geneid | 9969 |
---|---|
ensemblid | ENSG00000108510.10 |
hgncid | 22474 |
symbol | MED13 |
name | mediator complex subunit 13 |
refseq_nuc | NM_005121.3 |
refseq_prot | NP_005112.2 |
ensembl_nuc | ENST00000397786.7 |
ensembl_prot | ENSP00000380888.2 |
mane_status | MANE Select |
chr | chr17 |
start | 61942605 |
end | 62065278 |
strand | - |
ver | v1.2 |
region | chr17:61942605-62065278 |
region5000 | chr17:61937605-62070278 |
regionname0 | MED13_chr17_61942605_62065278 |
regionname5000 | MED13_chr17_61937605_62070278 |
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 | 1/1 | 2174 | 310 | 71 | 43 | 152 | 6 | 36 | 120 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0002 | 0/0 | 2174 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0003 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0004 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0005 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0006 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0007 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0008 | 0/0 | 2174 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0009 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0010 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0011 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
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 | 6525 | 182 | 28 | 31 | 91 | 5 | 26 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0002 | 0/0 | 6525 | 62 | 0 | 1 | 59 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0003 | 0/0 | 6525 | 40 | 24 | 8 | 2 | 1 | 5 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0004 | 0/0 | 6525 | 8 | 8 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0005 | 0/0 | 6525 | 7 | 7 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0006 | 0/0 | 6525 | 5 | 4 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0007 | 0/0 | 6525 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0008 | 0/0 | 6525 | 2 | 0 | 0 | 0 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0009 | 0/0 | 6525 | 2 | 2 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0010 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0011 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0012 | 1/0 | 6525 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0013 | 0/0 | 6525 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0014 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0015 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0016 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0017 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0018 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0019 | 0/0 | 6525 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0020 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0021 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0022 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0023 | 0/0 | 6525 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
c0024 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
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 | 1/1 | 3937 | 227 | 72 | 31 | 101 | 2 | 19 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0002 | 0/0 | 3935 | 45 | 1 | 6 | 26 | 0 | 12 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0003 | 0/0 | 3938 | 7 | 0 | 3 | 0 | 2 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0004 | 0/0 | 3937 | 6 | 0 | 0 | 6 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0005 | 0/0 | 3935 | 4 | 4 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0006 | 0/0 | 3937 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0007 | 0/0 | 3937 | 3 | 0 | 1 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0008 | 0/0 | 3936 | 3 | 0 | 0 | 2 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0009 | 0/0 | 3937 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0010 | 0/0 | 3935 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0011 | 0/0 | 3938 | 2 | 0 | 1 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0012 | 0/0 | 3935 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0013 | 0/0 | 3934 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0014 | 0/0 | 3937 | 2 | 0 | 2 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0015 | 0/0 | 3937 | 2 | 1 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0016 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0017 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0018 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0019 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0020 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0021 | 0/0 | 3922 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0022 | 0/0 | 3936 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0023 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0024 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0025 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0026 | 0/0 | 3937 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0027 | 0/0 | 3937 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0028 | 0/0 | 3937 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
t0029 | 0/0 | 3937 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
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 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 6525 | 182 | 28 | 31 | 91 | 5 | 26 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002 | 0/0 | 6525 | 62 | 0 | 1 | 59 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0003 | 0/0 | 6525 | 40 | 24 | 8 | 2 | 1 | 5 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0004 | 0/0 | 6525 | 8 | 8 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0006 | 0/0 | 6525 | 5 | 4 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0007 | 0/0 | 6525 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0008 | 0/0 | 6525 | 2 | 0 | 0 | 0 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0009 | 0/0 | 6525 | 2 | 2 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0012 | 1/0 | 6525 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0013 | 0/0 | 6525 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0016 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0017 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0018 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0021 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0002c0005 | 0/0 | 6525 | 7 | 7 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0003c0010 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0004c0023 | 0/0 | 6525 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0005c0020 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0006c0022 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0007c0019 | 0/0 | 6525 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0008c0015 | 0/0 | 6525 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0009c0014 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0010c0011 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0011c0024 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10461 | 103 | 26 | 19 | 47 | 1 | 9 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0002 | 0/0 | 10459 | 45 | 1 | 6 | 26 | 0 | 12 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0003 | 0/0 | 10462 | 7 | 0 | 3 | 0 | 2 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0004 | 0/0 | 10461 | 6 | 0 | 0 | 6 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0007 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0008 | 0/0 | 10460 | 2 | 0 | 0 | 1 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0010 | 0/0 | 10459 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0011 | 0/0 | 10462 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0012 | 0/0 | 10459 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0013 | 0/0 | 10458 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0014 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0015 | 0/0 | 10461 | 2 | 1 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0016 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0018 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0019 | 0/0 | 10459 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0020 | 0/0 | 10459 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0021 | 0/0 | 10446 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0022 | 0/0 | 10460 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0025 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0001t0027 | 0/0 | 10461 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0001 | 0/0 | 10461 | 56 | 0 | 1 | 53 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0009 | 0/0 | 10461 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0011 | 0/0 | 10462 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0023 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0024 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0002t0026 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0003t0001 | 0/0 | 10461 | 34 | 20 | 8 | 0 | 1 | 5 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0003t0006 | 0/0 | 10461 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0003t0007 | 0/0 | 10461 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0003t0029 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0004t0001 | 0/0 | 10461 | 8 | 8 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0006t0001 | 0/0 | 10461 | 4 | 3 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0006t0028 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0007t0005 | 0/0 | 10459 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0008t0001 | 0/0 | 10461 | 2 | 0 | 0 | 0 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0009t0001 | 0/0 | 10461 | 2 | 2 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0012t0001 | 1/0 | 10461 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0013t0001 | 0/0 | 10461 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0016t0001 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0017t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0018t0001 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0001c0021t0017 | 0/0 | 10459 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0002c0005t0001 | 0/0 | 10461 | 7 | 7 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0003c0010t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0004c0023t0001 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0005c0020t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0006c0022t0005 | 0/0 | 10459 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0007c0019t0008 | 0/0 | 10460 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0008c0015t0014 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0009c0014t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0010c0011t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
a0011c0024t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | copy fasta | chr17 | 61937605 | 62070278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0012g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0012g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0013g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0014g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0015g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0015g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0016g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0018g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0019g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0021g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0027g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0023g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0026g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0028g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0008t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0009t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0009t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0012t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0013t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0016t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0017t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0018t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0021t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0003c0010t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0004c0023t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0005c0020t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0006c0022t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0007c0019t0008g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0008c0015t0014g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0009c0014t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0010c0011t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0011c0024t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0027 | g0224 | EUR | GBR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0293 | EUR | GBR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00438 | hp2 | a0001 | c0003 | t0007 | g0298 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0043 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00597 | hp2 | a0001 | c0003 | t0007 | g0325 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00639 | hp1 | a0001 | c0006 | t0001 | g0113 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0309 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0297 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0256 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01168 | hp2 | a0001 | c0001 | t0014 | g0237 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0303 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01358 | hp2 | a0008 | c0015 | t0014 | g0199 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0292 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01517 | hp1 | a0001 | c0001 | t0022 | g0223 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0291 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01884 | hp1 | a0001 | c0003 | t0006 | g0094 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0326 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0164 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01952 | hp1 | a0001 | c0016 | t0001 | g0255 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0307 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02027 | hp2 | a0001 | c0001 | t0025 | g0008 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02055 | hp1 | a0001 | c0006 | t0001 | g0114 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02055 | hp2 | a0001 | c0004 | t0001 | g0081 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02056 | hp2 | a0001 | c0001 | t0012 | g0146 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02080 | hp1 | a0001 | c0001 | t0019 | g0131 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02083 | hp1 | a0001 | c0002 | t0024 | g0037 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02145 | hp1 | a0010 | c0011 | t0001 | g0239 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02148 | hp1 | a0001 | c0018 | t0001 | g0055 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0296 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | CDX | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02257 | hp1 | a0006 | c0022 | t0005 | g0011 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02257 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0232 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0003 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0080 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02572 | hp2 | a0001 | c0009 | t0001 | g0204 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02630 | hp1 | a0001 | c0006 | t0028 | g0102 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02630 | hp2 | a0001 | c0017 | t0001 | g0322 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0308 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02717 | hp1 | a0001 | c0003 | t0029 | g0091 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0163 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02735 | hp2 | a0001 | c0001 | t0008 | g0318 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02809 | hp2 | a0002 | c0005 | t0001 | g0121 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02895 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02896 | hp2 | a0001 | c0009 | t0001 | g0200 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02970 | hp1 | a0011 | c0024 | t0001 | g0320 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0122 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03017 | hp1 | a0001 | c0008 | t0001 | g0213 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03017 | hp2 | a0001 | c0001 | t0021 | g0129 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03130 | hp2 | a0003 | c0010 | t0001 | g0007 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0301 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0103 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03209 | hp1 | a0001 | c0003 | t0006 | g0093 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03209 | hp2 | a0002 | c0005 | t0001 | g0004 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03486 | hp1 | a0001 | c0003 | t0006 | g0092 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0289 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0305 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03491 | hp2 | a0001 | c0001 | t0015 | g0219 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0306 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0074 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03540 | hp2 | a0001 | c0007 | t0005 | g0010 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03579 | hp1 | a0001 | c0021 | t0017 | g0013 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03579 | hp2 | a0002 | c0005 | t0001 | g0005 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03654 | hp2 | a0001 | c0013 | t0001 | g0304 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0294 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0299 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03834 | hp2 | a0001 | c0008 | t0001 | g0210 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0202 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18906 | hp2 | a0005 | c0020 | t0001 | g0104 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18942 | hp1 | a0007 | c0019 | t0008 | g0310 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18946 | hp1 | a0001 | c0002 | t0026 | g0034 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18949 | hp2 | a0001 | c0002 | t0023 | g0039 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0270 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18968 | hp2 | a0001 | c0001 | t0020 | g0135 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18973 | hp2 | a0001 | c0001 | t0018 | g0212 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18982 | hp2 | a0001 | c0001 | t0013 | g0316 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18983 | hp2 | a0001 | c0001 | t0016 | g0252 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18994 | hp1 | a0001 | c0002 | t0011 | g0099 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19005 | hp1 | a0001 | c0002 | t0009 | g0069 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0115 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19043 | hp2 | a0009 | c0014 | t0001 | g0192 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19058 | hp2 | a0004 | c0023 | t0001 | g0216 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19079 | hp2 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19081 | hp1 | a0001 | c0001 | t0013 | g0120 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19084 | hp1 | a0001 | c0001 | t0012 | g0143 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19091 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19240 | hp1 | a0001 | c0007 | t0005 | g0012 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | ASW | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA21309 | hp1 | a0001 | c0007 | t0005 | g0009 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0238 | REF | REF | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
homoSapiens_grch38 | hp1 | a0001 | c0012 | t0001 | g0241 | REF | REF | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61952972
|
G | A | 1 | a0002 | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.6110C>T | p.Ala2037Val | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/30 | 6183/10461 | 6110/6525 | 2037/2174 | chr17 | 61952972 | ||
chr17:61956452
|
T | A | 1 | a0009 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5510A>T | p.Lys1837Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/30 | 5583/10461 | 5510/6525 | 1837/2174 | chr17 | 61956452 | ||
chr17:61962895
|
C | T | 1 | a0009 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.4921G>A | p.Val1641Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 4994/10461 | 4921/6525 | 1641/2174 | chr17 | 61962895 | ||
chr17:61965027
|
G | A | 1 | a0008 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.4823C>T | p.Pro1608Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4896/10461 | 4823/6525 | 1608/2174 | chr17 | 61965027 | ||
chr17:61984758
|
T | C | 1 | a0007 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2584A>G | p.Thr862Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 14/30 | 2657/10461 | 2584/6525 | 862/2174 | chr17 | 61984758 | ||
chr17:62010647
|
T | C | 1 | a0006 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1870A>G | p.Lys624Glu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1943/10461 | 1870/6525 | 624/2174 | chr17 | 62010647 | ||
chr17:62010859
|
G | A | 1 | a0005 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1658C>T | p.Ser553Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1731/10461 | 1658/6525 | 553/2174 | chr17 | 62010859 | ||
chr17:62033864
|
A | C | 1 | a0010 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.737T>G | p.Leu246Trp | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/30 | 810/10461 | 737/6525 | 246/2174 | chr17 | 62033864 | ||
chr17:62033887
|
C | A | 1 | a0004 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.714G>T | p.Gln238His | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/30 | 787/10461 | 714/6525 | 238/2174 | chr17 | 62033887 | ||
chr17:62063085
|
T | C | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.283A>G | p.Ile95Val | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/30 | 356/10461 | 283/6525 | 95/2174 | chr17 | 62063085 | ||
chr17:62063099
|
C | T | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.269G>A | p.Ser90Asn | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/30 | 342/10461 | 269/6525 | 90/2174 | chr17 | 62063099 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61953049
|
G | A | 1 | a0001c0013 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.6033C>T | p.Ile2011Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/30 | 6106/10461 | 6033/6525 | 2011/2174 | chr17 | 61953049 | ||
chr17:61955422
|
A | G | 1 | a0003c0010 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.5928T>C | p.Tyr1976Tyr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/30 | 6001/10461 | 5928/6525 | 1976/2174 | chr17 | 61955422 | ||
chr17:61955530
|
C | T | 2 | a0001c0007a0006c0022 | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
synonymous_variant | LOW | c.5820G>A | p.Thr1940Thr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/30 | 5893/10461 | 5820/6525 | 1940/2174 | chr17 | 61955530 | ||
chr17:61961088
|
T | C | 1 | a0001c0017 | 1 | HG02630.hp2 | splice_region_variant&synonymous_variant | LOW | c.5259A>G | p.Arg1753Arg | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/30 | 5332/10461 | 5259/6525 | 1753/2174 | chr17 | 61961088 | ||
chr17:61962857
|
G | A | 1 | a0001c0018 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.4959C>T | p.Asp1653Asp | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 5032/10461 | 4959/6525 | 1653/2174 | chr17 | 61962857 | ||
chr17:61962968
|
C | T | 8 | a0001c0002a0001c0003a0001c0006others(5): Show | 113 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
synonymous_variant | LOW | c.4848G>A | p.Thr1616Thr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 4921/10461 | 4848/6525 | 1616/2174 | chr17 | 61962968 | ||
chr17:61965074
|
T | C | 1 | a0001c0004 | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.4776A>G | p.Leu1592Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4849/10461 | 4776/6525 | 1592/2174 | chr17 | 61965074 | ||
chr17:61965329
|
T | C | 1 | a0001c0016 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.4521A>G | p.Ala1507Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4594/10461 | 4521/6525 | 1507/2174 | chr17 | 61965329 | ||
chr17:61965407
|
G | A | 1 | a0001c0017 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.4443C>T | p.Ala1481Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4516/10461 | 4443/6525 | 1481/2174 | chr17 | 61965407 | ||
chr17:61966523
|
G | A | 23 | a0001c0001a0001c0002a0001c0003others(20): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
synonymous_variant | LOW | c.4320C>T | p.Asp1440Asp | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/30 | 4393/10461 | 4320/6525 | 1440/2174 | chr17 | 61966523 | ||
chr17:61966568
|
T | C | 2 | a0001c0002a0001c0018 | 63 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
synonymous_variant | LOW | c.4275A>G | p.Lys1425Lys | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/30 | 4348/10461 | 4275/6525 | 1425/2174 | chr17 | 61966568 | ||
chr17:62011188
|
T | C | 1 | a0001c0006 | 5 | HG00639.hp1 HG02055.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.1329A>G | p.Ala443Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1402/10461 | 1329/6525 | 443/2174 | chr17 | 62011188 | ||
chr17:62029621
|
T | C | 3 | a0001c0007a0001c0021a0006c0022 | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
synonymous_variant | LOW | c.1203A>G | p.Leu401Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/30 | 1276/10461 | 1203/6525 | 401/2174 | chr17 | 62029621 | ||
chr17:62031619
|
G | A | 1 | a0001c0009 | 2 | HG02572.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.834C>T | p.Tyr278Tyr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/30 | 907/10461 | 834/6525 | 278/2174 | chr17 | 62031619 | ||
chr17:62052653
|
C | G | 1 | a0001c0008 | 2 | HG03017.hp1 HG03834.hp2 |
synonymous_variant | LOW | c.354G>C | p.Leu118Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/30 | 427/10461 | 354/6525 | 118/2174 | chr17 | 62052653 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61942656
|
GT | G | 5 | a0001c0001t0013a0001c0001t0022a0001c0007t0005others(2): Show | 8 | HG01517.hp1 HG02257.hp1 HG03540.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3811delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3811 | chr17 | 61942656 | |||||
chr17:61942662
|
T | G | 2 | a0001c0001t0007a0001c0003t0007 | 3 | HG00438.hp2 HG00597.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3806A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3806 | chr17 | 61942662 | |||||
chr17:61942669
|
T | A | 2 | a0001c0001t0020a0001c0002t0023 | 2 | NA18949.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3799 | chr17 | 61942669 | |||||
chr17:61942670
|
A | T | 2 | a0001c0001t0014a0008c0015t0014 | 2 | HG01168.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3798T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3798 | chr17 | 61942670 | |||||
chr17:61942732
|
G | A | 1 | a0001c0002t0024 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3736 | chr17 | 61942732 | |||||
chr17:61942776
|
AAAG | A | 7 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(4): Show | 54 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3689_*3691delCTT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3689 | chr17 | 61942776 | |||||
chr17:61943057
|
A | G | 2 | a0001c0001t0010a0001c0001t0012 | 4 | HG02056.hp2 NA19079.hp2 NA19084.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3411 | chr17 | 61943057 | |||||
chr17:61943631
|
A | G | 2 | a0001c0003t0006a0001c0003t0029 | 4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2837T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2837 | chr17 | 61943631 | |||||
chr17:61944017
|
G | A | 1 | a0001c0001t0015 | 2 | HG02280.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2451C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2451 | chr17 | 61944017 | |||||
chr17:61944233
|
G | A | 7 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(4): Show | 59 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2235C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2235 | chr17 | 61944233 | |||||
chr17:61944234
|
T | C | 3 | a0001c0007t0005a0001c0021t0017a0006c0022t0005 | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2234 | chr17 | 61944234 | |||||
chr17:61944288
|
GTAAAGTC others(6): Show |
G | 1 | a0001c0001t0021 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2167_*2179delAATA others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2167 | chr17 | 61944288 | |||||
chr17:61944372
|
G | GT | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(7): Show | 63 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2095dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2095 | chr17 | 61944372 | |||||
chr17:61944372
|
GT | G | 5 | a0001c0001t0008a0001c0007t0005a0001c0021t0017others(2): Show | 8 | HG02257.hp1 HG02735.hp2 HG03540.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2095delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2095 | chr17 | 61944372 | |||||
chr17:61944392
|
G | T | 1 | a0001c0002t0009 | 2 | HG00558.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2076C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2076 | chr17 | 61944392 | |||||
chr17:61944454
|
T | C | 3 | a0001c0007t0005a0001c0021t0017a0006c0022t0005 | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2014A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2014 | chr17 | 61944454 | |||||
chr17:61944530
|
T | C | 1 | a0001c0001t0025 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1938 | chr17 | 61944530 | |||||
chr17:61944587
|
G | A | 3 | a0001c0007t0005a0001c0021t0017a0006c0022t0005 | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1881C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1881 | chr17 | 61944587 | |||||
chr17:61944680
|
A | G | 1 | a0001c0001t0019 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1788 | chr17 | 61944680 | |||||
chr17:61944780
|
G | T | 1 | a0001c0001t0018 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1688 | chr17 | 61944780 | |||||
chr17:61944955
|
G | A | 1 | a0001c0002t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1513C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1513 | chr17 | 61944955 | |||||
chr17:61945522
|
G | A | 3 | a0001c0007t0005a0001c0021t0017a0006c0022t0005 | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*946C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 946 | chr17 | 61945522 | |||||
chr17:61945557
|
C | G | 1 | a0001c0001t0004 | 6 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*911G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 911 | chr17 | 61945557 | |||||
chr17:61945654
|
T | C | 1 | a0001c0001t0027 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 814 | chr17 | 61945654 | |||||
chr17:61946282
|
A | G | 1 | a0001c0021t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 186 | chr17 | 61946282 | |||||
chr17:61946390
|
A | C | 1 | a0001c0001t0016 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 78 | chr17 | 61946390 | |||||
chr17:61946416
|
G | A | 1 | a0001c0006t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 52 | chr17 | 61946416 | |||||
chr17:61946435
|
G | A | 1 | a0001c0003t0029 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 33 | chr17 | 61946435 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61946608
|
G | C | 1 | a0001c0001t0007g0002 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.6393-8C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 29/29 | chr17 | 61946608 | ||||||
chr17:61947030
|
C | G | 30 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(27): Show | 30 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.6292-13G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947030 | ||||||
chr17:61947194
|
G | GT | 8 | a0001c0001t0001g0235a0001c0001t0001g0283a0001c0001t0007g0002others(5): Show | 8 | HG01099.hp1 HG01109.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.6292-178dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947194 | ||||||
chr17:61947199
|
T | G | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6292-182A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947199 | ||||||
chr17:61947200
|
T | G | 1 | a0001c0002t0001g0062 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.6292-183A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947200 | ||||||
chr17:61947244
|
G | T | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6292-227C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947244 | ||||||
chr17:61947341
|
T | C | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6292-324A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947341 | ||||||
chr17:61947408
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6292-391G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947408 | ||||||
chr17:61947497
|
G | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6292-480C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947497 | ||||||
chr17:61947553
|
G | A | 1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6292-536C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947553 | ||||||
chr17:61947650
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6292-633C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947650 | ||||||
chr17:61948006
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6292-989A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948006 | ||||||
chr17:61948059
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6292-1042G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948059 | ||||||
chr17:61948203
|
A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6292-1186T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948203 | ||||||
chr17:61948384
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6292-1367A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948384 | ||||||
chr17:61948761
|
AAC | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6292-1746_6292-174 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948761 | ||||||
chr17:61948776
|
G | A | 3 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0017 | 3 | HG03669.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.6292-1759C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948776 | ||||||
chr17:61948808
|
C | G | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6292-1791G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948808 | ||||||
chr17:61948816
|
G | C | 1 | a0001c0001t0002g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6292-1799C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948816 | ||||||
chr17:61948861
|
C | A | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6292-1844G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948861 | ||||||
chr17:61949328
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6291+1497G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949328 | ||||||
chr17:61949329
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6291+1496C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949329 | ||||||
chr17:61949474
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.6291+1351C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949474 | ||||||
chr17:61949562
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6291+1263C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949562 | ||||||
chr17:61949597
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6291+1228A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949597 | ||||||
chr17:61949632
|
T | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6291+1193A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949632 | ||||||
chr17:61949708
|
G | A | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.6291+1117C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949708 | ||||||
chr17:61949732
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6291+1093C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949732 | ||||||
chr17:61949744
|
G | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.6291+1081C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949744 | ||||||
chr17:61949751
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0188others(2): Show | 5 | NA18612.hp2 NA18946.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.6291+1074C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949751 | ||||||
chr17:61949780
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6291+1045G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949780 | ||||||
chr17:61949824
|
T | C | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6291+1001A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949824 | ||||||
chr17:61949878
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0007g0002 | 2 | HG01099.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6291+947A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949878 | ||||||
chr17:61949905
|
A | G | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.6291+920T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949905 | ||||||
chr17:61949967
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6291+858C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949967 | ||||||
chr17:61950285
|
A | C | 1 | a0001c0002t0001g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6291+540T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950285 | ||||||
chr17:61950385
|
G | GT | 10 | a0001c0001t0001g0254a0001c0003t0001g0089a0001c0003t0001g0090others(7): Show | 10 | HG01358.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.6291+439dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950385 | ||||||
chr17:61950386
|
T | G | 1 | a0001c0002t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6291+439A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950386 | ||||||
chr17:61950388
|
T | G | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6291+437A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950388 | ||||||
chr17:61950418
|
T | C | 1 | a0001c0001t0015g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6291+407A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950418 | ||||||
chr17:61950509
|
G | A | 2 | a0001c0001t0003g0290a0001c0001t0003g0295 | 2 | HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.6291+316C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950509 | ||||||
chr17:61950516
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6291+309A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950516 | ||||||
chr17:61950532
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6291+293G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950532 | ||||||
chr17:61950703
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6291+122G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950703 | ||||||
chr17:61951257
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6118-259T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951257 | ||||||
chr17:61951444
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.6118-446G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951444 | ||||||
chr17:61951484
|
A | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.6118-486T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951484 | ||||||
chr17:61951515
|
T | C | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.6118-517A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951515 | ||||||
chr17:61951665
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6118-667A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951665 | ||||||
chr17:61951975
|
G | A | 1 | a0001c0001t0018g0212 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6118-977C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951975 | ||||||
chr17:61952168
|
C | T | 2 | a0001c0004t0001g0163a0001c0004t0001g0164 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6117+797G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952168 | ||||||
chr17:61952172
|
C | T | 2 | a0001c0002t0009g0043a0001c0002t0009g0069 | 2 | HG00558.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.6117+793G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952172 | ||||||
chr17:61952330
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6117+635C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952330 | ||||||
chr17:61952571
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.6117+394G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952571 | ||||||
chr17:61952616
|
C | G | 36 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0165others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.6117+349G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952616 | ||||||
chr17:61952753
|
C | T | 8 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0059others(5): Show | 8 | HG02027.hp1 NA18960.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.6117+212G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952753 | ||||||
chr17:61952835
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6117+130G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952835 | ||||||
chr17:61952930
|
C | T | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6117+35G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952930 | ||||||
chr17:61953513
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0196 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.5969-400T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953513 | ||||||
chr17:61953795
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5969-682T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953795 | ||||||
chr17:61953929
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.5969-816G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953929 | ||||||
chr17:61954083
|
G | A | 1 | a0001c0001t0016g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5969-970C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954083 | ||||||
chr17:61954118
|
C | T | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5969-1005G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954118 | ||||||
chr17:61954132
|
G | C | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5969-1019C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954132 | ||||||
chr17:61954250
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5968+1132C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954250 | ||||||
chr17:61954413
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.5968+969A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954413 | ||||||
chr17:61954528
|
G | A | 7 | a0001c0001t0002g0134a0001c0001t0002g0153a0001c0001t0002g0154others(4): Show | 7 | HG00438.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.5968+854C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954528 | ||||||
chr17:61954670
|
G | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5968+712C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954670 | ||||||
chr17:61954714
|
C | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.5968+668G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954714 | ||||||
chr17:61954770
|
G | A | 1 | a0001c0001t0008g0270 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5968+612C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954770 | ||||||
chr17:61954840
|
A | G | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5968+542T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954840 | ||||||
chr17:61954903
|
T | C | 1 | a0001c0006t0028g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5968+479A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954903 | ||||||
chr17:61954969
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5968+413C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954969 | ||||||
chr17:61955003
|
A | G | 1 | a0001c0003t0001g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5968+379T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955003 | ||||||
chr17:61955020
|
T | G | 60 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5968+362A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955020 | ||||||
chr17:61955120
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5968+262G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955120 | ||||||
chr17:61955147
|
CTCT | C | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5968+232_5968+234d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955147 | ||||||
chr17:61955280
|
T | C | 1 | a0001c0002t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5968+102A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955280 | ||||||
chr17:61955289
|
A | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5968+93T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955289 | ||||||
chr17:61955304
|
TCA | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.5968+76_5968+77del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955304 | ||||||
chr17:61955646
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5782+34C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 25/29 | chr17 | 61955646 | ||||||
chr17:61955855
|
T | TA | 34 | a0001c0001t0001g0084a0001c0001t0001g0166a0001c0001t0001g0167others(31): Show | 34 | HG00639.hp1 HG01346.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.5624-18dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | ||||||
chr17:61955855
|
T | TAA | 10 | a0001c0001t0001g0230a0001c0001t0001g0251a0001c0001t0001g0315others(7): Show | 10 | HG00642.hp1 HG01109.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.5624-19_5624-18dup others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | ||||||
chr17:61955855
|
TA | T | 13 | a0001c0001t0001g0218a0001c0001t0002g0133a0001c0001t0002g0152others(10): Show | 13 | HG01109.hp1 HG02451.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.5624-18delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | ||||||
chr17:61956292
|
A | T | 1 | a0001c0001t0016g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5623+47T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61956292 | ||||||
chr17:61956679
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5481-198T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956679 | ||||||
chr17:61956854
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5481-373A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956854 | ||||||
chr17:61956872
|
G | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.5481-391C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956872 | ||||||
chr17:61956877
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5481-396G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956877 | ||||||
chr17:61956889
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5481-408A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956889 | ||||||
chr17:61956995
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5481-514T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956995 | ||||||
chr17:61957002
|
T | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.5481-521A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957002 | ||||||
chr17:61957139
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5481-658G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957139 | ||||||
chr17:61957165
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5481-684C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957165 | ||||||
chr17:61957195
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0245 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5481-714G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957195 | ||||||
chr17:61957255
|
C | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.5481-774G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957255 | ||||||
chr17:61957280
|
A | C | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5481-799T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957280 | ||||||
chr17:61957334
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0002g0158a0001c0001t0013g0316 | 3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.5481-853G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957334 | ||||||
chr17:61957344
|
A | G | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5481-863T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957344 | ||||||
chr17:61957356
|
A | AT | 15 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5481-876dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957356 | ||||||
chr17:61957419
|
T | C | 3 | a0001c0003t0001g0201a0001c0003t0001g0202a0001c0003t0001g0203 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5481-938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957419 | ||||||
chr17:61957485
|
G | A | 30 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(27): Show | 30 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.5481-1004C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957485 | ||||||
chr17:61957590
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5481-1109G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957590 | ||||||
chr17:61957833
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5481-1352G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957833 | ||||||
chr17:61957834
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5481-1353T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957834 | ||||||
chr17:61957884
|
A | C | 1 | a0001c0001t0003g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5481-1403T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957884 | ||||||
chr17:61957951
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5481-1470C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957951 | ||||||
chr17:61957989
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5481-1508G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957989 | ||||||
chr17:61958075
|
A | G | 2 | a0001c0003t0001g0095a0001c0003t0001g0323 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5481-1594T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958075 | ||||||
chr17:61958143
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5481-1662G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958143 | ||||||
chr17:61958188
|
C | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5481-1707G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958188 | ||||||
chr17:61958208
|
C | T | 8 | a0001c0003t0001g0089a0001c0003t0001g0090a0001c0003t0001g0095others(5): Show | 8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.5481-1727G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958208 | ||||||
chr17:61958348
|
G | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0125 | 2 | NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.5481-1867C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958348 | ||||||
chr17:61958417
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5481-1936G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958417 | ||||||
chr17:61958488
|
A | G | 102 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(99): Show | 102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.5481-2007T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958488 | ||||||
chr17:61958577
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5481-2096G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958577 | ||||||
chr17:61958901
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5480+1966T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958901 | ||||||
chr17:61959349
|
A | C | 1 | a0001c0003t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5480+1518T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959349 | ||||||
chr17:61959496
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5480+1371A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959496 | ||||||
chr17:61959630
|
C | T | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.5480+1237G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959630 | ||||||
chr17:61959726
|
C | CT | 10 | a0001c0001t0001g0082a0001c0001t0001g0195a0001c0001t0001g0215others(7): Show | 10 | HG01978.hp2 HG02109.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.5480+1140dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | ||||||
chr17:61959726
|
CT | C | 183 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0183others(180): Show | 183 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.5480+1140delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | ||||||
chr17:61959726
|
CTT | C | 9 | a0001c0001t0002g0138a0001c0002t0001g0030a0001c0002t0001g0059others(6): Show | 9 | HG01175.hp1 HG01993.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.5480+1139_5480+114 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | ||||||
chr17:61959746
|
T | G | 7 | a0001c0001t0001g0184a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG00642.hp2 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.5480+1121A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959746 | ||||||
chr17:61959768
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5480+1099C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959768 | ||||||
chr17:61959789
|
T | C | 202 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(199): Show | 202 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.5480+1078A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959789 | ||||||
chr17:61959946
|
G | A | 1 | a0002c0005t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5480+921C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959946 | ||||||
chr17:61960239
|
T | C | 4 | a0001c0003t0006g0092a0001c0003t0006g0093a0001c0003t0006g0094others(1): Show | 4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5480+628A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960239 | ||||||
chr17:61960256
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5480+611A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960256 | ||||||
chr17:61960296
|
C | G | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5480+571G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960296 | ||||||
chr17:61960330
|
G | A | 9 | a0001c0003t0001g0014a0001c0003t0001g0089a0001c0003t0001g0090others(6): Show | 9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.5480+537C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960330 | ||||||
chr17:61960502
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5480+365C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960502 | ||||||
chr17:61960721
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5480+146G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960721 | ||||||
chr17:61960817
|
C | T | 2 | a0001c0001t0002g0127a0001c0001t0002g0137 | 2 | NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5480+50G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960817 | ||||||
chr17:61960849
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5480+18A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960849 | ||||||
chr17:61961194
|
T | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5257-104A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961194 | ||||||
chr17:61961253
|
G | C | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5257-163C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961253 | ||||||
chr17:61961481
|
C | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.5256+107G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961481 | ||||||
chr17:61961519
|
CA | C | 158 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(155): Show | 158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.5256+68delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | ||||||
chr17:61961519
|
CAA | C | 26 | a0001c0001t0010g0149a0001c0002t0001g0001a0001c0002t0001g0096others(23): Show | 26 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.5256+67_5256+68del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | ||||||
chr17:61961519
|
CAAA | C | 11 | a0001c0003t0001g0112a0001c0003t0001g0201a0001c0003t0001g0202others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5256+66_5256+68del others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | ||||||
chr17:61961790
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5065-11A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961790 | ||||||
chr17:61961872
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5065-93T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961872 | ||||||
chr17:61961899
|
A | T | 60 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5065-120T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961899 | ||||||
chr17:61961911
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5065-132A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961911 | ||||||
chr17:61962054
|
G | A | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.5065-275C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962054 | ||||||
chr17:61962076
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065-297T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962076 | ||||||
chr17:61962141
|
C | G | 1 | a0001c0002t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5065-362G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962141 | ||||||
chr17:61962178
|
C | G | 91 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0016others(88): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.5065-399G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962178 | ||||||
chr17:61962243
|
G | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0265a0001c0001t0001g0266others(3): Show | 6 | HG00558.hp1 NA18948.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-464C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962243 | ||||||
chr17:61962248
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5065-469A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962248 | ||||||
chr17:61962307
|
A | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5064+445T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962307 | ||||||
chr17:61962343
|
T | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.5064+409A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962343 | ||||||
chr17:61962363
|
G | A | 60 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5064+389C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962363 | ||||||
chr17:61962478
|
C | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5064+274G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962478 | ||||||
chr17:61962634
|
A | G | 31 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(28): Show | 31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.5064+118T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962634 | ||||||
chr17:61962745
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp2 | splice_region_variant&intron_variant | LOW | c.5064+7G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962745 | ||||||
chr17:61963046
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4845-75A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963046 | ||||||
chr17:61963166
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4845-195T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963166 | ||||||
chr17:61963202
|
CA | C | 152 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(149): Show | 152 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.4845-232delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963202
|
CAA | C | 107 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0190others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.4845-233_4845-232d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963202
|
CAAA | C | 6 | a0001c0002t0001g0018a0001c0002t0001g0042a0001c0002t0001g0048others(3): Show | 6 | HG02027.hp1 HG02132.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.4845-234_4845-232d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963202
|
CAAAAA | C | 6 | a0001c0004t0001g0071a0001c0004t0001g0073a0001c0004t0001g0074others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4845-236_4845-232d others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963202
|
CAAAAAAA | C | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4845-238_4845-232d others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963202
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4845-243_4845-232d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | ||||||
chr17:61963227
|
A | G | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4845-256T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963227 | ||||||
chr17:61963229
|
A | AGAAAGAA others(3): Show |
4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-259_4845-258i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963229 | ||||||
chr17:61963231
|
G | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-260C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963231 | ||||||
chr17:61963235
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4845-264C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963235 | ||||||
chr17:61963261
|
TAGGGTA | T | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.4845-296_4845-291d others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963261 | ||||||
chr17:61963436
|
T | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4845-465A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963436 | ||||||
chr17:61963458
|
C | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0284a0001c0001t0002g0116others(1): Show | 4 | HG02896.hp1 HG04184.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-487G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963458 | ||||||
chr17:61963591
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4845-620G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963591 | ||||||
chr17:61964000
|
A | G | 2 | a0001c0002t0001g0019a0001c0002t0001g0317 | 2 | NA18965.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4844+1006T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964000 | ||||||
chr17:61964232
|
A | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4844+774T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964232 | ||||||
chr17:61964302
|
A | G | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4844+704T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964302 | ||||||
chr17:61964408
|
C | T | 1 | a0001c0003t0001g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4844+598G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964408 | ||||||
chr17:61964486
|
G | T | 5 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0136others(2): Show | 5 | HG00642.hp1 HG01433.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.4844+520C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964486 | ||||||
chr17:61964554
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4844+452C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964554 | ||||||
chr17:61964688
|
C | T | 1 | a0001c0002t0001g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4844+318G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964688 | ||||||
chr17:61964836
|
T | G | 1 | a0001c0001t0012g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4844+170A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964836 | ||||||
chr17:61964893
|
A | G | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.4844+113T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964893 | ||||||
chr17:61964912
|
C | T | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4844+94G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964912 | ||||||
chr17:61964953
|
A | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4844+53T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964953 | ||||||
chr17:61965591
|
T | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4382-123A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965591 | ||||||
chr17:61965752
|
T | C | 1 | a0001c0002t0023g0039 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4382-284A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965752 | ||||||
chr17:61965951
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4382-483A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965951 | ||||||
chr17:61965990
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4381+472T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965990 | ||||||
chr17:61966029
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4381+433G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966029 | ||||||
chr17:61966121
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4381+341A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966121 | ||||||
chr17:61966210
|
C | T | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4381+252G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966210 | ||||||
chr17:61966245
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4381+217C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966245 | ||||||
chr17:61966898
|
A | C | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.4192-247T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61966898 | ||||||
chr17:61967447
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4191+588A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967447 | ||||||
chr17:61967581
|
A | G | 1 | a0001c0002t0001g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4191+454T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967581 | ||||||
chr17:61967805
|
C | T | 1 | a0001c0003t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4191+230G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967805 | ||||||
chr17:61967809
|
C | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4191+226G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967809 | ||||||
chr17:61967898
|
C | A | 1 | a0001c0001t0001g0246 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4191+137G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967898 | ||||||
chr17:61967934
|
C | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.4191+101G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967934 | ||||||
chr17:61968313
|
T | TTTTATTT others(1): Show |
62 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0018others(59): Show | 62 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.3968-63_3968-56dup others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968313 | ||||||
chr17:61968313
|
T | TTTTATTT others(5): Show |
3 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0049 | 3 | NA18612.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.3968-67_3968-56dup others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968313 | ||||||
chr17:61968316
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3968-58A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968316 | ||||||
chr17:61968412
|
G | GCC | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3968-156_3968-155d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968412 | ||||||
chr17:61968472
|
C | T | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3968-214G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968472 | ||||||
chr17:61968516
|
C | T | 1 | a0001c0007t0005g0010 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3968-258G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968516 | ||||||
chr17:61968528
|
G | A | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3968-270C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968528 | ||||||
chr17:61968748
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3968-490G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968748 | ||||||
chr17:61968915
|
C | G | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.3968-657G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968915 | ||||||
chr17:61969279
|
G | A | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.3968-1021C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969279 | ||||||
chr17:61969365
|
AC | A | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3968-1108delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969365 | ||||||
chr17:61969366
|
C | A | 270 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.3968-1108G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969366 | ||||||
chr17:61969416
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3968-1158G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969416 | ||||||
chr17:61969576
|
C | T | 1 | a0001c0018t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3968-1318G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969576 | ||||||
chr17:61969653
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3968-1395C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969653 | ||||||
chr17:61969761
|
C | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3968-1503G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969761 | ||||||
chr17:61970281
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3968-2023T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970281 | ||||||
chr17:61970631
|
A | G | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.3967+2096T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970631 | ||||||
chr17:61970679
|
C | CA | 35 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0088others(32): Show | 35 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.3967+2047dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | ||||||
chr17:61970679
|
CA | C | 91 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(88): Show | 91 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.3967+2047delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | ||||||
chr17:61970679
|
CAA | C | 77 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0002g0128others(74): Show | 77 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.3967+2046_3967+204 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | ||||||
chr17:61970726
|
G | GT | 208 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(205): Show | 208 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.3967+2000dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970726 | ||||||
chr17:61970726
|
G | GTT | 22 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(19): Show | 22 | HG01175.hp1 HG01346.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3967+1999_3967+200 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970726 | ||||||
chr17:61970960
|
G | T | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3967+1767C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970960 | ||||||
chr17:61971113
|
T | A | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.3967+1614A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971113 | ||||||
chr17:61971221
|
T | A | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3967+1506A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971221 | ||||||
chr17:61971275
|
CT | C | 6 | a0001c0001t0001g0315a0001c0001t0002g0152a0001c0002t0001g0048others(3): Show | 6 | HG01346.hp2 HG02145.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3967+1451delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971275 | ||||||
chr17:61971278
|
T | G | 7 | a0001c0001t0001g0261a0001c0001t0004g0260a0001c0001t0004g0262others(4): Show | 7 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.3967+1449A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971278 | ||||||
chr17:61971317
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3967+1410G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971317 | ||||||
chr17:61971592
|
C | T | 7 | a0001c0002t0001g0022a0001c0002t0001g0030a0001c0002t0001g0032others(4): Show | 7 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.3967+1135G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971592 | ||||||
chr17:61971593
|
G | A | 1 | a0001c0003t0001g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3967+1134C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971593 | ||||||
chr17:61971596
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3967+1131C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971596 | ||||||
chr17:61971599
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3967+1128A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971599 | ||||||
chr17:61971649
|
T | G | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3967+1078A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971649 | ||||||
chr17:61971791
|
G | A | 1 | a0001c0003t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3967+936C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971791 | ||||||
chr17:61971850
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3967+877A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971850 | ||||||
chr17:61971856
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3967+871G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971856 | ||||||
chr17:61971875
|
G | A | 31 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(28): Show | 31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.3967+852C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971875 | ||||||
chr17:61971906
|
C | G | 1 | a0001c0001t0020g0135 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3967+821G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971906 | ||||||
chr17:61972168
|
A | G | 2 | a0001c0001t0001g0287a0004c0023t0001g0216 | 2 | NA18972.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.3967+559T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61972168 | ||||||
chr17:61972663
|
T | C | 1 | a0001c0003t0006g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3967+64A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61972663 | ||||||
chr17:61972948
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3806-60A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61972948 | ||||||
chr17:61973073
|
T | G | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3806-185A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973073 | ||||||
chr17:61973181
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3806-293A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973181 | ||||||
chr17:61973289
|
A | G | 2 | a0001c0002t0001g0036a0001c0002t0001g0064 | 2 | NA18960.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3806-401T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973289 | ||||||
chr17:61973731
|
C | T | 1 | a0001c0003t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3806-843G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973731 | ||||||
chr17:61973859
|
T | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-971A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973859 | ||||||
chr17:61973931
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3806-1043G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973931 | ||||||
chr17:61973959
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3806-1071C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973959 | ||||||
chr17:61974309
|
TGGGA | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-1425_3806-142 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974309 | ||||||
chr17:61974330
|
T | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0245 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3806-1442A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974330 | ||||||
chr17:61974392
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-1504G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974392 | ||||||
chr17:61974397
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3806-1509G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974397 | ||||||
chr17:61974542
|
T | G | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3806-1654A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974542 | ||||||
chr17:61974550
|
T | TG | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.3806-1663_3806-166 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974550 | ||||||
chr17:61974723
|
C | T | 2 | a0001c0001t0015g0219a0001c0001t0015g0232 | 2 | HG02280.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3806-1835G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974723 | ||||||
chr17:61974782
|
T | A | 1 | a0001c0001t0019g0131 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3806-1894A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974782 | ||||||
chr17:61974975
|
A | C | 4 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0031others(1): Show | 4 | NA18983.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3806-2087T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974975 | ||||||
chr17:61975005
|
C | A | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.3806-2117G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975005 | ||||||
chr17:61975139
|
T | TA | 19 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(16): Show | 19 | HG02155.hp2 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.3806-2252dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975139 | ||||||
chr17:61975154
|
T | A | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3806-2266A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975154 | ||||||
chr17:61975154
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3806-2266A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975154 | ||||||
chr17:61975214
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3806-2326G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975214 | ||||||
chr17:61975505
|
T | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2617A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975505 | ||||||
chr17:61975609
|
T | C | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.3806-2721A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975609 | ||||||
chr17:61975630
|
A | C | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-2742T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975630 | ||||||
chr17:61975676
|
A | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975676 | ||||||
chr17:61975762
|
T | A | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3806-2874A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975762 | ||||||
chr17:61975842
|
C | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2954G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975842 | ||||||
chr17:61975885
|
A | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2997T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975885 | ||||||
chr17:61975934
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3806-3046A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975934 | ||||||
chr17:61976011
|
C | T | 1 | a0001c0003t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3806-3123G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976011 | ||||||
chr17:61976012
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-3124C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976012 | ||||||
chr17:61976023
|
A | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-3135T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976023 | ||||||
chr17:61976094
|
T | C | 5 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0113others(2): Show | 5 | HG00639.hp1 HG02055.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-3206A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976094 | ||||||
chr17:61976197
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3806-3309G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976197 | ||||||
chr17:61976198
|
G | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3806-3310C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976198 | ||||||
chr17:61976256
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0011g0075 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3806-3368A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976256 | ||||||
chr17:61976743
|
G | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-3855C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976743 | ||||||
chr17:61976896
|
C | G | 83 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(80): Show | 83 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.3806-4008G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976896 | ||||||
chr17:61977090
|
C | A | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.3806-4202G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977090 | ||||||
chr17:61977192
|
T | G | 1 | a0001c0006t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3806-4304A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977192 | ||||||
chr17:61977298
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3806-4410A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977298 | ||||||
chr17:61977475
|
G | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3806-4587C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977475 | ||||||
chr17:61977540
|
C | G | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-4652G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977540 | ||||||
chr17:61977744
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3805+4454C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977744 | ||||||
chr17:61977824
|
C | G | 78 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(75): Show | 78 | HG00140.hp1 HG00558.hp1 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.3805+4374G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977824 | ||||||
chr17:61977880
|
G | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+4318C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977880 | ||||||
chr17:61978151
|
C | CT | 61 | a0001c0001t0001g0287a0001c0001t0002g0116a0001c0001t0002g0117others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.3805+4046dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978151 | ||||||
chr17:61978250
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3805+3948T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978250 | ||||||
chr17:61978347
|
G | C | 6 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+3851C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978347 | ||||||
chr17:61978453
|
G | T | 11 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3805+3745C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978453 | ||||||
chr17:61978525
|
TG | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3805+3672delC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978525 | ||||||
chr17:61978585
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0287others(1): Show | 4 | HG02155.hp2 HG02523.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.3805+3613T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978585 | ||||||
chr17:61978769
|
CT | C | 6 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0187others(3): Show | 6 | NA18612.hp2 NA18946.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+3428delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978769 | ||||||
chr17:61978902
|
T | C | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3805+3296A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978902 | ||||||
chr17:61979068
|
T | G | 1 | a0001c0002t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3805+3130A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979068 | ||||||
chr17:61979386
|
C | T | 6 | a0001c0001t0002g0128a0001c0007t0005g0009a0001c0007t0005g0010others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+2812G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979386 | ||||||
chr17:61979547
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3805+2651C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979547 | ||||||
chr17:61979749
|
C | A | 1 | a0001c0003t0007g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3805+2449G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979749 | ||||||
chr17:61979951
|
G | A | 1 | a0001c0003t0007g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3805+2247C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979951 | ||||||
chr17:61980144
|
A | G | 103 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0016others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3805+2054T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980144 | ||||||
chr17:61980194
|
AAAAC | A | 8 | a0001c0001t0002g0142a0001c0001t0002g0145a0001c0001t0002g0147others(5): Show | 8 | HG01081.hp1 HG01109.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.3805+2000_3805+200 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980194 | ||||||
chr17:61980277
|
C | G | 1 | a0001c0003t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3805+1921G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980277 | ||||||
chr17:61980310
|
T | C | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3805+1888A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980310 | ||||||
chr17:61980359
|
T | G | 12 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3805+1839A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980359 | ||||||
chr17:61980528
|
C | A | 1 | a0001c0003t0001g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3805+1670G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980528 | ||||||
chr17:61980655
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3805+1543T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980655 | ||||||
chr17:61980832
|
C | T | 12 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3805+1366G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980832 | ||||||
chr17:61980908
|
A | G | 2 | a0002c0005t0001g0121a0002c0005t0001g0122 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3805+1290T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980908 | ||||||
chr17:61980956
|
C | A | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+1242G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980956 | ||||||
chr17:61981024
|
A | AT | 20 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(17): Show | 20 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.3805+1173dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981024 | ||||||
chr17:61981057
|
C | T | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.3805+1141G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981057 | ||||||
chr17:61981441
|
T | TCTAAATG others(20): Show |
2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3805+756_3805+757i others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981441 | ||||||
chr17:61981548
|
T | C | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3805+650A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981548 | ||||||
chr17:61981621
|
A | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+577T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981621 | ||||||
chr17:61981808
|
T | G | 1 | a0001c0001t0002g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3805+390A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981808 | ||||||
chr17:61981828
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0165a0001c0001t0001g0170others(4): Show | 7 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3805+370A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981828 | ||||||
chr17:61981897
|
T | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0044 | 2 | NA18945.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.3805+301A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981897 | ||||||
chr17:61983341
|
A | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2889-227T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983341 | ||||||
chr17:61983730
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2888+441G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983730 | ||||||
chr17:61983731
|
C | CT | 68 | a0001c0001t0001g0233a0001c0001t0001g0240a0001c0001t0001g0242others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2888+439dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | ||||||
chr17:61983731
|
CT | C | 87 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2888+439delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | ||||||
chr17:61983731
|
CTT | C | 8 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0096others(5): Show | 8 | HG02257.hp1 HG03540.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.2888+438_2888+439d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | ||||||
chr17:61983798
|
G | A | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2888+373C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983798 | ||||||
chr17:61984132
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2888+39T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61984132 | ||||||
chr17:61984584
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2691+67A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 14/29 | chr17 | 61984584 | ||||||
chr17:61984964
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2476+36C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 13/29 | chr17 | 61984964 | ||||||
chr17:61985191
|
A | C | 2 | a0001c0001t0010g0149a0001c0001t0010g0150 | 2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2386-101T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985191 | ||||||
chr17:61985231
|
T | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2386-141A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985231 | ||||||
chr17:61985244
|
T | C | 4 | a0001c0003t0001g0293a0001c0003t0001g0297a0001c0003t0001g0307others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-154A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985244 | ||||||
chr17:61985287
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2386-197C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985287 | ||||||
chr17:61985348
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2386-258T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985348 | ||||||
chr17:61985581
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2386-491C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985581 | ||||||
chr17:61985593
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2386-503G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985593 | ||||||
chr17:61985661
|
A | G | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2386-571T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985661 | ||||||
chr17:61986001
|
C | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-911G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986001 | ||||||
chr17:61986393
|
G | A | 1 | a0001c0002t0001g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2385+614C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986393 | ||||||
chr17:61986407
|
C | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2385+600G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986407 | ||||||
chr17:61987308
|
G | A | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(7): Show | 10 | HG00140.hp2 HG01346.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.2264-180C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987308 | ||||||
chr17:61987463
|
C | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2264-335G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987463 | ||||||
chr17:61987547
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2264-419A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987547 | ||||||
chr17:61987603
|
T | C | 1 | a0001c0001t0004g0275 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2264-475A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987603 | ||||||
chr17:61987781
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2264-653C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987781 | ||||||
chr17:61987889
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2264-761G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987889 | ||||||
chr17:61987918
|
T | C | 9 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0027others(6): Show | 9 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.2264-790A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987918 | ||||||
chr17:61988133
|
A | G | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2264-1005T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988133 | ||||||
chr17:61988281
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2264-1153C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988281 | ||||||
chr17:61988282
|
T | C | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2264-1154A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988282 | ||||||
chr17:61988423
|
T | C | 5 | a0001c0002t0001g0070a0001c0002t0001g0096a0001c0002t0001g0098others(2): Show | 5 | HG02148.hp1 NA18956.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264-1295A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988423 | ||||||
chr17:61988705
|
A | G | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2264-1577T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988705 | ||||||
chr17:61988735
|
GT | G | 7 | a0001c0001t0001g0079a0001c0001t0011g0075a0001c0007t0005g0009others(4): Show | 7 | HG02257.hp1 HG02300.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2264-1608delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988735 | ||||||
chr17:61988765
|
T | C | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2264-1637A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988765 | ||||||
chr17:61988965
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2264-1837G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988965 | ||||||
chr17:61989014
|
C | CT | 11 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0273others(8): Show | 11 | HG01109.hp2 HG01346.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.2264-1887dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989014 | ||||||
chr17:61989014
|
CT | C | 31 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(28): Show | 31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2264-1887delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989014 | ||||||
chr17:61989043
|
G | A | 1 | a0001c0001t0021g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2264-1915C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989043 | ||||||
chr17:61989129
|
A | G | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2264-2001T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989129 | ||||||
chr17:61989176
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264-2048C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989176 | ||||||
chr17:61989427
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2264-2299G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989427 | ||||||
chr17:61989467
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2264-2339A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989467 | ||||||
chr17:61989478
|
A | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2264-2350T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989478 | ||||||
chr17:61989710
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2264-2582T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989710 | ||||||
chr17:61990172
|
T | C | 1 | a0001c0001t0027g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2263+2368A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990172 | ||||||
chr17:61990264
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2263+2276A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990264 | ||||||
chr17:61990337
|
T | C | 1 | a0001c0004t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2263+2203A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990337 | ||||||
chr17:61990589
|
C | CTATA | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2263+1947_2263+195 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990589 | ||||||
chr17:61990602
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0314 | 2 | HG04199.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2263+1938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990602 | ||||||
chr17:61990604
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1936G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990604 | ||||||
chr17:61990612
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2263+1928G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990612 | ||||||
chr17:61990615
|
T | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1925A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990615 | ||||||
chr17:61990616
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1924A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990616 | ||||||
chr17:61990627
|
G | GTA | 15 | a0001c0001t0001g0082a0001c0001t0001g0249a0001c0001t0001g0253others(12): Show | 15 | HG00558.hp1 HG01516.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.2263+1911_2263+191 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTATA | 14 | a0001c0001t0001g0182a0001c0001t0001g0258a0001c0001t0001g0266others(11): Show | 14 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2263+1909_2263+191 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTATATA | 5 | a0001c0001t0001g0315a0001c0007t0005g0009a0001c0007t0005g0010others(2): Show | 5 | HG01346.hp2 HG02257.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2263+1907_2263+191 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTATATAT others(7): Show |
1 | a0001c0003t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2263+1899_2263+191 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTATATAT others(15): Show |
1 | a0001c0016t0001g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2263+1891_2263+191 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTATGTGT others(15): Show |
1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTGTATA | 6 | a0002c0005t0001g0004a0002c0005t0001g0005a0002c0005t0001g0006others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2263+1912_2263+191 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTGTATAT others(3): Show |
1 | a0001c0003t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
G | GTGTATAT others(9): Show |
1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
GTA | G | 70 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(67): Show | 70 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2263+1911_2263+191 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990627
|
GTATA | G | 3 | a0001c0001t0002g0126a0001c0001t0003g0250a0011c0024t0001g0320 | 3 | HG02970.hp1 HG03490.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2263+1909_2263+191 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | ||||||
chr17:61990629
|
A | G | 9 | a0001c0001t0001g0179a0001c0001t0001g0261a0001c0001t0004g0260others(6): Show | 9 | HG02148.hp2 HG03130.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.2263+1911T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990629 | ||||||
chr17:61990633
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2263+1907T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990633 | ||||||
chr17:61990650
|
T | C | 2 | a0001c0001t0001g0162a0001c0003t0001g0112 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2263+1890A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TAC | 6 | a0001c0001t0002g0142a0001c0001t0002g0145a0001c0001t0002g0147others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2263+1888_2263+188 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TATATATA others(3): Show |
13 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0108others(10): Show | 13 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TATATATA others(5): Show |
2 | a0001c0003t0001g0107a0001c0006t0001g0113 | 2 | HG00639.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TATATATA others(7): Show |
1 | a0001c0006t0001g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2263+1889_2263+189 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TATATATA others(9): Show |
2 | a0001c0003t0001g0201a0001c0003t0001g0203 | 2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990650
|
T | TATATATA others(15): Show |
1 | a0001c0003t0001g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2263+1889_2263+189 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | ||||||
chr17:61990699
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2263+1841A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990699 | ||||||
chr17:61990879
|
G | A | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2263+1661C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990879 | ||||||
chr17:61990931
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0158a0001c0001t0013g0316 | 3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2263+1609C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990931 | ||||||
chr17:61991055
|
C | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2263+1485G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991055 | ||||||
chr17:61991200
|
T | C | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.2263+1340A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991200 | ||||||
chr17:61991548
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2263+992G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991548 | ||||||
chr17:61991648
|
T | C | 2 | a0001c0001t0010g0149a0001c0001t0010g0150 | 2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2263+892A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991648 | ||||||
chr17:61991797
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0229 | 2 | NA18982.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2263+743A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991797 | ||||||
chr17:61991844
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG00642.hp2 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2263+696G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991844 | ||||||
chr17:61991847
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2263+693A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991847 | ||||||
chr17:61991934
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2263+606G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991934 | ||||||
chr17:61991980
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2263+560C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991980 | ||||||
chr17:61992160
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2263+380A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992160 | ||||||
chr17:61992213
|
T | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2263+327A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992213 | ||||||
chr17:61992248
|
C | T | 1 | a0002c0005t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2263+292G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992248 | ||||||
chr17:61992264
|
G | A | 1 | a0001c0001t0016g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2263+276C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992264 | ||||||
chr17:61992642
|
T | G | 1 | a0001c0003t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2182-21A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992642 | ||||||
chr17:61992750
|
G | GT | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-130dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992750 | ||||||
chr17:61992779
|
C | CT | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-159dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992779 | ||||||
chr17:61992788
|
G | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2182-167C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992788 | ||||||
chr17:61992831
|
C | T | 1 | a0001c0002t0001g0022 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2182-210G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992831 | ||||||
chr17:61992846
|
T | G | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-225A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992846 | ||||||
chr17:61992847
|
G | C | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-226C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992847 | ||||||
chr17:61992848
|
C | A | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-227G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992848 | ||||||
chr17:61992851
|
C | T | 11 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(8): Show | 11 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2182-230G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992851 | ||||||
chr17:61992864
|
G | GT | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-244dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992864 | ||||||
chr17:61992872
|
A | AT | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.2182-252dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992872 | ||||||
chr17:61992925
|
C | T | 1 | a0001c0003t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2182-304G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992925 | ||||||
chr17:61993000
|
T | C | 2 | a0002c0005t0001g0121a0002c0005t0001g0122 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2182-379A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993000 | ||||||
chr17:61993039
|
A | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182-418T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993039 | ||||||
chr17:61993105
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2182-484A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993105 | ||||||
chr17:61993196
|
C | CT | 57 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(54): Show | 57 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.2182-576dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993196 | ||||||
chr17:61993196
|
C | CTT | 6 | a0001c0001t0001g0079a0001c0002t0001g0057a0001c0003t0001g0112others(3): Show | 6 | HG00544.hp1 HG01891.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.2182-577_2182-576d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993196 | ||||||
chr17:61993199
|
TC | T | 8 | a0001c0001t0002g0117a0001c0001t0002g0124a0001c0001t0002g0206others(5): Show | 8 | NA18945.hp1 NA18968.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182-579delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993199 | ||||||
chr17:61993200
|
C | T | 195 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(192): Show | 195 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.2182-579G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993200 | ||||||
chr17:61993202
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2182-581A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993202 | ||||||
chr17:61993667
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2182-1046G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993667 | ||||||
chr17:61993696
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2182-1075C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993696 | ||||||
chr17:61993709
|
C | G | 11 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0187others(8): Show | 11 | HG00544.hp2 HG00597.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.2182-1088G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993709 | ||||||
chr17:61993793
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2182-1172A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993793 | ||||||
chr17:61993804
|
G | A | 1 | a0001c0001t0018g0212 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2182-1183C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993804 | ||||||
chr17:61993891
|
T | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+1261A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993891 | ||||||
chr17:61993919
|
G | A | 56 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2181+1233C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993919 | ||||||
chr17:61993937
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1215T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993937 | ||||||
chr17:61993948
|
C | A | 1 | a0001c0003t0001g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181+1204G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | ||||||
chr17:61993948
|
CA | C | 93 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(90): Show | 93 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.2181+1203delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | ||||||
chr17:61993948
|
CAA | C | 54 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2181+1202_2181+120 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | ||||||
chr17:61993952
|
A | C | 1 | a0001c0001t0025g0008 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2181+1200T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993952 | ||||||
chr17:61993980
|
C | T | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1172G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993980 | ||||||
chr17:61994004
|
A | AT | 7 | a0001c0001t0001g0276a0001c0002t0001g0022a0001c0004t0001g0072others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2181+1147dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994004 | ||||||
chr17:61994120
|
T | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+1032A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994120 | ||||||
chr17:61994394
|
A | G | 4 | a0001c0003t0001g0293a0001c0003t0001g0297a0001c0003t0001g0307others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+758T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994394 | ||||||
chr17:61994410
|
C | T | 14 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0025others(11): Show | 14 | HG00423.hp2 HG00558.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.2181+742G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994410 | ||||||
chr17:61994471
|
A | C | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181+681T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994471 | ||||||
chr17:61994591
|
A | G | 1 | a0002c0005t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2181+561T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994591 | ||||||
chr17:61994606
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181+546G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994606 | ||||||
chr17:61994856
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2181+296C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994856 | ||||||
chr17:61994922
|
G | C | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+230C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994922 | ||||||
chr17:61995000
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2181+152G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995000 | ||||||
chr17:61995018
|
A | G | 4 | a0001c0003t0001g0293a0001c0003t0001g0297a0001c0003t0001g0307others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+134T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995018 | ||||||
chr17:61995030
|
T | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2181+122A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995030 | ||||||
chr17:61995070
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2181+82T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995070 | ||||||
chr17:61995371
|
T | TA | 4 | a0001c0003t0001g0294a0001c0003t0001g0299a0001c0003t0001g0305others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1968-7dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995371 | ||||||
chr17:61995619
|
T | G | 2 | a0001c0003t0001g0302a0001c0003t0001g0303 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968-254A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995619 | ||||||
chr17:61995659
|
A | C | 1 | a0001c0006t0001g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1968-294T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995659 | ||||||
chr17:61995958
|
T | C | 2 | a0001c0001t0002g0148a0001c0001t0021g0129 | 2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1968-593A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995958 | ||||||
chr17:61995967
|
C | T | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(5): Show | 8 | HG01346.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-602G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995967 | ||||||
chr17:61995971
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-606A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995971 | ||||||
chr17:61995972
|
C | T | 2 | a0002c0005t0001g0004a0002c0005t0001g0006 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1968-607G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995972 | ||||||
chr17:61996316
|
C | A | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1968-951G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996316 | ||||||
chr17:61996421
|
G | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-1056C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996421 | ||||||
chr17:61996506
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1968-1141G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996506 | ||||||
chr17:61996826
|
C | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-1461G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996826 | ||||||
chr17:61996873
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-1508A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996873 | ||||||
chr17:61997014
|
C | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-1649G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997014 | ||||||
chr17:61997065
|
T | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-1700A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997065 | ||||||
chr17:61997393
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1968-2028T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997393 | ||||||
chr17:61997410
|
T | C | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-2045A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997410 | ||||||
chr17:61997787
|
C | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-2422G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997787 | ||||||
chr17:61997894
|
T | C | 2 | a0001c0003t0001g0302a0001c0003t0001g0303 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968-2529A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997894 | ||||||
chr17:61998253
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0002g0160 | 2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1968-2888A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998253 | ||||||
chr17:61998560
|
CAAAT | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-3199_1968-319 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998560 | ||||||
chr17:61998592
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1968-3227G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998592 | ||||||
chr17:61998596
|
C | CT | 54 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0168others(51): Show | 54 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1968-3232dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998596 | ||||||
chr17:61998596
|
C | CTT | 19 | a0001c0001t0001g0175a0001c0003t0001g0105a0001c0003t0001g0106others(16): Show | 19 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1968-3233_1968-323 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998596 | ||||||
chr17:61998678
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1968-3313G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998678 | ||||||
chr17:61998706
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-3341G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998706 | ||||||
chr17:61998717
|
G | A | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-3352C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998717 | ||||||
chr17:61998839
|
TCCTCCCA others(6): Show |
T | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1968-3487_1968-347 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998839 | ||||||
chr17:61998887
|
C | T | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1968-3522G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998887 | ||||||
chr17:61998925
|
CT | C | 92 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(89): Show | 92 | HG00140.hp1 HG00558.hp1 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.1968-3561delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | ||||||
chr17:61998925
|
CTT | C | 217 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(214): Show | 217 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.1968-3562_1968-356 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | ||||||
chr17:61998925
|
CTTT | C | 13 | a0001c0001t0002g0117a0001c0001t0002g0128a0001c0001t0002g0136others(10): Show | 13 | HG00642.hp1 HG02132.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968-3563_1968-356 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | ||||||
chr17:61998931
|
T | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | NA18985.hp1 NA19005.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1968-3566A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998931 | ||||||
chr17:61998953
|
G | A | 2 | a0002c0005t0001g0121a0002c0005t0001g0122 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1968-3588C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998953 | ||||||
chr17:61999158
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-3793A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999158 | ||||||
chr17:61999171
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1968-3806A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999171 | ||||||
chr17:61999180
|
A | C | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1968-3815T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999180 | ||||||
chr17:61999356
|
A | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1968-3991T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999356 | ||||||
chr17:61999536
|
G | A | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-4171C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999536 | ||||||
chr17:61999726
|
A | G | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1968-4361T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999726 | ||||||
chr17:61999807
|
A | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-4442T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999807 | ||||||
chr17:61999878
|
G | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-4513C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999878 | ||||||
chr17:62000060
|
A | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1968-4695T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000060 | ||||||
chr17:62000101
|
A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1968-4736T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000101 | ||||||
chr17:62000491
|
A | G | 101 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1968-5126T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000491 | ||||||
chr17:62000492
|
A | G | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1968-5127T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000492 | ||||||
chr17:62000539
|
G | A | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-5174C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000539 | ||||||
chr17:62000677
|
T | A | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1968-5312A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000677 | ||||||
chr17:62001353
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1968-5988C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001353 | ||||||
chr17:62001382
|
C | CACATCAC others(3): Show |
2 | a0001c0001t0001g0246a0001c0001t0001g0276 | 2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6018_1968-601 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001382 | ||||||
chr17:62001384
|
A | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0276 | 2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6019T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001384 | ||||||
chr17:62001386
|
A | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0276 | 2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6021T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001386 | ||||||
chr17:62001387
|
C | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0276 | 2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6022G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001387 | ||||||
chr17:62001597
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-6232G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001597 | ||||||
chr17:62001620
|
A | C | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968-6255T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001620 | ||||||
chr17:62001674
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1968-6309A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001674 | ||||||
chr17:62001678
|
G | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-6313C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001678 | ||||||
chr17:62001749
|
A | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0032 | 2 | NA18961.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1968-6384T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001749 | ||||||
chr17:62001822
|
C | T | 1 | a0001c0003t0001g0302 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1968-6457G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001822 | ||||||
chr17:62001931
|
C | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1968-6566G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001931 | ||||||
chr17:62002298
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-6933A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002298 | ||||||
chr17:62002400
|
A | C | 4 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0051others(1): Show | 4 | NA18946.hp1 NA18951.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7035T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002400 | ||||||
chr17:62002489
|
C | CA | 105 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0083others(102): Show | 105 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1968-7125dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | ||||||
chr17:62002489
|
C | CAA | 10 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0162others(7): Show | 10 | HG01109.hp2 HG01175.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1968-7126_1968-712 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | ||||||
chr17:62002489
|
CAAAA | C | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-7128_1968-712 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | ||||||
chr17:62002528
|
C | G | 1 | a0001c0002t0001g0070 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1968-7163G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002528 | ||||||
chr17:62002563
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1968-7198G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002563 | ||||||
chr17:62002701
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7336G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002701 | ||||||
chr17:62002707
|
G | GA | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-7343dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002707 | ||||||
chr17:62002781
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1968-7416A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002781 | ||||||
chr17:62002886
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7521T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002886 | ||||||
chr17:62002944
|
T | C | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1968-7579A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002944 | ||||||
chr17:62003109
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1967+7441C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003109 | ||||||
chr17:62003148
|
A | AT | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1967+7401dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003148 | ||||||
chr17:62003149
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1967+7401A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003149 | ||||||
chr17:62003191
|
AT | A | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1967+7358delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003191 | ||||||
chr17:62003364
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1967+7186C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003364 | ||||||
chr17:62003417
|
C | T | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1967+7133G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003417 | ||||||
chr17:62003599
|
C | CA | 14 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0180others(11): Show | 14 | HG01175.hp2 HG02040.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1967+6950dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAA | 29 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(26): Show | 29 | HG00639.hp1 HG01952.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1967+6948_1967+695 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAAA | 18 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0118others(15): Show | 18 | HG01109.hp2 HG01346.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1967+6947_1967+695 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAAAA | 8 | a0001c0001t0002g0119a0001c0001t0002g0133a0001c0001t0002g0145others(5): Show | 8 | HG01081.hp1 HG01099.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967+6946_1967+695 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAAAAA | 107 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0123others(104): Show | 107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1967+6945_1967+695 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAAAAAA | 27 | a0001c0001t0002g0124a0001c0001t0002g0130a0001c0001t0002g0138others(24): Show | 27 | HG01175.hp1 HG01433.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1967+6944_1967+695 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0002g0147a0001c0001t0002g0205a0001c0001t0002g0206others(6): Show | 9 | HG02027.hp1 HG02257.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.1967+6943_1967+695 others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62003599
|
CA | C | 24 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0182others(21): Show | 24 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967+6950delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | ||||||
chr17:62004054
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1967+6496A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004054 | ||||||
chr17:62004246
|
T | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1967+6304A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004246 | ||||||
chr17:62004262
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1967+6288T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004262 | ||||||
chr17:62004280
|
A | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+6270T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004280 | ||||||
chr17:62004321
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1967+6229T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004321 | ||||||
chr17:62004611
|
G | C | 1 | a0001c0002t0001g0070 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1967+5939C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004611 | ||||||
chr17:62004832
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+5718G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004832 | ||||||
chr17:62004845
|
T | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1967+5705A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004845 | ||||||
chr17:62004847
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1967+5703C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004847 | ||||||
chr17:62004897
|
CT | C | 7 | a0001c0001t0001g0197a0001c0001t0001g0281a0001c0006t0001g0101others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+5652delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | ||||||
chr17:62004897
|
CTT | C | 68 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0088others(65): Show | 68 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1967+5651_1967+565 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | ||||||
chr17:62004897
|
CTTT | C | 171 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(168): Show | 171 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1967+5650_1967+565 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | ||||||
chr17:62004908
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1967+5642A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004908 | ||||||
chr17:62004931
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967+5619C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004931 | ||||||
chr17:62004987
|
G | A | 3 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0161 | 3 | NA18965.hp2 NA19012.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1967+5563C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004987 | ||||||
chr17:62005385
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0251 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1967+5165G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005385 | ||||||
chr17:62005523
|
G | T | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1967+5027C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005523 | ||||||
chr17:62005538
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1967+5012C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005538 | ||||||
chr17:62005555
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4995C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005555 | ||||||
chr17:62005566
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1967+4984T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005566 | ||||||
chr17:62005587
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967+4963G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005587 | ||||||
chr17:62005610
|
TAA | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1967+4938_1967+493 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005610 | ||||||
chr17:62005815
|
A | T | 4 | a0001c0003t0001g0294a0001c0003t0001g0299a0001c0003t0001g0305others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+4735T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005815 | ||||||
chr17:62005847
|
G | T | 95 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(92): Show | 95 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1967+4703C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005847 | ||||||
chr17:62005934
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4616C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005934 | ||||||
chr17:62005980
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4570C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005980 | ||||||
chr17:62006023
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1967+4527T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006023 | ||||||
chr17:62006198
|
G | GGACTTAA others(7): Show |
5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+4351_1967+435 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006198 | ||||||
chr17:62006213
|
G | A | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1967+4337C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006213 | ||||||
chr17:62006270
|
T | TA | 16 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0002g0130others(13): Show | 16 | HG01891.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1967+4279dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006270 | ||||||
chr17:62006270
|
TA | T | 9 | a0001c0001t0001g0083a0001c0001t0001g0276a0001c0002t0001g0042others(6): Show | 9 | HG01884.hp2 HG02040.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1967+4279delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006270 | ||||||
chr17:62006284
|
A | AG | 17 | a0001c0001t0001g0194a0001c0001t0001g0222a0001c0001t0001g0244others(14): Show | 17 | HG00558.hp1 HG00597.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1967+4265dupC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006284 | ||||||
chr17:62006285
|
G | A | 80 | a0001c0001t0001g0315a0001c0001t0002g0116a0001c0001t0002g0117others(77): Show | 80 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1967+4265C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006285 | ||||||
chr17:62006353
|
A | T | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1967+4197T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006353 | ||||||
chr17:62006374
|
C | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+4176G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006374 | ||||||
chr17:62006613
|
TTC | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1967+3935_1967+393 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006613 | ||||||
chr17:62006692
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+3858G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006692 | ||||||
chr17:62006904
|
G | A | 3 | a0001c0003t0001g0109a0001c0003t0001g0111a0001c0003t0001g0115 | 3 | HG02559.hp2 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1967+3646C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006904 | ||||||
chr17:62007112
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1967+3438C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007112 | ||||||
chr17:62007112
|
G | C | 2 | a0001c0004t0001g0163a0001c0004t0001g0164 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1967+3438C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007112 | ||||||
chr17:62007120
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1967+3430T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007120 | ||||||
chr17:62007273
|
C | T | 5 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1967+3277G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007273 | ||||||
chr17:62007368
|
A | T | 1 | a0001c0001t0001g0267 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1967+3182T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007368 | ||||||
chr17:62007436
|
A | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0251 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1967+3114T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007436 | ||||||
chr17:62007461
|
C | G | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1967+3089G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007461 | ||||||
chr17:62007575
|
G | A | 1 | a0001c0007t0005g0009 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1967+2975C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007575 | ||||||
chr17:62007582
|
T | C | 65 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0016others(62): Show | 65 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1967+2968A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007582 | ||||||
chr17:62007585
|
A | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1967+2965T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007585 | ||||||
chr17:62007634
|
G | C | 1 | a0001c0001t0002g0247 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1967+2916C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007634 | ||||||
chr17:62007729
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0196 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1967+2821G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007729 | ||||||
chr17:62007797
|
A | G | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1967+2753T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007797 | ||||||
chr17:62008016
|
C | CA | 10 | a0001c0001t0001g0086a0001c0001t0001g0186a0001c0001t0001g0195others(7): Show | 10 | HG01175.hp2 HG02523.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.1967+2533dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAA | 6 | a0001c0003t0001g0014a0001c0003t0001g0089a0001c0003t0001g0095others(3): Show | 6 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967+2529_1967+253 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAA | 52 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1967+2528_1967+253 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA | 41 | a0001c0001t0001g0077a0001c0001t0001g0118a0001c0001t0003g0290others(38): Show | 41 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1967+2527_1967+253 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(3): Show |
19 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(16): Show | 19 | HG00438.hp1 HG02071.hp1 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.1967+2524_1967+253 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(4): Show |
26 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(23): Show | 26 | HG00423.hp1 HG00642.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1967+2523_1967+253 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0128a0001c0001t0002g0145a0001c0001t0002g0147others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967+2522_1967+253 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0082a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG02976.hp2 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1967+2521_1967+253 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(7): Show |
1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1967+2520_1967+253 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0240a0001c0003t0001g0256a0001c0016t0001g0255others(1): Show | 4 | HG01109.hp2 HG01952.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+2518_1967+253 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0245 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1967+2517_1967+253 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(11): Show |
3 | a0001c0004t0001g0163a0001c0004t0001g0164a0002c0005t0001g0005 | 3 | HG01891.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1967+2516_1967+253 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(13): Show |
2 | a0001c0004t0001g0073a0002c0005t0001g0289 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1967+2514_1967+253 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(14): Show |
3 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0074 | 3 | HG03516.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1967+2533_1967+253 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(15): Show |
1 | a0001c0004t0001g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(16): Show |
1 | a0002c0005t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(17): Show |
1 | a0002c0005t0001g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(28): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(19): Show |
1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(25): Show |
1 | a0001c0003t0001g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(36): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(28): Show |
1 | a0002c0005t0001g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(39): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
C | CAAAAAAA others(29): Show |
1 | a0002c0005t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(40): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008016
|
CAA | C | 17 | a0001c0001t0001g0276a0001c0003t0001g0106a0001c0003t0001g0107others(14): Show | 17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1967+2532_1967+253 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | ||||||
chr17:62008039
|
T | C | 101 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1967+2511A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008039 | ||||||
chr17:62008043
|
C | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+2507G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008043 | ||||||
chr17:62008058
|
C | G | 1 | a0001c0002t0001g0050 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1967+2492G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008058 | ||||||
chr17:62008074
|
T | G | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1967+2476A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008074 | ||||||
chr17:62008125
|
G | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2425C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008125 | ||||||
chr17:62008266
|
A | C | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1967+2284T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008266 | ||||||
chr17:62008295
|
G | T | 1 | a0001c0001t0012g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1967+2255C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008295 | ||||||
chr17:62008304
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1967+2246G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008304 | ||||||
chr17:62008305
|
G | A | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2245C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008305 | ||||||
chr17:62008317
|
C | CA | 13 | a0001c0001t0001g0180a0001c0001t0001g0194a0001c0001t0001g0195others(10): Show | 13 | HG00597.hp1 HG03195.hp1 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.1967+2232dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(2): Show |
54 | a0001c0001t0002g0117a0001c0001t0002g0119a0001c0001t0002g0124others(51): Show | 54 | HG00423.hp2 HG00642.hp1 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.1967+2224_1967+223 others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(3): Show |
69 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245others(66): Show | 69 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1967+2223_1967+223 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(4): Show |
36 | a0001c0001t0002g0125a0001c0001t0002g0132a0001c0001t0002g0134others(33): Show | 36 | HG00438.hp1 HG00639.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1967+2222_1967+223 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0148others(9): Show | 12 | HG00438.hp2 HG00544.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1967+2221_1967+223 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0079a0001c0001t0002g0312a0001c0001t0011g0075others(4): Show | 7 | HG01978.hp1 HG02293.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2220_1967+223 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0053a0001c0003t0001g0303 | 2 | HG01243.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1967+2219_1967+223 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1967+2216_1967+223 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(13): Show |
1 | a0001c0007t0005g0010 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1967+2213_1967+223 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(14): Show |
1 | a0001c0007t0005g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1967+2212_1967+223 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(16): Show |
1 | a0006c0022t0005g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1967+2210_1967+223 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
C | CAAAAAAA others(21): Show |
1 | a0001c0007t0005g0009 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1967+2232_1967+223 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
CA | C | 8 | a0001c0001t0001g0118a0001c0001t0001g0183a0001c0001t0001g0187others(5): Show | 8 | HG01168.hp1 HG01168.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1967+2232delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008317
|
CAAAA | C | 7 | a0001c0001t0001g0315a0001c0004t0001g0071a0001c0004t0001g0072others(4): Show | 7 | HG01346.hp2 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967+2229_1967+223 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | ||||||
chr17:62008449
|
G | A | 2 | a0001c0008t0001g0210a0001c0008t0001g0213 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1967+2101C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008449 | ||||||
chr17:62008611
|
G | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+1939C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008611 | ||||||
chr17:62008699
|
C | G | 1 | a0001c0006t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1967+1851G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008699 | ||||||
chr17:62008861
|
A | G | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+1689T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008861 | ||||||
chr17:62009025
|
C | A | 208 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(205): Show | 208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1967+1525G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009025 | ||||||
chr17:62009147
|
G | C | 38 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0165others(35): Show | 38 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1967+1403C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009147 | ||||||
chr17:62009226
|
T | C | 3 | a0001c0003t0001g0302a0001c0003t0001g0303a0001c0013t0001g0304 | 3 | HG01243.hp2 HG03654.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1967+1324A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009226 | ||||||
chr17:62009324
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1967+1226C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009324 | ||||||
chr17:62009328
|
G | A | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1967+1222C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009328 | ||||||
chr17:62009565
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1967+985C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009565 | ||||||
chr17:62009624
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+926T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009624 | ||||||
chr17:62009653
|
G | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+897C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009653 | ||||||
chr17:62009721
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1967+829A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009721 | ||||||
chr17:62009834
|
T | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1967+716A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009834 | ||||||
chr17:62009837
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+713C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009837 | ||||||
chr17:62009847
|
T | C | 1 | a0001c0002t0001g0100 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1967+703A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009847 | ||||||
chr17:62009859
|
G | A | 1 | a0001c0008t0001g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1967+691C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009859 | ||||||
chr17:62009894
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1967+656C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009894 | ||||||
chr17:62009988
|
G | A | 65 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0016others(62): Show | 65 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1967+562C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009988 | ||||||
chr17:62010107
|
A | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+443T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010107 | ||||||
chr17:62010121
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1967+429G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010121 | ||||||
chr17:62010149
|
A | G | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1967+401T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010149 | ||||||
chr17:62010153
|
G | A | 5 | a0001c0001t0002g0152a0001c0007t0005g0009a0001c0007t0005g0010others(2): Show | 5 | HG02257.hp1 HG02698.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1967+397C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010153 | ||||||
chr17:62010168
|
C | T | 8 | a0001c0003t0001g0089a0001c0003t0001g0090a0001c0003t0001g0095others(5): Show | 8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967+382G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010168 | ||||||
chr17:62010216
|
C | CA | 7 | a0001c0001t0002g0156a0001c0004t0001g0071a0001c0004t0001g0072others(4): Show | 7 | HG02055.hp2 HG02071.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967+333dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010216 | ||||||
chr17:62010279
|
T | C | 1 | a0001c0001t0027g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1967+271A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010279 | ||||||
chr17:62011317
|
C | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1284-84G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011317 | ||||||
chr17:62011318
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1284-85C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011318 | ||||||
chr17:62011346
|
C | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-113G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011346 | ||||||
chr17:62011401
|
T | C | 9 | a0001c0003t0001g0014a0001c0003t0001g0089a0001c0003t0001g0090others(6): Show | 9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-168A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011401 | ||||||
chr17:62011454
|
C | G | 1 | a0001c0003t0001g0296 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1284-221G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011454 | ||||||
chr17:62011457
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1284-224T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011457 | ||||||
chr17:62011550
|
T | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-317A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011550 | ||||||
chr17:62011877
|
G | A | 14 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(11): Show | 14 | HG02027.hp1 HG02293.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.1284-644C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011877 | ||||||
chr17:62011911
|
A | G | 17 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(14): Show | 17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1284-678T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011911 | ||||||
chr17:62011975
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-742C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011975 | ||||||
chr17:62012088
|
C | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1284-855G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012088 | ||||||
chr17:62012215
|
C | CA | 7 | a0001c0001t0002g0134a0001c0001t0002g0153a0001c0001t0002g0154others(4): Show | 7 | HG00438.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-983dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012215 | ||||||
chr17:62012327
|
C | CT | 14 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0167others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1284-1095dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | ||||||
chr17:62012327
|
C | CTT | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-1096_1284-109 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | ||||||
chr17:62012327
|
CT | C | 64 | a0001c0001t0001g0183a0001c0001t0001g0211a0001c0001t0001g0227others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1284-1095delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | ||||||
chr17:62012327
|
CTT | C | 31 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0003t0001g0105others(28): Show | 31 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1284-1096_1284-109 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | ||||||
chr17:62012359
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-1126G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012359 | ||||||
chr17:62012422
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-1189C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012422 | ||||||
chr17:62012542
|
C | T | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-1309G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012542 | ||||||
chr17:62012552
|
A | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078 | 3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284-1319T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012552 | ||||||
chr17:62012619
|
C | T | 1 | a0001c0003t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1284-1386G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012619 | ||||||
chr17:62012620
|
G | A | 1 | a0001c0008t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284-1387C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012620 | ||||||
chr17:62012621
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284-1388A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012621 | ||||||
chr17:62012696
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1284-1463A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012696 | ||||||
chr17:62012705
|
C | CT | 5 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-1473dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012705 | ||||||
chr17:62012724
|
C | A | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-1491G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012724 | ||||||
chr17:62012760
|
C | T | 1 | a0001c0001t0021g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1284-1527G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012760 | ||||||
chr17:62012800
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1284-1567A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012800 | ||||||
chr17:62012838
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1284-1605C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012838 | ||||||
chr17:62012888
|
G | T | 2 | a0001c0002t0001g0064a0001c0002t0001g0066 | 2 | NA18960.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1284-1655C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012888 | ||||||
chr17:62013166
|
A | C | 2 | a0001c0001t0002g0147a0001c0001t0003g0144 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1284-1933T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013166 | ||||||
chr17:62013338
|
C | T | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-2105G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013338 | ||||||
chr17:62013637
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1284-2404G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013637 | ||||||
chr17:62013780
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1284-2547G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013780 | ||||||
chr17:62013854
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-2621G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013854 | ||||||
chr17:62014040
|
C | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1284-2807G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014040 | ||||||
chr17:62014042
|
C | T | 6 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-2809G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014042 | ||||||
chr17:62014130
|
T | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284-2897A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014130 | ||||||
chr17:62014169
|
T | C | 5 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-2936A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014169 | ||||||
chr17:62014308
|
T | TTATATAT others(3): Show |
1 | a0001c0006t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1284-3076_1284-307 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | ||||||
chr17:62014308
|
T | TTATATAT others(5): Show |
5 | a0001c0003t0001g0112a0001c0006t0001g0101a0001c0006t0001g0103others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | ||||||
chr17:62014308
|
T | TTATATAT others(7): Show |
2 | a0001c0003t0001g0105a0001c0003t0001g0108 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | ||||||
chr17:62014308
|
T | TTATATAT others(9): Show |
8 | a0001c0003t0001g0106a0001c0003t0001g0109a0001c0003t0001g0111others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | ||||||
chr17:62014308
|
T | TTATATAT others(11): Show |
3 | a0001c0003t0001g0107a0001c0003t0001g0110a0001c0003t0001g0115 | 3 | HG02809.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | ||||||
chr17:62014310
|
T | A | 21 | a0001c0001t0001g0315a0001c0003t0001g0105a0001c0003t0001g0106others(18): Show | 21 | HG00639.hp1 HG01346.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1284-3077A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTA | 89 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1284-3079_1284-307 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATA | 73 | a0001c0001t0002g0134a0001c0001t0002g0153a0001c0001t0002g0154others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1284-3081_1284-307 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATATA | 5 | a0001c0001t0001g0189a0001c0002t0001g0052a0001c0002t0001g0053others(2): Show | 5 | HG01109.hp2 HG02056.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-3083_1284-307 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATATAT others(5): Show |
4 | a0001c0004t0001g0073a0001c0004t0001g0074a0001c0004t0001g0080others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-3089_1284-307 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATATAT others(7): Show |
2 | a0001c0004t0001g0071a0001c0004t0001g0072 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1284-3091_1284-307 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATATAT others(31): Show |
1 | a0001c0004t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1284-3078_1284-307 others(42): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014310
|
T | TTATATAT others(57): Show |
1 | a0001c0004t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1284-3078_1284-307 others(68): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | ||||||
chr17:62014379
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-3146G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014379 | ||||||
chr17:62014520
|
T | C | 31 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(28): Show | 31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1284-3287A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014520 | ||||||
chr17:62014545
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1284-3312C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014545 | ||||||
chr17:62014596
|
C | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-3363G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014596 | ||||||
chr17:62014658
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3425A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014658 | ||||||
chr17:62014672
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3439A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014672 | ||||||
chr17:62014996
|
G | A | 24 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0182others(21): Show | 24 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1284-3763C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014996 | ||||||
chr17:62015215
|
G | A | 5 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0136others(2): Show | 5 | HG00642.hp1 HG01433.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3982C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015215 | ||||||
chr17:62015397
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-4164C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015397 | ||||||
chr17:62015504
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-4271C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015504 | ||||||
chr17:62015708
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1284-4475C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015708 | ||||||
chr17:62015786
|
T | C | 57 | a0001c0001t0001g0279a0001c0001t0002g0116a0001c0001t0002g0117others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1284-4553A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015786 | ||||||
chr17:62015819
|
T | TAC | 3 | a0001c0002t0009g0043a0001c0002t0024g0037a0001c0021t0017g0013 | 3 | HG00558.hp2 HG02083.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284-4588_1284-458 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015819 | ||||||
chr17:62015825
|
C | CACTA | 98 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(95): Show | 98 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1284-4593_1284-459 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015825 | ||||||
chr17:62015833
|
A | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-4600T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015833 | ||||||
chr17:62015834
|
T | C | 94 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(91): Show | 94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1284-4601A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015834 | ||||||
chr17:62015836
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-4603G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015836 | ||||||
chr17:62015865
|
GTA | G | 7 | a0001c0003t0001g0297a0002c0005t0001g0003a0002c0005t0001g0004others(4): Show | 7 | HG01099.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-4634_1284-463 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015865 | ||||||
chr17:62015867
|
A | ATG | 112 | a0001c0001t0001g0118a0001c0001t0003g0290a0001c0001t0003g0291others(109): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1284-4636_1284-463 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015867 | ||||||
chr17:62015879
|
A | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0027a0001c0002t0001g0028others(5): Show | 8 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4646T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015879 | ||||||
chr17:62015888
|
C | T | 109 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(106): Show | 109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1284-4655G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015888 | ||||||
chr17:62015890
|
C | T | 8 | a0001c0002t0001g0018a0001c0002t0001g0027a0001c0002t0001g0028others(5): Show | 8 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4657G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015890 | ||||||
chr17:62015902
|
T | C | 10 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0027others(7): Show | 10 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284-4669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015902 | ||||||
chr17:62015915
|
C | CACACACA others(9): Show |
1 | a0001c0001t0002g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1284-4683_1284-468 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CACATACA others(3): Show |
1 | a0001c0001t0002g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1284-4683_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CAT | 7 | a0001c0001t0001g0172a0001c0001t0001g0231a0001c0001t0001g0249others(4): Show | 7 | HG01358.hp1 HG01516.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-4684_1284-468 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATAT | 6 | a0001c0001t0001g0169a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00558.hp1 HG01346.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284-4686_1284-468 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATAT | 7 | a0001c0001t0001g0084a0001c0001t0001g0168a0001c0001t0001g0171others(4): Show | 7 | HG01934.hp1 HG01993.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284-4688_1284-468 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(1): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0258a0001c0001t0001g0261 | 3 | NA18948.hp1 NA18980.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1284-4690_1284-468 others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0276 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1284-4692_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(5): Show |
2 | a0001c0001t0004g0260a0001c0001t0004g0275 | 2 | NA18952.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1284-4694_1284-468 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0193 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1284-4696_1284-468 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(9): Show |
1 | a0001c0002t0001g0042 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1284-4698_1284-468 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
C | CATATATA others(15): Show |
1 | a0001c0001t0001g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1284-4704_1284-468 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0246 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1284-4692_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015915
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0001g0257 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1284-4696_1284-468 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | ||||||
chr17:62015917
|
T | C | 88 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(85): Show | 88 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1284-4684A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015917 | ||||||
chr17:62015917
|
T | TATATATA others(28): Show |
1 | a0001c0007t0005g0009 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1284-4685_1284-468 others(39): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015917 | ||||||
chr17:62015919
|
T | C | 15 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(12): Show | 15 | HG00438.hp1 HG00639.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284-4686A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015919 | ||||||
chr17:62015921
|
T | C | 2 | a0001c0001t0002g0119a0001c0001t0002g0138 | 2 | HG01175.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1284-4688A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015921 | ||||||
chr17:62015923
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1284-4690A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015923 | ||||||
chr17:62015925
|
T | TACACACA others(20): Show |
3 | a0001c0007t0005g0010a0001c0007t0005g0012a0006c0022t0005g0011 | 3 | HG02257.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1284-4693_1284-469 others(31): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015925 | ||||||
chr17:62015930
|
ATATATAT others(19): Show |
A | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0269 | 3 | NA18950.hp2 NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1284-4723_1284-469 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015930 | ||||||
chr17:62015932
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0008g0270 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1284-4724_1284-470 others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015932 | ||||||
chr17:62015932
|
ATATATAT others(33): Show |
A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-4739_1284-470 others(44): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015932 | ||||||
chr17:62015934
|
A | T | 2 | a0001c0002t0001g0038a0001c0003t0001g0309 | 2 | HG00639.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1284-4701T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015934 | ||||||
chr17:62015934
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-470 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015934 | ||||||
chr17:62015936
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0182a0001c0001t0001g0251 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1284-4726_1284-470 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | ||||||
chr17:62015936
|
ATATATAT others(17): Show |
A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-4727_1284-470 others(28): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | ||||||
chr17:62015936
|
ATATATAT others(24): Show |
A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1284-4734_1284-470 others(35): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | ||||||
chr17:62015938
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0015g0219 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1284-4727_1284-470 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015938 | ||||||
chr17:62015938
|
ATATATAT others(19): Show |
A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-4731_1284-470 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015938 | ||||||
chr17:62015940
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0233a0001c0001t0001g0243 | 2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1284-4727_1284-470 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015940 | ||||||
chr17:62015940
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1284-4728_1284-470 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015940 | ||||||
chr17:62015942
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284-4726_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | ||||||
chr17:62015942
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0022g0223 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1284-4727_1284-471 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | ||||||
chr17:62015942
|
ATATATAT others(15): Show |
A | 3 | a0001c0001t0001g0209a0001c0001t0002g0136a0001c0001t0002g0141 | 3 | HG00642.hp1 HG01433.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | ||||||
chr17:62015944
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0284 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-471 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | ||||||
chr17:62015944
|
ATATATAT others(13): Show |
A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-4731_1284-471 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | ||||||
chr17:62015944
|
ATATATAT others(15): Show |
A | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-471 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | ||||||
chr17:62015946
|
ATATATAT others(10): Show |
A | 1 | a0001c0016t0001g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1284-4730_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | ||||||
chr17:62015946
|
ATATATAT others(11): Show |
A | 2 | a0002c0005t0001g0003a0002c0005t0001g0005 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | ||||||
chr17:62015946
|
ATATATAT others(12): Show |
A | 4 | a0001c0001t0002g0128a0001c0003t0001g0201a0001c0003t0001g0202others(1): Show | 4 | HG02717.hp2 HG02735.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-4732_1284-471 others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | ||||||
chr17:62015948
|
A | T | 5 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0003t0001g0296others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4715T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015948
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0176a0001c0001t0001g0184 | 2 | HG00642.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1284-4725_1284-471 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015948
|
ATATATAT others(8): Show |
A | 1 | a0001c0003t0001g0256 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1284-4730_1284-471 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015948
|
ATATATAT others(9): Show |
A | 2 | a0002c0005t0001g0004a0002c0005t0001g0006 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015948
|
ATATATAT others(13): Show |
A | 1 | a0001c0003t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1284-4735_1284-471 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015948
|
ATATATAT others(14): Show |
A | 1 | a0001c0002t0001g0038 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1284-4736_1284-471 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | ||||||
chr17:62015950
|
A | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0067a0001c0003t0001g0303 | 3 | HG01243.hp2 NA18954.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1284-4717T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0287a0008c0015t0014g0199 | 2 | HG01358.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1284-4727_1284-471 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-4729_1284-471 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(8): Show |
A | 1 | a0001c0006t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1284-4732_1284-471 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(9): Show |
A | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-471 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(10): Show |
A | 1 | a0001c0003t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1284-4734_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015950
|
ATATATTT others(14): Show |
A | 1 | a0001c0002t0024g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1284-4738_1284-471 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | ||||||
chr17:62015951
|
TATA | T | 13 | a0001c0001t0003g0290a0001c0001t0003g0295a0001c0001t0003g0300others(10): Show | 13 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284-4721_1284-471 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015951 | ||||||
chr17:62015952
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1284-4719T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | ||||||
chr17:62015952
|
ATATTTTT others(5): Show |
A | 1 | a0002c0005t0001g0122 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1284-4731_1284-472 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | ||||||
chr17:62015952
|
ATATTTTT others(6): Show |
A | 5 | a0001c0001t0002g0130a0001c0001t0010g0150a0001c0003t0001g0112others(2): Show | 5 | HG01891.hp2 HG02602.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4732_1284-472 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | ||||||
chr17:62015952
|
ATATTTTT others(8): Show |
A | 1 | a0001c0003t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1284-4734_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | ||||||
chr17:62015953
|
TA | T | 22 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0002t0001g0001others(19): Show | 22 | HG00597.hp2 HG02027.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.1284-4721delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015953 | ||||||
chr17:62015954
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0272 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0026g0034 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0041 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0244 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
A | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0246a0001c0002t0001g0030others(1): Show | 4 | HG01934.hp2 HG01993.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4721T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
AT | A | 10 | a0001c0001t0001g0087a0001c0001t0001g0162a0001c0001t0001g0177others(7): Show | 10 | HG00438.hp1 HG02071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4722delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATT | A | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0194others(7): Show | 10 | HG00140.hp1 HG00597.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTT | A | 15 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0001g0226others(12): Show | 15 | HG01099.hp1 HG01175.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284-4724_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTT | A | 10 | a0001c0001t0001g0082a0001c0001t0001g0170a0001c0001t0001g0183others(7): Show | 10 | HG01168.hp1 HG02922.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284-4725_1284-472 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTT | A | 19 | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0186others(16): Show | 19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1284-4726_1284-472 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT | A | 9 | a0001c0001t0001g0088a0001c0001t0001g0220a0001c0001t0002g0154others(6): Show | 9 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-4728_1284-472 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(2): Show |
A | 8 | a0001c0001t0001g0076a0001c0003t0001g0090a0001c0003t0001g0095others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4730_1284-472 others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(4): Show | 7 | HG02055.hp2 HG02300.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284-4731_1284-472 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0010g0149a0001c0006t0001g0101a0001c0006t0001g0103others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-4732_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0004t0001g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-472 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0003t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1284-4734_1284-472 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1284-4735_1284-472 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015954
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0003t0001g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1284-4736_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | ||||||
chr17:62015955
|
T | TA | 9 | a0001c0001t0001g0083a0001c0001t0002g0119a0001c0001t0002g0126others(6): Show | 9 | HG02622.hp1 HG03540.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | ||||||
chr17:62015955
|
T | TATA | 12 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0278others(9): Show | 12 | HG02056.hp2 HG02083.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | ||||||
chr17:62015955
|
T | TATATA | 3 | a0001c0001t0001g0173a0001c0001t0002g0139a0001c0001t0002g0247 | 3 | HG01928.hp1 NA18948.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | ||||||
chr17:62015955
|
T | TATATATA | 5 | a0001c0001t0002g0207a0001c0001t0012g0143a0001c0001t0021g0129others(2): Show | 5 | HG02572.hp1 HG02970.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | ||||||
chr17:62015955
|
T | TATATATA others(4): Show |
3 | a0001c0001t0001g0189a0001c0001t0003g0250a0001c0001t0025g0008 | 3 | HG02027.hp2 HG02895.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | ||||||
chr17:62015956
|
T | A | 44 | a0001c0001t0001g0084a0001c0001t0001g0168a0001c0001t0001g0169others(41): Show | 44 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1284-4723A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015956 | ||||||
chr17:62015957
|
T | A | 77 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0162others(74): Show | 77 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1284-4724A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015957 | ||||||
chr17:62015957
|
T | TA | 16 | a0001c0002t0001g0020a0001c0002t0001g0023a0001c0002t0001g0027others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-4725_1284-472 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015957 | ||||||
chr17:62015958
|
T | A | 41 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(38): Show | 41 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1284-4725A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015958 | ||||||
chr17:62015959
|
T | A | 104 | a0001c0001t0001g0087a0001c0001t0001g0173a0001c0001t0001g0174others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1284-4726A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015959 | ||||||
chr17:62015959
|
T | TATA | 10 | a0001c0002t0001g0015a0001c0002t0001g0017a0001c0002t0001g0019others(7): Show | 10 | HG00544.hp1 HG02080.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4727_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015959 | ||||||
chr17:62015960
|
T | A | 45 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0085others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1284-4727A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015960 | ||||||
chr17:62015961
|
T | A | 120 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0186others(117): Show | 120 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1284-4728A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015961 | ||||||
chr17:62015962
|
T | A | 32 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0183others(29): Show | 32 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1284-4729A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015962 | ||||||
chr17:62015963
|
T | A | 123 | a0001c0001t0001g0195a0001c0001t0001g0245a0001c0001t0002g0119others(120): Show | 123 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284-4730A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015963 | ||||||
chr17:62015964
|
T | A | 25 | a0001c0001t0001g0082a0001c0001t0001g0240a0001c0001t0002g0132others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1284-4731A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015964 | ||||||
chr17:62015965
|
T | A | 118 | a0001c0001t0001g0076a0001c0001t0002g0119a0001c0001t0002g0126others(115): Show | 118 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1284-4732A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015965 | ||||||
chr17:62015966
|
T | A | 20 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(17): Show | 20 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1284-4733A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015966 | ||||||
chr17:62015967
|
T | A | 100 | a0001c0001t0001g0076a0001c0001t0002g0134a0001c0001t0002g0145others(97): Show | 100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1284-4734A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015967 | ||||||
chr17:62015968
|
T | A | 13 | a0001c0001t0001g0079a0001c0001t0002g0161a0001c0001t0011g0075others(10): Show | 13 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284-4735A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015968 | ||||||
chr17:62015969
|
T | A | 72 | a0001c0001t0002g0145a0001c0002t0001g0001a0001c0002t0001g0015others(69): Show | 72 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1284-4736A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015969 | ||||||
chr17:62015969
|
T | TATATATA others(6): Show |
1 | a0001c0002t0001g0016 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1284-4737_1284-473 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015969 | ||||||
chr17:62015970
|
T | A | 9 | a0001c0002t0001g0022a0001c0002t0001g0030a0001c0002t0001g0032others(6): Show | 9 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-4737A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015970 | ||||||
chr17:62015971
|
T | A | 16 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0023others(13): Show | 16 | HG02132.hp1 HG02622.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-4738A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015971 | ||||||
chr17:62015993
|
C | T | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-4760G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015993 | ||||||
chr17:62016061
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG03130.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4828G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016061 | ||||||
chr17:62016165
|
C | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4932G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016165 | ||||||
chr17:62016172
|
C | CA | 22 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(19): Show | 22 | HG01952.hp1 HG02071.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1284-4940dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016172 | ||||||
chr17:62016174
|
AC | A | 3 | a0001c0001t0001g0315a0001c0003t0001g0106a0010c0011t0001g0239 | 3 | HG01346.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1284-4942delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016174 | ||||||
chr17:62016175
|
C | A | 104 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(101): Show | 104 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.1284-4942G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016175 | ||||||
chr17:62016177
|
A | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0137 | 2 | NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1284-4944T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016177 | ||||||
chr17:62016178
|
C | A | 107 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1284-4945G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016178 | ||||||
chr17:62016181
|
A | C | 102 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0230others(99): Show | 102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1284-4948T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016181 | ||||||
chr17:62016183
|
A | C | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1284-4950T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016183 | ||||||
chr17:62016371
|
G | C | 1 | a0001c0003t0001g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1284-5138C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016371 | ||||||
chr17:62016521
|
T | C | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-5288A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016521 | ||||||
chr17:62016522
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-5289G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016522 | ||||||
chr17:62016666
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1284-5433T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016666 | ||||||
chr17:62016785
|
G | C | 1 | a0001c0007t0005g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1284-5552C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016785 | ||||||
chr17:62017033
|
T | A | 31 | a0001c0002t0001g0018a0001c0002t0001g0023a0001c0002t0001g0027others(28): Show | 31 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1284-5800A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017033 | ||||||
chr17:62017179
|
T | C | 1 | a0001c0003t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1284-5946A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017179 | ||||||
chr17:62017219
|
T | TA | 88 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0001g0324others(85): Show | 88 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1284-5987dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | ||||||
chr17:62017219
|
T | TAA | 16 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(13): Show | 16 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-5988_1284-598 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | ||||||
chr17:62017219
|
TA | T | 72 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(69): Show | 72 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1284-5987delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | ||||||
chr17:62017243
|
A | G | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG02258.hp1 HG02300.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-6010T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017243 | ||||||
chr17:62017303
|
G | A | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1284-6070C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017303 | ||||||
chr17:62017352
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1284-6119T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017352 | ||||||
chr17:62017378
|
G | C | 4 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0012g0143others(1): Show | 4 | HG02056.hp2 NA19079.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-6145C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017378 | ||||||
chr17:62017446
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1284-6213A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017446 | ||||||
chr17:62017546
|
T | C | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-6313A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017546 | ||||||
chr17:62017813
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-6580A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017813 | ||||||
chr17:62017870
|
T | C | 2 | a0001c0003t0007g0298a0001c0003t0007g0325 | 2 | HG00438.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1284-6637A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017870 | ||||||
chr17:62017941
|
T | C | 1 | a0001c0002t0023g0039 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1284-6708A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017941 | ||||||
chr17:62017954
|
G | A | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1284-6721C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017954 | ||||||
chr17:62018136
|
G | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-6903C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018136 | ||||||
chr17:62018224
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1284-6991A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018224 | ||||||
chr17:62018355
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1284-7122T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018355 | ||||||
chr17:62018359
|
C | G | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG02258.hp1 HG02300.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-7126G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018359 | ||||||
chr17:62018438
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0238 | 2 | HG01167.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1284-7205G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018438 | ||||||
chr17:62018446
|
T | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-7213A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018446 | ||||||
chr17:62018561
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-7328T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018561 | ||||||
chr17:62018575
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-7342C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018575 | ||||||
chr17:62018715
|
C | CA | 122 | a0001c0001t0001g0088a0001c0001t0001g0175a0001c0001t0001g0176others(119): Show | 122 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1284-7483dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018715 | ||||||
chr17:62018715
|
CA | C | 8 | a0001c0001t0002g0205a0002c0005t0001g0003a0002c0005t0001g0004others(5): Show | 8 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-7483delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018715 | ||||||
chr17:62018888
|
A | C | 39 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0162others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1284-7655T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018888 | ||||||
chr17:62018954
|
GATCC | G | 4 | a0001c0003t0001g0293a0001c0003t0001g0297a0001c0003t0001g0307others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-7725_1284-772 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018954 | ||||||
chr17:62019201
|
T | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1284-7968A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019201 | ||||||
chr17:62019384
|
TATAA | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284-8155_1284-815 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019384 | ||||||
chr17:62019390
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1284-8157A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019390 | ||||||
chr17:62019428
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1284-8195A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019428 | ||||||
chr17:62019441
|
A | G | 1 | a0001c0002t0023g0039 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1284-8208T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019441 | ||||||
chr17:62019720
|
G | A | 85 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(82): Show | 85 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1284-8487C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019720 | ||||||
chr17:62019746
|
C | CT | 11 | a0001c0001t0001g0253a0001c0001t0002g0138a0001c0001t0002g0312others(8): Show | 11 | HG01175.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1284-8514dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019746 | ||||||
chr17:62019845
|
G | A | 1 | a0001c0003t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1284-8612C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019845 | ||||||
chr17:62019947
|
C | A | 8 | a0001c0003t0001g0089a0001c0003t0001g0090a0001c0003t0001g0095others(5): Show | 8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-8714G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019947 | ||||||
chr17:62019948
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1284-8715C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019948 | ||||||
chr17:62020035
|
C | T | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-8802G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020035 | ||||||
chr17:62020231
|
CT | C | 105 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(102): Show | 105 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1284-8999delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020231 | ||||||
chr17:62020256
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1284-9023T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020256 | ||||||
chr17:62020296
|
C | A | 97 | a0001c0001t0001g0191a0001c0001t0003g0290a0001c0001t0003g0291others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1284-9063G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020296 | ||||||
chr17:62020438
|
A | G | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+9103T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020438 | ||||||
chr17:62020533
|
C | T | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1283+9008G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020533 | ||||||
chr17:62020560
|
T | C | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1283+8981A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020560 | ||||||
chr17:62020580
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1283+8961G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020580 | ||||||
chr17:62020600
|
C | T | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283+8941G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020600 | ||||||
chr17:62020601
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1283+8940C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020601 | ||||||
chr17:62020633
|
C | G | 1 | a0001c0001t0002g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1283+8908G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020633 | ||||||
chr17:62020658
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+8883G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020658 | ||||||
chr17:62020685
|
C | CT | 11 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0246others(8): Show | 11 | HG00423.hp1 HG00642.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1283+8855dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020685 | ||||||
chr17:62020685
|
CT | C | 9 | a0001c0001t0001g0175a0001c0001t0001g0230a0001c0001t0001g0258others(6): Show | 9 | HG01168.hp1 HG01168.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1283+8855delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020685 | ||||||
chr17:62020687
|
T | C | 1 | a0001c0018t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1283+8854A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020687 | ||||||
chr17:62020703
|
T | C | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+8838A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020703 | ||||||
chr17:62020706
|
TA | T | 9 | a0001c0001t0002g0116a0001c0001t0002g0145a0001c0001t0002g0247others(6): Show | 9 | HG01081.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+8834delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020706 | ||||||
chr17:62020707
|
A | T | 185 | a0001c0001t0001g0082a0001c0001t0001g0191a0001c0001t0001g0209others(182): Show | 185 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.1283+8834T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020707 | ||||||
chr17:62020726
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+8815A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020726 | ||||||
chr17:62020733
|
C | G | 2 | a0001c0003t0001g0095a0001c0003t0001g0323 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1283+8808G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020733 | ||||||
chr17:62020741
|
T | G | 2 | a0001c0003t0001g0095a0001c0003t0001g0323 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1283+8800A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020741 | ||||||
chr17:62020849
|
T | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG00423.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1283+8692A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020849 | ||||||
chr17:62020872
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1283+8669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020872 | ||||||
chr17:62020895
|
T | G | 29 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+8646A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020895 | ||||||
chr17:62021066
|
G | A | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+8475C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021066 | ||||||
chr17:62021255
|
G | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+8286C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021255 | ||||||
chr17:62021278
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1283+8263G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021278 | ||||||
chr17:62021284
|
ACCTCCCG others(93): Show |
A | 2 | a0001c0002t0001g0038a0001c0002t0001g0321 | 2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1283+8157_1283+825 others(104): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021284 | ||||||
chr17:62021344
|
A | G | 323 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(320): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.1283+8197T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021344 | ||||||
chr17:62021356
|
C | T | 202 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(199): Show | 202 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1283+8185G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021356 | ||||||
chr17:62021360
|
C | T | 1 | a0001c0001t0012g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1283+8181G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021360 | ||||||
chr17:62021375
|
TCCCCACC others(42): Show |
T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+8117_1283+816 others(53): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021375 | ||||||
chr17:62021391
|
G | A | 100 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(97): Show | 100 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1283+8150C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021391 | ||||||
chr17:62021408
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0003g0250 | 2 | HG01358.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1283+8133C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021408 | ||||||
chr17:62021428
|
C | A | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1283+8113G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021428 | ||||||
chr17:62021503
|
C | T | 24 | a0001c0002t0024g0037a0001c0003t0001g0105a0001c0003t0001g0106others(21): Show | 24 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1283+8038G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021503 | ||||||
chr17:62021504
|
G | A | 11 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(8): Show | 11 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1283+8037C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021504 | ||||||
chr17:62021521
|
C | T | 2 | a0001c0001t0002g0136a0001c0001t0002g0141 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1283+8020G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021521 | ||||||
chr17:62021628
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1283+7913G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021628 | ||||||
chr17:62021777
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+7764G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021777 | ||||||
chr17:62021797
|
G | A | 2 | a0002c0005t0001g0121a0002c0005t0001g0122 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1283+7744C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021797 | ||||||
chr17:62021939
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+7602G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021939 | ||||||
chr17:62021982
|
C | A | 1 | a0002c0005t0001g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1283+7559G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021982 | ||||||
chr17:62022152
|
A | C | 1 | a0001c0001t0001g0244 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1283+7389T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022152 | ||||||
chr17:62022165
|
C | CA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(6): Show | 9 | HG01106.hp1 HG01346.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+7375dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022165 | ||||||
chr17:62022172
|
A | T | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+7369T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022172 | ||||||
chr17:62022173
|
AAAT | A | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022173 | ||||||
chr17:62022174
|
A | AAT | 60 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0166others(57): Show | 60 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | ||||||
chr17:62022174
|
A | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0162a0001c0001t0001g0165others(2): Show | 5 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1283+7367T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | ||||||
chr17:62022174
|
AAT | A | 90 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(87): Show | 90 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | ||||||
chr17:62022175
|
AT | A | 90 | a0001c0001t0001g0191a0001c0001t0003g0290a0001c0001t0003g0291others(87): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1283+7365delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022175 | ||||||
chr17:62022175
|
ATAT | A | 3 | a0001c0001t0001g0118a0001c0001t0002g0157a0001c0001t0020g0135 | 3 | HG02258.hp1 NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1283+7363_1283+736 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022175 | ||||||
chr17:62022176
|
T | A | 46 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1283+7365A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022176 | ||||||
chr17:62022178
|
T | A | 182 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(179): Show | 182 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1283+7363A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022178 | ||||||
chr17:62022180
|
T | A | 99 | a0001c0001t0001g0191a0001c0001t0002g0123a0001c0001t0002g0124others(96): Show | 99 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1283+7361A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022180 | ||||||
chr17:62022182
|
T | A | 3 | a0001c0003t0001g0109a0001c0003t0001g0111a0001c0003t0001g0115 | 3 | HG02559.hp2 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1283+7359A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022182 | ||||||
chr17:62022216
|
G | A | 97 | a0001c0001t0001g0191a0001c0001t0003g0290a0001c0001t0003g0291others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+7325C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022216 | ||||||
chr17:62022447
|
C | A | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+7094G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022447 | ||||||
chr17:62022588
|
A | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+6953T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022588 | ||||||
chr17:62022675
|
A | G | 14 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(11): Show | 14 | HG02155.hp2 HG02280.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1283+6866T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022675 | ||||||
chr17:62022751
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1283+6790A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022751 | ||||||
chr17:62022875
|
A | T | 324 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(321): Show | 324 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.1283+6666T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022875 | ||||||
chr17:62023017
|
A | T | 1 | a0001c0002t0001g0070 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1283+6524T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023017 | ||||||
chr17:62023112
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1283+6429C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023112 | ||||||
chr17:62023317
|
T | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+6224A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023317 | ||||||
chr17:62023604
|
C | T | 4 | a0001c0003t0006g0092a0001c0003t0006g0093a0001c0003t0006g0094others(1): Show | 4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+5937G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023604 | ||||||
chr17:62023698
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+5843G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023698 | ||||||
chr17:62023735
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1283+5806C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023735 | ||||||
chr17:62023739
|
GCC | G | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+5800_1283+580 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023739 | ||||||
chr17:62023745
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1283+5796G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023745 | ||||||
chr17:62023800
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0245 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1283+5741T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023800 | ||||||
chr17:62023864
|
A | T | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1283+5677T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023864 | ||||||
chr17:62023944
|
C | T | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+5597G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023944 | ||||||
chr17:62023958
|
A | G | 3 | a0001c0001t0002g0151a0001c0001t0002g0158a0001c0001t0013g0316 | 3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1283+5583T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023958 | ||||||
chr17:62023985
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1283+5556A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023985 | ||||||
chr17:62024020
|
T | C | 10 | a0001c0001t0001g0246a0001c0001t0001g0258a0001c0001t0001g0265others(7): Show | 10 | HG00558.hp1 HG02083.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1283+5521A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024020 | ||||||
chr17:62024021
|
G | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1283+5520C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024021 | ||||||
chr17:62024023
|
C | CT | 102 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(99): Show | 102 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1283+5517dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024023 | ||||||
chr17:62024023
|
C | CTT | 97 | a0001c0001t0001g0191a0001c0001t0002g0157a0001c0001t0003g0290others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+5516_1283+551 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024023 | ||||||
chr17:62024078
|
C | T | 29 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+5463G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024078 | ||||||
chr17:62024091
|
C | G | 1 | a0001c0004t0001g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1283+5450G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024091 | ||||||
chr17:62024181
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0229 | 2 | NA18982.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1283+5360G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024181 | ||||||
chr17:62024210
|
A | T | 2 | a0001c0002t0001g0038a0001c0002t0001g0321 | 2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1283+5331T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024210 | ||||||
chr17:62024211
|
T | G | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1283+5330A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024211 | ||||||
chr17:62024382
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1283+5159G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024382 | ||||||
chr17:62024487
|
G | A | 97 | a0001c0001t0001g0191a0001c0001t0003g0290a0001c0001t0003g0291others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+5054C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024487 | ||||||
chr17:62024534
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1283+5007T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024534 | ||||||
chr17:62024655
|
T | C | 29 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(26): Show | 29 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+4886A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024655 | ||||||
chr17:62024661
|
A | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+4880T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024661 | ||||||
chr17:62024714
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0196 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1283+4827A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024714 | ||||||
chr17:62025127
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1283+4414C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025127 | ||||||
chr17:62025336
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+4205G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025336 | ||||||
chr17:62025416
|
C | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+4125G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025416 | ||||||
chr17:62025606
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1283+3935C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025606 | ||||||
chr17:62025618
|
C | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+3923G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025618 | ||||||
chr17:62025641
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1283+3900C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025641 | ||||||
chr17:62025668
|
T | A | 209 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(206): Show | 209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+3873A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025668 | ||||||
chr17:62025695
|
C | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+3846G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025695 | ||||||
chr17:62025753
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1283+3788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025753 | ||||||
chr17:62025820
|
C | T | 1 | a0002c0005t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1283+3721G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025820 | ||||||
chr17:62026272
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0013g0120 | 2 | NA19058.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1283+3269C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026272 | ||||||
chr17:62026478
|
T | TA | 9 | a0001c0001t0001g0228a0001c0002t0001g0052a0001c0003t0001g0323others(6): Show | 9 | HG02056.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+3062dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026478 | ||||||
chr17:62026545
|
C | T | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1283+2996G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026545 | ||||||
chr17:62026791
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+2750G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026791 | ||||||
chr17:62026901
|
A | G | 1 | a0001c0004t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1283+2640T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026901 | ||||||
chr17:62026970
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1283+2571G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026970 | ||||||
chr17:62027108
|
A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1283+2433T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027108 | ||||||
chr17:62027264
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1283+2277C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027264 | ||||||
chr17:62027311
|
G | A | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+2230C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027311 | ||||||
chr17:62027312
|
C | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+2229G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027312 | ||||||
chr17:62027399
|
C | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+2142G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027399 | ||||||
chr17:62027531
|
C | A | 1 | a0001c0008t0001g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1283+2010G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027531 | ||||||
chr17:62027536
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1283+2005G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027536 | ||||||
chr17:62027606
|
T | C | 1 | a0004c0023t0001g0216 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1283+1935A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027606 | ||||||
chr17:62027623
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1283+1918A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027623 | ||||||
chr17:62027713
|
A | T | 15 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0025others(12): Show | 15 | HG00423.hp2 HG00558.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1283+1828T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027713 | ||||||
chr17:62027770
|
T | C | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1283+1771A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027770 | ||||||
chr17:62027865
|
A | AT | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+1675dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027865 | ||||||
chr17:62027869
|
C | A | 7 | a0001c0001t0001g0258a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG00558.hp1 NA18948.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1283+1672G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027869 | ||||||
chr17:62028099
|
G | A | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+1442C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028099 | ||||||
chr17:62028110
|
C | G | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+1431G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028110 | ||||||
chr17:62028112
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1283+1429C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028112 | ||||||
chr17:62028283
|
A | G | 1 | a0001c0001t0015g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1283+1258T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028283 | ||||||
chr17:62028323
|
A | G | 1 | a0001c0004t0001g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1283+1218T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028323 | ||||||
chr17:62028489
|
T | C | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+1052A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028489 | ||||||
chr17:62028553
|
T | TA | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+987dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028553 | ||||||
chr17:62028560
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1283+981T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028560 | ||||||
chr17:62028623
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | NA18945.hp1 NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1283+918A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028623 | ||||||
chr17:62028679
|
T | TA | 8 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0001g0231others(5): Show | 8 | HG01106.hp2 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1283+861dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028679 | ||||||
chr17:62028679
|
TA | T | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0002c0005t0001g0003others(3): Show | 6 | HG00558.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1283+861delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028679 | ||||||
chr17:62028804
|
C | G | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1283+737G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028804 | ||||||
chr17:62028863
|
A | G | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+678T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028863 | ||||||
chr17:62028907
|
T | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1283+634A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028907 | ||||||
chr17:62029038
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+503T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029038 | ||||||
chr17:62029041
|
A | G | 1 | a0001c0001t0003g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1283+500T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029041 | ||||||
chr17:62029105
|
G | C | 1 | a0001c0003t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1283+436C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029105 | ||||||
chr17:62029315
|
A | G | 1 | a0001c0001t0014g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1283+226T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029315 | ||||||
chr17:62029420
|
TC | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+120delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029420 | ||||||
chr17:62029474
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1283+67C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029474 | ||||||
chr17:62029484
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1283+57A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029484 | ||||||
chr17:62029493
|
G | A | 27 | a0001c0001t0001g0082a0001c0003t0001g0105a0001c0003t0001g0106others(24): Show | 27 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1283+48C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029493 | ||||||
chr17:62029511
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+30A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029511 | ||||||
chr17:62030194
|
T | C | 2 | a0001c0001t0002g0147a0001c0001t0003g0144 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1010-181A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030194 | ||||||
chr17:62030309
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-296C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030309 | ||||||
chr17:62030522
|
A | T | 1 | a0001c0001t0003g0300 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1010-509T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030522 | ||||||
chr17:62031151
|
G | C | 1 | a0001c0002t0001g0015 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1009+293C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62031151 | ||||||
chr17:62031197
|
G | A | 1 | a0001c0002t0001g0038 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1009+247C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62031197 | ||||||
chr17:62031675
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.815-37G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031675 | ||||||
chr17:62031680
|
T | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-42A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031680 | ||||||
chr17:62031796
|
CT | C | 55 | a0001c0001t0001g0082a0001c0001t0001g0226a0001c0001t0002g0116others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815-159delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031796 | ||||||
chr17:62032167
|
C | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0288 | 2 | NA18980.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.815-529G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032167 | ||||||
chr17:62032479
|
G | GA | 12 | a0001c0001t0001g0191a0001c0001t0001g0211a0001c0001t0001g0214others(9): Show | 12 | HG00140.hp1 HG01109.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.815-842dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032479 | ||||||
chr17:62032479
|
GA | G | 29 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0022others(26): Show | 29 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.815-842delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032479 | ||||||
chr17:62032516
|
C | T | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.815-878G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032516 | ||||||
chr17:62032583
|
C | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-945G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032583 | ||||||
chr17:62033045
|
A | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.814+742T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033045 | ||||||
chr17:62033068
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.814+719A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033068 | ||||||
chr17:62033076
|
G | T | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.814+711C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033076 | ||||||
chr17:62033090
|
T | G | 3 | a0001c0001t0002g0151a0001c0001t0002g0158a0001c0001t0013g0316 | 3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.814+697A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033090 | ||||||
chr17:62033140
|
G | A | 1 | a0001c0008t0001g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.814+647C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033140 | ||||||
chr17:62033401
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.814+386A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033401 | ||||||
chr17:62033416
|
A | G | 2 | a0001c0003t0001g0305a0001c0003t0001g0306 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.814+371T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033416 | ||||||
chr17:62033565
|
T | C | 2 | a0001c0001t0010g0149a0001c0001t0010g0150 | 2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.814+222A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033565 | ||||||
chr17:62033751
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.814+36G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033751 | ||||||
chr17:62034107
|
A | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.617-123T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034107 | ||||||
chr17:62034486
|
CA | C | 233 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(230): Show | 233 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.617-503delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034486 | ||||||
chr17:62034496
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.617-512T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034496 | ||||||
chr17:62034666
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.617-682A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034666 | ||||||
chr17:62034680
|
A | G | 1 | a0004c0023t0001g0216 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.617-696T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034680 | ||||||
chr17:62034731
|
G | T | 1 | a0001c0002t0001g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.616+732C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034731 | ||||||
chr17:62035104
|
G | C | 1 | a0001c0018t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.616+359C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62035104 | ||||||
chr17:62035116
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.616+347C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62035116 | ||||||
chr17:62035722
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0007g0002 | 2 | HG01099.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.471-114G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62035722 | ||||||
chr17:62035881
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.471-273T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62035881 | ||||||
chr17:62036090
|
C | CT | 93 | a0001c0001t0003g0290a0001c0001t0003g0295a0001c0001t0003g0300others(90): Show | 93 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.471-483dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036090 | ||||||
chr17:62036105
|
A | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0285 | 3 | NA18948.hp2 NA18966.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.471-497T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036105 | ||||||
chr17:62036373
|
G | A | 20 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(17): Show | 20 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.471-765C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036373 | ||||||
chr17:62036424
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-816A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036424 | ||||||
chr17:62036460
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-852C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036460 | ||||||
chr17:62036466
|
T | G | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.471-858A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036466 | ||||||
chr17:62036481
|
A | AGAAAATA others(352): Show |
1 | a0001c0003t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471-874_471-873ins others(359): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036481 | ||||||
chr17:62036862
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-1254C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036862 | ||||||
chr17:62036869
|
G | C | 2 | a0002c0005t0001g0121a0002c0005t0001g0122 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.471-1261C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036869 | ||||||
chr17:62037065
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.471-1457T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037065 | ||||||
chr17:62037162
|
C | T | 4 | a0001c0003t0006g0092a0001c0003t0006g0093a0001c0003t0006g0094others(1): Show | 4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-1554G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037162 | ||||||
chr17:62037419
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-1811G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037419 | ||||||
chr17:62037495
|
T | C | 1 | a0001c0002t0001g0023 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.471-1887A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037495 | ||||||
chr17:62037522
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.471-1914C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037522 | ||||||
chr17:62037528
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-1920C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037528 | ||||||
chr17:62037666
|
C | CA | 8 | a0001c0001t0001g0082a0001c0001t0001g0209a0001c0001t0001g0240others(5): Show | 8 | HG01346.hp2 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.471-2059dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037666 | ||||||
chr17:62037666
|
CA | C | 6 | a0001c0001t0001g0171a0001c0001t0001g0175a0001c0007t0005g0009others(3): Show | 6 | HG01993.hp1 HG02257.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471-2059delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037666 | ||||||
chr17:62037673
|
A | T | 1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.471-2065T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037673 | ||||||
chr17:62037955
|
C | CA | 7 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0268others(4): Show | 7 | HG03195.hp1 NA18946.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2348dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
C | CAA | 42 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0018others(39): Show | 42 | HG00558.hp2 HG00639.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.471-2349_471-2348d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
C | CAAA | 22 | a0001c0002t0001g0001a0001c0002t0001g0017a0001c0002t0001g0023others(19): Show | 22 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.471-2350_471-2348d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
C | CAAAA | 18 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0295others(15): Show | 18 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.471-2351_471-2348d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
C | CAAAAA | 7 | a0001c0002t0001g0057a0001c0002t0001g0065a0001c0002t0001g0317others(4): Show | 7 | HG00544.hp1 HG01884.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2352_471-2348d others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
CA | C | 69 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00544.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.471-2348delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
CAA | C | 18 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0082others(15): Show | 18 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.471-2349_471-2348d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
CAAA | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0118others(4): Show | 7 | HG01346.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2350_471-2348d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0003t0001g0202a0001c0003t0001g0203 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.471-2359_471-2348d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62037955
|
CAAAAAAA others(6): Show |
C | 83 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(80): Show | 83 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.471-2360_471-2348d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | ||||||
chr17:62038421
|
G | GCATTTTA others(27): Show |
4 | a0001c0003t0001g0294a0001c0003t0001g0299a0001c0003t0001g0305others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-2847_471-2814d others(36): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038421 | ||||||
chr17:62038431
|
AT | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-2824delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038431 | ||||||
chr17:62038433
|
A | G | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-2825T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038433 | ||||||
chr17:62038746
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-3138G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038746 | ||||||
chr17:62038830
|
AT | A | 25 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0003t0001g0105others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.471-3223delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038830 | ||||||
chr17:62038887
|
CTGGCCTC others(7): Show |
C | 1 | a0001c0003t0001g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.471-3293_471-3280d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038887 | ||||||
chr17:62039026
|
G | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.471-3418C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039026 | ||||||
chr17:62039084
|
T | C | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.471-3476A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039084 | ||||||
chr17:62039226
|
A | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-3618T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039226 | ||||||
chr17:62039239
|
G | A | 208 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(205): Show | 208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.471-3631C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039239 | ||||||
chr17:62039346
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-3738C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039346 | ||||||
chr17:62039383
|
A | T | 1 | a0001c0001t0002g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.471-3775T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039383 | ||||||
chr17:62039388
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.471-3780A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039388 | ||||||
chr17:62039552
|
TA | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-3945delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039552 | ||||||
chr17:62039586
|
GA | G | 7 | a0001c0001t0001g0184a0001c0001t0001g0198a0001c0001t0001g0230others(4): Show | 7 | HG00642.hp2 HG01168.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-3979delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039586 | ||||||
chr17:62039587
|
A | AT | 12 | a0001c0001t0001g0087a0001c0001t0001g0162a0001c0001t0001g0167others(9): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.471-3980dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | ||||||
chr17:62039587
|
AT | A | 67 | a0001c0001t0001g0209a0001c0001t0001g0245a0001c0001t0001g0315others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.471-3980delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | ||||||
chr17:62039587
|
ATT | A | 97 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.471-3981_471-3980d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | ||||||
chr17:62039653
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0321 | 2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.471-4045C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039653 | ||||||
chr17:62039737
|
G | A | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.471-4129C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039737 | ||||||
chr17:62039842
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.471-4234C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039842 | ||||||
chr17:62039881
|
G | T | 1 | a0001c0003t0006g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.471-4273C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039881 | ||||||
chr17:62039930
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.471-4322T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039930 | ||||||
chr17:62040317
|
C | T | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-4709G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040317 | ||||||
chr17:62040417
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471-4809G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040417 | ||||||
chr17:62040594
|
T | C | 1 | a0001c0003t0001g0297 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.471-4986A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040594 | ||||||
chr17:62040602
|
G | A | 1 | a0001c0001t0016g0252 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.471-4994C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040602 | ||||||
chr17:62040758
|
A | C | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.471-5150T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040758 | ||||||
chr17:62041174
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.471-5566A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041174 | ||||||
chr17:62041235
|
A | G | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.471-5627T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041235 | ||||||
chr17:62041244
|
TG | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-5637delC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041244 | ||||||
chr17:62041333
|
T | C | 1 | a0001c0003t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.471-5725A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041333 | ||||||
chr17:62041349
|
G | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-5741C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041349 | ||||||
chr17:62041408
|
CATAAAA | C | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.471-5806_471-5801d others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041408 | ||||||
chr17:62041743
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471-6135T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041743 | ||||||
chr17:62041885
|
C | T | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.471-6277G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041885 | ||||||
chr17:62041964
|
T | C | 1 | a0001c0002t0024g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.471-6356A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041964 | ||||||
chr17:62042176
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.471-6568T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042176 | ||||||
chr17:62042318
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-6710G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042318 | ||||||
chr17:62042432
|
C | T | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.471-6824G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042432 | ||||||
chr17:62042433
|
A | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-6825T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042433 | ||||||
chr17:62042444
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01167.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.471-6836G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042444 | ||||||
chr17:62042474
|
A | G | 2 | a0001c0001t0002g0119a0001c0001t0002g0155 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.471-6866T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042474 | ||||||
chr17:62042554
|
T | C | 103 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.471-6946A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042554 | ||||||
chr17:62042560
|
C | CA | 112 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0188others(109): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.471-6953dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | ||||||
chr17:62042560
|
C | CAA | 26 | a0001c0001t0002g0119a0001c0001t0003g0295a0001c0002t0001g0015others(23): Show | 26 | HG00639.hp1 HG01243.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.471-6954_471-6953d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | ||||||
chr17:62042560
|
C | CAAA | 11 | a0001c0003t0001g0106a0001c0003t0001g0107a0001c0003t0001g0110others(8): Show | 11 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.471-6955_471-6953d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | ||||||
chr17:62042582
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.471-6974G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042582 | ||||||
chr17:62042590
|
C | A | 1 | a0001c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.471-6982G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042590 | ||||||
chr17:62042839
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.471-7231C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042839 | ||||||
chr17:62043156
|
C | CA | 28 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0176others(25): Show | 28 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.471-7549dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAA | 43 | a0001c0001t0001g0088a0001c0001t0001g0177a0001c0001t0001g0182others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.471-7550_471-7549d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAA | 27 | a0001c0001t0003g0290a0001c0001t0003g0292a0001c0001t0003g0295others(24): Show | 27 | HG00423.hp2 HG01106.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.471-7551_471-7549d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAAA | 6 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245others(3): Show | 6 | HG01099.hp2 HG02080.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.471-7552_471-7549d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAAAAAA others(4): Show |
1 | a0001c0007t0005g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.471-7559_471-7549d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAAAAAA others(5): Show |
1 | a0001c0007t0005g0010 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.471-7560_471-7549d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAAAAAA others(7): Show |
1 | a0006c0022t0005g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.471-7562_471-7549d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
C | CAAAAAAA others(11): Show |
1 | a0001c0007t0005g0009 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471-7566_471-7549d others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
CA | C | 82 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(79): Show | 82 | HG00140.hp1 HG00558.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.471-7549delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0001g0041a0001c0002t0001g0052 | 2 | HG02056.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.471-7560_471-7549d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043156
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-7563_471-7549d others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | ||||||
chr17:62043168
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.471-7577_471-7561d others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043168 | ||||||
chr17:62043179
|
A | G | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-7571T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043179 | ||||||
chr17:62043181
|
A | AG | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG01891.hp1 HG02055.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.471-7574_471-7573i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | ||||||
chr17:62043181
|
A | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0001g0315 | 3 | HG01346.hp2 HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.471-7573T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | ||||||
chr17:62043181
|
AAAAG | A | 50 | a0001c0001t0001g0272a0001c0001t0001g0279a0001c0001t0002g0116others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.471-7577_471-7574d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | ||||||
chr17:62043182
|
AAAG | A | 7 | a0001c0001t0002g0140a0001c0001t0002g0147a0001c0001t0002g0160others(4): Show | 7 | HG01109.hp1 HG02056.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-7577_471-7575d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043182 | ||||||
chr17:62043193
|
G | A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.471-7585C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043193 | ||||||
chr17:62043224
|
C | A | 1 | a0001c0002t0001g0041 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.471-7616G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043224 | ||||||
chr17:62043271
|
G | A | 1 | a0001c0003t0001g0302 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.471-7663C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043271 | ||||||
chr17:62044232
|
TA | T | 26 | a0001c0001t0001g0079a0001c0001t0001g0194a0001c0001t0001g0215others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.470+8304delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044232 | ||||||
chr17:62044462
|
T | C | 1 | a0001c0002t0001g0066 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.470+8075A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044462 | ||||||
chr17:62044468
|
C | T | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+8069G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044468 | ||||||
chr17:62044594
|
T | C | 2 | a0001c0004t0001g0163a0001c0004t0001g0164 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.470+7943A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044594 | ||||||
chr17:62044697
|
T | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+7840A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044697 | ||||||
chr17:62044739
|
T | G | 1 | a0001c0003t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.470+7798A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044739 | ||||||
chr17:62044783
|
T | A | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.470+7754A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044783 | ||||||
chr17:62045019
|
CAAA | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0165a0001c0001t0001g0170others(4): Show | 7 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+7515_470+7517d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045019 | ||||||
chr17:62045039
|
AT | A | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+7497delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045039 | ||||||
chr17:62045097
|
G | A | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+7440C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045097 | ||||||
chr17:62045112
|
A | G | 1 | a0001c0018t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.470+7425T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045112 | ||||||
chr17:62045174
|
T | A | 3 | a0001c0003t0001g0201a0001c0003t0001g0202a0001c0003t0001g0203 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.470+7363A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045174 | ||||||
chr17:62045445
|
C | T | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.470+7092G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045445 | ||||||
chr17:62045472
|
A | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+7065T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045472 | ||||||
chr17:62046097
|
A | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+6440T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046097 | ||||||
chr17:62046219
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.470+6318C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046219 | ||||||
chr17:62046248
|
T | A | 3 | a0001c0003t0001g0201a0001c0003t0001g0202a0001c0003t0001g0203 | 3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.470+6289A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046248 | ||||||
chr17:62046280
|
GA | G | 7 | a0001c0001t0001g0261a0001c0001t0004g0260a0001c0001t0004g0262others(4): Show | 7 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+6256delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046280 | ||||||
chr17:62046755
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470+5782A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046755 | ||||||
chr17:62046950
|
A | G | 102 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(99): Show | 102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.470+5587T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046950 | ||||||
chr17:62047033
|
CT | C | 201 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(198): Show | 201 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.470+5503delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047033 | ||||||
chr17:62047140
|
A | G | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+5397T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047140 | ||||||
chr17:62047188
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.470+5349A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047188 | ||||||
chr17:62047208
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+5329A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047208 | ||||||
chr17:62047221
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+5316T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047221 | ||||||
chr17:62047228
|
G | A | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.470+5309C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047228 | ||||||
chr17:62047470
|
T | C | 324 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(321): Show | 324 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(321): Show |
intron_variant | MODIFIER | c.470+5067A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047470 | ||||||
chr17:62047582
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.470+4955T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047582 | ||||||
chr17:62047655
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+4882C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047655 | ||||||
chr17:62047685
|
C | T | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4852G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047685 | ||||||
chr17:62047694
|
C | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.470+4843G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047694 | ||||||
chr17:62047793
|
A | G | 1 | a0001c0003t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.470+4744T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047793 | ||||||
chr17:62047849
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.470+4688G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047849 | ||||||
chr17:62048019
|
T | TATATAC | 47 | a0001c0001t0001g0082a0001c0001t0001g0197a0001c0001t0003g0290others(44): Show | 47 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.470+4512_470+4517d others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048019 | ||||||
chr17:62048019
|
T | TATATACA others(5): Show |
5 | a0001c0001t0001g0079a0001c0001t0021g0129a0001c0002t0001g0042others(2): Show | 5 | HG02818.hp2 HG03017.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+4506_470+4517d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048019 | ||||||
chr17:62048037
|
CATATACA others(5): Show |
C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4488_470+4499d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048037 | ||||||
chr17:62048039
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+4498A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048039 | ||||||
chr17:62048043
|
C | CAT | 15 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(12): Show | 15 | HG01261.hp2 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.470+4492_470+4493d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATAT | 5 | a0001c0004t0001g0074a0002c0005t0001g0003a0002c0005t0001g0004others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+4490_470+4493d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(1): Show |
19 | a0001c0002t0001g0001a0001c0002t0001g0020a0001c0002t0001g0024others(16): Show | 19 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(3): Show |
11 | a0001c0001t0001g0076a0001c0001t0003g0291a0001c0001t0003g0292others(8): Show | 11 | HG01516.hp1 HG01517.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(7): Show |
1 | a0001c0001t0011g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(9): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0003t0001g0293 | 3 | HG00140.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.470+4493_470+4494i others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(13): Show |
1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(5): Show |
3 | a0001c0002t0001g0019a0001c0002t0001g0054a0001c0003t0001g0089 | 3 | HG02965.hp2 NA18965.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.470+4493_470+4494i others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(7): Show |
17 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0002t0001g0018others(14): Show | 17 | HG01934.hp2 HG01993.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(9): Show |
7 | a0001c0002t0001g0029a0001c0002t0001g0044a0001c0002t0001g0049others(4): Show | 7 | HG01928.hp2 HG02080.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATACA others(11): Show |
1 | a0001c0002t0001g0028 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATATA others(1): Show |
4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+4486_470+4493d others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
C | CATATATA others(7): Show |
1 | a0001c0002t0001g0027 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.470+4480_470+4493d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048043
|
CAT | C | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG03130.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+4492_470+4493d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | ||||||
chr17:62048045
|
T | TATAC | 7 | a0001c0001t0002g0128a0001c0001t0002g0148a0001c0002t0001g0025others(4): Show | 7 | HG02572.hp2 HG02735.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+4491_470+4492i others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | ||||||
chr17:62048045
|
T | TATACATA others(3): Show |
58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.470+4491_470+4492i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | ||||||
chr17:62048045
|
T | TATACATA others(15): Show |
1 | a0001c0003t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.470+4491_470+4492i others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | ||||||
chr17:62048047
|
T | TAC | 4 | a0001c0003t0001g0296a0001c0003t0001g0302a0001c0003t0001g0303others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4489_470+4490i others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048047 | ||||||
chr17:62048049
|
T | C | 4 | a0001c0001t0001g0259a0001c0001t0025g0008a0001c0002t0001g0047others(1): Show | 4 | HG02027.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4488A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048049 | ||||||
chr17:62048051
|
T | C | 2 | a0001c0001t0002g0128a0001c0002t0001g0026 | 2 | HG02735.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.470+4486A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048051 | ||||||
chr17:62048056
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0238others(3): Show | 6 | HG01167.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.470+4481T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048056 | ||||||
chr17:62048057
|
T | C | 1 | a0001c0003t0006g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.470+4480A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048057 | ||||||
chr17:62048058
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0242a0001c0001t0001g0261others(7): Show | 10 | HG03669.hp2 HG06807.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.470+4479T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048058 | ||||||
chr17:62048064
|
G | A | 101 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.470+4473C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048064 | ||||||
chr17:62048077
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.470+4460A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048077 | ||||||
chr17:62048166
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0162 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.470+4371C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048166 | ||||||
chr17:62048221
|
C | T | 21 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(18): Show | 21 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.470+4316G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048221 | ||||||
chr17:62048242
|
T | C | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+4295A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048242 | ||||||
chr17:62048265
|
C | T | 1 | a0001c0001t0008g0318 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.470+4272G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048265 | ||||||
chr17:62048266
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4271C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048266 | ||||||
chr17:62048302
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4235C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048302 | ||||||
chr17:62048394
|
G | C | 7 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+4143C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048394 | ||||||
chr17:62048398
|
C | CA | 26 | a0001c0001t0001g0088a0001c0001t0001g0166a0001c0001t0001g0167others(23): Show | 26 | HG00642.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.470+4138dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | ||||||
chr17:62048398
|
CA | C | 40 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 40 | HG01167.hp2 HG01433.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.470+4138delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | ||||||
chr17:62048398
|
CAA | C | 160 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0002g0116others(157): Show | 160 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.470+4137_470+4138d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | ||||||
chr17:62048398
|
CAAA | C | 6 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0002t0001g0001others(3): Show | 6 | HG01109.hp2 HG01952.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.470+4136_470+4138d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | ||||||
chr17:62048398
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.470+4126_470+4138d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | ||||||
chr17:62048445
|
G | C | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4092C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048445 | ||||||
chr17:62048463
|
A | G | 1 | a0001c0002t0001g0026 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.470+4074T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048463 | ||||||
chr17:62048536
|
A | G | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.470+4001T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048536 | ||||||
chr17:62048543
|
C | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0287others(1): Show | 4 | HG02155.hp2 HG02523.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+3994G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048543 | ||||||
chr17:62048680
|
T | C | 6 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.470+3857A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048680 | ||||||
chr17:62048903
|
A | G | 5 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+3634T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048903 | ||||||
chr17:62049078
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+3451_470+3458d others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(2): Show |
7 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+3450_470+3458d others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(3): Show |
4 | a0001c0002t0001g0050a0001c0003t0001g0256a0001c0016t0001g0255others(1): Show | 4 | HG01109.hp2 HG01952.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+3449_470+3458d others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(4): Show |
12 | a0001c0001t0002g0155a0001c0001t0002g0157a0001c0002t0001g0001others(9): Show | 12 | HG01891.hp1 HG02723.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.470+3448_470+3458d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(5): Show |
104 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.470+3447_470+3458d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(6): Show |
30 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245others(27): Show | 30 | HG00423.hp1 HG00438.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.470+3446_470+3458d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(7): Show |
18 | a0001c0001t0002g0125a0001c0001t0002g0148a0001c0001t0010g0149others(15): Show | 18 | HG00544.hp1 HG01891.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.470+3445_470+3458d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(8): Show |
5 | a0001c0002t0001g0053a0001c0003t0001g0109a0001c0003t0001g0110others(2): Show | 5 | HG02559.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+3444_470+3458d others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(11): Show |
1 | a0001c0004t0001g0074 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.470+3458_470+3459i others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(13): Show |
1 | a0001c0004t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.470+3458_470+3459i others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.470+3458_470+3459i others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049078
|
C | CAAAAAAA others(20): Show |
2 | a0003c0010t0001g0007a0009c0014t0001g0192 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.470+3458_470+3459i others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | ||||||
chr17:62049261
|
C | A | 203 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(200): Show | 203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+3276G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049261 | ||||||
chr17:62049342
|
G | A | 23 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0182others(20): Show | 23 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.470+3195C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049342 | ||||||
chr17:62049411
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.470+3126C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049411 | ||||||
chr17:62049539
|
C | G | 2 | a0001c0001t0002g0311a0001c0001t0002g0312 | 2 | HG02293.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.470+2998G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049539 | ||||||
chr17:62049586
|
GA | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+2950delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049586 | ||||||
chr17:62049626
|
G | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+2911C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049626 | ||||||
chr17:62049635
|
G | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.470+2902C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049635 | ||||||
chr17:62049669
|
C | T | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.470+2868G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049669 | ||||||
chr17:62049683
|
G | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.470+2854C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049683 | ||||||
chr17:62049801
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2736C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049801 | ||||||
chr17:62049822
|
C | T | 1 | a0001c0003t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.470+2715G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049822 | ||||||
chr17:62049892
|
T | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2645A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049892 | ||||||
chr17:62049930
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.470+2597_470+2606d others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049930
|
C | CAAAAAAA others(4): Show |
107 | a0001c0001t0001g0315a0001c0001t0003g0290a0001c0001t0003g0291others(104): Show | 107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.470+2596_470+2606d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049930
|
C | CAAAAAAA others(5): Show |
17 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0020others(14): Show | 17 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.470+2595_470+2606d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049930
|
C | CAAAAAAA others(6): Show |
8 | a0001c0003t0001g0307a0001c0004t0001g0071a0001c0004t0001g0072others(5): Show | 8 | HG01891.hp1 HG01978.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.470+2594_470+2606d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049930
|
C | CAAAAAAA others(7): Show |
2 | a0001c0004t0001g0074a0001c0004t0001g0080 | 2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.470+2606_470+2607i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049930
|
C | CAAAAAAA others(8): Show |
1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+2606_470+2607i others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | ||||||
chr17:62049943
|
A | AAAAAAAA others(3): Show |
1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2593_470+2594i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049943 | ||||||
chr17:62050232
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.470+2305G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050232 | ||||||
chr17:62050471
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470+2066A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050471 | ||||||
chr17:62050645
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0011g0075 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.470+1892C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050645 | ||||||
chr17:62050789
|
A | G | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.470+1748T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050789 | ||||||
chr17:62051072
|
T | A | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+1465A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051072 | ||||||
chr17:62051304
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470+1233C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051304 | ||||||
chr17:62051338
|
A | G | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.470+1199T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051338 | ||||||
chr17:62051635
|
A | AAAAC | 101 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.470+898_470+901dup others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051635 | ||||||
chr17:62051853
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.470+684C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051853 | ||||||
chr17:62051896
|
T | C | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+641A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051896 | ||||||
chr17:62052066
|
T | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.470+471A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052066 | ||||||
chr17:62052194
|
T | G | 1 | a0001c0002t0001g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.470+343A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052194 | ||||||
chr17:62052248
|
G | A | 1 | a0001c0002t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.470+289C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052248 | ||||||
chr17:62052382
|
T | TA | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0324others(9): Show | 12 | HG01978.hp2 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.470+154dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052382 | ||||||
chr17:62052427
|
A | C | 1 | a0001c0001t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.470+110T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052427 | ||||||
chr17:62052514
|
C | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+23G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052514 | ||||||
chr17:62052710
|
A | G | 1 | a0003c0010t0001g0007 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.302-5T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62052710 | ||||||
chr17:62053041
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-336G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053041 | ||||||
chr17:62053127
|
G | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.302-422C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053127 | ||||||
chr17:62053218
|
T | G | 1 | a0001c0007t0005g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.302-513A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053218 | ||||||
chr17:62053286
|
A | G | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-581T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053286 | ||||||
chr17:62053683
|
T | C | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.302-978A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053683 | ||||||
chr17:62053873
|
A | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG00423.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.302-1168T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053873 | ||||||
chr17:62053958
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.302-1253G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053958 | ||||||
chr17:62053988
|
C | T | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1283G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053988 | ||||||
chr17:62054200
|
G | A | 22 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.302-1495C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054200 | ||||||
chr17:62054319
|
A | C | 1 | a0001c0001t0011g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.302-1614T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054319 | ||||||
chr17:62054689
|
A | C | 1 | a0001c0001t0018g0212 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.302-1984T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054689 | ||||||
chr17:62054745
|
C | A | 8 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-2040G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054745 | ||||||
chr17:62054765
|
G | C | 19 | a0001c0003t0001g0105a0001c0003t0001g0106a0001c0003t0001g0107others(16): Show | 19 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.302-2060C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054765 | ||||||
chr17:62054863
|
G | C | 1 | a0001c0001t0002g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.302-2158C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054863 | ||||||
chr17:62055142
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.302-2437G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055142 | ||||||
chr17:62055369
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.302-2664C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055369 | ||||||
chr17:62055397
|
C | A | 3 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0161 | 3 | NA18965.hp2 NA19012.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.302-2692G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055397 | ||||||
chr17:62055408
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.302-2703T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055408 | ||||||
chr17:62055446
|
T | C | 1 | a0001c0003t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-2741A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055446 | ||||||
chr17:62055716
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.302-3011C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055716 | ||||||
chr17:62055740
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.302-3035A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055740 | ||||||
chr17:62055770
|
C | T | 5 | a0001c0004t0001g0071a0001c0004t0001g0072a0001c0004t0001g0073others(2): Show | 5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-3065G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055770 | ||||||
chr17:62055837
|
T | C | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.302-3132A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055837 | ||||||
chr17:62055943
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.302-3238T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055943 | ||||||
chr17:62056048
|
A | G | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.302-3343T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056048 | ||||||
chr17:62056164
|
G | A | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-3459C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056164 | ||||||
chr17:62056179
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302-3474C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056179 | ||||||
chr17:62056253
|
CGTT | C | 53 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(50): Show | 53 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.302-3551_302-3549d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056253 | ||||||
chr17:62056393
|
T | C | 97 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.302-3688A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056393 | ||||||
chr17:62056603
|
C | CT | 199 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(196): Show | 199 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.302-3899dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056603 | ||||||
chr17:62056610
|
T | TC | 4 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(1): Show | 4 | HG00544.hp1 HG02056.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-3906_302-3905i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056610 | ||||||
chr17:62056926
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302-4221G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056926 | ||||||
chr17:62057174
|
A | G | 9 | a0001c0003t0001g0014a0001c0003t0001g0089a0001c0003t0001g0090others(6): Show | 9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-4469T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057174 | ||||||
chr17:62057179
|
T | C | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.302-4474A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057179 | ||||||
chr17:62057234
|
TTA | T | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4531_302-4530d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057234 | ||||||
chr17:62057536
|
T | C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4831A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057536 | ||||||
chr17:62057550
|
CAAT | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(52): Show | 55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.302-4848_302-4846d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057550 | ||||||
chr17:62057822
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.302-5117C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057822 | ||||||
chr17:62057916
|
C | T | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301+5151G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057916 | ||||||
chr17:62058035
|
C | A | 325 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(322): Show | 325 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(322): Show |
intron_variant | MODIFIER | c.301+5032G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058035 | ||||||
chr17:62058221
|
T | A | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301+4846A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058221 | ||||||
chr17:62058437
|
C | G | 4 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(1): Show | 4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4630G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058437 | ||||||
chr17:62058437
|
C | T | 1 | a0001c0003t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.301+4630G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058437 | ||||||
chr17:62058508
|
G | A | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301+4559C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058508 | ||||||
chr17:62058520
|
C | CA | 22 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(19): Show | 22 | HG00544.hp1 HG01243.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.301+4546dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058520 | ||||||
chr17:62058520
|
CA | C | 6 | a0001c0001t0001g0165a0001c0001t0001g0211a0001c0002t0001g0018others(3): Show | 6 | HG02132.hp1 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+4546delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058520 | ||||||
chr17:62058537
|
A | G | 3 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0017 | 3 | HG03669.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.301+4530T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058537 | ||||||
chr17:62058539
|
A | AG | 56 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.301+4527_301+4528i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058539 | ||||||
chr17:62058539
|
A | G | 2 | a0001c0001t0013g0120a0001c0008t0001g0210 | 2 | HG03834.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.301+4528T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058539 | ||||||
chr17:62058807
|
G | A | 94 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(91): Show | 94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.301+4260C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058807 | ||||||
chr17:62059139
|
C | T | 1 | a0001c0001t0004g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.301+3928G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059139 | ||||||
chr17:62059206
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.301+3861T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059206 | ||||||
chr17:62059286
|
C | T | 94 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(91): Show | 94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.301+3781G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059286 | ||||||
chr17:62059398
|
T | C | 1 | a0001c0002t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.301+3669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059398 | ||||||
chr17:62059427
|
T | C | 1 | a0001c0001t0004g0275 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.301+3640A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059427 | ||||||
chr17:62059430
|
C | G | 1 | a0001c0001t0004g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.301+3637G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059430 | ||||||
chr17:62059482
|
G | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+3585C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059482 | ||||||
chr17:62059630
|
G | C | 1 | a0001c0021t0017g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301+3437C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059630 | ||||||
chr17:62059724
|
T | C | 207 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(204): Show | 207 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.301+3343A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059724 | ||||||
chr17:62059782
|
C | T | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.301+3285G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059782 | ||||||
chr17:62059822
|
A | C | 1 | a0001c0016t0001g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.301+3245T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059822 | ||||||
chr17:62059854
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+3213C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059854 | ||||||
chr17:62059925
|
A | C | 2 | a0001c0004t0001g0163a0001c0004t0001g0164 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.301+3142T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059925 | ||||||
chr17:62059925
|
A | G | 1 | a0010c0011t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301+3142T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059925 | ||||||
chr17:62060058
|
G | A | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+3009C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060058 | ||||||
chr17:62060104
|
G | A | 5 | a0001c0002t0001g0001a0001c0002t0001g0063a0001c0002t0001g0064others(2): Show | 5 | HG02027.hp1 NA18960.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+2963C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060104 | ||||||
chr17:62060282
|
G | A | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+2785C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060282 | ||||||
chr17:62060286
|
C | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+2781G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060286 | ||||||
chr17:62060448
|
G | A | 1 | a0001c0013t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.301+2619C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060448 | ||||||
chr17:62060462
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.301+2605A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060462 | ||||||
chr17:62060475
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+2592G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060475 | ||||||
chr17:62060486
|
G | A | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+2581C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060486 | ||||||
chr17:62060508
|
T | C | 9 | a0001c0002t0001g0001a0001c0002t0001g0059a0001c0002t0001g0060others(6): Show | 9 | HG02027.hp1 HG02040.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+2559A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060508 | ||||||
chr17:62060600
|
A | G | 100 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(97): Show | 100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.301+2467T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060600 | ||||||
chr17:62060620
|
G | A | 84 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.301+2447C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060620 | ||||||
chr17:62060620
|
G | C | 1 | a0009c0014t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+2447C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060620 | ||||||
chr17:62060621
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.301+2446G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060621 | ||||||
chr17:62060632
|
G | A | 1 | a0001c0006t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.301+2435C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060632 | ||||||
chr17:62060644
|
C | CA | 22 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(19): Show | 22 | HG00544.hp2 HG00597.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.301+2422dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060644 | ||||||
chr17:62060644
|
CA | C | 89 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(86): Show | 89 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.301+2422delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060644 | ||||||
chr17:62060930
|
C | T | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+2137G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060930 | ||||||
chr17:62060968
|
G | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2099C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060968 | ||||||
chr17:62060972
|
T | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2095A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060972 | ||||||
chr17:62060973
|
ACAGGCGT others(29): Show |
A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2058_301+2093d others(38): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060973 | ||||||
chr17:62061011
|
T | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2056A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061011 | ||||||
chr17:62061016
|
A | C | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2051T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061016 | ||||||
chr17:62061018
|
G | T | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2049C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061018 | ||||||
chr17:62061020
|
T | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2047A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061020 | ||||||
chr17:62061024
|
A | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2043T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061024 | ||||||
chr17:62061130
|
AACCTAGA others(29): Show |
A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1901_301+1936d others(38): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061130 | ||||||
chr17:62061168
|
A | T | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1899T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061168 | ||||||
chr17:62061171
|
G | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1896C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061171 | ||||||
chr17:62061172
|
C | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1895G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061172 | ||||||
chr17:62061177
|
C | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1890G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061177 | ||||||
chr17:62061211
|
A | G | 2 | a0001c0001t0001g0082a0003c0010t0001g0007 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.301+1856T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061211 | ||||||
chr17:62061371
|
GA | G | 85 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(82): Show | 85 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.301+1695delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061371 | ||||||
chr17:62061443
|
T | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1624A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061443 | ||||||
chr17:62061448
|
A | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1619T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061448 | ||||||
chr17:62061450
|
A | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1617T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061450 | ||||||
chr17:62061451
|
G | T | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1616C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061451 | ||||||
chr17:62061497
|
C | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1570G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061497 | ||||||
chr17:62061499
|
A | C | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1568T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061499 | ||||||
chr17:62061505
|
C | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1562G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061505 | ||||||
chr17:62061539
|
G | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1528C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061539 | ||||||
chr17:62061552
|
A | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1515T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061552 | ||||||
chr17:62061553
|
T | C | 58 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+1514A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061553 | ||||||
chr17:62061554
|
A | T | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1513T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061554 | ||||||
chr17:62061557
|
T | G | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1510A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061557 | ||||||
chr17:62061570
|
T | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1497A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061570 | ||||||
chr17:62061579
|
TTCAACAA others(5): Show |
T | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1476_301+1487d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061579 | ||||||
chr17:62061592
|
T | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1475A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061592 | ||||||
chr17:62061594
|
C | A | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1473G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061594 | ||||||
chr17:62061620
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.301+1447T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061620 | ||||||
chr17:62062027
|
C | G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.301+1040G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062027 | ||||||
chr17:62062139
|
A | T | 96 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.301+928T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062139 | ||||||
chr17:62062164
|
G | A | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+903C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062164 | ||||||
chr17:62062209
|
T | C | 1 | a0001c0001t0002g0311 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.301+858A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062209 | ||||||
chr17:62062289
|
C | T | 14 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(11): Show | 14 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+778G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062289 | ||||||
chr17:62062460
|
CTCT | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0238others(3): Show | 6 | HG01167.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+604_301+606del others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062460 | ||||||
chr17:62062578
|
AACACACA others(20): Show |
A | 1 | a0001c0003t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+462_301+488del others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062578 | ||||||
chr17:62062578
|
AACACACA others(26): Show |
A | 1 | a0001c0002t0001g0288 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.301+456_301+488del others(33): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062578 | ||||||
chr17:62062589
|
ACACACAC others(4): Show |
A | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+467_301+477del others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062589 | ||||||
chr17:62062590
|
CACACACA others(13): Show |
C | 5 | a0001c0007t0005g0009a0001c0007t0005g0010a0001c0007t0005g0012others(2): Show | 5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+457_301+476del others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062590 | ||||||
chr17:62062598
|
CACCACA | C | 5 | a0001c0003t0001g0201a0001c0003t0001g0202a0001c0003t0001g0203others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+463_301+468del others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | ||||||
chr17:62062598
|
CACCACAC others(1): Show |
C | 29 | a0001c0002t0001g0096a0001c0002t0001g0098a0001c0002t0001g0100others(26): Show | 29 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.301+461_301+468del others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | ||||||
chr17:62062598
|
CACCACAC others(3): Show |
C | 80 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(77): Show | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.301+459_301+468del others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | ||||||
chr17:62062599
|
A | C | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.301+468T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062599 | ||||||
chr17:62062599
|
AC | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0287a0001c0017t0001g0322 | 3 | HG02109.hp1 HG02630.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.301+467delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062599 | ||||||
chr17:62062600
|
C | A | 2 | a0001c0003t0001g0256a0001c0016t0001g0255 | 2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.301+467G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
C | CA | 56 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.301+466_301+467ins others(1): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
C | CCA | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0251others(5): Show | 8 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+465_301+466dup others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
C | CCACA | 25 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(22): Show | 25 | HG00558.hp1 HG01516.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.301+463_301+466dup others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
C | CCACACA | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01167.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+461_301+466dup others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
CCA | C | 32 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0001t0001g0214others(29): Show | 32 | HG00140.hp1 HG01168.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.301+465_301+466del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
CCACA | C | 41 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(38): Show | 41 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.301+463_301+466del others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062600
|
CCACACA | C | 19 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(16): Show | 19 | HG01243.hp1 HG01934.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.301+461_301+466del others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | ||||||
chr17:62062602
|
A | AC | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(4): Show | 7 | HG02293.hp1 HG03486.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+464dupG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062602 | ||||||
chr17:62062603
|
CA | C | 50 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0002g0116others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.301+463delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062603 | ||||||
chr17:62062616
|
A | C | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+451T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062616 | ||||||
chr17:62062759
|
C | T | 1 | a0001c0001t0025g0008 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.301+308G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062759 | ||||||
chr17:62062790
|
G | A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+277C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062790 | ||||||
chr17:62063564
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67-263C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063564 | ||||||
chr17:62063601
|
G | C | 21 | a0001c0001t0003g0290a0001c0001t0003g0291a0001c0001t0003g0292others(18): Show | 21 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-300C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063601 | ||||||
chr17:62063717
|
A | T | 4 | a0002c0005t0001g0003a0002c0005t0001g0004a0002c0005t0001g0005others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-416T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063717 | ||||||
chr17:62064002
|
T | C | 1 | a0007c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.67-701A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064002 | ||||||
chr17:62064034
|
G | A | 2 | a0001c0001t0002g0311a0001c0001t0002g0312 | 2 | HG02293.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.67-733C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064034 | ||||||
chr17:62064194
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.67-893C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064194 | ||||||
chr17:62064201
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67-900A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064201 | ||||||
chr17:62064255
|
C | T | 1 | a0001c0001t0007g0002 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.66+885G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064255 | ||||||
chr17:62064342
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+798C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064342 | ||||||
chr17:62064608
|
A | G | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+532T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064608 | ||||||
chr17:62064726
|
G | A | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.66+414C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064726 | ||||||
chr17:62064740
|
A | G | 1 | a0001c0002t0001g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.66+400T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064740 | ||||||
chr17:62064760
|
T | C | 1 | a0001c0002t0001g0317 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.66+380A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064760 | ||||||
chr17:62064813
|
G | A | 1 | a0001c0001t0008g0318 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.66+327C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064813 | ||||||
chr17:62064833
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+307G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064833 | ||||||
chr17:62064849
|
G | A | 1 | a0011c0024t0001g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.66+291C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064849 | ||||||
chr17:62064880
|
T | G | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.66+260A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064880 | ||||||
chr17:62064904
|
G | A | 1 | a0001c0017t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+236C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064904 | ||||||
chr17:62065011
|
G | A | 2 | a0001c0001t0001g0324a0001c0003t0001g0323 | 2 | HG01978.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.66+129C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065011 | ||||||
chr17:62065019
|
G | A | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.66+121C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065019 | ||||||
chr17:62065110
|
C | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+30G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065110 |