1 | a0012c0021t0002g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1384-70C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121234 | ||||||
chr17:78121280 | T | C | 320 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1384-116A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121280 | ||||||
chr17:78121320 | A | G | 294 | a0001c0001t0001g0008a0001c0001t0001g0238a0001c0001t0001g0254others(291): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1384-156T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121320 | ||||||
chr17:78121379 | G | A | 2 | a0001c0001t0003g0271a0001c0001t0004g0272 | 2 | HG00558.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1383+177C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121379 | ||||||
chr17:78121420 | A | G | 17 | a0002c0002t0015g0236a0004c0006t0007g0035a0004c0006t0007g0036others(14): Show | 17 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1383+136T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121420 | ||||||
chr17:78121436 | G | A | 37 | a0001c0001t0001g0263a0001c0001t0001g0267a0001c0001t0001g0270others(34): Show | 37 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1383+120C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121436 | ||||||
chr17:78121489 | G | C | 106 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0263others(103): Show | 107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1383+67C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 11/19 | chr17 | 78121489 | ||||||
chr17:78121719 | C | T | 2 | a0002c0002t0002g0092a0005c0004t0003g0204 | 2 | HG01934.hp1 HG02895.hp1 |
splice_region_variant&intron_variant | LOW | c.1228-8G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78121719 | ||||||
chr17:78121820 | AAC | A | 11 | a0002c0002t0015g0236a0004c0006t0007g0035a0004c0006t0007g0036others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-111_1228-110d others(4): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78121820 | ||||||
chr17:78121890 | G | A | 324 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(321): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1228-179C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78121890 | ||||||
chr17:78122160 | G | A | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1227+445C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122160 | ||||||
chr17:78122192 | C | T | 6 | a0007c0007t0002g0060a0007c0007t0002g0061a0007c0007t0002g0062others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+413G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122192 | ||||||
chr17:78122289 | C | T | 4 | a0004c0006t0002g0042a0004c0006t0002g0043a0004c0006t0006g0041others(1): Show | 4 | HG02056.hp1 NA18946.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+316G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122289 | ||||||
chr17:78122293 | A | G | 1 | a0001c0001t0013g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1227+312T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122293 | ||||||
chr17:78122342 | C | T | 51 | a0001c0001t0001g0277a0001c0001t0008g0089a0001c0001t0013g0083others(48): Show | 53 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1227+263G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122342 | ||||||
chr17:78122345 | G | A | 1 | a0001c0001t0030g0341 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1227+260C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122345 | ||||||
chr17:78122357 | C | T | 1 | a0001c0001t0063g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1227+248G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122357 | ||||||
chr17:78122372 | G | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1227+233C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122372 | ||||||
chr17:78122373 | C | T | 51 | a0001c0001t0001g0277a0001c0001t0008g0089a0001c0001t0013g0083others(48): Show | 53 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1227+232G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122373 | ||||||
chr17:78122408 | G | A | 49 | a0001c0001t0001g0277a0001c0001t0008g0089a0001c0001t0013g0083others(46): Show | 51 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.1227+197C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122408 | ||||||
chr17:78122415 | G | C | 2 | a0001c0001t0015g0273a0001c0001t0015g0274 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1227+190C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122415 | ||||||
chr17:78122440 | C | G | 1 | a0001c0005t0003g0421 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1227+165G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122440 | ||||||
chr17:78122441 | G | C | 1 | a0001c0005t0003g0421 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1227+164C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122441 | ||||||
chr17:78122474 | G | A | 9 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0006g0071others(6): Show | 9 | HG01106.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1227+131C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122474 | ||||||
chr17:78122504 | C | T | 3 | a0004c0006t0007g0039a0004c0006t0009g0038a0004c0006t0013g0040 | 3 | HG02486.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1227+101G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122504 | ||||||
chr17:78122542 | T | C | 2 | a0002c0002t0006g0113a0002c0002t0006g0114 | 2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1227+63A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122542 | ||||||
chr17:78122578 | C | G | 1 | a0012c0021t0002g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1227+27G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 10/19 | chr17 | 78122578 | ||||||
chr17:78122753 | G | C | 36 | a0001c0001t0002g0150a0002c0002t0002g0116a0002c0002t0002g0117others(33): Show | 37 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.1083-4C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78122753 | ||||||
chr17:78122806 | G | C | 61 | a0001c0001t0002g0150a0002c0002t0002g0092a0002c0002t0002g0093others(58): Show | 62 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1083-57C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78122806 | ||||||
chr17:78122907 | C | G | 1 | a0004c0010t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1083-158G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78122907 | ||||||
chr17:78123014 | G | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0254a0001c0001t0001g0255others(42): Show | 46 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1083-265C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123014 | ||||||
chr17:78123212 | C | T | 63 | a0001c0001t0056g0158a0003c0003t0001g0349a0003c0003t0001g0350others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1083-463G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123212 | ||||||
chr17:78123267 | C | G | 1 | a0004c0012t0041g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1083-518G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123267 | ||||||
chr17:78123339 | G | A | 6 | a0007c0007t0002g0060a0007c0007t0002g0061a0007c0007t0002g0062others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083-590C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123339 | ||||||
chr17:78123381 | G | A | 47 | a0001c0001t0001g0277a0001c0001t0008g0089a0001c0001t0013g0083others(44): Show | 49 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1082+608C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123381 | ||||||
chr17:78123412 | T | C | 1 | a0002c0002t0002g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1082+577A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123412 | ||||||
chr17:78123414 | G | A | 1 | a0001c0001t0055g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1082+575C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123414 | ||||||
chr17:78123463 | A | ATGAATGA others(131): Show |
1 | a0005c0004t0082g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1082+388_1082+525d others(140): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123463 | ||||||
chr17:78123486 | A | AATGGGTG others(127): Show |
34 | a0002c0002t0015g0236a0002c0002t0069g0422a0005c0004t0001g0206others(31): Show | 35 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1082+369_1082+502d others(136): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123486 | ||||||
chr17:78123486 | A | AATGGGTG others(261): Show |
3 | a0005c0004t0003g0198a0005c0004t0003g0199a0005c0004t0003g0200 | 3 | NA18944.hp1 NA18956.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1082+502_1082+503i others(270): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123486 | ||||||
chr17:78123488 | T | C | 1 | a0001c0005t0001g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1082+501A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123488 | ||||||
chr17:78123516 | G | A | 1 | a0001c0001t0063g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1082+473C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123516 | ||||||
chr17:78123531 | A | G | 10 | a0001c0001t0007g0081a0001c0001t0008g0089a0001c0001t0013g0083others(7): Show | 10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082+458T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123531 | ||||||
chr17:78123532 | G | A | 10 | a0001c0001t0007g0081a0001c0001t0008g0089a0001c0001t0013g0083others(7): Show | 10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082+457C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123532 | ||||||
chr17:78123532 | G | GATGGATG others(65): Show |
12 | a0004c0006t0007g0032a0004c0006t0007g0035a0004c0006t0007g0036others(9): Show | 12 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082+385_1082+456d others(74): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123532 | ||||||
chr17:78123548 | GATGGGTG others(57): Show |
G | 10 | a0001c0001t0007g0081a0001c0001t0008g0089a0001c0001t0013g0083others(7): Show | 10 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1082+377_1082+440d others(66): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123548 | ||||||
chr17:78123604 | A | AATGGATG others(55): Show |
1 | a0005c0004t0033g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1082+384_1082+385i others(64): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123604 | ||||||
chr17:78123612 | A | AATGGGTG others(1): Show |
96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1082+369_1082+376d others(10): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123612 | ||||||
chr17:78123612 | A | G | 1 | a0006c0016t0037g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1082+377T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123612 | ||||||
chr17:78123666 | A | ATGGATGG others(18): Show |
1 | a0022c0031t0004g0423 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1082+298_1082+322d others(27): Show |
TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123666 | ||||||
chr17:78123736 | C | A | 431 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(428): Show | 440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.1082+253G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123736 | ||||||
chr17:78123761 | T | C | 5 | a0002c0002t0002g0070a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG01074.hp1 HG01106.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082+228A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123761 | ||||||
chr17:78123790 | T | C | 7 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0077others(4): Show | 7 | HG01243.hp2 HG01257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082+199A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123790 | ||||||
chr17:78123802 | T | C | 1 | a0014c0036t0029g0412 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1082+187A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123802 | ||||||
chr17:78123849 | T | C | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1082+140A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123849 | ||||||
chr17:78123984 | A | G | 207 | a0001c0001t0001g0008a0001c0001t0001g0254a0001c0001t0001g0255others(204): Show | 211 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(208): Show |
splice_region_variant&intron_variant | LOW | c.1082+5T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 9/19 | chr17 | 78123984 | ||||||
chr17:78124318 | A | C | 7 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0077others(4): Show | 7 | HG01243.hp2 HG01257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-139T>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/19 | chr17 | 78124318 | ||||||
chr17:78124367 | G | A | 6 | a0007c0007t0002g0060a0007c0007t0002g0061a0007c0007t0002g0062others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+157C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/19 | chr17 | 78124367 | ||||||
chr17:78124377 | G | A | 1 | a0005c0004t0082g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.891+147C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/19 | chr17 | 78124377 | ||||||
chr17:78124418 | G | A | 1 | a0003c0003t0003g0414 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.891+106C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/19 | chr17 | 78124418 | ||||||
chr17:78124452 | C | T | 5 | a0002c0002t0002g0070a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG01074.hp1 HG01106.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+72G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 8/19 | chr17 | 78124452 | ||||||
chr17:78125113 | T | C | 2 | a0004c0006t0024g0027a0004c0006t0024g0028 | 2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.536+45A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 6/19 | chr17 | 78125113 | ||||||
chr17:78125289 | C | A | 1 | a0002c0002t0002g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.431-26G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125289 | ||||||
chr17:78125318 | C | T | 1 | a0005c0004t0003g0196 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.431-55G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125318 | ||||||
chr17:78125361 | G | A | 1 | a0005c0004t0090g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.431-98C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125361 | ||||||
chr17:78125476 | C | T | 1 | a0005c0004t0082g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.431-213G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125476 | ||||||
chr17:78125477 | G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0415a0001c0001t0001g0416others(3): Show | 7 | HG00099.hp2 HG01167.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-214C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125477 | ||||||
chr17:78125679 | C | T | 10 | a0001c0001t0001g0238a0001c0005t0001g0239a0001c0005t0001g0240others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+47G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125679 | ||||||
chr17:78125700 | T | A | 5 | a0002c0002t0002g0070a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG01074.hp1 HG01106.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+26A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 5/19 | chr17 | 78125700 | ||||||
chr17:78125997 | T | C | 63 | a0001c0001t0002g0150a0002c0002t0002g0092a0002c0002t0002g0093others(60): Show | 64 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.272-113A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 4/19 | chr17 | 78125997 | ||||||
chr17:78126023 | A | G | 5 | a0002c0002t0002g0070a0002c0002t0002g0072a0002c0002t0002g0073others(2): Show | 5 | HG01074.hp1 HG01106.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-139T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 4/19 | chr17 | 78126023 | ||||||
chr17:78126139 | A | G | 45 | a0005c0004t0001g0152a0005c0004t0001g0153a0005c0004t0001g0206others(42): Show | 47 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.271+138T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 4/19 | chr17 | 78126139 | ||||||
chr17:78126385 | T | C | 1 | a0001c0005t0003g0421 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.182-19A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 3/19 | chr17 | 78126385 | ||||||
chr17:78126390 | A | G | 1 | a0003c0003t0003g0193 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.182-24T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 3/19 | chr17 | 78126390 | ||||||
chr17:78126438 | G | C | 1 | a0002c0002t0069g0422 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.182-72C>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 3/19 | chr17 | 78126438 | ||||||
chr17:78126518 | G | A | 1 | a0022c0031t0004g0423 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.181+6C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 3/19 | chr17 | 78126518 | ||||||
chr17:78126666 | G | A | 3 | a0003c0009t0014g0424a0003c0009t0014g0425a0003c0009t0014g0426 | 3 | NA18959.hp2 NA18973.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.57-18C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 2/19 | chr17 | 78126666 | ||||||
chr17:78127061 | C | T | 1 | a0005c0004t0087g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-74-155G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127061 | ||||||
chr17:78127262 | C | T | 8 | a0001c0005t0003g0183a0001c0005t0003g0186a0001c0005t0003g0187others(5): Show | 8 | NA18943.hp2 NA18968.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74-356G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127262 | ||||||
chr17:78127349 | A | G | 1 | a0001c0001t0001g0428 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-74-443T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127349 | ||||||
chr17:78127382 | C | G | 51 | a0002c0002t0002g0067a0002c0002t0002g0068a0002c0002t0013g0059others(48): Show | 51 | HG01070.hp1 HG01074.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.-74-476G>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127382 | ||||||
chr17:78127398 | CA | C | 6 | a0004c0006t0002g0019a0004c0006t0002g0020a0004c0006t0002g0021others(3): Show | 6 | NA18939.hp1 NA18953.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74-493delT | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127398 | ||||||
chr17:78127411 | C | T | 3 | a0001c0001t0022g0180a0001c0005t0016g0181a0001c0005t0071g0182 | 3 | HG01943.hp2 HG01993.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-74-505G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127411 | ||||||
chr17:78127447 | A | G | 42 | a0002c0002t0013g0059a0004c0006t0002g0019a0004c0006t0002g0020others(39): Show | 42 | HG01070.hp1 HG01074.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.-74-541T>C | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127447 | ||||||
chr17:78127594 | T | A | 1 | a0004c0011t0008g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-74-688A>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127594 | ||||||
chr17:78127777 | G | A | 1 | a0005c0004t0005g0427 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-75+835C>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127777 | ||||||
chr17:78127873 | C | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0428a0001c0001t0001g0430others(6): Show | 10 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-75+739G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78127873 | ||||||
chr17:78128185 | C | A | 1 | a0008c0013t0032g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-75+427G>T | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78128185 | ||||||
chr17:78128189 | A | T | 2 | a0005c0018t0027g0017a0005c0018t0027g0018 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-75+423T>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78128189 | ||||||
chr17:78128280 | C | T | 1 | a0008c0013t0032g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-75+332G>A | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78128280 | ||||||
chr17:78128359 | T | C | 400 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(397): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.-75+253A>G | TMC6 | ENSG00000141524.19 | transcript | ENST00000590602.6 | protein_coding | 1/19 | chr17 | 78128359 |