geneid | 84899 |
---|---|
ensemblid | ENSG00000125247.16 |
hgncid | 25904 |
symbol | TMTC4 |
name | transmembrane O-mannosyltransferase targeting cadherins 4 |
refseq_nuc | NM_032813.5 |
refseq_prot | NP_116202.2 |
ensembl_nuc | ENST00000342624.10 |
ensembl_prot | ENSP00000343871.5 |
mane_status | MANE Select |
chr | chr13 |
start | 100603625 |
end | 100674795 |
strand | - |
ver | v1.2 |
region | chr13:100603625-100674795 |
region5000 | chr13:100598625-100679795 |
regionname0 | TMTC4_chr13_100603625_100674795 |
regionname5000 | TMTC4_chr13_100598625_100679795 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 760 | 203 | 57 | 52 | 55 | 13 | 25 | 42 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002 | 0/1 | 760 | 123 | 32 | 11 | 63 | 3 | 13 | 44 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003 | 0/0 | 760 | 10 | 0 | 0 | 8 | 0 | 2 | 7 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0004 | 0/0 | 760 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0005 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0006 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0007 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0008 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0009 | 0/0 | 760 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0010 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0011 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2283 | 122 | 32 | 10 | 63 | 3 | 13 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0002 | 0/0 | 2283 | 90 | 5 | 23 | 44 | 5 | 13 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0003 | 1/0 | 2283 | 49 | 29 | 9 | 1 | 2 | 7 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0004 | 0/0 | 2283 | 47 | 19 | 19 | 2 | 4 | 3 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0005 | 0/0 | 2283 | 10 | 0 | 0 | 8 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0006 | 0/0 | 2283 | 6 | 0 | 0 | 4 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0007 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0008 | 0/0 | 2283 | 3 | 0 | 0 | 3 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0009 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0010 | 0/0 | 2283 | 2 | 0 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0011 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0012 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0013 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0014 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0015 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0016 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0017 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0018 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0019 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0020 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0021 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
c0022 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1629 | 156 | 36 | 41 | 53 | 7 | 19 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0002 | 0/1 | 1629 | 111 | 25 | 10 | 56 | 4 | 15 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0003 | 1/0 | 1629 | 40 | 11 | 10 | 10 | 5 | 3 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0004 | 0/0 | 1629 | 9 | 5 | 0 | 4 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0005 | 0/0 | 1629 | 7 | 0 | 0 | 5 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0006 | 0/0 | 1629 | 5 | 5 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0007 | 0/0 | 1629 | 4 | 4 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0008 | 0/0 | 1629 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0009 | 0/0 | 1629 | 2 | 0 | 0 | 1 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0010 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0011 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0012 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0013 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0014 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0015 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0016 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
t0017 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 2283 | 90 | 5 | 23 | 44 | 5 | 13 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003 | 1/0 | 2283 | 49 | 29 | 9 | 1 | 2 | 7 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004 | 0/0 | 2283 | 47 | 19 | 19 | 2 | 4 | 3 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0005 | 0/0 | 2283 | 10 | 0 | 0 | 8 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0009 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0010 | 0/0 | 2283 | 2 | 0 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0017 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0018 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0020 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001 | 0/1 | 2283 | 122 | 32 | 10 | 63 | 3 | 13 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0015 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0006 | 0/0 | 2283 | 6 | 0 | 0 | 4 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0008 | 0/0 | 2283 | 3 | 0 | 0 | 3 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0021 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0004c0007 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0005c0011 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0006c0013 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0007c0014 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0008c0019 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0009c0016 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0010c0012 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0011c0022 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 3911 | 63 | 1 | 18 | 33 | 3 | 8 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0002 | 0/0 | 3911 | 2 | 0 | 0 | 1 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0003 | 0/0 | 3911 | 18 | 1 | 4 | 8 | 2 | 3 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0004 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0005 | 0/0 | 3911 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0008 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0009 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0014 | 0/0 | 3911 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0002t0017 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003t0001 | 0/0 | 3911 | 30 | 16 | 8 | 1 | 0 | 5 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003t0002 | 0/0 | 3911 | 5 | 2 | 0 | 0 | 1 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003t0003 | 1/0 | 3911 | 11 | 8 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003t0008 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0003t0010 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0001 | 0/0 | 3911 | 32 | 11 | 14 | 2 | 2 | 3 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0002 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0003 | 0/0 | 3911 | 9 | 2 | 5 | 0 | 2 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0007 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0011 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0004t0013 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0005t0001 | 0/0 | 3911 | 10 | 0 | 0 | 8 | 0 | 2 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0009t0001 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0009t0002 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0010t0001 | 0/0 | 3911 | 2 | 0 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0017t0001 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0018t0001 | 0/0 | 3911 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0001c0020t0001 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0001 | 0/0 | 3911 | 4 | 4 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0002 | 0/1 | 3911 | 98 | 19 | 9 | 54 | 3 | 12 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0004 | 0/0 | 3911 | 7 | 4 | 0 | 3 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0005 | 0/0 | 3911 | 6 | 0 | 0 | 5 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0006 | 0/0 | 3911 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0007 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0015 | 0/0 | 3911 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0001t0016 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0002c0015t0002 | 0/0 | 3911 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0006t0001 | 0/0 | 3911 | 5 | 0 | 0 | 4 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0006t0009 | 0/0 | 3911 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0008t0001 | 0/0 | 3911 | 3 | 0 | 0 | 3 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0003c0021t0001 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0004c0007t0002 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0004c0007t0006 | 0/0 | 3911 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0005c0011t0001 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0006c0013t0003 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0007c0014t0002 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0008c0019t0001 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0009c0016t0012 | 0/0 | 3911 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0010c0012t0004 | 0/0 | 3911 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
a0011c0022t0003 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | copy fasta | chr13 | 100598625 | 100679795 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0014g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0002t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0003t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0004t0013g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0009t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0009t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0010t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0010t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0017t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0001c0020t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0015g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0002c0015t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0006t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0008t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0008t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0003c0021t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0004c0007t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0004c0007t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0004c0007t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0005c0011t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0006c0013t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0007c0014t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0008c0019t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0009c0016t0012g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0010c0012t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
a0011c0022t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0002 | g0285 | EUR | GBR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0066 | EUR | GBR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00140 | hp2 | a0001 | c0004 | t0003 | g0048 | EUR | GBR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0026 | EUR | FIN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00323 | hp2 | a0001 | c0018 | t0001 | g0192 | EUR | FIN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00408 | hp2 | a0002 | c0001 | t0002 | g0291 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00423 | hp2 | a0002 | c0001 | t0002 | g0306 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00438 | hp2 | a0002 | c0001 | t0002 | g0307 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00544 | hp1 | a0002 | c0001 | t0002 | g0332 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00621 | hp1 | a0002 | c0001 | t0002 | g0233 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00673 | hp1 | a0002 | c0001 | t0002 | g0225 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00673 | hp2 | a0002 | c0001 | t0002 | g0304 | EAS | CHS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00735 | hp1 | a0001 | c0010 | t0001 | g0129 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00735 | hp2 | a0002 | c0001 | t0002 | g0296 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0024 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01069 | hp2 | a0002 | c0001 | t0002 | g0269 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01070 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01071 | hp2 | a0002 | c0001 | t0002 | g0270 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01081 | hp1 | a0001 | c0004 | t0001 | g0039 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01081 | hp2 | a0001 | c0002 | t0014 | g0162 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0197 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01106 | hp1 | a0002 | c0001 | t0002 | g0272 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0206 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01168 | hp1 | a0001 | c0004 | t0001 | g0086 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01168 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0030 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0020 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01192 | hp2 | a0002 | c0001 | t0002 | g0313 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01243 | hp2 | a0009 | c0016 | t0012 | g0112 | AMR | PUR | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0025 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01256 | hp1 | a0002 | c0001 | t0002 | g0256 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01256 | hp2 | a0001 | c0003 | t0003 | g0054 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01257 | hp1 | a0002 | c0001 | t0002 | g0260 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01358 | hp1 | a0001 | c0004 | t0003 | g0046 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0203 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01433 | hp2 | a0001 | c0004 | t0003 | g0017 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0037 | AMR | CLM | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0027 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01516 | hp1 | a0002 | c0001 | t0002 | g0243 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0208 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01517 | hp2 | a0002 | c0001 | t0002 | g0261 | EUR | IBS | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01884 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01884 | hp2 | a0002 | c0001 | t0004 | g0011 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01891 | hp1 | a0002 | c0001 | t0002 | g0259 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0106 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01928 | hp1 | a0002 | c0001 | t0002 | g0295 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01943 | hp2 | a0002 | c0015 | t0002 | g0294 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01952 | hp1 | a0001 | c0004 | t0001 | g0040 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0029 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01975 | hp2 | a0001 | c0004 | t0001 | g0113 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0034 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0088 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG01981 | hp2 | a0001 | c0004 | t0003 | g0035 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0297 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02015 | hp1 | a0002 | c0001 | t0002 | g0251 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02015 | hp2 | a0002 | c0001 | t0002 | g0005 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02027 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02027 | hp2 | a0002 | c0001 | t0002 | g0333 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02055 | hp1 | a0001 | c0020 | t0001 | g0107 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02055 | hp2 | a0002 | c0001 | t0002 | g0230 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02056 | hp1 | a0008 | c0019 | t0001 | g0157 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02056 | hp2 | a0002 | c0001 | t0002 | g0334 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02071 | hp1 | a0002 | c0001 | t0002 | g0005 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02071 | hp2 | a0001 | c0002 | t0009 | g0128 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02074 | hp2 | a0002 | c0001 | t0016 | g0327 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02080 | hp1 | a0002 | c0001 | t0004 | g0278 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02080 | hp2 | a0002 | c0001 | t0002 | g0324 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02083 | hp1 | a0003 | c0021 | t0001 | g0119 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0339 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02129 | hp1 | a0002 | c0001 | t0002 | g0290 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0253 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02132 | hp2 | a0002 | c0001 | t0004 | g0293 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02135 | hp1 | a0002 | c0001 | t0002 | g0301 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02145 | hp1 | a0002 | c0001 | t0006 | g0210 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0061 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02148 | hp1 | a0001 | c0004 | t0001 | g0038 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02148 | hp2 | a0001 | c0004 | t0003 | g0036 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0059 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02258 | hp1 | a0001 | c0003 | t0010 | g0078 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02258 | hp2 | a0001 | c0003 | t0003 | g0131 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02280 | hp1 | a0002 | c0001 | t0002 | g0238 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02300 | hp1 | a0001 | c0004 | t0003 | g0043 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02300 | hp2 | a0002 | c0001 | t0015 | g0264 | AMR | PEL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02451 | hp1 | a0001 | c0004 | t0007 | g0214 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02451 | hp2 | a0001 | c0003 | t0003 | g0084 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02572 | hp1 | a0002 | c0001 | t0002 | g0014 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0022 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0083 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02630 | hp2 | a0001 | c0003 | t0003 | g0076 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02647 | hp1 | a0002 | c0001 | t0001 | g0060 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02647 | hp2 | a0002 | c0001 | t0002 | g0340 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02698 | hp1 | a0002 | c0001 | t0002 | g0321 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02717 | hp1 | a0002 | c0001 | t0002 | g0012 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02717 | hp2 | a0002 | c0001 | t0002 | g0218 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0108 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02735 | hp1 | a0003 | c0006 | t0009 | g0120 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02738 | hp1 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02809 | hp1 | a0002 | c0001 | t0002 | g0265 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02818 | hp1 | a0002 | c0001 | t0002 | g0292 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02818 | hp2 | a0002 | c0001 | t0002 | g0315 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02886 | hp1 | a0002 | c0001 | t0004 | g0325 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02886 | hp2 | a0001 | c0004 | t0013 | g0221 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02895 | hp1 | a0001 | c0002 | t0008 | g0146 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0326 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02896 | hp2 | a0001 | c0003 | t0003 | g0092 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0090 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02897 | hp2 | a0001 | c0002 | t0008 | g0151 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02922 | hp2 | a0002 | c0001 | t0007 | g0335 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02965 | hp1 | a0002 | c0001 | t0007 | g0257 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02965 | hp2 | a0004 | c0007 | t0006 | g0318 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0062 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02976 | hp2 | a0001 | c0003 | t0010 | g0077 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03017 | hp1 | a0002 | c0001 | t0002 | g0222 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03017 | hp2 | a0002 | c0001 | t0002 | g0274 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03098 | hp1 | a0001 | c0003 | t0008 | g0089 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03098 | hp2 | a0002 | c0001 | t0004 | g0229 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03130 | hp1 | a0001 | c0004 | t0002 | g0211 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03130 | hp2 | a0001 | c0004 | t0011 | g0063 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03139 | hp1 | a0002 | c0001 | t0002 | g0268 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0213 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03225 | hp2 | a0001 | c0017 | t0001 | g0216 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03239 | hp1 | a0001 | c0003 | t0002 | g0065 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0198 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03453 | hp1 | a0001 | c0004 | t0003 | g0031 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03453 | hp2 | a0002 | c0001 | t0006 | g0329 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03486 | hp1 | a0002 | c0001 | t0002 | g0341 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03490 | hp1 | a0002 | c0001 | t0002 | g0330 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03516 | hp2 | a0004 | c0007 | t0006 | g0236 | AFR | ESN | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03540 | hp1 | a0001 | c0004 | t0007 | g0212 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03540 | hp2 | a0002 | c0001 | t0002 | g0258 | AFR | GWD | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0091 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03579 | hp2 | a0002 | c0001 | t0004 | g0015 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03654 | hp2 | a0002 | c0001 | t0002 | g0317 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0045 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03669 | hp2 | a0003 | c0006 | t0001 | g0117 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03688 | hp1 | a0002 | c0001 | t0002 | g0227 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0288 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03704 | hp1 | a0001 | c0005 | t0001 | g0111 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0080 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03710 | hp2 | a0002 | c0001 | t0002 | g0273 | SAS | PJL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03831 | hp1 | a0002 | c0001 | t0002 | g0262 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0049 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03834 | hp1 | a0001 | c0002 | t0005 | g0287 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0056 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03942 | hp1 | a0001 | c0003 | t0002 | g0067 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03942 | hp2 | a0002 | c0001 | t0005 | g0275 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0205 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04115 | hp2 | a0002 | c0001 | t0002 | g0244 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04184 | hp1 | a0002 | c0001 | t0002 | g0331 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | BEB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04199 | hp1 | a0001 | c0005 | t0001 | g0099 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0057 | SAS | STU | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18522 | hp2 | a0002 | c0001 | t0002 | g0247 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18906 | hp1 | a0002 | c0001 | t0002 | g0228 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18906 | hp2 | a0001 | c0003 | t0003 | g0095 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18943 | hp1 | a0002 | c0001 | t0002 | g0314 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18944 | hp2 | a0003 | c0006 | t0001 | g0118 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18945 | hp2 | a0002 | c0001 | t0002 | g0271 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18946 | hp2 | a0002 | c0001 | t0002 | g0299 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18947 | hp1 | a0011 | c0022 | t0003 | g0173 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18947 | hp2 | a0002 | c0001 | t0002 | g0298 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18949 | hp2 | a0002 | c0001 | t0002 | g0338 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18951 | hp2 | a0003 | c0006 | t0001 | g0116 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18952 | hp1 | a0002 | c0001 | t0002 | g0252 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18953 | hp2 | a0002 | c0001 | t0002 | g0323 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18956 | hp2 | a0002 | c0001 | t0002 | g0235 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18960 | hp2 | a0002 | c0001 | t0002 | g0311 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18963 | hp1 | a0003 | c0008 | t0001 | g0123 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18963 | hp2 | a0001 | c0005 | t0001 | g0102 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18967 | hp1 | a0003 | c0008 | t0001 | g0121 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18968 | hp1 | a0003 | c0008 | t0001 | g0122 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18968 | hp2 | a0002 | c0001 | t0002 | g0309 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18969 | hp1 | a0002 | c0001 | t0002 | g0276 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18970 | hp1 | a0002 | c0001 | t0002 | g0254 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0242 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18979 | hp1 | a0002 | c0001 | t0002 | g0312 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0281 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18982 | hp1 | a0002 | c0001 | t0005 | g0249 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18982 | hp2 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18983 | hp2 | a0007 | c0014 | t0002 | g0267 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18988 | hp2 | a0002 | c0001 | t0002 | g0263 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18989 | hp1 | a0002 | c0001 | t0005 | g0250 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0100 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18991 | hp1 | a0002 | c0001 | t0005 | g0231 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18991 | hp2 | a0002 | c0001 | t0002 | g0322 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18993 | hp1 | a0002 | c0001 | t0002 | g0310 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18993 | hp2 | a0001 | c0005 | t0001 | g0104 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18995 | hp1 | a0002 | c0001 | t0002 | g0337 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18995 | hp2 | a0006 | c0013 | t0003 | g0180 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18998 | hp1 | a0002 | c0001 | t0002 | g0300 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18998 | hp2 | a0002 | c0001 | t0002 | g0224 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA18999 | hp2 | a0002 | c0001 | t0002 | g0280 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19004 | hp1 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19004 | hp2 | a0002 | c0001 | t0004 | g0279 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19006 | hp1 | a0002 | c0001 | t0002 | g0283 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19010 | hp1 | a0002 | c0001 | t0002 | g0240 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19011 | hp1 | a0002 | c0001 | t0002 | g0255 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19011 | hp2 | a0002 | c0001 | t0002 | g0302 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19030 | hp1 | a0004 | c0007 | t0002 | g0226 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19030 | hp2 | a0002 | c0001 | t0002 | g0320 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19043 | hp2 | a0002 | c0001 | t0002 | g0013 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19057 | hp1 | a0002 | c0001 | t0002 | g0303 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19058 | hp2 | a0002 | c0001 | t0002 | g0239 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19060 | hp2 | a0002 | c0001 | t0005 | g0232 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19062 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19062 | hp2 | a0002 | c0001 | t0005 | g0277 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19063 | hp2 | a0001 | c0005 | t0001 | g0098 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19064 | hp1 | a0003 | c0006 | t0001 | g0124 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19064 | hp2 | a0001 | c0005 | t0001 | g0101 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19066 | hp1 | a0002 | c0001 | t0002 | g0308 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19066 | hp2 | a0002 | c0001 | t0002 | g0319 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19067 | hp1 | a0002 | c0001 | t0002 | g0282 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19067 | hp2 | a0002 | c0001 | t0002 | g0336 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0289 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19079 | hp2 | a0002 | c0001 | t0002 | g0234 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19080 | hp2 | a0002 | c0001 | t0002 | g0305 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19081 | hp1 | a0003 | c0006 | t0001 | g0115 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19081 | hp2 | a0002 | c0001 | t0002 | g0286 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0105 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0103 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19085 | hp2 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19087 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19090 | hp1 | a0001 | c0005 | t0001 | g0171 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19240 | hp1 | a0002 | c0001 | t0006 | g0328 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | YRI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20129 | hp1 | a0001 | c0002 | t0017 | g0167 | AFR | ASW | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0064 | AFR | ASW | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20752 | hp1 | a0001 | c0004 | t0003 | g0042 | EUR | TSI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0148 | EUR | TSI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20805 | hp1 | a0001 | c0003 | t0003 | g0052 | EUR | TSI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20805 | hp2 | a0001 | c0010 | t0001 | g0160 | EUR | TSI | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20905 | hp1 | a0002 | c0001 | t0002 | g0245 | SAS | GIH | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20905 | hp2 | a0002 | c0001 | t0002 | g0284 | SAS | GIH | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0178 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0018 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG02559 | hp2 | a0002 | c0001 | t0002 | g0266 | AFR | ACB | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0114 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG03471 | hp2 | a0001 | c0009 | t0002 | g0215 | AFR | MSL | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG06807 | hp1 | a0005 | c0011 | t0001 | g0217 | AFR | USA | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | USA | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20300 | hp1 | a0001 | c0009 | t0001 | g0009 | AFR | USA | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA20300 | hp2 | a0010 | c0012 | t0004 | g0246 | AFR | USA | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA21309 | hp1 | a0002 | c0001 | t0002 | g0223 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0237 | REF | REF | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0096 | REF | REF | TMTC4_chr13_100598625_100679795 | TMTC4 | chr13 | 100598625 | 100679795 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:100612441
|
A | G | 1 | a0009 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2021T>C | p.Met674Thr | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/19 | 2280/3911 | 2021/2283 | 674/760 | chr13 | 100612441 | ||
chr13:100625792
|
G | T | 1 | a0007 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1687C>A | p.Gln563Lys | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 14/19 | 1946/3911 | 1687/2283 | 563/760 | chr13 | 100625792 | ||
chr13:100634807
|
T | C | 1 | a0008 | 1 | HG02056.hp1 | missense_variant&splice_region_variant | MODERATE | c.1504A>G | p.Lys502Glu | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/19 | 1763/3911 | 1504/2283 | 502/760 | chr13 | 100634807 | ||
chr13:100635086
|
C | T | 4 | a0002a0005a0007others(1): Show | 126 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
missense_variant | MODERATE | c.1312G>A | p.Val438Ile | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 11/19 | 1571/3911 | 1312/2283 | 438/760 | chr13 | 100635086 | ||
chr13:100637624
|
C | T | 1 | a0006 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.913G>A | p.Val305Met | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/19 | 1172/3911 | 913/2283 | 305/760 | chr13 | 100637624 | ||
chr13:100637696
|
C | T | 2 | a0004a0010 | 4 | HG02965.hp2 HG03516.hp2 NA19030.hp1 others(1): Show |
missense_variant | MODERATE | c.841G>A | p.Gly281Ser | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/19 | 1100/3911 | 841/2283 | 281/760 | chr13 | 100637696 | ||
chr13:100642311
|
C | T | 1 | a0005 | 1 | HG06807.hp1 | missense_variant&splice_region_variant | MODERATE | c.641G>A | p.Ser214Asn | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/19 | 900/3911 | 641/2283 | 214/760 | chr13 | 100642311 | ||
chr13:100668725
|
T | C | 1 | a0003 | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
missense_variant | MODERATE | c.73A>G | p.Thr25Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/19 | 332/3911 | 73/2283 | 25/760 | chr13 | 100668725 | ||
chr13:100668781
|
T | C | 1 | a0011 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.17A>G | p.His6Arg | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/19 | 276/3911 | 17/2283 | 6/760 | chr13 | 100668781 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:100605126
|
A | G | 2 | a0001c0018a0001c0020 | 2 | HG00323.hp2 HG02055.hp1 |
synonymous_variant | LOW | c.2151T>C | p.Arg717Arg | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 2410/3911 | 2151/2283 | 717/760 | chr13 | 100605126 | ||
chr13:100614392
|
C | T | 3 | a0001c0009a0004c0007a0010c0012 | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
synonymous_variant | LOW | c.1875G>A | p.Ala625Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/19 | 2134/3911 | 1875/2283 | 625/760 | chr13 | 100614392 | ||
chr13:100614410
|
G | A | 1 | a0003c0021 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1857C>T | p.His619His | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/19 | 2116/3911 | 1857/2283 | 619/760 | chr13 | 100614410 | ||
chr13:100625658
|
C | G | 1 | a0002c0015 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.1713G>C | p.Ala571Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/19 | 1972/3911 | 1713/2283 | 571/760 | chr13 | 100625658 | ||
chr13:100625796
|
A | G | 1 | a0010c0012 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1683T>C | p.Ala561Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 14/19 | 1942/3911 | 1683/2283 | 561/760 | chr13 | 100625796 | ||
chr13:100625820
|
T | C | 2 | a0003c0006a0003c0021 | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
synonymous_variant | LOW | c.1659A>G | p.Glu553Glu | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 14/19 | 1918/3911 | 1659/2283 | 553/760 | chr13 | 100625820 | ||
chr13:100634925
|
G | A | 1 | a0001c0017 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1386C>T | p.Ala462Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/19 | 1645/3911 | 1386/2283 | 462/760 | chr13 | 100634925 | ||
chr13:100635111
|
T | C | 20 | a0001c0002a0001c0004a0001c0005others(17): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
synonymous_variant | LOW | c.1287A>G | p.Ala429Ala | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 11/19 | 1546/3911 | 1287/2283 | 429/760 | chr13 | 100635111 | ||
chr13:100635150
|
G | A | 6 | a0001c0002a0001c0010a0001c0018others(3): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
synonymous_variant | LOW | c.1248C>T | p.Pro416Pro | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 11/19 | 1507/3911 | 1248/2283 | 416/760 | chr13 | 100635150 | ||
chr13:100636726
|
G | A | 1 | a0001c0020 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1008C>T | p.Asn336Asn | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/19 | 1267/3911 | 1008/2283 | 336/760 | chr13 | 100636726 | ||
chr13:100637657
|
G | A | 1 | a0001c0005 | 10 | HG03704.hp1 HG04199.hp1 NA18963.hp2 others(7): Show |
synonymous_variant | LOW | c.880C>T | p.Leu294Leu | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/19 | 1139/3911 | 880/2283 | 294/760 | chr13 | 100637657 | ||
chr13:100656400
|
G | A | 1 | a0001c0010 | 2 | HG00735.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.621C>T | p.Tyr207Tyr | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/19 | 880/3911 | 621/2283 | 207/760 | chr13 | 100656400 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:100603691
|
C | T | 1 | a0001c0004t0013 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 1303 | chr13 | 100603691 | |||||
chr13:100603711
|
A | G | 4 | a0001c0002t0005a0001c0002t0009a0002c0001t0005others(1): Show | 9 | HG02071.hp2 HG02735.hp1 HG03834.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1283T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 1283 | chr13 | 100603711 | |||||
chr13:100603942
|
G | C | 5 | a0001c0002t0008a0001c0002t0017a0001c0003t0008others(2): Show | 8 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1052C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 1052 | chr13 | 100603942 | |||||
chr13:100604050
|
G | T | 1 | a0009c0016t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 944 | chr13 | 100604050 | |||||
chr13:100604158
|
T | C | 1 | a0002c0001t0015 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*836A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 836 | chr13 | 100604158 | |||||
chr13:100604173
|
A | G | 3 | a0001c0003t0010a0002c0001t0006a0004c0007t0006 | 7 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*821T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 821 | chr13 | 100604173 | |||||
chr13:100604309
|
T | A | 31 | a0001c0002t0001a0001c0002t0002a0001c0002t0014others(28): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*685A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 685 | chr13 | 100604309 | |||||
chr13:100604319
|
C | T | 1 | a0001c0004t0011 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 675 | chr13 | 100604319 | |||||
chr13:100604361
|
C | A | 1 | a0001c0002t0014 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*633G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 19/19 | 633 | chr13 | 100604361 | |||||
chr13:100670368
|
G | C | 19 | a0001c0002t0002a0001c0002t0004a0001c0002t0005others(16): Show | 138 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(135): Show |
5_prime_UTR_variant | MODIFIER | c.-6C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/19 | 6 | chr13 | 100670368 | |||||
chr13:100670379
|
C | A | 1 | a0002c0001t0016 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/19 | 17 | chr13 | 100670379 | |||||
chr13:100670481
|
G | A | 1 | a0001c0002t0017 | 1 | NA20129.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-119C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/19 | chr13 | 100670481 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:100605149
|
TAGC | T | 7 | a0001c0003t0010g0077a0001c0003t0010g0078a0002c0001t0006g0210others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02965.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2135-10_2135-8delG others(2): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605149 | ||||||
chr13:100605194
|
G | T | 13 | a0001c0002t0008g0146a0001c0002t0008g0151a0001c0002t0017g0167others(10): Show | 13 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.2135-52C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605194 | ||||||
chr13:100605257
|
A | G | 1 | a0007c0014t0002g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2135-115T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605257 | ||||||
chr13:100605413
|
A | G | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2135-271T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605413 | ||||||
chr13:100605434
|
T | C | 6 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2135-292A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605434 | ||||||
chr13:100605728
|
G | A | 1 | a0001c0004t0002g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2135-586C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605728 | ||||||
chr13:100605802
|
A | G | 2 | a0001c0002t0001g0130a0001c0002t0001g0170 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2134+556T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100605802 | ||||||
chr13:100606074
|
T | C | 5 | a0001c0003t0003g0095a0002c0001t0004g0011a0002c0001t0004g0015others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2134+284A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100606074 | ||||||
chr13:100606171
|
G | A | 5 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2134+187C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100606171 | ||||||
chr13:100606224
|
C | T | 1 | a0001c0003t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2134+134G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100606224 | ||||||
chr13:100606269
|
T | C | 1 | a0001c0003t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2134+89A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100606269 | ||||||
chr13:100606294
|
A | G | 3 | a0001c0003t0003g0091a0001c0004t0003g0031a0010c0012t0004g0246 | 3 | HG03453.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2134+64T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 18/18 | chr13 | 100606294 | ||||||
chr13:100606580
|
C | A | 1 | a0001c0004t0001g0016 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2065-153G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606580 | ||||||
chr13:100606619
|
G | A | 9 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0005g0231others(6): Show | 9 | HG02071.hp2 HG02735.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-192C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606619 | ||||||
chr13:100606640
|
G | A | 1 | a0001c0004t0011g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2065-213C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606640 | ||||||
chr13:100606682
|
G | T | 34 | a0001c0002t0001g0041a0001c0002t0001g0135a0001c0002t0001g0139others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2065-255C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606682 | ||||||
chr13:100606704
|
G | C | 1 | a0001c0004t0003g0048 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2065-277C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606704 | ||||||
chr13:100606727
|
G | A | 1 | a0002c0001t0002g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2065-300C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606727 | ||||||
chr13:100606805
|
T | C | 3 | a0001c0004t0001g0047a0001c0004t0001g0085a0002c0001t0002g0230 | 3 | HG02055.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2065-378A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606805 | ||||||
chr13:100606840
|
C | A | 1 | a0001c0004t0003g0036 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2065-413G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606840 | ||||||
chr13:100606988
|
T | C | 9 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0005g0231others(6): Show | 9 | HG02071.hp2 HG02735.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.2065-561A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100606988 | ||||||
chr13:100607173
|
A | G | 93 | a0001c0002t0001g0041a0001c0002t0001g0135a0001c0002t0001g0139others(90): Show | 94 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2065-746T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607173 | ||||||
chr13:100607244
|
T | C | 1 | a0002c0001t0002g0273 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2065-817A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607244 | ||||||
chr13:100607346
|
G | A | 5 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2065-919C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607346 | ||||||
chr13:100607415
|
G | A | 1 | a0001c0004t0011g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2065-988C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607415 | ||||||
chr13:100607466
|
G | A | 8 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-1039C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607466 | ||||||
chr13:100607516
|
C | CA | 9 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0003g0091others(6): Show | 9 | HG02257.hp2 HG02738.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.2065-1090dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607516 | ||||||
chr13:100607516
|
CA | C | 64 | a0001c0002t0001g0200a0001c0002t0003g0004a0001c0002t0003g0174others(61): Show | 65 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2065-1090delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607516 | ||||||
chr13:100607526
|
AAAAAAAT others(158): Show |
A | 3 | a0001c0004t0001g0220a0001c0004t0013g0221a0001c0017t0001g0216 | 3 | HG02257.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2065-1264_2065-110 others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607526 | ||||||
chr13:100607698
|
T | C | 44 | a0001c0002t0001g0148a0001c0002t0001g0153a0001c0002t0001g0175others(41): Show | 45 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2065-1271A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607698 | ||||||
chr13:100607702
|
G | A | 2 | a0002c0001t0002g0235a0002c0001t0002g0286 | 2 | NA18956.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2065-1275C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607702 | ||||||
chr13:100607878
|
G | A | 14 | a0001c0002t0005g0287a0001c0002t0008g0146a0001c0002t0008g0151others(11): Show | 14 | HG02071.hp2 HG02451.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.2065-1451C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607878 | ||||||
chr13:100607889
|
G | A | 1 | a0002c0001t0002g0282 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2065-1462C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607889 | ||||||
chr13:100607971
|
C | T | 1 | a0004c0007t0002g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2065-1544G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607971 | ||||||
chr13:100607972
|
G | C | 3 | a0001c0003t0003g0091a0001c0004t0003g0031a0010c0012t0004g0246 | 3 | HG03453.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2065-1545C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100607972 | ||||||
chr13:100608100
|
A | T | 1 | a0004c0007t0002g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2065-1673T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608100 | ||||||
chr13:100608116
|
A | C | 1 | a0002c0001t0002g0281 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2065-1689T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608116 | ||||||
chr13:100608246
|
G | A | 10 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(7): Show | 10 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2065-1819C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608246 | ||||||
chr13:100608605
|
T | C | 1 | a0002c0001t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2065-2178A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608605 | ||||||
chr13:100608813
|
C | A | 1 | a0001c0009t0002g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2065-2386G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608813 | ||||||
chr13:100608886
|
G | A | 1 | a0001c0002t0014g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2065-2459C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100608886 | ||||||
chr13:100609113
|
T | C | 113 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(110): Show | 115 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2065-2686A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609113 | ||||||
chr13:100609193
|
C | T | 1 | a0001c0004t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2065-2766G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609193 | ||||||
chr13:100609219
|
G | A | 1 | a0002c0001t0002g0310 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2065-2792C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609219 | ||||||
chr13:100609328
|
C | T | 325 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.2065-2901G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609328 | ||||||
chr13:100609480
|
T | C | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2064+2918A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609480 | ||||||
chr13:100609597
|
C | T | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+2801G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609597 | ||||||
chr13:100609623
|
T | C | 1 | a0001c0003t0002g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2064+2775A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609623 | ||||||
chr13:100609653
|
A | T | 1 | a0001c0002t0001g0219 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2064+2745T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609653 | ||||||
chr13:100609668
|
A | AAT | 173 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2064+2728_2064+272 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609668 | ||||||
chr13:100609671
|
G | A | 205 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2064+2727C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609671 | ||||||
chr13:100609676
|
T | TAC | 37 | a0001c0002t0001g0139a0001c0002t0001g0149a0001c0002t0001g0163others(34): Show | 38 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.2064+2721_2064+272 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609676 | ||||||
chr13:100609676
|
T | TACAC | 65 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(62): Show | 66 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2064+2721_2064+272 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609676 | ||||||
chr13:100609678
|
T | C | 104 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2064+2720A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609678 | ||||||
chr13:100609678
|
T | TACACAC | 8 | a0001c0002t0004g0316a0001c0002t0005g0287a0001c0002t0009g0128others(5): Show | 8 | HG02027.hp1 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2064+2719_2064+272 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609678 | ||||||
chr13:100609680
|
T | C | 115 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2064+2718A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609680 | ||||||
chr13:100609680
|
T | TAC | 17 | a0001c0002t0001g0143a0001c0003t0003g0091a0001c0004t0001g0021others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2064+2716_2064+271 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609680 | ||||||
chr13:100609680
|
T | TACAC | 26 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(23): Show | 26 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2064+2714_2064+271 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609680 | ||||||
chr13:100609680
|
T | TATAC | 5 | a0001c0002t0001g0142a0001c0002t0001g0193a0001c0009t0002g0215others(2): Show | 5 | HG02145.hp1 HG03471.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+2717_2064+271 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609680 | ||||||
chr13:100609682
|
C | T | 1 | a0002c0001t0002g0295 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2064+2716G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609682 | ||||||
chr13:100609701
|
A | C | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2064+2697T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609701 | ||||||
chr13:100609784
|
A | G | 104 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2064+2614T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609784 | ||||||
chr13:100609974
|
G | A | 1 | a0002c0001t0002g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2064+2424C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100609974 | ||||||
chr13:100610299
|
G | A | 5 | a0002c0001t0002g0224a0002c0001t0002g0240a0002c0001t0002g0276others(2): Show | 5 | NA18953.hp2 NA18969.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+2099C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100610299 | ||||||
chr13:100610491
|
T | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+1907A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100610491 | ||||||
chr13:100610514
|
C | T | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+1884G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100610514 | ||||||
chr13:100610648
|
C | T | 1 | a0002c0001t0002g0283 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2064+1750G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100610648 | ||||||
chr13:100611127
|
C | T | 4 | a0001c0002t0001g0186a0001c0002t0003g0181a0001c0002t0003g0182others(1): Show | 4 | HG00438.hp1 HG00738.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+1271G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611127 | ||||||
chr13:100611311
|
C | T | 104 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2064+1087G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611311 | ||||||
chr13:100611327
|
T | C | 1 | a0002c0001t0004g0325 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2064+1071A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611327 | ||||||
chr13:100611453
|
C | T | 2 | a0001c0003t0001g0051a0002c0001t0002g0313 | 2 | HG01192.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2064+945G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611453 | ||||||
chr13:100611457
|
C | T | 103 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(100): Show | 105 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2064+941G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611457 | ||||||
chr13:100611510
|
G | A | 174 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.2064+888C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611510 | ||||||
chr13:100611512
|
G | A | 1 | a0001c0003t0003g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2064+886C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611512 | ||||||
chr13:100611541
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2064+857G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611541 | ||||||
chr13:100611571
|
C | T | 1 | a0002c0001t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2064+827G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611571 | ||||||
chr13:100611599
|
A | C | 1 | a0002c0001t0002g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2064+799T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611599 | ||||||
chr13:100611674
|
T | A | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2064+724A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611674 | ||||||
chr13:100611800
|
A | G | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2064+598T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611800 | ||||||
chr13:100611869
|
T | C | 1 | a0001c0004t0001g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2064+529A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611869 | ||||||
chr13:100611932
|
G | T | 1 | a0001c0004t0013g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2064+466C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100611932 | ||||||
chr13:100612024
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2064+374C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612024 | ||||||
chr13:100612097
|
C | T | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2064+301G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612097 | ||||||
chr13:100612180
|
C | A | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+218G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612180 | ||||||
chr13:100612183
|
C | T | 3 | a0001c0003t0003g0091a0001c0004t0001g0032a0001c0004t0003g0031 | 3 | HG02723.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2064+215G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612183 | ||||||
chr13:100612369
|
C | T | 3 | a0001c0002t0003g0178a0001c0003t0003g0054a0001c0003t0003g0131 | 3 | HG01256.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2064+29G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612369 | ||||||
chr13:100612379
|
C | T | 176 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2064+19G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 17/18 | chr13 | 100612379 | ||||||
chr13:100612557
|
C | T | 5 | a0001c0002t0009g0128a0002c0001t0002g0334a0003c0006t0001g0116others(2): Show | 5 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1952-47G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612557 | ||||||
chr13:100612654
|
T | TAC | 46 | a0001c0002t0001g0189a0001c0002t0001g0196a0001c0003t0001g0002others(43): Show | 47 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1952-146_1952-145d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
T | TACAC | 6 | a0001c0002t0002g0339a0001c0002t0004g0316a0001c0003t0001g0049others(3): Show | 6 | HG02027.hp1 HG02083.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1952-148_1952-145d others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
T | TACACAC | 5 | a0001c0002t0001g0132a0001c0002t0001g0142a0001c0002t0001g0150others(2): Show | 5 | HG02129.hp2 HG02818.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1952-150_1952-145d others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TAC | T | 23 | a0001c0002t0001g0184a0001c0003t0001g0058a0001c0003t0001g0081others(20): Show | 23 | HG01074.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1952-146_1952-145d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACAC | T | 17 | a0001c0002t0001g0008a0001c0002t0001g0207a0001c0002t0001g0209others(14): Show | 17 | HG00544.hp2 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1952-148_1952-145d others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACAC | T | 109 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1952-150_1952-145d others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACACA others(1): Show |
T | 6 | a0001c0002t0001g0136a0001c0002t0001g0161a0001c0002t0001g0219others(3): Show | 6 | HG00423.hp1 HG02004.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1952-152_1952-145d others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACACA others(3): Show |
T | 2 | a0004c0007t0006g0236a0004c0007t0006g0318 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1952-154_1952-145d others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACACA others(5): Show |
T | 1 | a0001c0004t0001g0024 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1952-156_1952-145d others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACACA others(7): Show |
T | 14 | a0001c0002t0001g0143a0001c0004t0001g0021a0001c0004t0001g0022others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1952-158_1952-145d others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612654
|
TACACACA others(13): Show |
T | 1 | a0001c0002t0003g0181 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1952-164_1952-145d others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612654 | ||||||
chr13:100612661
|
A | G | 2 | a0004c0007t0002g0226a0010c0012t0004g0246 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1952-151T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612661 | ||||||
chr13:100612663
|
A | G | 4 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(1): Show | 4 | HG03471.hp2 NA19030.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1952-153T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612663 | ||||||
chr13:100612665
|
A | G | 4 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0006g0236others(1): Show | 4 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1952-155T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612665 | ||||||
chr13:100612667
|
A | G | 3 | a0001c0009t0001g0009a0004c0007t0006g0236a0004c0007t0006g0318 | 3 | HG02965.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1952-157T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612667 | ||||||
chr13:100612892
|
T | C | 1 | a0001c0017t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1952-382A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100612892 | ||||||
chr13:100613183
|
T | C | 2 | a0002c0001t0002g0230a0002c0001t0002g0247 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1952-673A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613183 | ||||||
chr13:100613185
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1952-675C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613185 | ||||||
chr13:100613304
|
C | T | 2 | a0001c0005t0001g0099a0001c0005t0001g0111 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1952-794G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613304 | ||||||
chr13:100613317
|
G | C | 1 | a0001c0004t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1952-807C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613317 | ||||||
chr13:100613731
|
C | T | 14 | a0001c0002t0001g0143a0001c0004t0001g0021a0001c0004t0001g0022others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1951+585G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613731 | ||||||
chr13:100613839
|
G | GC | 24 | a0001c0002t0001g0184a0001c0002t0001g0219a0001c0002t0003g0182others(21): Show | 24 | HG00438.hp1 HG01261.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1951+476dupG | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613839 | ||||||
chr13:100613925
|
C | T | 1 | a0002c0001t0002g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1951+391G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613925 | ||||||
chr13:100613946
|
T | C | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1951+370A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613946 | ||||||
chr13:100613989
|
G | A | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1951+327C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100613989 | ||||||
chr13:100614036
|
T | C | 3 | a0001c0003t0003g0091a0001c0004t0001g0032a0001c0004t0003g0031 | 3 | HG02723.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1951+280A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614036 | ||||||
chr13:100614061
|
A | G | 1 | a0001c0004t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1951+255T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614061 | ||||||
chr13:100614103
|
C | T | 1 | a0002c0001t0002g0313 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1951+213G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614103 | ||||||
chr13:100614114
|
C | T | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1951+202G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614114 | ||||||
chr13:100614128
|
C | T | 1 | a0002c0001t0002g0244 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1951+188G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614128 | ||||||
chr13:100614222
|
G | A | 3 | a0004c0007t0002g0226a0004c0007t0006g0236a0004c0007t0006g0318 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1951+94C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614222 | ||||||
chr13:100614259
|
G | A | 2 | a0001c0004t0011g0063a0001c0004t0013g0221 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1951+57C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614259 | ||||||
chr13:100614275
|
G | A | 3 | a0001c0004t0001g0220a0001c0004t0007g0212a0001c0004t0007g0214 | 3 | HG02257.hp1 HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1951+41C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 16/18 | chr13 | 100614275 | ||||||
chr13:100614497
|
TA | T | 6 | a0001c0002t0001g0142a0001c0002t0003g0206a0001c0003t0001g0071others(3): Show | 6 | HG00323.hp2 HG01106.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837-68delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100614497 | ||||||
chr13:100614509
|
A | G | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1837-79T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100614509 | ||||||
chr13:100614632
|
T | C | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1837-202A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100614632 | ||||||
chr13:100614903
|
G | T | 1 | a0002c0001t0002g0280 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1837-473C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100614903 | ||||||
chr13:100614947
|
A | G | 29 | a0001c0002t0005g0287a0001c0002t0009g0128a0001c0003t0001g0074others(26): Show | 29 | HG01192.hp2 HG01891.hp2 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.1837-517T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100614947 | ||||||
chr13:100615180
|
C | G | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1837-750G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615180 | ||||||
chr13:100615237
|
A | G | 38 | a0001c0002t0001g0184a0001c0002t0001g0189a0002c0001t0002g0005others(35): Show | 39 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.1837-807T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615237 | ||||||
chr13:100615282
|
C | T | 17 | a0001c0002t0005g0287a0001c0002t0009g0128a0001c0003t0002g0326others(14): Show | 17 | HG01192.hp2 HG02056.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1837-852G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615282 | ||||||
chr13:100615329
|
G | T | 1 | a0001c0002t0001g0097 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1837-899C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615329 | ||||||
chr13:100615337
|
C | T | 2 | a0002c0001t0002g0230a0002c0001t0002g0247 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1837-907G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615337 | ||||||
chr13:100615349
|
G | C | 1 | a0001c0004t0001g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1837-919C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615349 | ||||||
chr13:100615396
|
C | A | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1837-966G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615396 | ||||||
chr13:100615401
|
G | A | 5 | a0001c0002t0001g0163a0001c0004t0003g0036a0001c0004t0003g0042others(2): Show | 5 | HG00140.hp2 HG01358.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1837-971C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615401 | ||||||
chr13:100615432
|
C | T | 1 | a0001c0002t0003g0206 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1837-1002G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615432 | ||||||
chr13:100615440
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1837-1010C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615440 | ||||||
chr13:100615534
|
C | T | 3 | a0001c0002t0003g0178a0001c0003t0003g0054a0001c0003t0003g0131 | 3 | HG01256.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1837-1104G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615534 | ||||||
chr13:100615546
|
A | C | 7 | a0001c0003t0001g0082a0001c0003t0001g0088a0001c0004t0001g0113others(4): Show | 7 | HG01975.hp2 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-1116T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615546 | ||||||
chr13:100615649
|
C | T | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1837-1219G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615649 | ||||||
chr13:100615840
|
G | T | 1 | a0002c0001t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1837-1410C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615840 | ||||||
chr13:100615865
|
C | G | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-1435G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615865 | ||||||
chr13:100615967
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1837-1537G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100615967 | ||||||
chr13:100616062
|
A | AT | 14 | a0001c0002t0001g0143a0001c0002t0001g0156a0001c0004t0001g0022others(11): Show | 14 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1837-1633dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616062 | ||||||
chr13:100616062
|
AT | A | 34 | a0001c0002t0005g0287a0001c0002t0009g0128a0001c0003t0001g0074others(31): Show | 34 | HG01192.hp2 HG01358.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1837-1633delA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616062 | ||||||
chr13:100616348
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1837-1918C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616348 | ||||||
chr13:100616453
|
G | A | 13 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1837-2023C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616453 | ||||||
chr13:100616528
|
C | A | 1 | a0002c0001t0002g0241 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1837-2098G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616528 | ||||||
chr13:100616959
|
C | T | 188 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1837-2529G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100616959 | ||||||
chr13:100617110
|
C | T | 1 | a0002c0001t0002g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1837-2680G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617110 | ||||||
chr13:100617127
|
A | AT | 118 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1837-2698dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617127 | ||||||
chr13:100617127
|
A | ATT | 7 | a0001c0004t0001g0108a0001c0009t0001g0009a0001c0009t0002g0215others(4): Show | 7 | HG02723.hp2 HG02965.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-2699_1837-269 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617127 | ||||||
chr13:100617127
|
A | ATTTT | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-2701_1837-269 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617127 | ||||||
chr13:100617292
|
G | T | 1 | a0001c0003t0001g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1837-2862C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617292 | ||||||
chr13:100617353
|
C | T | 14 | a0001c0002t0005g0287a0001c0002t0009g0128a0001c0004t0001g0085others(11): Show | 14 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-2923G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617353 | ||||||
chr13:100617546
|
G | C | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-3116C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617546 | ||||||
chr13:100617707
|
C | T | 188 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0132others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1837-3277G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617707 | ||||||
chr13:100617743
|
C | T | 14 | a0001c0002t0005g0287a0001c0002t0009g0128a0001c0004t0001g0085others(11): Show | 14 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1837-3313G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100617743 | ||||||
chr13:100618211
|
T | C | 1 | a0001c0004t0003g0017 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1837-3781A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618211 | ||||||
chr13:100618220
|
T | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-3790A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618220 | ||||||
chr13:100618224
|
G | A | 1 | a0002c0001t0002g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1837-3794C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618224 | ||||||
chr13:100618400
|
C | T | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1837-3970G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618400 | ||||||
chr13:100618436
|
A | C | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1837-4006T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618436 | ||||||
chr13:100618450
|
T | G | 2 | a0001c0004t0011g0063a0001c0004t0013g0221 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1837-4020A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618450 | ||||||
chr13:100618451
|
C | CT | 16 | a0001c0002t0001g0125a0001c0002t0003g0181a0001c0002t0003g0206others(13): Show | 16 | HG01106.hp2 HG01192.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1837-4022dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618451 | ||||||
chr13:100618451
|
C | CTT | 8 | a0001c0002t0001g0184a0001c0002t0001g0189a0002c0001t0002g0005others(5): Show | 9 | HG00408.hp2 HG00673.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-4023_1837-402 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618451 | ||||||
chr13:100618453
|
TG | T | 88 | a0001c0002t0001g0041a0001c0002t0001g0127a0001c0002t0001g0132others(85): Show | 89 | HG00099.hp2 HG00323.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.1837-4024delC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618453 | ||||||
chr13:100618454
|
G | C | 13 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1837-4024C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618454 | ||||||
chr13:100618454
|
G | T | 219 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(216): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1837-4024C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618454 | ||||||
chr13:100618471
|
A | T | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1837-4041T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618471 | ||||||
chr13:100618476
|
C | A | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1837-4046G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618476 | ||||||
chr13:100618533
|
G | C | 1 | a0001c0003t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1837-4103C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618533 | ||||||
chr13:100618536
|
G | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-4106C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618536 | ||||||
chr13:100618643
|
G | C | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-4213C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618643 | ||||||
chr13:100618647
|
T | C | 1 | a0002c0001t0002g0234 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1837-4217A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618647 | ||||||
chr13:100618739
|
G | T | 1 | a0001c0009t0002g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1837-4309C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618739 | ||||||
chr13:100618803
|
G | T | 2 | a0001c0002t0005g0287a0003c0006t0009g0120 | 2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1837-4373C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618803 | ||||||
chr13:100618813
|
C | T | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-4383G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618813 | ||||||
chr13:100618819
|
T | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-4389A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618819 | ||||||
chr13:100618849
|
C | T | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1837-4419G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618849 | ||||||
chr13:100618916
|
G | A | 1 | a0001c0004t0003g0017 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1837-4486C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100618916 | ||||||
chr13:100619018
|
T | C | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-4588A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619018 | ||||||
chr13:100619032
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1837-4602C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619032 | ||||||
chr13:100619064
|
C | T | 1 | a0001c0002t0005g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1837-4634G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619064 | ||||||
chr13:100619068
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1837-4638G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619068 | ||||||
chr13:100619101
|
C | G | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-4671G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619101 | ||||||
chr13:100619102
|
G | A | 3 | a0004c0007t0002g0226a0004c0007t0006g0236a0004c0007t0006g0318 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1837-4672C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619102 | ||||||
chr13:100619194
|
T | C | 7 | a0001c0004t0001g0085a0001c0009t0001g0009a0001c0009t0002g0215others(4): Show | 7 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-4764A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619194 | ||||||
chr13:100619203
|
C | T | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1837-4773G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619203 | ||||||
chr13:100619264
|
A | T | 1 | a0001c0003t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1837-4834T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619264 | ||||||
chr13:100619281
|
CAG | C | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-4853_1837-485 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619281 | ||||||
chr13:100619328
|
G | GAC | 7 | a0001c0003t0001g0110a0001c0004t0001g0045a0001c0004t0001g0108others(4): Show | 7 | HG02055.hp1 HG02056.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-4900_1837-489 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
G | GACAC | 7 | a0001c0003t0001g0074a0001c0003t0001g0081a0001c0003t0001g0087others(4): Show | 7 | HG01261.hp1 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1837-4902_1837-489 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
G | GACACAC | 5 | a0001c0003t0001g0083a0001c0003t0001g0094a0001c0003t0001g0109others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837-4904_1837-489 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GAC | G | 22 | a0001c0002t0001g0134a0001c0002t0001g0140a0001c0002t0001g0141others(19): Show | 22 | HG00642.hp1 HG01978.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1837-4900_1837-489 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACAC | G | 79 | a0001c0002t0001g0003a0001c0002t0001g0041a0001c0002t0001g0097others(76): Show | 81 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1837-4902_1837-489 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACAC | G | 20 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008others(17): Show | 20 | HG00609.hp2 HG01081.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1837-4904_1837-489 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(1): Show |
G | 28 | a0001c0002t0001g0149a0001c0002t0001g0199a0001c0002t0003g0174others(25): Show | 29 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1837-4906_1837-489 others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(3): Show |
G | 131 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0142others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1837-4908_1837-489 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(5): Show |
G | 19 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(16): Show | 19 | HG00735.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1837-4910_1837-489 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(7): Show |
G | 1 | a0001c0004t0003g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1837-4912_1837-489 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(9): Show |
G | 4 | a0001c0002t0001g0132a0004c0007t0002g0226a0004c0007t0006g0236others(1): Show | 4 | HG02965.hp2 HG03516.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1837-4914_1837-489 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619328
|
GACACACA others(15): Show |
G | 1 | a0001c0003t0002g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1837-4920_1837-489 others(26): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619328 | ||||||
chr13:100619602
|
C | A | 7 | a0001c0002t0005g0287a0001c0002t0009g0128a0002c0001t0002g0334others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-5172G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619602 | ||||||
chr13:100619643
|
A | AAC | 118 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1837-5215_1837-521 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619643 | ||||||
chr13:100619698
|
G | C | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1837-5268C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619698 | ||||||
chr13:100619751
|
G | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837-5321C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619751 | ||||||
chr13:100619761
|
C | T | 2 | a0001c0005t0001g0099a0001c0005t0001g0111 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1837-5331G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619761 | ||||||
chr13:100619878
|
C | T | 7 | a0002c0001t0002g0300a0002c0001t0002g0302a0002c0001t0002g0303others(4): Show | 7 | NA18968.hp2 NA18991.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-5448G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100619878 | ||||||
chr13:100620111
|
T | C | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1836+5424A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620111 | ||||||
chr13:100620124
|
T | C | 1 | a0001c0002t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1836+5411A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620124 | ||||||
chr13:100620207
|
C | T | 1 | a0001c0004t0011g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1836+5328G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620207 | ||||||
chr13:100620237
|
T | C | 325 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1836+5298A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620237 | ||||||
chr13:100620304
|
C | A | 1 | a0001c0004t0002g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1836+5231G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620304 | ||||||
chr13:100620355
|
G | A | 1 | a0001c0002t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1836+5180C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620355 | ||||||
chr13:100620424
|
G | A | 1 | a0002c0001t0002g0307 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1836+5111C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620424 | ||||||
chr13:100620650
|
C | G | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1836+4885G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620650 | ||||||
chr13:100620651
|
G | A | 1 | a0001c0002t0017g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1836+4884C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620651 | ||||||
chr13:100620730
|
C | T | 6 | a0001c0009t0001g0009a0001c0009t0002g0215a0004c0007t0002g0226others(3): Show | 6 | HG02965.hp2 HG03471.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1836+4805G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620730 | ||||||
chr13:100620828
|
A | C | 2 | a0001c0018t0001g0192a0011c0022t0003g0173 | 2 | HG00323.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1836+4707T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620828 | ||||||
chr13:100620828
|
AAAAC | A | 7 | a0001c0009t0001g0009a0001c0009t0002g0215a0002c0001t0001g0060others(4): Show | 7 | HG02647.hp1 HG02965.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+4703_1836+470 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620828 | ||||||
chr13:100620927
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1836+4608G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100620927 | ||||||
chr13:100621023
|
T | A | 322 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1836+4512A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621023 | ||||||
chr13:100621030
|
C | T | 1 | a0002c0001t0004g0325 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1836+4505G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621030 | ||||||
chr13:100621075
|
C | A | 5 | a0001c0009t0001g0009a0004c0007t0002g0226a0004c0007t0006g0236others(2): Show | 5 | HG02965.hp2 HG03516.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+4460G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621075 | ||||||
chr13:100621345
|
C | A | 119 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(116): Show | 121 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1836+4190G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621345 | ||||||
chr13:100621448
|
T | C | 8 | a0001c0002t0001g0041a0001c0003t0002g0066a0001c0009t0001g0009others(5): Show | 8 | HG00099.hp2 HG01099.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+4087A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621448 | ||||||
chr13:100621477
|
G | A | 2 | a0001c0004t0001g0085a0002c0001t0002g0313 | 2 | HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1836+4058C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621477 | ||||||
chr13:100621574
|
T | C | 6 | a0001c0002t0005g0287a0002c0001t0002g0334a0003c0006t0001g0116others(3): Show | 6 | HG02056.hp2 HG02083.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+3961A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621574 | ||||||
chr13:100621582
|
C | T | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1836+3953G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621582 | ||||||
chr13:100621780
|
T | C | 1 | a0002c0001t0002g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1836+3755A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621780 | ||||||
chr13:100621878
|
C | T | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1836+3657G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100621878 | ||||||
chr13:100622015
|
G | T | 1 | a0001c0004t0001g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1836+3520C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622015 | ||||||
chr13:100622166
|
T | G | 1 | a0002c0001t0002g0334 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1836+3369A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622166 | ||||||
chr13:100622270
|
C | G | 13 | a0001c0002t0001g0041a0001c0003t0002g0326a0001c0004t0001g0085others(10): Show | 13 | HG01099.hp2 HG01192.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1836+3265G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622270 | ||||||
chr13:100622380
|
G | A | 7 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+3155C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622380 | ||||||
chr13:100622435
|
A | G | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1836+3100T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622435 | ||||||
chr13:100622457
|
G | A | 1 | a0001c0003t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1836+3078C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622457 | ||||||
chr13:100622547
|
T | C | 9 | a0001c0002t0017g0167a0001c0003t0001g0083a0001c0003t0001g0093others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1836+2988A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622547 | ||||||
chr13:100622603
|
A | G | 4 | a0002c0001t0002g0302a0002c0001t0002g0308a0002c0001t0002g0309others(1): Show | 4 | NA18968.hp2 NA19011.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1836+2932T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622603 | ||||||
chr13:100622607
|
T | C | 2 | a0001c0002t0003g0183a0001c0002t0003g0194 | 2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1836+2928A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622607 | ||||||
chr13:100622609
|
T | A | 188 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1836+2926A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622609 | ||||||
chr13:100622610
|
G | A | 300 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(297): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1836+2925C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622610 | ||||||
chr13:100622648
|
C | A | 1 | a0001c0017t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1836+2887G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622648 | ||||||
chr13:100622656
|
A | T | 1 | a0001c0002t0001g0145 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1836+2879T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622656 | ||||||
chr13:100622681
|
T | C | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1836+2854A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622681 | ||||||
chr13:100622685
|
C | T | 316 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(313): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1836+2850G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622685 | ||||||
chr13:100622711
|
T | C | 1 | a0001c0009t0002g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1836+2824A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622711 | ||||||
chr13:100622751
|
A | G | 31 | a0001c0003t0001g0074a0001c0003t0001g0075a0001c0003t0001g0079others(28): Show | 32 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1836+2784T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622751 | ||||||
chr13:100622777
|
T | A | 8 | a0001c0004t0001g0016a0001c0004t0001g0034a0001c0004t0001g0037others(5): Show | 8 | HG01081.hp1 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1836+2758A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622777 | ||||||
chr13:100622796
|
C | CT | 3 | a0004c0007t0002g0226a0004c0007t0006g0236a0004c0007t0006g0318 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1836+2738dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622796 | ||||||
chr13:100622817
|
T | C | 104 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1836+2718A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622817 | ||||||
chr13:100622872
|
G | A | 150 | a0001c0002t0001g0179a0001c0002t0001g0184a0001c0002t0001g0189others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1836+2663C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622872 | ||||||
chr13:100622873
|
T | C | 1 | a0001c0003t0003g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1836+2662A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622873 | ||||||
chr13:100622877
|
C | T | 1 | a0001c0002t0009g0128 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1836+2658G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100622877 | ||||||
chr13:100623601
|
C | T | 114 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(111): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1836+1934G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623601 | ||||||
chr13:100623640
|
G | GT | 87 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0097others(84): Show | 89 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1836+1894dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623640 | ||||||
chr13:100623640
|
G | GTT | 60 | a0002c0001t0001g0059a0002c0001t0001g0061a0002c0001t0001g0062others(57): Show | 60 | HG00438.hp2 HG00673.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1836+1893_1836+189 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623640 | ||||||
chr13:100623640
|
G | GTTT | 21 | a0002c0001t0002g0233a0002c0001t0002g0240a0002c0001t0002g0242others(18): Show | 21 | HG00544.hp1 HG00621.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1836+1892_1836+189 others(7): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623640 | ||||||
chr13:100623644
|
TG | T | 29 | a0001c0004t0001g0001a0001c0004t0001g0019a0001c0004t0001g0022others(26): Show | 30 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1836+1890delC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623644 | ||||||
chr13:100623645
|
G | GT | 8 | a0001c0003t0001g0072a0001c0003t0001g0073a0001c0003t0001g0081others(5): Show | 8 | HG01891.hp2 HG01981.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+1889dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623645 | ||||||
chr13:100623645
|
G | T | 261 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(258): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1836+1890C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623645 | ||||||
chr13:100623645
|
GT | G | 15 | a0001c0003t0001g0002a0001c0003t0001g0051a0001c0003t0001g0055others(12): Show | 16 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1836+1889delA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623645 | ||||||
chr13:100623649
|
T | G | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1836+1886A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623649 | ||||||
chr13:100623650
|
T | G | 7 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(4): Show | 7 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+1885A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623650 | ||||||
chr13:100623712
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0001g0163 | 2 | HG01358.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1836+1823C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623712 | ||||||
chr13:100623745
|
G | A | 1 | a0001c0002t0001g0219 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1836+1790C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623745 | ||||||
chr13:100623753
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1836+1782C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623753 | ||||||
chr13:100623797
|
C | T | 114 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(111): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1836+1738G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623797 | ||||||
chr13:100623824
|
T | C | 1 | a0001c0004t0001g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1836+1711A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623824 | ||||||
chr13:100623829
|
C | T | 1 | a0002c0001t0002g0323 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1836+1706G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100623829 | ||||||
chr13:100624046
|
G | C | 1 | a0002c0001t0002g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1836+1489C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624046 | ||||||
chr13:100624315
|
T | C | 1 | a0001c0002t0003g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1836+1220A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624315 | ||||||
chr13:100624343
|
AAAAAAAA others(4): Show |
A | 97 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(94): Show | 99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1836+1181_1836+119 others(15): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624343 | ||||||
chr13:100624344
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1836+1181_1836+119 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624344 | ||||||
chr13:100624354
|
T | TA | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1836+1180dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624354 | ||||||
chr13:100624354
|
T | TAA | 41 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(38): Show | 42 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1836+1179_1836+118 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624354 | ||||||
chr13:100624354
|
T | TAAA | 25 | a0001c0004t0001g0016a0001c0004t0001g0034a0001c0004t0001g0037others(22): Show | 25 | HG00140.hp2 HG01081.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1836+1178_1836+118 others(7): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624354 | ||||||
chr13:100624354
|
T | TAAAA | 116 | a0001c0004t0001g0113a0002c0001t0001g0059a0002c0001t0001g0060others(113): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1836+1177_1836+118 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624354 | ||||||
chr13:100624373
|
G | T | 10 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(7): Show | 10 | HG03704.hp1 HG04199.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.1836+1162C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624373 | ||||||
chr13:100624449
|
G | A | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1836+1086C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624449 | ||||||
chr13:100624503
|
T | G | 1 | a0002c0001t0002g0235 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1836+1032A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624503 | ||||||
chr13:100624571
|
AAAAC | A | 291 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(288): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1836+960_1836+963d others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624571 | ||||||
chr13:100624630
|
A | G | 124 | a0001c0004t0001g0113a0002c0001t0001g0059a0002c0001t0001g0060others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1836+905T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624630 | ||||||
chr13:100624856
|
A | G | 1 | a0001c0002t0009g0128 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1836+679T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624856 | ||||||
chr13:100624859
|
G | A | 123 | a0001c0004t0001g0113a0002c0001t0001g0059a0002c0001t0001g0060others(120): Show | 124 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1836+676C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624859 | ||||||
chr13:100624887
|
G | A | 115 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(112): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1836+648C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100624887 | ||||||
chr13:100625129
|
G | A | 2 | a0003c0006t0001g0115a0003c0006t0001g0124 | 2 | NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1836+406C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100625129 | ||||||
chr13:100625160
|
G | A | 114 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(111): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1836+375C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100625160 | ||||||
chr13:100625265
|
C | T | 1 | a0002c0001t0002g0299 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1836+270G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100625265 | ||||||
chr13:100625452
|
G | GT | 4 | a0001c0004t0001g0085a0001c0004t0001g0108a0001c0004t0011g0063others(1): Show | 4 | HG02723.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1836+82dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100625452 | ||||||
chr13:100625454
|
G | A | 1 | a0001c0004t0001g0023 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1836+81C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 15/18 | chr13 | 100625454 | ||||||
chr13:100625738
|
G | C | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1694+47C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 14/18 | chr13 | 100625738 | ||||||
chr13:100625932
|
C | G | 3 | a0002c0001t0002g0276a0002c0001t0002g0312a0002c0001t0002g0323 | 3 | NA18953.hp2 NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1587-40G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 13/18 | chr13 | 100625932 | ||||||
chr13:100625933
|
A | T | 1 | a0001c0002t0017g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1587-41T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 13/18 | chr13 | 100625933 | ||||||
chr13:100625947
|
A | T | 1 | a0001c0002t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1587-55T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 13/18 | chr13 | 100625947 | ||||||
chr13:100626154
|
C | A | 1 | a0001c0003t0001g0053 | 1 | HG01361.hp2 | splice_region_variant&intron_variant | LOW | c.1507-4G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100626154 | ||||||
chr13:100626502
|
T | C | 1 | a0002c0001t0002g0336 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1507-352A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100626502 | ||||||
chr13:100626837
|
T | C | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1507-687A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100626837 | ||||||
chr13:100626985
|
C | G | 1 | a0002c0001t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1507-835G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100626985 | ||||||
chr13:100627130
|
T | C | 1 | a0001c0002t0001g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1507-980A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627130 | ||||||
chr13:100627186
|
C | G | 1 | a0001c0004t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1507-1036G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627186 | ||||||
chr13:100627199
|
T | A | 1 | a0002c0001t0004g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1507-1049A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627199 | ||||||
chr13:100627288
|
C | T | 125 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(122): Show | 126 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1507-1138G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627288 | ||||||
chr13:100627299
|
C | T | 4 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(1): Show | 4 | HG00099.hp2 HG03239.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507-1149G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627299 | ||||||
chr13:100627452
|
A | G | 1 | a0001c0004t0001g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1507-1302T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627452 | ||||||
chr13:100627834
|
C | T | 124 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(121): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1507-1684G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100627834 | ||||||
chr13:100628037
|
G | A | 273 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(270): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1507-1887C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628037 | ||||||
chr13:100628068
|
G | C | 5 | a0002c0001t0005g0231a0002c0001t0005g0232a0002c0001t0005g0249others(2): Show | 5 | NA18982.hp1 NA18989.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-1918C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628068 | ||||||
chr13:100628133
|
C | A | 1 | a0002c0001t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1507-1983G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628133 | ||||||
chr13:100628278
|
A | C | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507-2128T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628278 | ||||||
chr13:100628281
|
T | C | 46 | a0002c0001t0002g0224a0002c0001t0002g0225a0002c0001t0002g0233others(43): Show | 46 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1507-2131A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628281 | ||||||
chr13:100628375
|
TTC | T | 28 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(25): Show | 29 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1507-2227_1507-222 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628375 | ||||||
chr13:100628379
|
G | A | 1 | a0001c0004t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1507-2229C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628379 | ||||||
chr13:100628488
|
C | T | 1 | a0002c0001t0002g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1507-2338G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628488 | ||||||
chr13:100628566
|
T | C | 133 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(130): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1507-2416A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628566 | ||||||
chr13:100628646
|
G | C | 130 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1507-2496C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628646 | ||||||
chr13:100628761
|
A | T | 154 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(151): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1507-2611T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628761 | ||||||
chr13:100628827
|
C | A | 1 | a0003c0006t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1507-2677G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628827 | ||||||
chr13:100628858
|
G | T | 1 | a0002c0001t0002g0291 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1507-2708C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628858 | ||||||
chr13:100628870
|
C | G | 5 | a0002c0001t0002g0265a0002c0001t0006g0210a0002c0001t0006g0328others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-2720G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628870 | ||||||
chr13:100628952
|
C | T | 33 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(30): Show | 34 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1507-2802G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100628952 | ||||||
chr13:100629139
|
ACT | A | 21 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(18): Show | 22 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1507-2991_1507-299 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629139 | ||||||
chr13:100629140
|
CTCTG | C | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1507-2994_1507-299 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629140 | ||||||
chr13:100629213
|
C | T | 40 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(37): Show | 41 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1507-3063G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629213 | ||||||
chr13:100629321
|
A | G | 40 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019others(37): Show | 41 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1507-3171T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629321 | ||||||
chr13:100629352
|
T | C | 8 | a0001c0004t0001g0016a0001c0004t0001g0034a0001c0004t0001g0037others(5): Show | 8 | HG01081.hp1 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1507-3202A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629352 | ||||||
chr13:100629365
|
C | A | 1 | a0002c0001t0002g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1507-3215G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629365 | ||||||
chr13:100629388
|
C | A | 1 | a0004c0007t0002g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1507-3238G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629388 | ||||||
chr13:100629595
|
G | C | 1 | a0001c0002t0003g0178 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1507-3445C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629595 | ||||||
chr13:100629703
|
A | G | 1 | a0001c0002t0001g0153 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1507-3553T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629703 | ||||||
chr13:100629744
|
A | C | 2 | a0001c0002t0001g0140a0001c0002t0001g0141 | 2 | NA19074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1507-3594T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629744 | ||||||
chr13:100629799
|
G | A | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1507-3649C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629799 | ||||||
chr13:100629807
|
T | A | 62 | a0002c0001t0002g0012a0002c0001t0002g0013a0002c0001t0002g0014others(59): Show | 62 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1507-3657A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629807 | ||||||
chr13:100629837
|
T | C | 3 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019 | 4 | HG02486.hp1 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1507-3687A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629837 | ||||||
chr13:100629905
|
G | A | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1507-3755C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100629905 | ||||||
chr13:100630019
|
CTGTGTGT others(1): Show |
C | 101 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(98): Show | 103 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1507-3877_1507-387 others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630019 | ||||||
chr13:100630019
|
CTGTGTGT others(3): Show |
C | 101 | a0001c0004t0001g0220a0001c0004t0002g0211a0001c0004t0013g0221others(98): Show | 102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1507-3879_1507-387 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630019 | ||||||
chr13:100630019
|
CTGTGTGT others(5): Show |
C | 10 | a0002c0001t0002g0012a0002c0001t0002g0234a0002c0001t0002g0258others(7): Show | 10 | HG02004.hp1 HG02717.hp1 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507-3881_1507-387 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630019 | ||||||
chr13:100630019
|
CTGTGTGT others(7): Show |
C | 50 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0004t0001g0001others(47): Show | 51 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1507-3883_1507-387 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630019 | ||||||
chr13:100630019
|
CTGTGTGT others(9): Show |
C | 2 | a0002c0001t0002g0224a0002c0001t0002g0240 | 2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1507-3885_1507-387 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630019 | ||||||
chr13:100630021
|
GTGTGTA | G | 13 | a0001c0002t0001g0186a0001c0002t0001g0200a0001c0002t0001g0201others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1507-3877_1507-387 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630021 | ||||||
chr13:100630027
|
A | G | 12 | a0001c0004t0001g0085a0001c0004t0001g0108a0001c0004t0003g0010others(9): Show | 12 | HG01884.hp1 HG02083.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1507-3877T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630027 | ||||||
chr13:100630027
|
ATGTG | A | 40 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(37): Show | 41 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1507-3881_1507-387 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630027 | ||||||
chr13:100630031
|
G | A | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507-3881C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630031 | ||||||
chr13:100630037
|
G | A | 10 | a0001c0002t0001g0186a0001c0002t0001g0200a0001c0002t0001g0201others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1507-3887C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630037 | ||||||
chr13:100630039
|
G | A | 86 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(83): Show | 88 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1507-3889C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630039 | ||||||
chr13:100630041
|
G | A | 2 | a0001c0004t0001g0220a0001c0004t0013g0221 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1507-3891C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630041 | ||||||
chr13:100630045
|
G | A | 49 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0004t0001g0001others(46): Show | 50 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1507-3895C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630045 | ||||||
chr13:100630057
|
G | T | 1 | a0002c0001t0002g0248 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1507-3907C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630057 | ||||||
chr13:100630065
|
G | A | 11 | a0001c0004t0001g0108a0001c0004t0002g0211a0001c0004t0002g0213others(8): Show | 11 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1507-3915C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630065 | ||||||
chr13:100630067
|
A | G | 13 | a0001c0004t0001g0108a0001c0004t0002g0211a0001c0004t0002g0213others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1507-3917T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630067 | ||||||
chr13:100630067
|
ATGTGTG | A | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507-3923_1507-391 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630067 | ||||||
chr13:100630100
|
A | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1507-3950T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630100 | ||||||
chr13:100630220
|
T | C | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1507-4070A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630220 | ||||||
chr13:100630264
|
A | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1507-4114T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630264 | ||||||
chr13:100630366
|
T | C | 55 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(52): Show | 56 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1507-4216A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630366 | ||||||
chr13:100630535
|
T | C | 1 | a0002c0001t0007g0335 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1506+4270A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630535 | ||||||
chr13:100630536
|
A | C | 2 | a0002c0001t0002g0230a0002c0001t0002g0247 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1506+4269T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630536 | ||||||
chr13:100630568
|
A | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+4237T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630568 | ||||||
chr13:100630965
|
T | C | 123 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(120): Show | 124 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1506+3840A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630965 | ||||||
chr13:100630977
|
A | G | 1 | a0001c0002t0003g0181 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1506+3828T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100630977 | ||||||
chr13:100631040
|
C | A | 8 | a0001c0005t0001g0098a0001c0005t0001g0100a0001c0005t0001g0101others(5): Show | 8 | NA18963.hp2 NA18989.hp2 NA18993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1506+3765G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631040 | ||||||
chr13:100631243
|
A | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+3562T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631243 | ||||||
chr13:100631502
|
T | G | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1506+3303A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631502 | ||||||
chr13:100631593
|
T | C | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+3212A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631593 | ||||||
chr13:100631594
|
G | A | 100 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(97): Show | 102 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1506+3211C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631594 | ||||||
chr13:100631699
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1506+3106A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631699 | ||||||
chr13:100631771
|
T | A | 1 | a0001c0002t0001g0188 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1506+3034A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631771 | ||||||
chr13:100631781
|
G | A | 1 | a0002c0001t0002g0313 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1506+3024C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631781 | ||||||
chr13:100631837
|
C | CA | 9 | a0001c0003t0002g0326a0001c0003t0003g0092a0003c0006t0001g0115others(6): Show | 9 | HG02083.hp1 HG02735.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506+2967dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631837 | ||||||
chr13:100631841
|
A | G | 35 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(32): Show | 36 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1506+2964T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631841 | ||||||
chr13:100631902
|
A | G | 59 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(56): Show | 60 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1506+2903T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631902 | ||||||
chr13:100631915
|
T | C | 2 | a0001c0002t0001g0186a0001c0002t0003g0182 | 2 | HG00438.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1506+2890A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631915 | ||||||
chr13:100631949
|
G | A | 33 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(30): Show | 34 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1506+2856C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631949 | ||||||
chr13:100631995
|
T | G | 2 | a0003c0006t0001g0117a0003c0006t0009g0120 | 2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1506+2810A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100631995 | ||||||
chr13:100632005
|
T | TAAG | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2797_1506+279 others(7): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632005 | ||||||
chr13:100632015
|
C | CCA | 27 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0126others(24): Show | 28 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1506+2788_1506+278 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
C | CCACA | 4 | a0001c0002t0001g0007a0001c0002t0001g0152a0001c0003t0001g0002others(1): Show | 5 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1506+2786_1506+278 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
C | CCACACAC others(1): Show |
3 | a0001c0003t0001g0070a0001c0003t0002g0326a0001c0003t0003g0092 | 3 | HG02630.hp1 HG02896.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1506+2782_1506+278 others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
C | CCACACAC others(3): Show |
1 | a0001c0003t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1506+2780_1506+278 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
C | CCACACAC others(5): Show |
1 | a0001c0003t0001g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1506+2778_1506+278 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
C | CCACACAC others(7): Show |
1 | a0001c0003t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+2776_1506+278 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632015
|
CCACACAC others(3): Show |
C | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1506+2780_1506+278 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632015 | ||||||
chr13:100632029
|
ACACACAC others(29): Show |
A | 10 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0100others(7): Show | 10 | HG01243.hp2 HG01975.hp2 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.1506+2740_1506+277 others(40): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632029 | ||||||
chr13:100632029
|
ACACACAC others(33): Show |
A | 2 | a0001c0005t0001g0099a0001c0005t0001g0111 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1506+2736_1506+277 others(44): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632029 | ||||||
chr13:100632031
|
ACACACAC others(27): Show |
A | 3 | a0001c0004t0001g0020a0001c0004t0001g0032a0001c0004t0003g0031 | 3 | HG01175.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1506+2740_1506+277 others(38): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632031 | ||||||
chr13:100632031
|
ACACACAC others(29): Show |
A | 32 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(29): Show | 33 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1506+2738_1506+277 others(40): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632031 | ||||||
chr13:100632045
|
ACACACAC others(7): Show |
A | 1 | a0002c0001t0002g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1506+2746_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632045 | ||||||
chr13:100632045
|
ACACACAC others(9): Show |
A | 1 | a0002c0001t0005g0231 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1506+2744_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632045 | ||||||
chr13:100632047
|
A | T | 3 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0011g0063 | 3 | HG01884.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1506+2758T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632047 | ||||||
chr13:100632047
|
ACACACAC others(7): Show |
A | 11 | a0002c0001t0002g0251a0002c0001t0002g0280a0002c0001t0002g0298others(8): Show | 11 | HG00438.hp2 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+2744_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632047 | ||||||
chr13:100632049
|
A | T | 3 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0011g0063 | 3 | HG01884.hp1 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1506+2756T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632049
|
ACACACTC others(3): Show |
A | 1 | a0002c0001t0002g0241 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1506+2746_1506+275 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632049
|
ACACACTC others(5): Show |
A | 3 | a0002c0001t0002g0310a0002c0001t0002g0330a0002c0001t0004g0229 | 3 | HG03098.hp2 HG03490.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1506+2744_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632049
|
ACACACTC others(7): Show |
A | 77 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(74): Show | 78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1506+2742_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632049
|
ACACACTC others(9): Show |
A | 2 | a0002c0001t0002g0269a0002c0001t0002g0270 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1506+2740_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632049
|
ACACACTC others(11): Show |
A | 6 | a0002c0001t0002g0233a0002c0001t0002g0243a0002c0001t0002g0261others(3): Show | 6 | HG00621.hp1 HG01106.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1506+2738_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632049 | ||||||
chr13:100632051
|
A | T | 4 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0011g0063others(1): Show | 4 | HG01884.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+2754T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632051 | ||||||
chr13:100632051
|
ACACT | A | 4 | a0001c0002t0001g0133a0001c0002t0001g0136a0001c0002t0001g0144others(1): Show | 4 | HG01081.hp2 HG02698.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+2750_1506+275 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632051 | ||||||
chr13:100632051
|
ACACTCTC others(3): Show |
A | 1 | a0002c0001t0002g0323 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1506+2744_1506+275 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632051 | ||||||
chr13:100632051
|
ACACTCTC others(5): Show |
A | 11 | a0002c0001t0002g0013a0002c0001t0002g0014a0002c0001t0002g0259others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+2742_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632051 | ||||||
chr13:100632051
|
ACACTCTC others(7): Show |
A | 1 | a0002c0001t0002g0248 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1506+2740_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632051 | ||||||
chr13:100632053
|
A | ACACACAC others(17): Show |
1 | a0001c0003t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(28): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(21): Show |
1 | a0001c0003t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(32): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(15): Show |
3 | a0001c0003t0001g0087a0001c0003t0003g0084a0001c0003t0003g0095 | 3 | HG01261.hp1 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(26): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(19): Show |
1 | a0001c0003t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(30): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(13): Show |
5 | a0001c0003t0001g0068a0001c0003t0001g0071a0001c0003t0001g0082others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(24): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(11): Show |
1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(13): Show |
3 | a0001c0003t0002g0066a0001c0003t0003g0052a0001c0020t0001g0107 | 3 | HG00099.hp2 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(24): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(15): Show |
1 | a0001c0003t0003g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(26): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(9): Show |
1 | a0001c0003t0001g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(11): Show |
1 | a0001c0003t0002g0065 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(13): Show |
2 | a0001c0003t0001g0109a0001c0003t0008g0089 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(24): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(5): Show |
2 | a0001c0003t0001g0058a0001c0003t0002g0067 | 2 | HG01074.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(7): Show |
1 | a0001c0003t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(9): Show |
2 | a0001c0003t0001g0051a0001c0003t0002g0064 | 2 | NA19062.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(17): Show |
1 | a0001c0003t0001g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(28): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(7): Show |
2 | a0001c0003t0003g0054a0001c0003t0003g0131 | 2 | HG01256.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(9): Show |
2 | a0001c0002t0003g0206a0001c0003t0001g0049 | 2 | HG01106.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(11): Show |
1 | a0001c0002t0003g0004 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACAC others(13): Show |
1 | a0001c0002t0003g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(24): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACTC others(5): Show |
4 | a0001c0002t0001g0130a0001c0002t0001g0193a0001c0002t0001g0209others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACTC others(7): Show |
3 | a0001c0002t0003g0182a0001c0002t0003g0183a0001c0002t0003g0194 | 3 | HG00438.hp1 NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACTC others(9): Show |
3 | a0001c0002t0003g0198a0001c0004t0001g0220a0011c0022t0003g0173 | 3 | HG02257.hp1 HG03239.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACTC others(11): Show |
1 | a0001c0002t0001g0188 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACACTC others(17): Show |
1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(28): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(1): Show |
4 | a0001c0002t0001g0175a0001c0002t0001g0200a0001c0002t0001g0208others(1): Show | 4 | HG01516.hp2 HG01928.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(3): Show |
3 | a0001c0002t0001g0201a0001c0002t0001g0204a0001c0002t0001g0207 | 3 | HG00408.hp1 HG00642.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(5): Show |
5 | a0001c0002t0001g0186a0001c0002t0003g0178a0001c0002t0003g0181others(2): Show | 5 | HG00323.hp2 HG00738.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(7): Show |
4 | a0001c0002t0001g0185a0001c0002t0001g0190a0001c0002t0001g0196others(1): Show | 4 | HG01074.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(9): Show |
2 | a0001c0002t0001g0179a0001c0002t0003g0187 | 2 | HG00544.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(11): Show |
4 | a0001c0002t0001g0176a0001c0002t0001g0189a0001c0002t0003g0174others(1): Show | 4 | HG01975.hp1 HG02135.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+2751_1506+275 others(22): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACACTCTC others(13): Show |
1 | a0001c0002t0001g0184 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1506+2751_1506+275 others(24): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACTCTCTC others(7): Show |
1 | a0006c0013t0003g0180 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1506+2738_1506+275 others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | ACTCTCTC others(15): Show |
1 | a0001c0002t0017g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1506+2730_1506+275 others(26): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
A | T | 7 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0007g0212others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506+2752T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
ACT | A | 3 | a0001c0002t0001g0097a0001c0002t0001g0159a0001c0003t0001g0074 | 3 | HG03041.hp2 NA18946.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1506+2750_1506+275 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
ACTCT | A | 8 | a0001c0002t0001g0125a0001c0002t0001g0138a0001c0002t0001g0140others(5): Show | 8 | HG01943.hp1 HG02735.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506+2748_1506+275 others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
ACTCTCT | A | 10 | a0001c0002t0001g0134a0001c0002t0003g0202a0001c0004t0013g0221others(7): Show | 10 | HG00423.hp1 HG02083.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1506+2746_1506+275 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
ACTCTCTC others(3): Show |
A | 5 | a0001c0002t0001g0153a0002c0001t0002g0230a0002c0001t0002g0247others(2): Show | 5 | HG00099.hp1 HG02055.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1506+2742_1506+275 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632053
|
ACTCTCTC others(5): Show |
A | 4 | a0002c0001t0002g0228a0002c0001t0002g0268a0002c0001t0002g0315others(1): Show | 4 | HG02818.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506+2740_1506+275 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632053 | ||||||
chr13:100632055
|
T | A | 41 | a0001c0002t0001g0041a0001c0002t0001g0126a0001c0002t0001g0127others(38): Show | 42 | HG00609.hp1 HG00735.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1506+2750A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632055 | ||||||
chr13:100632057
|
T | A | 10 | a0001c0002t0001g0097a0001c0002t0001g0132a0001c0002t0001g0159others(7): Show | 11 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+2748A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632057 | ||||||
chr13:100632059
|
T | A | 6 | a0001c0002t0001g0125a0001c0002t0001g0166a0001c0003t0001g0074others(3): Show | 6 | HG01943.hp1 HG02735.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+2746A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632059 | ||||||
chr13:100632061
|
T | A | 10 | a0001c0002t0001g0134a0001c0002t0003g0202a0003c0006t0001g0115others(7): Show | 10 | HG00423.hp1 HG02083.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+2744A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632061 | ||||||
chr13:100632063
|
T | A | 9 | a0002c0001t0002g0258a0003c0006t0001g0115a0003c0006t0001g0116others(6): Show | 9 | HG02083.hp1 HG02735.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.1506+2742A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632063 | ||||||
chr13:100632065
|
T | A | 7 | a0001c0002t0001g0153a0003c0006t0001g0115a0003c0006t0001g0116others(4): Show | 7 | HG02083.hp1 HG03669.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506+2740A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632065 | ||||||
chr13:100632094
|
G | C | 1 | a0002c0001t0002g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1506+2711C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632094 | ||||||
chr13:100632113
|
C | T | 1 | a0001c0002t0014g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1506+2692G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632113 | ||||||
chr13:100632147
|
T | C | 47 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(44): Show | 48 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1506+2658A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632147 | ||||||
chr13:100632449
|
C | A | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2356G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632449 | ||||||
chr13:100632515
|
A | T | 53 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(50): Show | 54 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1506+2290T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632515 | ||||||
chr13:100632516
|
G | T | 1 | a0002c0001t0002g0340 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1506+2289C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632516 | ||||||
chr13:100632560
|
T | C | 1 | a0002c0001t0002g0280 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1506+2245A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632560 | ||||||
chr13:100632571
|
A | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2234T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632571 | ||||||
chr13:100632595
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1506+2210A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632595 | ||||||
chr13:100632645
|
C | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2160G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632645 | ||||||
chr13:100632708
|
T | G | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2097A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632708 | ||||||
chr13:100632767
|
C | T | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+2038G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632767 | ||||||
chr13:100632791
|
T | C | 1 | a0002c0001t0002g0313 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1506+2014A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632791 | ||||||
chr13:100632997
|
C | T | 5 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(2): Show | 5 | HG02451.hp1 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+1808G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100632997 | ||||||
chr13:100633095
|
C | T | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+1710G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633095 | ||||||
chr13:100633096
|
G | A | 1 | a0002c0001t0002g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1506+1709C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633096 | ||||||
chr13:100633139
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1506+1666G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633139 | ||||||
chr13:100633184
|
T | G | 1 | a0001c0004t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1506+1621A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633184 | ||||||
chr13:100633240
|
C | T | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506+1565G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633240 | ||||||
chr13:100633257
|
C | T | 1 | a0001c0003t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+1548G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633257 | ||||||
chr13:100633312
|
G | GA | 6 | a0001c0003t0001g0070a0001c0003t0001g0087a0001c0003t0001g0109others(3): Show | 6 | HG01243.hp1 HG01261.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+1492dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GA | G | 21 | a0001c0003t0001g0002a0001c0003t0001g0051a0001c0003t0001g0053others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1506+1492delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAA | G | 27 | a0001c0002t0001g0008a0001c0002t0001g0134a0001c0002t0001g0140others(24): Show | 27 | HG00423.hp1 HG00544.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1506+1491_1506+149 others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAA | G | 76 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(73): Show | 78 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1506+1490_1506+149 others(7): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAA | G | 10 | a0001c0004t0001g0113a0001c0005t0001g0099a0001c0005t0001g0100others(7): Show | 10 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+1487_1506+149 others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAAA | G | 11 | a0001c0004t0001g0032a0001c0004t0001g0033a0001c0004t0001g0039others(8): Show | 11 | HG01081.hp1 HG02083.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+1486_1506+149 others(11): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAAA others(1): Show |
G | 31 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(28): Show | 32 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1506+1485_1506+149 others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAAA others(2): Show |
G | 9 | a0002c0001t0001g0061a0002c0001t0002g0227a0002c0001t0002g0256others(6): Show | 9 | HG00423.hp2 HG01256.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1506+1484_1506+149 others(13): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAAA others(3): Show |
G | 114 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0062others(111): Show | 115 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1506+1483_1506+149 others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633312
|
GAAAAAAA others(5): Show |
G | 5 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(2): Show | 5 | HG02451.hp1 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+1481_1506+149 others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633312 | ||||||
chr13:100633316
|
A | G | 1 | a0001c0002t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1506+1489T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633316 | ||||||
chr13:100633323
|
A | G | 1 | a0002c0001t0002g0255 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1506+1482T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633323 | ||||||
chr13:100633385
|
G | A | 123 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(120): Show | 124 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1506+1420C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633385 | ||||||
chr13:100633683
|
C | T | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1506+1122G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633683 | ||||||
chr13:100633699
|
T | C | 2 | a0002c0001t0002g0289a0007c0014t0002g0267 | 2 | NA18983.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1506+1106A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633699 | ||||||
chr13:100633771
|
G | A | 54 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(51): Show | 55 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506+1034C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633771 | ||||||
chr13:100633829
|
TAAACATA others(1): Show |
T | 9 | a0002c0001t0002g0237a0002c0001t0002g0241a0002c0001t0002g0285others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506+968_1506+975d others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100633829 | ||||||
chr13:100634001
|
G | A | 47 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(44): Show | 48 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1506+804C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634001 | ||||||
chr13:100634012
|
C | T | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1506+793G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634012 | ||||||
chr13:100634045
|
C | T | 2 | a0001c0003t0001g0068a0001c0003t0001g0069 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1506+760G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634045 | ||||||
chr13:100634139
|
C | CA | 22 | a0001c0002t0009g0128a0001c0004t0001g0033a0001c0004t0001g0113others(19): Show | 22 | HG01243.hp2 HG01975.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1506+665dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634139 | ||||||
chr13:100634139
|
CA | C | 9 | a0001c0002t0001g0041a0001c0002t0001g0139a0001c0004t0001g0030others(6): Show | 9 | HG01099.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506+665delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634139 | ||||||
chr13:100634155
|
AGGTATAA others(4): Show |
A | 4 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(1): Show | 4 | HG02630.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+639_1506+649d others(13): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634155 | ||||||
chr13:100634204
|
C | T | 1 | a0001c0003t0001g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1506+601G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634204 | ||||||
chr13:100634206
|
G | A | 57 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(54): Show | 58 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1506+599C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634206 | ||||||
chr13:100634458
|
G | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0170 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1506+347C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634458 | ||||||
chr13:100634568
|
A | G | 296 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(293): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1506+237T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634568 | ||||||
chr13:100634583
|
A | G | 47 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(44): Show | 48 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1506+222T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634583 | ||||||
chr13:100634625
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0159 | 2 | NA18946.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1506+180C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634625 | ||||||
chr13:100634670
|
T | C | 296 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(293): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1506+135A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634670 | ||||||
chr13:100634720
|
G | A | 57 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(54): Show | 58 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1506+85C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 12/18 | chr13 | 100634720 | ||||||
chr13:100635325
|
T | C | 1 | a0001c0002t0002g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1203-130A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635325 | ||||||
chr13:100635385
|
A | G | 35 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(32): Show | 36 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1203-190T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635385 | ||||||
chr13:100635389
|
T | G | 1 | a0002c0001t0002g0313 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1203-194A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635389 | ||||||
chr13:100635397
|
T | C | 292 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(289): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1203-202A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635397 | ||||||
chr13:100635413
|
G | C | 1 | a0002c0001t0002g0337 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1203-218C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635413 | ||||||
chr13:100635440
|
C | G | 10 | a0001c0005t0001g0098a0001c0005t0001g0099a0001c0005t0001g0100others(7): Show | 10 | HG03704.hp1 HG04199.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.1203-245G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635440 | ||||||
chr13:100635662
|
T | C | 3 | a0003c0008t0001g0121a0003c0008t0001g0122a0003c0008t0001g0123 | 3 | NA18963.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1203-467A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635662 | ||||||
chr13:100635705
|
A | G | 57 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0018others(54): Show | 58 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1203-510T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635705 | ||||||
chr13:100635892
|
G | C | 1 | a0002c0001t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1202+640C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635892 | ||||||
chr13:100635912
|
C | T | 292 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(289): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1202+620G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100635912 | ||||||
chr13:100636116
|
T | G | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+416A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636116 | ||||||
chr13:100636194
|
TA | T | 12 | a0001c0004t0001g0113a0001c0005t0001g0098a0001c0005t0001g0099others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.1202+337delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636194 | ||||||
chr13:100636304
|
G | A | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1202+228C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636304 | ||||||
chr13:100636354
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1202+178G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636354 | ||||||
chr13:100636357
|
G | A | 1 | a0001c0004t0001g0044 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1202+175C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636357 | ||||||
chr13:100636434
|
G | C | 41 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0179others(38): Show | 42 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1202+98C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636434 | ||||||
chr13:100636458
|
T | C | 1 | a0002c0001t0002g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1202+74A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 10/18 | chr13 | 100636458 | ||||||
chr13:100636738
|
C | T | 149 | a0001c0002t0001g0184a0001c0003t0001g0002a0001c0003t0001g0049others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(148): Show |
splice_region_variant&intron_variant | LOW | c.1000-4G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100636738 | ||||||
chr13:100636872
|
G | A | 5 | a0002c0001t0002g0224a0002c0001t0002g0240a0002c0001t0002g0276others(2): Show | 5 | NA18953.hp2 NA18969.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-138C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100636872 | ||||||
chr13:100636908
|
A | G | 1 | a0002c0001t0004g0293 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1000-174T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100636908 | ||||||
chr13:100636995
|
G | T | 4 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(1): Show | 4 | HG02630.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-261C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100636995 | ||||||
chr13:100637283
|
T | G | 3 | a0003c0008t0001g0121a0003c0008t0001g0122a0003c0008t0001g0123 | 3 | NA18963.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.999+255A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100637283 | ||||||
chr13:100637341
|
C | T | 138 | a0001c0002t0002g0288a0001c0002t0005g0287a0001c0004t0001g0113others(135): Show | 139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.999+197G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100637341 | ||||||
chr13:100637455
|
G | A | 1 | a0002c0001t0002g0244 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.999+83C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 9/18 | chr13 | 100637455 | ||||||
chr13:100637715
|
C | T | 109 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(106): Show | 111 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.835-13G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 8/18 | chr13 | 100637715 | ||||||
chr13:100637744
|
C | A | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 254 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.835-42G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 8/18 | chr13 | 100637744 | ||||||
chr13:100637804
|
A | T | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.835-102T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 8/18 | chr13 | 100637804 | ||||||
chr13:100637862
|
T | C | 1 | a0002c0001t0005g0232 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.834+68A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 8/18 | chr13 | 100637862 | ||||||
chr13:100638172
|
T | C | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.742-150A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638172 | ||||||
chr13:100638189
|
T | C | 1 | a0001c0003t0001g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.742-167A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638189 | ||||||
chr13:100638201
|
T | C | 1 | a0001c0003t0001g0051 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.742-179A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638201 | ||||||
chr13:100638333
|
C | T | 1 | a0002c0001t0002g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.742-311G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638333 | ||||||
chr13:100638404
|
G | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0170 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.742-382C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638404 | ||||||
chr13:100638429
|
G | A | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-407C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638429 | ||||||
chr13:100638795
|
C | T | 5 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0118others(2): Show | 5 | HG02083.hp1 NA18944.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.742-773G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638795 | ||||||
chr13:100638978
|
C | T | 2 | a0001c0010t0001g0129a0001c0010t0001g0160 | 2 | HG00735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.742-956G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100638978 | ||||||
chr13:100639092
|
A | G | 14 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.742-1070T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639092 | ||||||
chr13:100639115
|
T | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0170 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.742-1093A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639115 | ||||||
chr13:100639168
|
G | A | 1 | a0001c0004t0001g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.742-1146C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639168 | ||||||
chr13:100639175
|
G | T | 1 | a0002c0001t0007g0335 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.742-1153C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639175 | ||||||
chr13:100639393
|
C | T | 14 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.742-1371G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639393 | ||||||
chr13:100639418
|
C | T | 1 | a0002c0001t0002g0308 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.742-1396G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639418 | ||||||
chr13:100639517
|
G | A | 2 | a0001c0004t0001g0113a0009c0016t0012g0112 | 2 | HG01243.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.742-1495C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639517 | ||||||
chr13:100639834
|
G | A | 34 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(31): Show | 35 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.742-1812C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639834 | ||||||
chr13:100639840
|
T | C | 8 | a0001c0004t0001g0113a0002c0001t0002g0228a0002c0001t0002g0258others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-1818A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639840 | ||||||
chr13:100639918
|
C | T | 1 | a0002c0001t0002g0291 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.742-1896G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639918 | ||||||
chr13:100639960
|
A | T | 2 | a0002c0001t0002g0243a0002c0001t0002g0261 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.742-1938T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100639960 | ||||||
chr13:100640172
|
T | C | 1 | a0001c0003t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.741+2039A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640172 | ||||||
chr13:100640402
|
A | G | 14 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.741+1809T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640402 | ||||||
chr13:100640507
|
G | A | 310 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(307): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.741+1704C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640507 | ||||||
chr13:100640580
|
T | C | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.741+1631A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640580 | ||||||
chr13:100640583
|
C | T | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.741+1628G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640583 | ||||||
chr13:100640736
|
C | G | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.741+1475G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640736 | ||||||
chr13:100640737
|
G | A | 14 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.741+1474C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640737 | ||||||
chr13:100640827
|
GA | G | 8 | a0001c0003t0001g0072a0001c0003t0001g0073a0001c0003t0001g0074others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+1383delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640827 | ||||||
chr13:100640828
|
A | G | 1 | a0001c0003t0010g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.741+1383T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100640828 | ||||||
chr13:100641051
|
C | A | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+1160G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641051 | ||||||
chr13:100641086
|
T | G | 271 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.741+1125A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641086 | ||||||
chr13:100641162
|
C | T | 1 | a0004c0007t0002g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.741+1049G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641162 | ||||||
chr13:100641334
|
G | T | 7 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(4): Show | 7 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+877C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641334 | ||||||
chr13:100641432
|
C | T | 1 | a0002c0001t0004g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.741+779G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641432 | ||||||
chr13:100641989
|
C | T | 4 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0011g0063others(1): Show | 4 | HG01884.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+222G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641989 | ||||||
chr13:100641996
|
T | G | 22 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(19): Show | 23 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.741+215A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100641996 | ||||||
chr13:100642013
|
A | G | 262 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.741+198T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100642013 | ||||||
chr13:100642050
|
T | C | 2 | a0002c0001t0002g0269a0002c0001t0002g0270 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.741+161A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100642050 | ||||||
chr13:100642174
|
C | G | 127 | a0001c0002t0001g0140a0001c0002t0001g0141a0001c0002t0002g0288others(124): Show | 128 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.741+37G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 7/18 | chr13 | 100642174 | ||||||
chr13:100642503
|
C | T | 3 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019 | 4 | HG02486.hp1 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-192G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642503 | ||||||
chr13:100642574
|
T | C | 337 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.641-263A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642574 | ||||||
chr13:100642594
|
G | A | 1 | a0003c0006t0001g0117 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-283C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642594 | ||||||
chr13:100642796
|
C | T | 6 | a0001c0004t0001g0034a0001c0004t0001g0037a0001c0004t0001g0038others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-485G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642796 | ||||||
chr13:100642828
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.641-517G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642828 | ||||||
chr13:100642899
|
C | A | 1 | a0001c0004t0011g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.641-588G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642899 | ||||||
chr13:100642987
|
G | A | 1 | a0001c0009t0001g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.641-676C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642987 | ||||||
chr13:100642996
|
C | G | 1 | a0001c0003t0001g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.641-685G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100642996 | ||||||
chr13:100643084
|
C | T | 1 | a0001c0002t0004g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.641-773G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643084 | ||||||
chr13:100643220
|
C | T | 3 | a0004c0007t0002g0226a0004c0007t0006g0236a0004c0007t0006g0318 | 3 | HG02965.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641-909G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643220 | ||||||
chr13:100643332
|
G | A | 1 | a0002c0001t0002g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.641-1021C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643332 | ||||||
chr13:100643367
|
C | T | 1 | a0002c0001t0002g0322 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.641-1056G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643367 | ||||||
chr13:100643434
|
C | T | 1 | a0002c0001t0002g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.641-1123G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643434 | ||||||
chr13:100643542
|
T | C | 1 | a0001c0002t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.641-1231A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643542 | ||||||
chr13:100643779
|
G | GGGTCAGC others(7): Show |
1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-1482_641-1469d others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643779 | ||||||
chr13:100643952
|
G | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0170 | 2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.641-1641C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643952 | ||||||
chr13:100643978
|
G | C | 1 | a0001c0017t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.641-1667C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100643978 | ||||||
chr13:100644098
|
C | CT | 16 | a0001c0002t0001g0125a0001c0002t0003g0174a0001c0003t0001g0050others(13): Show | 16 | HG01433.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.641-1788dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644098 | ||||||
chr13:100644098
|
CT | C | 15 | a0001c0002t0001g0041a0001c0002t0001g0097a0001c0002t0001g0155others(12): Show | 15 | HG01099.hp2 HG02451.hp1 HG03704.hp1 others(12): Show |
intron_variant | MODIFIER | c.641-1788delA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644098 | ||||||
chr13:100644174
|
C | T | 3 | a0001c0004t0001g0026a0001c0004t0001g0027a0001c0004t0001g0029 | 3 | HG00323.hp1 HG01515.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.641-1863G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644174 | ||||||
chr13:100644398
|
C | T | 2 | a0002c0001t0002g0289a0004c0007t0002g0226 | 2 | NA19030.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.641-2087G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644398 | ||||||
chr13:100644485
|
T | C | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.641-2174A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644485 | ||||||
chr13:100644496
|
G | A | 109 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(106): Show | 111 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.641-2185C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644496 | ||||||
chr13:100644550
|
T | C | 1 | a0002c0001t0004g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.641-2239A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644550 | ||||||
chr13:100644640
|
ATC | A | 3 | a0002c0001t0002g0280a0002c0001t0002g0307a0002c0001t0004g0279 | 3 | HG00438.hp2 NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.641-2331_641-2330d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644640 | ||||||
chr13:100644764
|
C | A | 1 | a0001c0002t0001g0163 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.641-2453G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644764 | ||||||
chr13:100644815
|
A | C | 7 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-2504T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644815 | ||||||
chr13:100644821
|
C | CT | 127 | a0001c0002t0001g0140a0001c0002t0001g0141a0001c0002t0002g0288others(124): Show | 128 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.641-2511dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644821 | ||||||
chr13:100644846
|
G | A | 4 | a0001c0004t0001g0085a0001c0004t0003g0010a0001c0004t0011g0063others(1): Show | 4 | HG01884.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-2535C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100644846 | ||||||
chr13:100645272
|
T | A | 1 | a0002c0001t0002g0238 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.641-2961A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645272 | ||||||
chr13:100645414
|
C | A | 2 | a0001c0002t0001g0186a0001c0002t0003g0182 | 2 | HG00438.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.641-3103G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645414 | ||||||
chr13:100645438
|
T | A | 1 | a0001c0017t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.641-3127A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645438 | ||||||
chr13:100645478
|
C | A | 1 | a0002c0001t0002g0234 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.641-3167G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645478 | ||||||
chr13:100645534
|
T | C | 5 | a0001c0004t0001g0085a0001c0004t0001g0108a0001c0004t0003g0010others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-3223A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645534 | ||||||
chr13:100645572
|
C | G | 110 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(107): Show | 112 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.641-3261G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645572 | ||||||
chr13:100645995
|
G | A | 1 | a0001c0003t0001g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.641-3684C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100645995 | ||||||
chr13:100646194
|
T | C | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.641-3883A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646194 | ||||||
chr13:100646215
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.641-3904G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646215 | ||||||
chr13:100646379
|
A | T | 1 | a0001c0004t0001g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.641-4068T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646379 | ||||||
chr13:100646515
|
G | A | 3 | a0001c0004t0001g0024a0001c0004t0001g0030a0001c0004t0001g0086 | 3 | HG01069.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.641-4204C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646515 | ||||||
chr13:100646667
|
C | G | 1 | a0001c0003t0001g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.641-4356G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646667 | ||||||
chr13:100646693
|
A | G | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.641-4382T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646693 | ||||||
chr13:100646699
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.641-4388A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646699 | ||||||
chr13:100646816
|
C | A | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.641-4505G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646816 | ||||||
chr13:100646860
|
CG | C | 4 | a0002c0001t0001g0059a0002c0001t0001g0060a0002c0001t0001g0061others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-4550delC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646860 | ||||||
chr13:100646861
|
G | T | 1 | a0002c0001t0002g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.641-4550C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646861 | ||||||
chr13:100646930
|
C | T | 324 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(321): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.641-4619G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100646930 | ||||||
chr13:100647164
|
G | C | 1 | a0001c0002t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.641-4853C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647164 | ||||||
chr13:100647297
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.641-4986G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647297 | ||||||
chr13:100647317
|
C | T | 320 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.641-5006G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647317 | ||||||
chr13:100647529
|
A | G | 3 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066 | 3 | HG00099.hp2 HG03239.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.641-5218T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647529 | ||||||
chr13:100647578
|
C | T | 1 | a0002c0001t0002g0248 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.641-5267G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647578 | ||||||
chr13:100647626
|
G | A | 310 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(307): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.641-5315C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647626 | ||||||
chr13:100647763
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-5452G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647763 | ||||||
chr13:100647771
|
T | C | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.641-5460A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647771 | ||||||
chr13:100647794
|
T | C | 1 | a0001c0004t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.641-5483A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647794 | ||||||
chr13:100647808
|
G | A | 37 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(34): Show | 38 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.641-5497C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647808 | ||||||
chr13:100647927
|
T | A | 2 | a0001c0003t0010g0077a0001c0003t0010g0078 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.641-5616A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647927 | ||||||
chr13:100647951
|
C | A | 1 | a0001c0004t0001g0001 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.641-5640G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647951 | ||||||
chr13:100647986
|
T | C | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.641-5675A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100647986 | ||||||
chr13:100648024
|
G | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-5713C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648024 | ||||||
chr13:100648259
|
A | C | 1 | a0001c0003t0003g0054 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.641-5948T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648259 | ||||||
chr13:100648283
|
T | C | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.641-5972A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648283 | ||||||
chr13:100648342
|
T | C | 36 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.641-6031A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648342 | ||||||
chr13:100648396
|
A | T | 1 | a0001c0002t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.641-6085T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648396 | ||||||
chr13:100648425
|
T | G | 122 | a0001c0002t0002g0288a0001c0002t0005g0287a0001c0004t0001g0113others(119): Show | 123 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.641-6114A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648425 | ||||||
chr13:100648452
|
G | A | 17 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(14): Show | 18 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.641-6141C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648452 | ||||||
chr13:100648611
|
G | C | 1 | a0002c0001t0002g0271 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.641-6300C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648611 | ||||||
chr13:100648749
|
G | A | 1 | a0001c0002t0003g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.641-6438C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100648749 | ||||||
chr13:100649152
|
C | T | 7 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-6841G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649152 | ||||||
chr13:100649190
|
G | T | 6 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-6879C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649190 | ||||||
chr13:100649218
|
C | T | 1 | a0002c0001t0002g0310 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.641-6907G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649218 | ||||||
chr13:100649327
|
T | G | 1 | a0002c0001t0002g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.641-7016A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649327 | ||||||
chr13:100649509
|
G | T | 1 | a0004c0007t0002g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640+6872C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649509 | ||||||
chr13:100649534
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640+6847G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649534 | ||||||
chr13:100649738
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.640+6643C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649738 | ||||||
chr13:100649762
|
A | AAAAT | 62 | a0001c0002t0001g0041a0001c0002t0001g0201a0001c0002t0002g0288others(59): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.640+6615_640+6618d others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649762 | ||||||
chr13:100649794
|
T | A | 1 | a0002c0001t0006g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.640+6587A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649794 | ||||||
chr13:100649849
|
T | C | 1 | a0002c0001t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.640+6532A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649849 | ||||||
chr13:100649941
|
A | G | 1 | a0001c0003t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.640+6440T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649941 | ||||||
chr13:100649975
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.640+6406G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100649975 | ||||||
chr13:100650082
|
GA | G | 22 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(19): Show | 23 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.640+6298delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650082 | ||||||
chr13:100650182
|
A | G | 22 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(19): Show | 23 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.640+6199T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650182 | ||||||
chr13:100650203
|
A | T | 1 | a0001c0002t0001g0188 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.640+6178T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650203 | ||||||
chr13:100650399
|
G | C | 2 | a0002c0001t0002g0230a0002c0001t0002g0247 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.640+5982C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650399 | ||||||
chr13:100650462
|
G | A | 268 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.640+5919C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650462 | ||||||
chr13:100650566
|
C | T | 1 | a0002c0001t0002g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.640+5815G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650566 | ||||||
chr13:100650569
|
G | T | 268 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.640+5812C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650569 | ||||||
chr13:100650579
|
C | T | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+5802G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650579 | ||||||
chr13:100650665
|
T | C | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+5716A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650665 | ||||||
chr13:100650855
|
T | G | 1 | a0001c0004t0013g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.640+5526A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650855 | ||||||
chr13:100650911
|
T | C | 1 | a0002c0001t0006g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.640+5470A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650911 | ||||||
chr13:100650927
|
T | G | 304 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.640+5454A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650927 | ||||||
chr13:100650962
|
A | C | 268 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.640+5419T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100650962 | ||||||
chr13:100651072
|
T | G | 2 | a0002c0001t0002g0273a0002c0001t0002g0274 | 2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.640+5309A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651072 | ||||||
chr13:100651094
|
T | C | 1 | a0001c0003t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.640+5287A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651094 | ||||||
chr13:100651136
|
C | T | 1 | a0001c0004t0013g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.640+5245G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651136 | ||||||
chr13:100651211
|
C | T | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640+5170G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651211 | ||||||
chr13:100651283
|
T | G | 1 | a0001c0004t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.640+5098A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651283 | ||||||
chr13:100651301
|
C | G | 111 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(108): Show | 113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.640+5080G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651301 | ||||||
chr13:100651372
|
T | C | 2 | a0002c0001t0002g0330a0002c0001t0002g0331 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.640+5009A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651372 | ||||||
chr13:100651402
|
G | A | 111 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(108): Show | 113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.640+4979C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651402 | ||||||
chr13:100651491
|
T | C | 1 | a0001c0003t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640+4890A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651491 | ||||||
chr13:100651496
|
C | CA | 8 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(5): Show | 8 | HG01981.hp1 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+4884dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651496 | ||||||
chr13:100651496
|
CA | C | 24 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0018others(21): Show | 25 | HG01081.hp1 HG01099.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.640+4884delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651496 | ||||||
chr13:100651496
|
CAA | C | 27 | a0001c0002t0001g0156a0001c0002t0001g0199a0001c0002t0001g0207others(24): Show | 27 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.640+4883_640+4884d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651496 | ||||||
chr13:100651496
|
CAAA | C | 211 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(208): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.640+4882_640+4884d others(5): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651496 | ||||||
chr13:100651496
|
CAAAA | C | 24 | a0001c0002t0001g0140a0001c0002t0001g0141a0001c0004t0002g0211others(21): Show | 24 | HG01256.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.640+4881_640+4884d others(6): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651496 | ||||||
chr13:100651570
|
A | C | 4 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(1): Show | 4 | HG02630.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+4811T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651570 | ||||||
chr13:100651582
|
C | G | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+4799G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651582 | ||||||
chr13:100651621
|
G | A | 36 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.640+4760C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651621 | ||||||
chr13:100651697
|
G | A | 1 | a0001c0002t0003g0198 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.640+4684C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651697 | ||||||
chr13:100651835
|
G | A | 147 | a0001c0002t0002g0288a0001c0002t0005g0287a0001c0003t0001g0002others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.640+4546C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651835 | ||||||
chr13:100651904
|
A | C | 1 | a0001c0002t0003g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.640+4477T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100651904 | ||||||
chr13:100652068
|
G | A | 1 | a0002c0001t0002g0235 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.640+4313C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652068 | ||||||
chr13:100652074
|
A | C | 47 | a0001c0002t0002g0288a0001c0002t0005g0287a0002c0001t0002g0005others(44): Show | 48 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.640+4307T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652074 | ||||||
chr13:100652102
|
T | C | 1 | a0001c0002t0001g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.640+4279A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652102 | ||||||
chr13:100652257
|
T | C | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+4124A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652257 | ||||||
chr13:100652300
|
G | A | 2 | a0001c0002t0001g0179a0001c0002t0001g0199 | 2 | NA18953.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.640+4081C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652300 | ||||||
chr13:100652350
|
G | A | 1 | a0001c0003t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.640+4031C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652350 | ||||||
chr13:100652786
|
TA | T | 51 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(48): Show | 52 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+3594delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652786 | ||||||
chr13:100652855
|
G | A | 1 | a0001c0003t0001g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.640+3526C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100652855 | ||||||
chr13:100653386
|
T | C | 1 | a0005c0011t0001g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640+2995A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653386 | ||||||
chr13:100653616
|
C | T | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.640+2765G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653616 | ||||||
chr13:100653633
|
T | C | 1 | a0002c0001t0002g0313 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.640+2748A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653633 | ||||||
chr13:100653745
|
GGT | G | 6 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+2634_640+2635d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653745 | ||||||
chr13:100653916
|
C | T | 1 | a0002c0001t0002g0284 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640+2465G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653916 | ||||||
chr13:100653917
|
T | C | 1 | a0001c0002t0001g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.640+2464A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653917 | ||||||
chr13:100653925
|
T | C | 4 | a0001c0003t0001g0050a0001c0003t0001g0056a0001c0003t0001g0057others(1): Show | 4 | HG01074.hp1 HG02738.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2456A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653925 | ||||||
chr13:100653946
|
A | C | 2 | a0001c0003t0001g0082a0001c0003t0001g0088 | 2 | HG01981.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.640+2435T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653946 | ||||||
chr13:100653946
|
A | T | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.640+2435T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653946 | ||||||
chr13:100653950
|
G | A | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.640+2431C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100653950 | ||||||
chr13:100654020
|
C | T | 1 | a0001c0003t0003g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640+2361G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654020 | ||||||
chr13:100654222
|
C | T | 4 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0118others(1): Show | 4 | NA18944.hp2 NA18951.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2159G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654222 | ||||||
chr13:100654353
|
C | T | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+2028G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654353 | ||||||
chr13:100654357
|
C | T | 3 | a0001c0002t0001g0176a0001c0002t0003g0183a0001c0002t0003g0194 | 3 | HG02135.hp2 NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.640+2024G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654357 | ||||||
chr13:100654364
|
G | C | 1 | a0002c0001t0006g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.640+2017C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654364 | ||||||
chr13:100654522
|
A | G | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.640+1859T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654522 | ||||||
chr13:100654541
|
T | C | 1 | a0001c0002t0003g0206 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.640+1840A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654541 | ||||||
chr13:100654645
|
G | T | 2 | a0001c0004t0001g0032a0001c0004t0003g0031 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.640+1736C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654645 | ||||||
chr13:100654735
|
C | T | 269 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(266): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.640+1646G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100654735 | ||||||
chr13:100655011
|
C | T | 145 | a0001c0002t0002g0288a0001c0002t0005g0287a0001c0003t0001g0002others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.640+1370G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655011 | ||||||
chr13:100655013
|
C | A | 36 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.640+1368G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655013 | ||||||
chr13:100655016
|
A | AT | 149 | a0001c0002t0001g0041a0001c0002t0001g0138a0001c0002t0002g0288others(146): Show | 151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.640+1364dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655016 | ||||||
chr13:100655016
|
A | ATT | 14 | a0001c0004t0001g0033a0001c0004t0001g0169a0001c0004t0003g0031others(11): Show | 14 | HG00642.hp2 HG01981.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+1363_640+1364d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655016 | ||||||
chr13:100655016
|
AT | A | 108 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(105): Show | 110 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.640+1364delA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655016 | ||||||
chr13:100655094
|
T | C | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+1287A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655094 | ||||||
chr13:100655114
|
C | T | 1 | a0001c0004t0001g0026 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.640+1267G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655114 | ||||||
chr13:100655133
|
T | C | 120 | a0001c0002t0002g0288a0001c0002t0005g0287a0002c0001t0002g0005others(117): Show | 121 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.640+1248A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655133 | ||||||
chr13:100655178
|
C | G | 36 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.640+1203G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655178 | ||||||
chr13:100655203
|
G | A | 1 | a0002c0001t0002g0315 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.640+1178C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655203 | ||||||
chr13:100655521
|
C | T | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+860G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655521 | ||||||
chr13:100655542
|
A | G | 270 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.640+839T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655542 | ||||||
chr13:100655545
|
T | G | 270 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.640+836A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655545 | ||||||
chr13:100655614
|
T | C | 263 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.640+767A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655614 | ||||||
chr13:100655633
|
C | A | 272 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.640+748G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655633 | ||||||
chr13:100655676
|
T | C | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+705A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655676 | ||||||
chr13:100655746
|
C | T | 37 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(34): Show | 38 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.640+635G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655746 | ||||||
chr13:100655785
|
GTAA | G | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+593_640+595del others(3): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655785 | ||||||
chr13:100655862
|
T | TG | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+518dupC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655862 | ||||||
chr13:100655894
|
T | C | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+487A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655894 | ||||||
chr13:100655950
|
A | G | 2 | a0002c0001t0002g0230a0002c0001t0002g0247 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.640+431T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100655950 | ||||||
chr13:100656199
|
C | T | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.640+182G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 6/18 | chr13 | 100656199 | ||||||
chr13:100656542
|
C | CT | 9 | a0001c0003t0001g0106a0001c0003t0008g0089a0001c0004t0001g0034others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-75dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTT | 166 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0008others(163): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.553-76_553-75dupAA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTT | 14 | a0001c0002t0001g0007a0001c0002t0001g0125a0001c0002t0001g0126others(11): Show | 14 | HG00544.hp1 HG00609.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-77_553-75dupAA others(1): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(3): Show |
1 | a0003c0006t0009g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.553-84_553-75dupAA others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(4): Show |
4 | a0003c0006t0001g0115a0003c0006t0001g0118a0003c0006t0001g0124others(1): Show | 4 | HG02083.hp1 NA18944.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-85_553-75dupAA others(9): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(5): Show |
4 | a0003c0006t0001g0116a0003c0006t0001g0117a0003c0008t0001g0122others(1): Show | 4 | HG03669.hp2 NA18951.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-86_553-75dupAA others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(6): Show |
1 | a0003c0008t0001g0121 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.553-87_553-75dupAA others(11): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(8): Show |
13 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(10): Show | 14 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-89_553-75dupAA others(13): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(9): Show |
4 | a0001c0003t0001g0053a0001c0003t0001g0080a0001c0003t0002g0067others(1): Show | 4 | HG01361.hp2 HG03471.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-90_553-75dupAA others(14): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(10): Show |
5 | a0001c0002t0001g0201a0001c0003t0001g0051a0001c0004t0002g0211others(2): Show | 5 | HG00408.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-91_553-75dupAA others(15): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(11): Show |
4 | a0001c0002t0001g0200a0001c0002t0017g0167a0001c0003t0003g0114others(1): Show | 4 | HG03471.hp1 HG06807.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-92_553-75dupAA others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(12): Show |
16 | a0001c0002t0001g0179a0001c0002t0001g0196a0001c0002t0001g0199others(13): Show | 17 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.553-75_553-74insAA others(17): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(13): Show |
14 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0188others(11): Show | 14 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.553-75_553-74insAA others(18): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(14): Show |
6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG00423.hp1 HG01074.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-75_553-74insAA others(19): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656542
|
C | CTTTTTTT others(15): Show |
3 | a0001c0002t0003g0181a0001c0002t0003g0182a0001c0002t0004g0316 | 3 | HG00438.hp1 HG02027.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.553-75_553-74insAA others(20): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656542 | ||||||
chr13:100656582
|
AC | A | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-115delG | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656582 | ||||||
chr13:100656729
|
A | G | 1 | a0002c0001t0002g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.553-261T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656729 | ||||||
chr13:100656838
|
C | T | 126 | a0001c0002t0002g0288a0001c0002t0002g0339a0001c0002t0005g0287others(123): Show | 127 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.553-370G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656838 | ||||||
chr13:100656928
|
A | G | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-460T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656928 | ||||||
chr13:100656932
|
T | C | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-464A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100656932 | ||||||
chr13:100657077
|
A | G | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-609T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657077 | ||||||
chr13:100657533
|
C | CG | 258 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(255): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.553-1066dupC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657533 | ||||||
chr13:100657533
|
C | G | 1 | a0002c0001t0002g0338 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.553-1065G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657533 | ||||||
chr13:100657553
|
T | C | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.553-1085A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657553 | ||||||
chr13:100657561
|
G | T | 1 | a0006c0013t0003g0180 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.553-1093C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657561 | ||||||
chr13:100657590
|
G | T | 340 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(337): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.553-1122C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657590 | ||||||
chr13:100657604
|
C | G | 23 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0003t0001g0002others(20): Show | 24 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.553-1136G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657604 | ||||||
chr13:100657847
|
A | T | 15 | a0002c0001t0002g0225a0002c0001t0002g0248a0002c0001t0002g0251others(12): Show | 15 | HG00544.hp1 HG00673.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.553-1379T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657847 | ||||||
chr13:100657861
|
C | T | 320 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.553-1393G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657861 | ||||||
chr13:100657928
|
G | A | 35 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(32): Show | 36 | HG00140.hp2 HG00323.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.553-1460C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100657928 | ||||||
chr13:100658167
|
A | C | 1 | a0001c0003t0008g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.553-1699T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658167 | ||||||
chr13:100658290
|
G | A | 249 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.553-1822C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658290 | ||||||
chr13:100658296
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.553-1828C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658296 | ||||||
chr13:100658362
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-1894A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658362 | ||||||
chr13:100658503
|
G | A | 249 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.553-2035C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658503 | ||||||
chr13:100658626
|
A | C | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2158T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658626 | ||||||
chr13:100658627
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2159C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658627 | ||||||
chr13:100658629
|
G | C | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2161C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658629 | ||||||
chr13:100658630
|
C | CTAACTTG others(70): Show |
1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2163_553-2162i others(79): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658630 | ||||||
chr13:100658688
|
A | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2220T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658688 | ||||||
chr13:100658732
|
TCTTTCTG others(96): Show |
T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2367_553-2265d others(2): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658732 | ||||||
chr13:100658838
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2370C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658838 | ||||||
chr13:100658860
|
C | G | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2392G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658860 | ||||||
chr13:100658861
|
A | C | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2393T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658861 | ||||||
chr13:100658929
|
G | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2461C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658929 | ||||||
chr13:100658930
|
A | G | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2462T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658930 | ||||||
chr13:100658931
|
G | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2463C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100658931 | ||||||
chr13:100659043
|
A | AT | 8 | a0002c0001t0005g0277a0003c0006t0001g0115a0003c0006t0001g0116others(5): Show | 8 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-2576dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659043 | ||||||
chr13:100659076
|
G | C | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2608C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659076 | ||||||
chr13:100659078
|
G | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2610C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659078 | ||||||
chr13:100659079
|
T | G | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2611A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659079 | ||||||
chr13:100659086
|
G | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2618C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659086 | ||||||
chr13:100659095
|
C | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2627G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659095 | ||||||
chr13:100659108
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2640C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659108 | ||||||
chr13:100659115
|
T | C | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2647A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659115 | ||||||
chr13:100659118
|
A | ATACTTTA others(3): Show |
1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2651_553-2650i others(12): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659118 | ||||||
chr13:100659122
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2654C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659122 | ||||||
chr13:100659123
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2655C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659123 | ||||||
chr13:100659124
|
C | T | 4 | a0001c0002t0001g0006a0002c0001t0002g0230a0002c0001t0002g0247others(1): Show | 4 | HG00609.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-2656G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659124 | ||||||
chr13:100659125
|
G | T | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2657C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659125 | ||||||
chr13:100659126
|
G | A | 1 | a0002c0001t0005g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.553-2658C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659126 | ||||||
chr13:100659416
|
C | T | 2 | a0001c0004t0001g0220a0001c0004t0013g0221 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.553-2948G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659416 | ||||||
chr13:100659457
|
T | C | 249 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.553-2989A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659457 | ||||||
chr13:100659634
|
C | T | 2 | a0002c0001t0002g0244a0002c0001t0002g0317 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.553-3166G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659634 | ||||||
chr13:100659677
|
G | C | 1 | a0002c0001t0002g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.553-3209C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659677 | ||||||
chr13:100659691
|
C | A | 1 | a0001c0002t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.553-3223G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100659691 | ||||||
chr13:100660040
|
T | C | 1 | a0001c0004t0001g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.552+2924A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660040 | ||||||
chr13:100660070
|
C | T | 1 | a0010c0012t0004g0246 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.552+2894G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660070 | ||||||
chr13:100660294
|
G | A | 1 | a0002c0001t0002g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.552+2670C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660294 | ||||||
chr13:100660306
|
A | G | 320 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.552+2658T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660306 | ||||||
chr13:100660330
|
CAAAAA | C | 80 | a0001c0002t0001g0164a0001c0002t0001g0219a0001c0002t0002g0288others(77): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.552+2629_552+2633d others(7): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660330 | ||||||
chr13:100660330
|
CAAAAAA | C | 169 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(166): Show | 171 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.552+2628_552+2633d others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660330 | ||||||
chr13:100660566
|
C | A | 4 | a0001c0003t0002g0326a0004c0007t0002g0226a0004c0007t0006g0236others(1): Show | 4 | HG02896.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+2398G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660566 | ||||||
chr13:100660657
|
A | AT | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.552+2306dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660657 | ||||||
chr13:100660657
|
A | ATT | 62 | a0001c0002t0001g0097a0001c0002t0001g0175a0001c0002t0001g0184others(59): Show | 63 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+2305_552+2306d others(4): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660657 | ||||||
chr13:100660657
|
A | ATTT | 10 | a0001c0002t0001g0176a0001c0002t0001g0179a0001c0002t0001g0204others(7): Show | 10 | HG00642.hp1 HG01433.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+2304_552+2306d others(5): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660657 | ||||||
chr13:100660673
|
T | TC | 7 | a0001c0004t0001g0020a0001c0004t0001g0026a0001c0004t0001g0027others(4): Show | 7 | HG00323.hp1 HG01175.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+2290_552+2291i others(3): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660673 | ||||||
chr13:100660796
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+2168C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660796 | ||||||
chr13:100660799
|
G | A | 1 | a0001c0004t0003g0036 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.552+2165C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660799 | ||||||
chr13:100660821
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.552+2143A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660821 | ||||||
chr13:100660840
|
G | A | 33 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(30): Show | 34 | HG00140.hp2 HG00323.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.552+2124C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660840 | ||||||
chr13:100660906
|
G | A | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.552+2058C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660906 | ||||||
chr13:100660914
|
G | A | 249 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.552+2050C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660914 | ||||||
chr13:100660930
|
G | A | 1 | a0002c0001t0002g0319 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.552+2034C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660930 | ||||||
chr13:100660980
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+1984A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100660980 | ||||||
chr13:100661219
|
T | C | 1 | a0001c0003t0003g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.552+1745A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661219 | ||||||
chr13:100661294
|
C | T | 1 | a0001c0002t0001g0132 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.552+1670G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661294 | ||||||
chr13:100661296
|
T | C | 249 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.552+1668A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661296 | ||||||
chr13:100661400
|
C | T | 1 | a0002c0001t0002g0241 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.552+1564G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661400 | ||||||
chr13:100661447
|
C | T | 1 | a0001c0004t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.552+1517G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661447 | ||||||
chr13:100661584
|
G | C | 1 | a0002c0001t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.552+1380C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661584 | ||||||
chr13:100661709
|
G | A | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.552+1255C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661709 | ||||||
chr13:100661750
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+1214A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661750 | ||||||
chr13:100661852
|
C | T | 71 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0179others(68): Show | 73 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.552+1112G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100661852 | ||||||
chr13:100662036
|
C | T | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.552+928G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662036 | ||||||
chr13:100662084
|
G | A | 1 | a0001c0004t0013g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.552+880C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662084 | ||||||
chr13:100662110
|
C | A | 1 | a0002c0001t0002g0320 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.552+854G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662110 | ||||||
chr13:100662298
|
A | G | 261 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.552+666T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662298 | ||||||
chr13:100662311
|
C | T | 2 | a0001c0004t0001g0220a0001c0004t0013g0221 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.552+653G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662311 | ||||||
chr13:100662412
|
T | G | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.552+552A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662412 | ||||||
chr13:100662467
|
C | A | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.552+497G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662467 | ||||||
chr13:100662498
|
T | C | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.552+466A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662498 | ||||||
chr13:100662717
|
C | T | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.552+247G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662717 | ||||||
chr13:100662723
|
G | C | 1 | a0002c0001t0002g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.552+241C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662723 | ||||||
chr13:100662901
|
C | T | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.552+63G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662901 | ||||||
chr13:100662921
|
G | A | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.552+43C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662921 | ||||||
chr13:100662944
|
C | T | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.552+20G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 5/18 | chr13 | 100662944 | ||||||
chr13:100663367
|
G | A | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.336-187C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 4/18 | chr13 | 100663367 | ||||||
chr13:100663644
|
G | A | 1 | a0001c0002t0001g0163 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.336-464C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 4/18 | chr13 | 100663644 | ||||||
chr13:100663969
|
G | A | 130 | a0001c0002t0001g0219a0001c0002t0002g0288a0001c0002t0002g0339others(127): Show | 131 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.335+252C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 4/18 | chr13 | 100663969 | ||||||
chr13:100664059
|
C | T | 251 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.335+162G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 4/18 | chr13 | 100664059 | ||||||
chr13:100664124
|
A | G | 134 | a0001c0002t0001g0219a0001c0002t0002g0288a0001c0002t0002g0339others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.335+97T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 4/18 | chr13 | 100664124 | ||||||
chr13:100664449
|
C | T | 1 | a0001c0004t0003g0042 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220-113G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100664449 | ||||||
chr13:100664702
|
C | T | 3 | a0001c0002t0001g0130a0001c0002t0001g0170a0001c0003t0003g0131 | 3 | HG01175.hp2 HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.220-366G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100664702 | ||||||
chr13:100665127
|
A | AC | 4 | a0001c0003t0001g0051a0001c0005t0001g0098a0001c0020t0001g0107others(1): Show | 4 | HG02055.hp1 NA19058.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-792dupG | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665127 | ||||||
chr13:100665369
|
A | G | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-1033T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665369 | ||||||
chr13:100665388
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-1052C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665388 | ||||||
chr13:100665666
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220-1330G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665666 | ||||||
chr13:100665696
|
C | A | 1 | a0001c0002t0003g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.220-1360G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665696 | ||||||
chr13:100665853
|
G | A | 2 | a0002c0001t0006g0328a0002c0001t0006g0329 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.220-1517C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665853 | ||||||
chr13:100665862
|
A | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-1526T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665862 | ||||||
chr13:100665882
|
C | T | 126 | a0001c0002t0001g0219a0001c0002t0002g0288a0001c0002t0002g0339others(123): Show | 127 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.220-1546G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100665882 | ||||||
chr13:100666062
|
G | A | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-1726C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666062 | ||||||
chr13:100666114
|
A | G | 1 | a0002c0001t0002g0238 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-1778T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666114 | ||||||
chr13:100666160
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-1824A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666160 | ||||||
chr13:100666173
|
T | C | 1 | a0001c0002t0001g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.220-1837A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666173 | ||||||
chr13:100666354
|
A | C | 1 | a0001c0002t0001g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-2018T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666354 | ||||||
chr13:100666493
|
G | T | 1 | a0001c0004t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+2086C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666493 | ||||||
chr13:100666498
|
C | T | 1 | a0001c0005t0001g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.219+2081G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666498 | ||||||
chr13:100666603
|
C | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+1976G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666603 | ||||||
chr13:100666683
|
G | C | 1 | a0002c0001t0002g0323 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219+1896C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666683 | ||||||
chr13:100666830
|
A | C | 2 | a0001c0004t0001g0085a0001c0004t0001g0108 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.219+1749T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666830 | ||||||
chr13:100666911
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.219+1668C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666911 | ||||||
chr13:100666916
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.219+1663C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666916 | ||||||
chr13:100666927
|
C | T | 121 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.219+1652G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666927 | ||||||
chr13:100666979
|
C | G | 311 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(308): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.219+1600G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100666979 | ||||||
chr13:100667039
|
T | C | 2 | a0001c0004t0001g0030a0001c0004t0001g0086 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.219+1540A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667039 | ||||||
chr13:100667092
|
A | G | 2 | a0001c0004t0001g0220a0001c0004t0013g0221 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.219+1487T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667092 | ||||||
chr13:100667156
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+1423C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667156 | ||||||
chr13:100667265
|
C | T | 308 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(305): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.219+1314G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667265 | ||||||
chr13:100667354
|
C | T | 1 | a0002c0001t0002g0237 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.219+1225G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667354 | ||||||
chr13:100667383
|
C | A | 1 | a0002c0001t0002g0324 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.219+1196G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667383 | ||||||
chr13:100667652
|
T | A | 1 | a0002c0001t0004g0325 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219+927A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667652 | ||||||
chr13:100667784
|
G | C | 1 | a0001c0003t0002g0326 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.219+795C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100667784 | ||||||
chr13:100668094
|
A | C | 6 | a0001c0004t0001g0034a0001c0004t0001g0037a0001c0004t0001g0038others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+485T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668094 | ||||||
chr13:100668187
|
C | T | 1 | a0001c0003t0003g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219+392G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668187 | ||||||
chr13:100668216
|
G | GT | 190 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(187): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.219+362dupA | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668216 | ||||||
chr13:100668216
|
G | GTT | 25 | a0001c0002t0001g0097a0001c0002t0001g0125a0001c0002t0001g0126others(22): Show | 25 | HG00642.hp1 HG00735.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.219+361_219+362dup others(2): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668216 | ||||||
chr13:100668316
|
C | T | 1 | a0002c0001t0002g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.219+263G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668316 | ||||||
chr13:100668488
|
A | G | 1 | a0001c0004t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+91T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 3/18 | chr13 | 100668488 | ||||||
chr13:100668813
|
T | C | 259 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.4-19A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100668813 | ||||||
chr13:100668917
|
ACAATTTG others(13): Show |
A | 1 | a0001c0002t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4-143_4-124delGGAA others(16): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100668917 | ||||||
chr13:100668952
|
C | G | 1 | a0011c0022t0003g0173 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.4-158G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100668952 | ||||||
chr13:100668990
|
C | T | 123 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(120): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.4-196G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100668990 | ||||||
chr13:100669034
|
C | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-240G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669034 | ||||||
chr13:100669044
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-250C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669044 | ||||||
chr13:100669056
|
G | A | 1 | a0001c0002t0001g0166 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4-262C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669056 | ||||||
chr13:100669106
|
T | C | 1 | a0002c0001t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4-312A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669106 | ||||||
chr13:100669229
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-435C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669229 | ||||||
chr13:100669433
|
A | G | 21 | a0001c0003t0001g0002a0001c0003t0001g0049a0001c0003t0001g0050others(18): Show | 22 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.4-639T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669433 | ||||||
chr13:100669439
|
TG | T | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.4-646delC | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669439 | ||||||
chr13:100669569
|
C | G | 1 | a0002c0001t0002g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4-775G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669569 | ||||||
chr13:100669585
|
G | A | 12 | a0001c0002t0001g0097a0001c0004t0001g0113a0001c0005t0001g0098others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+775C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669585 | ||||||
chr13:100669662
|
C | G | 13 | a0001c0002t0001g0097a0001c0004t0001g0113a0001c0005t0001g0098others(10): Show | 13 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+698G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669662 | ||||||
chr13:100669702
|
C | G | 238 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(235): Show | 241 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.3+658G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669702 | ||||||
chr13:100669724
|
G | A | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+636C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669724 | ||||||
chr13:100669761
|
C | T | 3 | a0001c0004t0001g0001a0001c0004t0001g0018a0001c0004t0001g0019 | 4 | HG02486.hp1 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+599G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669761 | ||||||
chr13:100669768
|
G | C | 94 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(91): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.3+592C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100669768 | ||||||
chr13:100670054
|
A | C | 3 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066 | 3 | HG00099.hp2 HG03239.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3+306T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100670054 | ||||||
chr13:100670091
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+269A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100670091 | ||||||
chr13:100670279
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3+81G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100670279 | ||||||
chr13:100670282
|
C | A | 12 | a0001c0002t0001g0097a0001c0004t0001g0113a0001c0005t0001g0098others(9): Show | 12 | HG01243.hp2 HG01975.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.3+78G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100670282 | ||||||
chr13:100670323
|
G | A | 1 | a0001c0003t0001g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3+37C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 2/18 | chr13 | 100670323 | ||||||
chr13:100670621
|
T | G | 232 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(229): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-207-52A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100670621 | ||||||
chr13:100670811
|
G | T | 101 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(98): Show | 103 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.-207-242C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100670811 | ||||||
chr13:100670957
|
C | A | 1 | a0001c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-207-388G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100670957 | ||||||
chr13:100670978
|
C | A | 1 | a0001c0004t0001g0169 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-207-409G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100670978 | ||||||
chr13:100671118
|
G | A | 2 | a0002c0001t0006g0328a0002c0001t0006g0329 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-207-549C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671118 | ||||||
chr13:100671238
|
C | T | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-207-669G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671238 | ||||||
chr13:100671294
|
G | T | 94 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(91): Show | 96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-207-725C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671294 | ||||||
chr13:100671413
|
G | A | 2 | a0002c0001t0002g0330a0002c0001t0002g0331 | 2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-207-844C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671413 | ||||||
chr13:100671439
|
TA | T | 9 | a0001c0003t0001g0072a0001c0003t0001g0073a0001c0003t0001g0074others(6): Show | 9 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-207-871delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671439 | ||||||
chr13:100671719
|
C | T | 4 | a0001c0003t0001g0068a0001c0003t0001g0069a0001c0003t0001g0070others(1): Show | 4 | HG02630.hp1 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207-1150G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671719 | ||||||
chr13:100671739
|
G | T | 126 | a0001c0002t0002g0288a0001c0002t0002g0339a0001c0002t0004g0316others(123): Show | 127 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-207-1170C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671739 | ||||||
chr13:100671817
|
G | A | 1 | a0001c0002t0003g0203 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-207-1248C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671817 | ||||||
chr13:100671839
|
G | C | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-207-1270C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671839 | ||||||
chr13:100671874
|
C | T | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-207-1305G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671874 | ||||||
chr13:100671876
|
C | CA | 24 | a0001c0002t0001g0172a0001c0003t0001g0106a0001c0003t0001g0109others(21): Show | 24 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-207-1308dupT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671876 | ||||||
chr13:100671876
|
CA | C | 110 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(107): Show | 113 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-207-1308delT | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100671876 | ||||||
chr13:100672024
|
C | A | 39 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0179others(36): Show | 40 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.-207-1455G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672024 | ||||||
chr13:100672046
|
C | T | 238 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(235): Show | 241 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.-207-1477G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672046 | ||||||
chr13:100672127
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1558C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672127 | ||||||
chr13:100672129
|
T | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1560A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672129 | ||||||
chr13:100672130
|
A | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1561T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672130 | ||||||
chr13:100672131
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1562C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672131 | ||||||
chr13:100672133
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1564A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672133 | ||||||
chr13:100672134
|
T | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1565A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672134 | ||||||
chr13:100672135
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1566A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672135 | ||||||
chr13:100672136
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1567A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672136 | ||||||
chr13:100672137
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1568C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672137 | ||||||
chr13:100672138
|
G | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1569C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672138 | ||||||
chr13:100672140
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1571C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672140 | ||||||
chr13:100672143
|
A | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1574T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672143 | ||||||
chr13:100672144
|
T | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1575A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672144 | ||||||
chr13:100672145
|
T | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1576A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672145 | ||||||
chr13:100672148
|
C | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1579G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672148 | ||||||
chr13:100672149
|
C | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1580G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672149 | ||||||
chr13:100672151
|
C | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1582G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672151 | ||||||
chr13:100672152
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1583A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672152 | ||||||
chr13:100672154
|
C | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1585G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672154 | ||||||
chr13:100672155
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1586A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672155 | ||||||
chr13:100672156
|
T | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1587A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672156 | ||||||
chr13:100672157
|
C | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1588G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672157 | ||||||
chr13:100672158
|
C | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1589G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672158 | ||||||
chr13:100672159
|
C | G | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1590G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672159 | ||||||
chr13:100672164
|
C | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1595G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672164 | ||||||
chr13:100672167
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1598C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672167 | ||||||
chr13:100672168
|
A | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1599T>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672168 | ||||||
chr13:100672177
|
C | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1608G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672177 | ||||||
chr13:100672180
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1611C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672180 | ||||||
chr13:100672181
|
G | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1612C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672181 | ||||||
chr13:100672182
|
G | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1613C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672182 | ||||||
chr13:100672184
|
G | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1615C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672184 | ||||||
chr13:100672186
|
A | C | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1617T>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672186 | ||||||
chr13:100672187
|
C | T | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-207-1618G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672187 | ||||||
chr13:100672275
|
C | T | 1 | a0002c0001t0002g0223 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-207-1706G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672275 | ||||||
chr13:100672540
|
G | A | 3 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209 | 3 | HG00642.hp1 HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-207-1971C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672540 | ||||||
chr13:100672785
|
C | G | 7 | a0001c0004t0002g0211a0001c0004t0002g0213a0001c0004t0007g0212others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-208+1959G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672785 | ||||||
chr13:100672798
|
A | G | 237 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(234): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-208+1946T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672798 | ||||||
chr13:100672889
|
A | G | 91 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(88): Show | 93 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-208+1855T>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672889 | ||||||
chr13:100672921
|
G | A | 1 | a0001c0003t0003g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-208+1823C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100672921 | ||||||
chr13:100673081
|
G | C | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-208+1663C>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673081 | ||||||
chr13:100673254
|
G | A | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-208+1490C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673254 | ||||||
chr13:100673663
|
T | A | 15 | a0001c0002t0001g0041a0001c0004t0001g0016a0001c0004t0001g0034others(12): Show | 15 | HG00140.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-208+1081A>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673663 | ||||||
chr13:100673711
|
T | C | 1 | a0001c0004t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-208+1033A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673711 | ||||||
chr13:100673743
|
C | T | 1 | a0001c0004t0003g0017 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-208+1001G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673743 | ||||||
chr13:100673796
|
C | T | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-208+948G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673796 | ||||||
chr13:100673954
|
T | C | 10 | a0003c0006t0001g0115a0003c0006t0001g0116a0003c0006t0001g0117others(7): Show | 10 | HG02083.hp1 HG02735.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.-208+790A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100673954 | ||||||
chr13:100674144
|
C | T | 127 | a0001c0002t0002g0288a0001c0002t0002g0339a0001c0002t0004g0316others(124): Show | 128 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-208+600G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674144 | ||||||
chr13:100674166
|
C | CCCCGGGC others(1): Show |
33 | a0001c0002t0001g0041a0001c0004t0001g0001a0001c0004t0001g0016others(30): Show | 34 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-208+570_-208+577d others(10): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674166 | ||||||
chr13:100674166
|
C | CCCCGGGC others(31): Show |
1 | a0001c0004t0003g0048 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-208+577_-208+578i others(40): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674166 | ||||||
chr13:100674185
|
T | C | 1 | a0002c0001t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-208+559A>G | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674185 | ||||||
chr13:100674205
|
T | G | 1 | a0001c0002t0001g0219 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-208+539A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674205 | ||||||
chr13:100674253
|
G | T | 1 | a0001c0004t0001g0016 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-208+491C>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674253 | ||||||
chr13:100674288
|
C | T | 126 | a0001c0002t0002g0288a0001c0002t0002g0339a0001c0002t0004g0316others(123): Show | 127 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-208+456G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674288 | ||||||
chr13:100674365
|
G | A | 2 | a0001c0004t0001g0220a0001c0004t0013g0221 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-208+379C>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674365 | ||||||
chr13:100674481
|
C | G | 2 | a0001c0004t0003g0010a0001c0009t0001g0009 | 2 | HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-208+263G>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674481 | ||||||
chr13:100674491
|
G | GCGGGCA | 102 | a0001c0002t0001g0003a0001c0002t0001g0006a0001c0002t0001g0007others(99): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-208+252_-208+253i others(8): Show |
TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674491 | ||||||
chr13:100674574
|
C | T | 3 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0008 | 3 | HG00609.hp2 NA18988.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-208+170G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674574 | ||||||
chr13:100674603
|
T | G | 2 | a0002c0001t0002g0340a0002c0001t0002g0341 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-208+141A>C | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674603 | ||||||
chr13:100674691
|
C | T | 1 | a0002c0001t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-208+53G>A | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674691 | ||||||
chr13:100674738
|
C | A | 121 | a0001c0002t0002g0288a0001c0002t0002g0339a0001c0002t0004g0316others(118): Show | 122 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.-208+6G>T | TMTC4 | ENSG00000125247.16 | transcript | ENST00000342624.10 | protein_coding | 1/18 | chr13 | 100674738 |