geneid | 51586 |
---|---|
ensemblid | ENSG00000099917.17 |
hgncid | 14248 |
symbol | MED15 |
name | mediator complex subunit 15 |
refseq_nuc | NM_001003891.3 |
refseq_prot | NP_001003891.1 |
ensembl_nuc | ENST00000263205.11 |
ensembl_prot | ENSP00000263205.7 |
mane_status | MANE Select |
chr | chr22 |
start | 20507610 |
end | 20587619 |
strand | + |
ver | v1.2 |
region | chr22:20507610-20587619 |
region5000 | chr22:20502610-20592619 |
regionname0 | MED15_chr22_20507610_20587619 |
regionname5000 | MED15_chr22_20502610_20592619 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 788 | 264 | 65 | 51 | 111 | 11 | 25 | 78 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002 | 0/0 | 789 | 51 | 9 | 8 | 21 | 4 | 9 | 16 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003 | 0/0 | 787 | 8 | 4 | 1 | 1 | 0 | 2 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0004 | 0/0 | 785 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0005 | 0/0 | 787 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0006 | 0/0 | 784 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0007 | 0/0 | 788 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0008 | 0/0 | 788 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0009 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0010 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0011 | 0/0 | 788 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0012 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0013 | 0/0 | 778 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0014 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0015 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2367 | 190 | 57 | 40 | 61 | 9 | 22 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0002 | 0/0 | 2367 | 61 | 0 | 7 | 49 | 2 | 3 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0003 | 0/0 | 2370 | 50 | 9 | 8 | 20 | 4 | 9 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0004 | 0/0 | 2367 | 8 | 7 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0005 | 0/0 | 2364 | 6 | 3 | 1 | 1 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0006 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0007 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0008 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0009 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0010 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0011 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0012 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0013 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0014 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0015 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0016 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0017 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0018 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0019 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0020 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0021 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0022 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0023 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0024 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
c0025 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 985 | 251 | 81 | 50 | 81 | 11 | 27 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0002 | 0/0 | 985 | 64 | 0 | 7 | 50 | 2 | 5 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0003 | 0/0 | 985 | 11 | 1 | 5 | 0 | 1 | 4 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0004 | 0/0 | 985 | 4 | 0 | 0 | 4 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0005 | 0/0 | 985 | 2 | 1 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0006 | 0/0 | 985 | 2 | 0 | 0 | 0 | 2 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0007 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0008 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0009 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0010 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0011 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0012 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
t0013 | 0/0 | 985 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2367 | 190 | 57 | 40 | 61 | 9 | 22 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0002 | 0/0 | 2367 | 61 | 0 | 7 | 49 | 2 | 3 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0004 | 0/0 | 2367 | 8 | 7 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0006 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0017 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0023 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0025 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002c0003 | 0/0 | 2370 | 50 | 9 | 8 | 20 | 4 | 9 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002c0014 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0005 | 0/0 | 2364 | 6 | 3 | 1 | 1 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0012 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0020 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0004c0009 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0004c0021 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0005c0011 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0006c0010 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0007c0008 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0008c0007 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0009c0024 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0010c0016 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0011c0019 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0012c0018 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0013c0015 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0014c0013 | 0/0 | 2379 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0015c0022 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3351 | 170 | 53 | 34 | 58 | 6 | 18 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0002 | 0/0 | 3351 | 3 | 0 | 0 | 3 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0003 | 0/0 | 3351 | 10 | 1 | 4 | 0 | 1 | 4 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0005 | 0/0 | 3351 | 2 | 1 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0006 | 0/0 | 3351 | 2 | 0 | 0 | 0 | 2 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0007 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0009 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0001t0013 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0002t0002 | 0/0 | 3351 | 56 | 0 | 7 | 44 | 2 | 3 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0002t0004 | 0/0 | 3351 | 4 | 0 | 0 | 4 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0002t0008 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0004t0001 | 0/0 | 3351 | 8 | 7 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0006t0001 | 0/0 | 3351 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0017t0001 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0023t0001 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0001c0025t0001 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002c0003t0001 | 0/0 | 3354 | 49 | 9 | 8 | 19 | 4 | 9 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002c0003t0012 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0002c0014t0001 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0005t0001 | 0/0 | 3348 | 4 | 2 | 1 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0005t0002 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0005t0010 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0012t0001 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0003c0020t0002 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0004c0009t0001 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0004c0021t0002 | 0/0 | 3342 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0005c0011t0001 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0006c0010t0001 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0007c0008t0002 | 0/0 | 3351 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0008c0007t0001 | 0/0 | 3351 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0009c0024t0001 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0010c0016t0001 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0011c0019t0001 | 0/0 | 3351 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0012c0018t0001 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0013c0015t0011 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0014c0013t0001 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
a0015c0022t0003 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | copy fasta | chr22 | 20502610 | 20592619 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0013g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0006t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0017t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0023t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0025t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0014t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0012t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0020t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0009t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0009t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0021t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0005c0011t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0005c0011t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0006c0010t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0006c0010t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0007c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0007c0008t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0008c0007t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0008c0007t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0009c0024t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0010c0016t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0011c0019t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0012c0018t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0013c0015t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0014c0013t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0015c0022t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0159 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0180 | EUR | FIN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0108 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00438 | hp2 | a0002 | c0014 | t0001 | g0191 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00733 | hp2 | a0002 | c0003 | t0001 | g0173 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0164 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00741 | hp1 | a0014 | c0013 | t0001 | g0189 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0172 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01070 | hp1 | a0008 | c0007 | t0001 | g0281 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0171 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01071 | hp2 | a0008 | c0007 | t0001 | g0282 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0174 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0161 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01167 | hp2 | a0001 | c0006 | t0001 | g0138 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01168 | hp2 | a0001 | c0023 | t0001 | g0183 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0135 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0163 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01243 | hp2 | a0015 | c0022 | t0003 | g0060 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0142 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0293 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01433 | hp2 | a0002 | c0003 | t0001 | g0150 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0286 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01515 | hp2 | a0002 | c0003 | t0001 | g0165 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01516 | hp1 | a0011 | c0019 | t0001 | g0091 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0242 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0283 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0243 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01952 | hp1 | a0001 | c0001 | t0013 | g0288 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01978 | hp1 | a0003 | c0005 | t0001 | g0322 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02055 | hp2 | a0003 | c0005 | t0010 | g0303 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02071 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0016 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0177 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02451 | hp1 | a0004 | c0009 | t0001 | g0213 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02572 | hp1 | a0003 | c0005 | t0001 | g0265 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02572 | hp2 | a0006 | c0010 | t0001 | g0279 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02602 | hp1 | a0003 | c0005 | t0002 | g0276 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0145 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0301 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0297 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0182 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0162 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0148 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0089 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02809 | hp2 | a0006 | c0010 | t0001 | g0277 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0298 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02886 | hp2 | a0012 | c0018 | t0001 | g0027 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0144 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02970 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0300 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0133 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03017 | hp2 | a0002 | c0003 | t0001 | g0170 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0302 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03139 | hp1 | a0003 | c0005 | t0001 | g0313 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03139 | hp2 | a0002 | c0003 | t0001 | g0299 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03225 | hp2 | a0003 | c0012 | t0001 | g0314 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0187 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03579 | hp1 | a0009 | c0024 | t0001 | g0311 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0184 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0274 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0168 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0253 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0134 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0167 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0223 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18522 | hp1 | a0005 | c0011 | t0001 | g0139 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0157 | EAS | CHB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18945 | hp2 | a0007 | c0008 | t0002 | g0218 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0178 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0155 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18977 | hp1 | a0010 | c0016 | t0001 | g0130 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18980 | hp1 | a0007 | c0008 | t0002 | g0217 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18993 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18995 | hp1 | a0004 | c0021 | t0002 | g0258 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0185 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19009 | hp1 | a0002 | c0003 | t0012 | g0175 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19009 | hp2 | a0003 | c0005 | t0001 | g0153 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0158 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19043 | hp1 | a0004 | c0009 | t0001 | g0214 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19070 | hp1 | a0001 | c0017 | t0001 | g0062 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0176 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19085 | hp1 | a0001 | c0002 | t0008 | g0222 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19086 | hp2 | a0013 | c0015 | t0011 | g0179 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0154 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19240 | hp1 | a0001 | c0025 | t0001 | g0087 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ASW | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0149 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20905 | hp2 | a0003 | c0020 | t0002 | g0239 | SAS | GIH | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0318 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18955 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA21309 | hp1 | a0005 | c0011 | t0001 | g0140 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0190 | REF | REF | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20564628
|
CCAG | C | 2 | a0005a0009 | 3 | HG03579.hp1 NA18522.hp1 NA21309.hp1 |
disruptive_inframe_deletion | MODERATE | c.654_656delGCA | p.Gln218del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/18 | 723/3351 | 654/2367 | 218/788 | INFO_REALIGN_3_PRIME | chr22 | 20564628 | |
chr22:20566526
|
A | ACAG | 2 | a0002a0013 | 52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
conservative_inframe_insertion | MODERATE | c.784_786dupCAG | p.Gln262dup | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 856/3351 | 787/2367 | 263/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | |
chr22:20566526
|
A | ACAGCAGC others(5): Show |
1 | a0014 | 1 | HG00741.hp1 | conservative_inframe_insertion | MODERATE | c.775_786dupCAGCAGCA others(4): Show |
p.Gln259_Gln262dup | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 856/3351 | 787/2367 | 263/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | |
chr22:20566526
|
ACAG | A | 2 | a0003a0009 | 9 | HG01978.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
conservative_inframe_deletion | MODERATE | c.784_786delCAG | p.Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 853/3351 | 784/2367 | 262/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | |
chr22:20566526
|
ACAGCAGC others(2): Show |
A | 1 | a0004 | 3 | HG02451.hp1 NA18995.hp1 NA19043.hp1 |
conservative_inframe_deletion | MODERATE | c.778_786delCAGCAGCA others(1): Show |
p.Gln260_Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 847/3351 | 778/2367 | 260/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | |
chr22:20566526
|
ACAGCAGC others(5): Show |
A | 1 | a0006 | 2 | HG02572.hp2 HG02809.hp2 |
conservative_inframe_deletion | MODERATE | c.775_786delCAGCAGCA others(4): Show |
p.Gln259_Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 844/3351 | 775/2367 | 259/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | |
chr22:20566537
|
A | G | 1 | a0015 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.761A>G | p.Gln254Arg | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 830/3351 | 761/2367 | 254/788 | chr22 | 20566537 | ||
chr22:20568611
|
A | C | 1 | a0007 | 2 | NA18945.hp2 NA18980.hp1 |
missense_variant | MODERATE | c.1132A>C | p.Met378Leu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/18 | 1201/3351 | 1132/2367 | 378/788 | chr22 | 20568611 | ||
chr22:20582641
|
T | C | 1 | a0010 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1303T>C | p.Ser435Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1372/3351 | 1303/2367 | 435/788 | chr22 | 20582641 | ||
chr22:20582695
|
C | G | 1 | a0011 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1357C>G | p.Gln453Glu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1426/3351 | 1357/2367 | 453/788 | chr22 | 20582695 | ||
chr22:20584874
|
C | T | 1 | a0008 | 2 | HG01070.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.1823C>T | p.Pro608Leu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 15/18 | 1892/3351 | 1823/2367 | 608/788 | chr22 | 20584874 | ||
chr22:20586669
|
C | T | 1 | a0013 | 1 | NA19086.hp2 | stop_gained | HIGH | c.2332C>T | p.Gln778* | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2401/3351 | 2332/2367 | 778/788 | chr22 | 20586669 | ||
chr22:20586675
|
G | A | 1 | a0012 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2338G>A | p.Val780Ile | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2407/3351 | 2338/2367 | 780/788 | chr22 | 20586675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20537195
|
C | T | 1 | a0001c0025 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.147C>T | p.Ala49Ala | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/18 | 216/3351 | 147/2367 | 49/788 | chr22 | 20537195 | ||
chr22:20555084
|
G | A | 1 | a0003c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.387G>A | p.Pro129Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/18 | 456/3351 | 387/2367 | 129/788 | chr22 | 20555084 | ||
chr22:20566526
|
A | G | 1 | a0001c0023 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.750A>G | p.Gln250Gln | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 819/3351 | 750/2367 | 250/788 | chr22 | 20566526 | ||
chr22:20582646
|
G | A | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1308G>A | p.Pro436Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1377/3351 | 1308/2367 | 436/788 | chr22 | 20582646 | ||
chr22:20582688
|
T | C | 1 | a0010c0016 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.1350T>C | p.Pro450Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1419/3351 | 1350/2367 | 450/788 | chr22 | 20582688 | ||
chr22:20582888
|
G | A | 1 | a0002c0014 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.1458G>A | p.Pro486Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 11/18 | 1527/3351 | 1458/2367 | 486/788 | chr22 | 20582888 | ||
chr22:20585113
|
G | A | 2 | a0001c0004a0005c0011 | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.1977G>A | p.Val659Val | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/18 | 2046/3351 | 1977/2367 | 659/788 | chr22 | 20585113 | ||
chr22:20585798
|
G | A | 4 | a0001c0002a0003c0020a0004c0021others(1): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
synonymous_variant | LOW | c.2202G>A | p.Pro734Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/18 | 2271/3351 | 2202/2367 | 734/788 | chr22 | 20585798 | ||
chr22:20586590
|
G | A | 1 | a0001c0017 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.2253G>A | p.Ser751Ser | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2322/3351 | 2253/2367 | 751/788 | chr22 | 20586590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20507647
|
G | A | 1 | a0001c0001t0007 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/18 | 32 | chr22 | 20507647 | |||||
chr22:20586725
|
C | T | 1 | a0001c0001t0013 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 21 | chr22 | 20586725 | |||||
chr22:20586752
|
C | T | 1 | a0001c0001t0006 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 48 | chr22 | 20586752 | |||||
chr22:20586755
|
C | T | 1 | a0002c0003t0012 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 51 | chr22 | 20586755 | |||||
chr22:20586785
|
C | T | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 81 | chr22 | 20586785 | |||||
chr22:20586908
|
G | A | 1 | a0001c0001t0005 | 2 | HG01346.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*204G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 204 | chr22 | 20586908 | |||||
chr22:20587139
|
G | A | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 435 | chr22 | 20587139 | |||||
chr22:20587163
|
T | C | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0004others(5): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*459T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 459 | chr22 | 20587163 | |||||
chr22:20587215
|
A | C | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 511 | chr22 | 20587215 | |||||
chr22:20587250
|
G | C | 1 | a0001c0001t0009 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 546 | chr22 | 20587250 | |||||
chr22:20587264
|
C | T | 2 | a0001c0001t0003a0015c0022t0003 | 11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*560C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 560 | chr22 | 20587264 | |||||
chr22:20587279
|
C | T | 1 | a0003c0005t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 575 | chr22 | 20587279 | |||||
chr22:20587380
|
C | T | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*676C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 676 | chr22 | 20587380 | |||||
chr22:20587445
|
A | T | 1 | a0001c0002t0004 | 4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*741A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 741 | chr22 | 20587445 | |||||
chr22:20587498
|
G | A | 1 | a0001c0002t0008 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 794 | chr22 | 20587498 | |||||
chr22:20587613
|
C | T | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 909 | chr22 | 20587613 | |||||
chr22:20587614
|
T | C | 1 | a0013c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 910 | chr22 | 20587614 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20507862
|
G | T | 11 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0323others(8): Show | 11 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+116G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507862 | ||||||
chr22:20507886
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.68+140C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507886 | ||||||
chr22:20507896
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+150C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507896 | ||||||
chr22:20508261
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68+515C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508261 | ||||||
chr22:20508286
|
G | T | 1 | a0001c0001t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.68+540G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508286 | ||||||
chr22:20508359
|
T | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.68+613T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508359 | ||||||
chr22:20508433
|
A | G | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+687A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508433 | ||||||
chr22:20508493
|
C | G | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+747C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508493 | ||||||
chr22:20508600
|
C | G | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+854C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508600 | ||||||
chr22:20508915
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.68+1169G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508915 | ||||||
chr22:20509092
|
G | C | 2 | a0002c0003t0001g0133a0002c0003t0001g0134 | 2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.68+1346G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509092 | ||||||
chr22:20509150
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG00544.hp1 NA18971.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1404C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509150 | ||||||
chr22:20509530
|
G | A | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+1784G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509530 | ||||||
chr22:20509598
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0006t0001g0135others(1): Show | 4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1852G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509598 | ||||||
chr22:20509624
|
C | T | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+1878C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509624 | ||||||
chr22:20509671
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+1925C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509671 | ||||||
chr22:20509757
|
T | C | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+2011T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509757 | ||||||
chr22:20509998
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68+2252C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509998 | ||||||
chr22:20510055
|
C | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2309C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510055 | ||||||
chr22:20510082
|
G | A | 2 | a0002c0003t0001g0149a0002c0003t0001g0150 | 2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.68+2336G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510082 | ||||||
chr22:20510088
|
T | G | 3 | a0002c0003t0001g0151a0002c0003t0001g0152a0003c0005t0001g0153 | 3 | NA18956.hp2 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.68+2342T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510088 | ||||||
chr22:20510105
|
A | G | 12 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(9): Show | 13 | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+2359A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510105 | ||||||
chr22:20510134
|
C | T | 5 | a0001c0004t0001g0144a0001c0004t0001g0145a0001c0004t0001g0146others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+2388C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510134 | ||||||
chr22:20510203
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.68+2457C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510203 | ||||||
chr22:20510254
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.68+2508C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510254 | ||||||
chr22:20510314
|
A | C | 5 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG01952.hp1 HG03927.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+2568A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510314 | ||||||
chr22:20510380
|
A | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2634A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510380 | ||||||
chr22:20510417
|
A | T | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+2671A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510417 | ||||||
chr22:20510557
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2811C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510557 | ||||||
chr22:20510653
|
C | T | 16 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(13): Show | 16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.68+2907C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510653 | ||||||
chr22:20510659
|
C | T | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.68+2913C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510659 | ||||||
chr22:20510790
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3044A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510790 | ||||||
chr22:20510858
|
A | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0123others(125): Show | 135 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+3112A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510858 | ||||||
chr22:20511004
|
A | C | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+3258A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511004 | ||||||
chr22:20511465
|
C | G | 1 | a0002c0014t0001g0191 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.68+3719C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511465 | ||||||
chr22:20511498
|
G | GA | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0124others(121): Show | 131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.68+3763dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511498 | |||||
chr22:20511812
|
C | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68+4066C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511812 | ||||||
chr22:20511944
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(133): Show | 144 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.68+4198G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511944 | ||||||
chr22:20511982
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.68+4236T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511982 | ||||||
chr22:20511988
|
C | CT | 18 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+4259dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0196others(82): Show | 91 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.68+4253_68+4259dup others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(11): Show | 14 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+4252_68+4259dup others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT others(2): Show |
7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+4251_68+4259dup others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT others(3): Show |
12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+4250_68+4259dup others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0285a0001c0001t0006g0286a0001c0006t0001g0138others(1): Show | 4 | HG01106.hp2 HG01167.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+4249_68+4259dup others(11): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20511988
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+4248_68+4259dup others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | |||||
chr22:20512006
|
G | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(281): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.68+4260G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512006 | ||||||
chr22:20512091
|
C | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4345C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512091 | ||||||
chr22:20512101
|
A | G | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+4355A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512101 | ||||||
chr22:20512277
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.68+4531T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512277 | ||||||
chr22:20512371
|
C | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4625C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512371 | ||||||
chr22:20512389
|
T | C | 1 | a0002c0003t0001g0154 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.68+4643T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512389 | ||||||
chr22:20512547
|
G | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4801G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512547 | ||||||
chr22:20512567
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68+4821G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512567 | ||||||
chr22:20512587
|
C | CT | 96 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0107others(93): Show | 100 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.68+4863dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | |||||
chr22:20512587
|
C | CTT | 6 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0001g0309others(3): Show | 6 | HG00408.hp1 HG02486.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+4862_68+4863dup others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | |||||
chr22:20512587
|
CT | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(29): Show | 35 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.68+4863delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | |||||
chr22:20512626
|
C | G | 1 | a0001c0004t0001g0144 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68+4880C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512626 | ||||||
chr22:20512758
|
A | AT | 12 | a0001c0001t0001g0105a0001c0001t0001g0295a0001c0001t0001g0296others(9): Show | 13 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+5026dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512758 | |||||
chr22:20512786
|
A | T | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.68+5040A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512786 | ||||||
chr22:20512795
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.68+5049T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512795 | ||||||
chr22:20512833
|
C | T | 18 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+5087C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512833 | ||||||
chr22:20512930
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0114a0011c0019t0001g0091 | 3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+5184C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512930 | ||||||
chr22:20512976
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68+5230G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512976 | ||||||
chr22:20512978
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.68+5232G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512978 | ||||||
chr22:20513040
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0114a0011c0019t0001g0091 | 3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+5294G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513040 | ||||||
chr22:20513282
|
CT | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.68+5551delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20513282 | |||||
chr22:20513282
|
CTT | C | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+5550_68+5551del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20513282 | |||||
chr22:20513732
|
C | T | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+5986C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513732 | ||||||
chr22:20513923
|
G | C | 1 | a0001c0001t0001g0320 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.68+6177G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513923 | ||||||
chr22:20513936
|
C | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+6190C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513936 | ||||||
chr22:20513965
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+6219G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513965 | ||||||
chr22:20513966
|
C | T | 1 | a0004c0009t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68+6220C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513966 | ||||||
chr22:20514009
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.68+6263C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514009 | ||||||
chr22:20514239
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+6493C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514239 | ||||||
chr22:20514307
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+6561A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514307 | ||||||
chr22:20514342
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68+6596A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514342 | ||||||
chr22:20514387
|
T | C | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+6641T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514387 | ||||||
chr22:20514419
|
T | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+6673T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514419 | ||||||
chr22:20514677
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+6931C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514677 | ||||||
chr22:20514678
|
G | A | 2 | a0005c0011t0001g0139a0005c0011t0001g0140 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68+6932G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514678 | ||||||
chr22:20514730
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.68+6984C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514730 | ||||||
chr22:20514813
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68+7067C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514813 | ||||||
chr22:20514849
|
G | T | 18 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+7103G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514849 | ||||||
chr22:20514898
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.68+7152G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514898 | ||||||
chr22:20514910
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+7164C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514910 | ||||||
chr22:20515188
|
C | T | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+7442C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515188 | ||||||
chr22:20515191
|
G | C | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+7445G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515191 | ||||||
chr22:20515222
|
A | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+7476A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515222 | ||||||
chr22:20515280
|
A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(30): Show | 36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+7534A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515280 | ||||||
chr22:20515463
|
TA | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(321): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.68+7729delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20515463 | |||||
chr22:20515514
|
G | C | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.68+7768G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515514 | ||||||
chr22:20515674
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+7928C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515674 | ||||||
chr22:20515678
|
G | A | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+7932G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515678 | ||||||
chr22:20515701
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+7955G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515701 | ||||||
chr22:20515741
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+7995G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515741 | ||||||
chr22:20515867
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+8121G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515867 | ||||||
chr22:20516001
|
A | AAAAC | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+8263_68+8266dup others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516001 | |||||
chr22:20516045
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68+8299G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516045 | ||||||
chr22:20516091
|
C | T | 1 | a0005c0011t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68+8345C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516091 | ||||||
chr22:20516102
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68+8356A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516102 | ||||||
chr22:20516141
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+8395C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516141 | ||||||
chr22:20516317
|
A | AAAT | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+8595_68+8597dup others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516317 | |||||
chr22:20516381
|
G | A | 1 | a0001c0002t0002g0006 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.68+8635G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516381 | ||||||
chr22:20516398
|
C | T | 5 | a0001c0004t0001g0144a0001c0004t0001g0145a0001c0004t0001g0146others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+8652C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516398 | ||||||
chr22:20516683
|
AT | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(30): Show | 36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+8939delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516683 | |||||
chr22:20516809
|
A | T | 1 | a0001c0002t0002g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.68+9063A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516809 | ||||||
chr22:20516853
|
A | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9107A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516853 | ||||||
chr22:20516884
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0199 | 3 | HG03710.hp2 HG04115.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.68+9138T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516884 | ||||||
chr22:20516905
|
T | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+9159T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516905 | ||||||
chr22:20517051
|
T | C | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+9305T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517051 | ||||||
chr22:20517103
|
A | AT | 71 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(68): Show | 75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.68+9371dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20517103 | |||||
chr22:20517106
|
T | A | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9360T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517106 | ||||||
chr22:20517383
|
C | T | 1 | a0014c0013t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.68+9637C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517383 | ||||||
chr22:20517456
|
C | T | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+9710C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517456 | ||||||
chr22:20517467
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+9721A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517467 | ||||||
chr22:20517677
|
A | G | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+9931A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517677 | ||||||
chr22:20517743
|
A | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9997A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517743 | ||||||
chr22:20517750
|
T | C | 1 | a0003c0012t0001g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.68+10004T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517750 | ||||||
chr22:20517823
|
G | C | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+10077G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517823 | ||||||
chr22:20517852
|
A | ATTT | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(30): Show | 36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+10112_68+10114d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20517852 | |||||
chr22:20518070
|
T | TGACATTG others(25): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0136others(104): Show | 113 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.68+10325_68+10356d others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518070 | |||||
chr22:20518070
|
T | TGACATTG others(25): Show |
1 | a0001c0002t0002g0261 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68+10332_68+10333i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518070 | |||||
chr22:20518075
|
T | TTGACGTG others(25): Show |
1 | a0006c0010t0001g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68+10356_68+10357i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518075 | |||||
chr22:20518080
|
G | GTGAGGGA others(25): Show |
5 | a0001c0002t0002g0216a0001c0002t0002g0219a0001c0002t0002g0220others(2): Show | 5 | HG00544.hp2 NA18941.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+10356_68+10357i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518080 | |||||
chr22:20518220
|
C | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0208others(7): Show | 10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+10474C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518220 | ||||||
chr22:20518228
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.68+10482C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518228 | ||||||
chr22:20518434
|
T | G | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+10688T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518434 | ||||||
chr22:20518504
|
A | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+10758A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518504 | ||||||
chr22:20518551
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.68+10805T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518551 | ||||||
chr22:20518551
|
T | TTGAG | 4 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(1): Show | 4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+10808_68+10811d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518551 | |||||
chr22:20518568
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+10822C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518568 | ||||||
chr22:20519106
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+11360G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519106 | ||||||
chr22:20519271
|
A | G | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+11525A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519271 | ||||||
chr22:20519325
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(324): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.68+11579T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519325 | ||||||
chr22:20519401
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68+11655T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519401 | ||||||
chr22:20519437
|
G | GT | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0084others(46): Show | 52 | HG01261.hp2 HG01891.hp1 HG01952.hp1 others(49): Show |
intron_variant | MODIFIER | c.68+11706dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20519437 | |||||
chr22:20519588
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+11842G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519588 | ||||||
chr22:20519605
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68+11859C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519605 | ||||||
chr22:20520161
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0308a0001c0001t0001g0309 | 4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+12415A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520161 | ||||||
chr22:20520209
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.68+12463A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520209 | ||||||
chr22:20520253
|
G | A | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.68+12507G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520253 | ||||||
chr22:20520268
|
T | C | 2 | a0005c0011t0001g0139a0005c0011t0001g0140 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68+12522T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520268 | ||||||
chr22:20520346
|
T | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+12600T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520346 | ||||||
chr22:20520417
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02083.hp2 NA18978.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+12671G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520417 | ||||||
chr22:20520689
|
T | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+12943T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520689 | ||||||
chr22:20520695
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+12949C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520695 | ||||||
chr22:20520866
|
A | G | 3 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143 | 3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68+13120A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520866 | ||||||
chr22:20520892
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.68+13146A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520892 | ||||||
chr22:20521025
|
T | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+13279T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521025 | ||||||
chr22:20521088
|
A | AT | 26 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(23): Show | 26 | HG00735.hp1 HG01981.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.68+13368dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521088
|
A | ATT | 29 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0192others(26): Show | 31 | HG00558.hp1 HG01255.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.68+13367_68+13368d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521088
|
A | ATTT | 54 | a0001c0001t0001g0001a0001c0001t0001g0196a0001c0001t0001g0206others(51): Show | 58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.68+13366_68+13368d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521088
|
A | ATTTT | 10 | a0001c0002t0002g0216a0001c0002t0002g0220a0001c0002t0002g0254others(7): Show | 10 | HG01358.hp1 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+13365_68+13368d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521088
|
AT | A | 17 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 18 | HG00099.hp2 HG00408.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+13368delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521088
|
ATTTT | A | 7 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0297others(4): Show | 7 | HG02647.hp2 HG02818.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+13365_68+13368d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | |||||
chr22:20521096
|
T | TTTTTTTT others(289): Show |
12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+13365_68+13366i others(298): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521096 | |||||
chr22:20521097
|
T | TTTTTTTT others(288): Show |
3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.68+13365_68+13366i others(297): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521097 | |||||
chr22:20521097
|
T | TTTTTTTT others(293): Show |
1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+13368_68+13369i others(302): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521097 | |||||
chr22:20521117
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.68+13371G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521117 | ||||||
chr22:20521119
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0136others(123): Show | 133 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.68+13373T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521119 | ||||||
chr22:20521198
|
G | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+13452G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521198 | ||||||
chr22:20521231
|
G | C | 2 | a0002c0003t0001g0157a0002c0003t0001g0158 | 2 | NA18747.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.68+13485G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521231 | ||||||
chr22:20521242
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+13496A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521242 | ||||||
chr22:20521283
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | NA18943.hp1 NA18950.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+13537G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521283 | ||||||
chr22:20521391
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+13645C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521391 | ||||||
chr22:20521400
|
G | GT | 7 | a0001c0001t0001g0196a0001c0001t0005g0292a0001c0001t0005g0293others(4): Show | 7 | HG01346.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+13659dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521400 | |||||
chr22:20521406
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0136others(124): Show | 134 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.68+13660G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521406 | ||||||
chr22:20521427
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.68+13681C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521427 | ||||||
chr22:20521490
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+13744G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521490 | ||||||
chr22:20521550
|
AT | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+13820delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521550 | |||||
chr22:20521656
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.68+13910A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521656 | ||||||
chr22:20521666
|
G | T | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG00423.hp1 HG02040.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+13920G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521666 | ||||||
chr22:20521675
|
C | T | 3 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0070 | 3 | HG01168.hp1 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.68+13929C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521675 | ||||||
chr22:20521676
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+13930G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521676 | ||||||
chr22:20521691
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68+13945T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521691 | ||||||
chr22:20521695
|
C | CTTAT | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+13986_68+13989d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521695
|
C | CTTATTTA others(1): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0003g0066others(3): Show | 6 | HG00438.hp2 HG00741.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+13982_68+13989d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521695
|
CTTAT | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0192others(33): Show | 37 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(34): Show |
intron_variant | MODIFIER | c.68+13986_68+13989d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521695
|
CTTATTTA others(1): Show |
C | 5 | a0001c0001t0001g0312a0001c0001t0005g0292a0001c0001t0005g0293others(2): Show | 5 | HG01346.hp1 HG02055.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+13982_68+13989d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521695
|
CTTATTTA others(5): Show |
C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+13978_68+13989d others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521695
|
CTTATTTA others(13): Show |
C | 77 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0228others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.68+13970_68+13989d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | |||||
chr22:20521713
|
T | G | 4 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(1): Show | 4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+13967T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521713 | ||||||
chr22:20521923
|
G | A | 1 | a0002c0003t0001g0302 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68+14177G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521923 | ||||||
chr22:20521988
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.68+14242C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521988 | ||||||
chr22:20522222
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0136others(124): Show | 134 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.68+14476A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522222 | ||||||
chr22:20522284
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+14538C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522284 | ||||||
chr22:20522309
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68+14563T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522309 | ||||||
chr22:20522317
|
A | G | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+14571A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522317 | ||||||
chr22:20522339
|
T | C | 2 | a0002c0003t0001g0185a0002c0003t0001g0186 | 2 | NA18967.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.68+14593T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522339 | ||||||
chr22:20522412
|
T | G | 1 | a0001c0002t0002g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68+14666T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522412 | ||||||
chr22:20522554
|
G | A | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-14563G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522554 | ||||||
chr22:20522675
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-14442G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522675 | ||||||
chr22:20522722
|
G | A | 1 | a0001c0002t0002g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.69-14395G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522722 | ||||||
chr22:20522938
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69-14179C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522938 | ||||||
chr22:20523016
|
A | T | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-14101A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523016 | ||||||
chr22:20523065
|
G | C | 1 | a0001c0001t0001g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.69-14052G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523065 | ||||||
chr22:20523155
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 5 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-13962A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523155 | ||||||
chr22:20523297
|
G | A | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.69-13820G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523297 | ||||||
chr22:20523314
|
A | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-13803A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523314 | ||||||
chr22:20523358
|
T | A | 9 | a0001c0001t0001g0296a0001c0001t0003g0066a0001c0001t0005g0292others(6): Show | 9 | HG01346.hp1 HG01934.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-13759T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523358 | ||||||
chr22:20523359
|
A | T | 2 | a0001c0002t0002g0252a0001c0002t0002g0273 | 2 | HG00621.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.69-13758A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523359 | ||||||
chr22:20523480
|
C | G | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-13637C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523480 | ||||||
chr22:20523626
|
C | G | 5 | a0001c0002t0002g0194a0001c0002t0002g0225a0001c0002t0002g0260others(2): Show | 5 | NA18948.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-13491C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523626 | ||||||
chr22:20523702
|
C | T | 1 | a0001c0002t0002g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.69-13415C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523702 | ||||||
chr22:20523769
|
T | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-13348T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523769 | ||||||
chr22:20523888
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.69-13229G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523888 | ||||||
chr22:20524072
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69-13045C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524072 | ||||||
chr22:20524084
|
T | C | 1 | a0003c0005t0001g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69-13033T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524084 | ||||||
chr22:20524473
|
C | G | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-12644C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524473 | ||||||
chr22:20524550
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-12567C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524550 | ||||||
chr22:20524613
|
T | TTTTTG | 12 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(9): Show | 13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-12489_69-12485d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20524613 | |||||
chr22:20524798
|
TTTTAGTA others(9): Show |
T | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-12299_69-12284d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20524798 | |||||
chr22:20524840
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-12277C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524840 | ||||||
chr22:20525080
|
G | A | 1 | a0002c0003t0001g0154 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.69-12037G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525080 | ||||||
chr22:20525320
|
G | GT | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(38): Show | 44 | HG01346.hp1 HG01891.hp1 HG01952.hp1 others(41): Show |
intron_variant | MODIFIER | c.69-11787dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525320 | |||||
chr22:20525501
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11616C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525501 | ||||||
chr22:20525530
|
C | CT | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0105others(4): Show | 7 | HG02135.hp1 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-11564dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | |||||
chr22:20525530
|
CT | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0266a0001c0001t0001g0289others(10): Show | 13 | HG00544.hp2 HG01346.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-11564delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | |||||
chr22:20525530
|
CTT | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0192a0001c0001t0001g0193others(85): Show | 91 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.69-11565_69-11564d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | |||||
chr22:20525530
|
CTTTTTTT | C | 14 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(11): Show | 14 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-11570_69-11564d others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | |||||
chr22:20525578
|
C | T | 3 | a0001c0002t0002g0248a0001c0002t0002g0249a0001c0002t0002g0271 | 3 | NA18943.hp2 NA18966.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.69-11539C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525578 | ||||||
chr22:20525602
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11515T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525602 | ||||||
chr22:20525694
|
G | A | 1 | a0002c0003t0001g0187 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.69-11423G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525694 | ||||||
chr22:20525717
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.69-11400G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525717 | ||||||
chr22:20525725
|
G | A | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-11392G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525725 | ||||||
chr22:20525746
|
G | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-11371G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525746 | ||||||
chr22:20525816
|
G | T | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69-11301G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525816 | ||||||
chr22:20525824
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-11293C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525824 | ||||||
chr22:20525832
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-11285G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525832 | ||||||
chr22:20525864
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11253G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525864 | ||||||
chr22:20526147
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-10970T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526147 | ||||||
chr22:20526423
|
C | T | 3 | a0001c0002t0002g0247a0007c0008t0002g0217a0007c0008t0002g0218 | 3 | HG02155.hp2 NA18945.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.69-10694C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526423 | ||||||
chr22:20526458
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-10659A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526458 | ||||||
chr22:20526611
|
A | T | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-10506A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526611 | ||||||
chr22:20526632
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-10485A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526632 | ||||||
chr22:20526824
|
G | A | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.69-10293G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526824 | ||||||
chr22:20527098
|
T | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00408.hp2 HG00423.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.69-10019T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527098 | ||||||
chr22:20527142
|
G | C | 1 | a0001c0001t0001g0324 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.69-9975G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527142 | ||||||
chr22:20527391
|
C | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(30): Show | 36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.69-9726C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527391 | ||||||
chr22:20527453
|
G | A | 4 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279others(1): Show | 4 | HG01255.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-9664G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527453 | ||||||
chr22:20527453
|
G | GT | 16 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0136others(13): Show | 16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-9656dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527453 | |||||
chr22:20527675
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-9442C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527675 | ||||||
chr22:20527734
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.69-9383C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527734 | ||||||
chr22:20527951
|
C | T | 1 | a0007c0008t0002g0218 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69-9166C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527951 | ||||||
chr22:20527956
|
CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0064others(109): Show | 118 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.69-9141delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527956 | |||||
chr22:20527956
|
CAA | C | 13 | a0001c0001t0001g0193a0001c0001t0001g0210a0001c0001t0001g0295others(10): Show | 14 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-9142_69-9141del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527956 | |||||
chr22:20528040
|
C | T | 4 | a0001c0001t0005g0292a0001c0001t0005g0293a0003c0005t0001g0313others(1): Show | 4 | HG01346.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-9077C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528040 | ||||||
chr22:20528041
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69-9076G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528041 | ||||||
chr22:20528102
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-9015C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528102 | ||||||
chr22:20528136
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-8981G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528136 | ||||||
chr22:20528160
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.69-8957C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528160 | ||||||
chr22:20528254
|
T | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-8863T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528254 | ||||||
chr22:20528322
|
C | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-8795C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528322 | ||||||
chr22:20528353
|
C | T | 1 | a0002c0003t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.69-8764C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528353 | ||||||
chr22:20528357
|
A | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-8760A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528357 | ||||||
chr22:20528448
|
GCA | G | 3 | a0001c0001t0001g0280a0001c0001t0001g0284a0003c0005t0010g0303 | 3 | HG00741.hp2 HG02055.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.69-8666_69-8665del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20528448 | |||||
chr22:20528542
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-8575C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528542 | ||||||
chr22:20528634
|
C | T | 1 | a0004c0021t0002g0258 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.69-8483C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528634 | ||||||
chr22:20528665
|
A | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0137others(15): Show | 19 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.69-8452A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528665 | ||||||
chr22:20528739
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.69-8378C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528739 | ||||||
chr22:20528742
|
C | T | 1 | a0002c0003t0001g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.69-8375C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528742 | ||||||
chr22:20529032
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.69-8085C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529032 | ||||||
chr22:20529035
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.69-8082C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529035 | ||||||
chr22:20529090
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-8027C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529090 | ||||||
chr22:20529162
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.69-7955T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529162 | ||||||
chr22:20529351
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(242): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.69-7766G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529351 | ||||||
chr22:20529367
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0212 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.69-7750C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529367 | ||||||
chr22:20529453
|
T | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-7664T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529453 | ||||||
chr22:20529603
|
T | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-7514T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529603 | ||||||
chr22:20529724
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-7393C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529724 | ||||||
chr22:20529774
|
TAGGG | T | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7341_69-7338del others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20529774 | |||||
chr22:20529779
|
A | C | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7338A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529779 | ||||||
chr22:20529783
|
G | T | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7334G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529783 | ||||||
chr22:20529784
|
G | A | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7333G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529784 | ||||||
chr22:20529787
|
TCAC | T | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7327_69-7325del others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20529787 | |||||
chr22:20529791
|
C | T | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7326C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529791 | ||||||
chr22:20529792
|
A | G | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7325A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529792 | ||||||
chr22:20529794
|
G | A | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7323G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529794 | ||||||
chr22:20529915
|
C | T | 1 | a0002c0003t0001g0176 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.69-7202C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529915 | ||||||
chr22:20529950
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-7167C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529950 | ||||||
chr22:20530006
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69-7111G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530006 | ||||||
chr22:20530013
|
C | T | 13 | a0001c0002t0002g0007a0001c0002t0002g0224a0001c0002t0002g0244others(10): Show | 14 | HG00558.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-7104C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530013 | ||||||
chr22:20530301
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.69-6816C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530301 | ||||||
chr22:20530546
|
T | C | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-6571T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530546 | ||||||
chr22:20530623
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(131): Show | 142 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.69-6494C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530623 | ||||||
chr22:20530714
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18971.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.69-6403G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530714 | ||||||
chr22:20530750
|
A | AG | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0285others(7): Show | 10 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-6366dupG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20530750 | |||||
chr22:20530768
|
G | A | 1 | a0004c0009t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69-6349G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530768 | ||||||
chr22:20530813
|
A | G | 2 | a0001c0001t0001g0312a0001c0002t0002g0251 | 2 | HG02165.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.69-6304A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530813 | ||||||
chr22:20530934
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.69-6183T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530934 | ||||||
chr22:20530971
|
A | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-6146A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530971 | ||||||
chr22:20531020
|
C | T | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.69-6097C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531020 | ||||||
chr22:20531131
|
C | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-5986C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531131 | ||||||
chr22:20531187
|
CTCAGTTT others(1): Show |
C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(163): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.69-5929_69-5922del others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531187 | ||||||
chr22:20531402
|
G | A | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-5715G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531402 | ||||||
chr22:20531991
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-5126G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531991 | ||||||
chr22:20532465
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-4652G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532465 | ||||||
chr22:20532793
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0137others(33): Show | 38 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.69-4324A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532793 | ||||||
chr22:20532879
|
G | T | 5 | a0001c0002t0002g0194a0001c0002t0002g0225a0001c0002t0002g0260others(2): Show | 5 | NA18948.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-4238G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532879 | ||||||
chr22:20532905
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-4212G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532905 | ||||||
chr22:20532963
|
T | G | 1 | a0001c0001t0002g0325 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.69-4154T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532963 | ||||||
chr22:20533067
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69-4050A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533067 | ||||||
chr22:20533246
|
C | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.69-3871C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533246 | ||||||
chr22:20533317
|
C | G | 8 | a0001c0002t0002g0008a0001c0002t0002g0240a0001c0002t0002g0241others(5): Show | 9 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-3800C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533317 | ||||||
chr22:20533327
|
G | A | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-3790G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533327 | ||||||
chr22:20533336
|
A | G | 2 | a0001c0002t0002g0238a0001c0002t0002g0262 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.69-3781A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533336 | ||||||
chr22:20533685
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0308a0001c0001t0001g0309 | 4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-3432C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533685 | ||||||
chr22:20533795
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-3322C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533795 | ||||||
chr22:20533880
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0047others(2): Show | 5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-3237C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533880 | ||||||
chr22:20534082
|
A | G | 1 | a0001c0025t0001g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.69-3035A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534082 | ||||||
chr22:20534127
|
T | C | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-2990T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534127 | ||||||
chr22:20534154
|
C | T | 2 | a0001c0002t0002g0269a0001c0002t0002g0275 | 2 | HG00544.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.69-2963C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534154 | ||||||
chr22:20534439
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0002g0291 | 2 | NA18956.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.69-2678A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534439 | ||||||
chr22:20534451
|
G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-2666G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534451 | ||||||
chr22:20534488
|
C | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-2629C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534488 | ||||||
chr22:20534541
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-2576G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534541 | ||||||
chr22:20534639
|
C | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0208others(7): Show | 10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-2478C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534639 | ||||||
chr22:20534640
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 277 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.69-2477A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534640 | ||||||
chr22:20534641
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-2476C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534641 | ||||||
chr22:20534646
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.69-2471A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534646 | ||||||
chr22:20534797
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.69-2320G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534797 | ||||||
chr22:20534815
|
A | G | 27 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(24): Show | 28 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.69-2302A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534815 | ||||||
chr22:20534817
|
T | C | 29 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(26): Show | 30 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.69-2300T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534817 | ||||||
chr22:20534984
|
G | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(177): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.69-2133G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534984 | ||||||
chr22:20535082
|
C | G | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-2035C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535082 | ||||||
chr22:20535319
|
A | G | 1 | a0001c0023t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.69-1798A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535319 | ||||||
chr22:20535352
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.69-1765A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535352 | ||||||
chr22:20535383
|
A | G | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-1734A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535383 | ||||||
chr22:20535399
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0088others(2): Show | 6 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-1718C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535399 | ||||||
chr22:20535563
|
CT | C | 13 | a0001c0001t0001g0228a0001c0001t0001g0295a0001c0001t0001g0296others(10): Show | 14 | HG01169.hp2 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.69-1540delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535563 | |||||
chr22:20535621
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-1496G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535621 | ||||||
chr22:20535639
|
C | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(263): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.69-1478C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535639 | ||||||
chr22:20535646
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-1471G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535646 | ||||||
chr22:20535660
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.69-1457T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535660 | ||||||
chr22:20535708
|
T | C | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-1409T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535708 | ||||||
chr22:20535716
|
T | C | 13 | a0001c0001t0001g0192a0001c0001t0001g0199a0001c0001t0001g0320others(10): Show | 13 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-1401T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535716 | ||||||
chr22:20535721
|
A | G | 16 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0001t0001g0268others(13): Show | 16 | HG00642.hp1 HG01081.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-1396A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535721 | ||||||
chr22:20535740
|
T | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0086others(35): Show | 39 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.69-1377T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535740 | ||||||
chr22:20535750
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0076others(1): Show | 4 | HG02735.hp1 HG03669.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-1367A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535750 | ||||||
chr22:20535758
|
A | G | 7 | a0001c0001t0001g0045a0002c0003t0001g0133a0002c0003t0001g0134others(4): Show | 7 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1359A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535758 | ||||||
chr22:20535772
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69-1345G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535772 | ||||||
chr22:20535831
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.69-1286C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535831 | ||||||
chr22:20535839
|
G | A | 1 | a0003c0012t0001g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69-1278G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535839 | ||||||
chr22:20535872
|
C | CT | 7 | a0001c0001t0001g0037a0001c0001t0001g0107a0001c0001t0001g0110others(4): Show | 7 | HG01433.hp2 HG03831.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-1222dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535872
|
CT | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0113others(57): Show | 63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.69-1222delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535872
|
CTT | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-1223_69-1222del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535872
|
CTTT | C | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(8): Show | 12 | HG01169.hp2 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.69-1224_69-1222del others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535872
|
CTTTTT | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.69-1226_69-1222del others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535872
|
CTTTTTT | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.69-1227_69-1222del others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | |||||
chr22:20535882
|
T | C | 12 | a0001c0001t0001g0039a0001c0001t0001g0077a0001c0001t0001g0198others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-1235T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535882 | ||||||
chr22:20535980
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.69-1137G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535980 | ||||||
chr22:20535998
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-1119T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535998 | ||||||
chr22:20536026
|
G | A | 1 | a0002c0003t0001g0167 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69-1091G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536026 | ||||||
chr22:20536242
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-875A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536242 | ||||||
chr22:20536272
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-845T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536272 | ||||||
chr22:20536284
|
A | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-833A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536284 | ||||||
chr22:20536359
|
G | T | 1 | a0001c0001t0001g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.69-758G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536359 | ||||||
chr22:20536370
|
G | A | 3 | a0001c0004t0001g0145a0001c0004t0001g0146a0001c0004t0001g0148 | 3 | HG02615.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.69-747G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536370 | ||||||
chr22:20536390
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0110a0001c0001t0001g0201 | 3 | HG03540.hp1 HG03834.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.69-727G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536390 | ||||||
chr22:20536511
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.69-606A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536511 | ||||||
chr22:20536792
|
G | A | 1 | a0004c0009t0001g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69-325G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536792 | ||||||
chr22:20536853
|
G | A | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-264G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536853 | ||||||
chr22:20536972
|
C | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.69-145C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536972 | ||||||
chr22:20537079
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-38T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20537079 | ||||||
chr22:20537093
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.69-24G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20537093 | ||||||
chr22:20537211
|
C | CCCTA | 65 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0113others(62): Show | 68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.156+8_156+11dupCCT others(1): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20537211 | |||||
chr22:20537258
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(278): Show | 291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.156+54A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537258 | ||||||
chr22:20537281
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(168): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.156+77G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537281 | ||||||
chr22:20537393
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0212 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.156+189G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537393 | ||||||
chr22:20537438
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+234C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537438 | ||||||
chr22:20537555
|
C | T | 65 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0113others(62): Show | 68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.156+351C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537555 | ||||||
chr22:20537641
|
G | T | 66 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0113others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.156+437G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537641 | ||||||
chr22:20537763
|
T | G | 1 | a0003c0005t0001g0153 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.156+559T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537763 | ||||||
chr22:20537786
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+582G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537786 | ||||||
chr22:20537803
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.156+599C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537803 | ||||||
chr22:20537930
|
C | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+726C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537930 | ||||||
chr22:20537936
|
T | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | NA18943.hp1 NA18950.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+732T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537936 | ||||||
chr22:20538026
|
C | T | 1 | a0002c0003t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.156+822C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538026 | ||||||
chr22:20538085
|
GC | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG02129.hp2 NA18950.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+883delC | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20538085 | |||||
chr22:20538143
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0104 | 2 | HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.156+939C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538143 | ||||||
chr22:20538304
|
C | T | 4 | a0001c0001t0003g0015a0001c0001t0003g0052a0001c0001t0003g0066others(1): Show | 4 | HG01243.hp2 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1100C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538304 | ||||||
chr22:20538310
|
C | T | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156+1106C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538310 | ||||||
chr22:20538451
|
T | G | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+1247T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538451 | ||||||
chr22:20538545
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0308a0001c0001t0001g0309 | 4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1341C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538545 | ||||||
chr22:20538626
|
T | C | 1 | a0001c0002t0002g0270 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.156+1422T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538626 | ||||||
chr22:20538693
|
G | A | 1 | a0002c0003t0001g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.156+1489G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538693 | ||||||
chr22:20538709
|
C | CGT | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+1517_156+1518d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20538709 | |||||
chr22:20538762
|
C | T | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156+1558C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538762 | ||||||
chr22:20538819
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.156+1615C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538819 | ||||||
chr22:20538853
|
C | G | 1 | a0001c0001t0001g0001 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.156+1649C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538853 | ||||||
chr22:20538907
|
G | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+1703G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538907 | ||||||
chr22:20538981
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0047others(2): Show | 5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+1777A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538981 | ||||||
chr22:20539287
|
T | TG | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(8): Show | 12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+2086dupG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20539287 | |||||
chr22:20539326
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+2122G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539326 | ||||||
chr22:20539480
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.156+2276G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539480 | ||||||
chr22:20539482
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(160): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.156+2278T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539482 | ||||||
chr22:20539627
|
C | G | 1 | a0001c0002t0002g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.156+2423C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539627 | ||||||
chr22:20539884
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+2680C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539884 | ||||||
chr22:20539915
|
G | C | 1 | a0002c0003t0001g0180 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.156+2711G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539915 | ||||||
chr22:20540135
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.156+2931G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540135 | ||||||
chr22:20540508
|
A | G | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+3304A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540508 | ||||||
chr22:20540737
|
C | A | 11 | a0001c0001t0001g0132a0001c0001t0003g0003a0001c0001t0003g0015others(8): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+3533C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540737 | ||||||
chr22:20540871
|
T | C | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.156+3667T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540871 | ||||||
chr22:20540892
|
T | TCAA | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(156): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.156+3713_156+3715d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20540892 | |||||
chr22:20540976
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+3772C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540976 | ||||||
chr22:20541085
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0106a0012c0018t0001g0027 | 3 | HG01891.hp2 HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.156+3881A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541085 | ||||||
chr22:20541239
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156+4035A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541239 | ||||||
chr22:20541342
|
A | G | 2 | a0002c0003t0001g0154a0013c0015t0011g0179 | 2 | NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.156+4138A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541342 | ||||||
chr22:20541353
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.156+4149A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541353 | ||||||
chr22:20541486
|
G | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156+4282G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541486 | ||||||
chr22:20541584
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.156+4380G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541584 | ||||||
chr22:20541640
|
C | T | 9 | a0002c0003t0001g0133a0002c0003t0001g0134a0002c0003t0001g0149others(6): Show | 9 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.156+4436C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541640 | ||||||
chr22:20541650
|
A | AT | 15 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0002t0002g0253others(12): Show | 16 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+4464dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541650 | |||||
chr22:20541650
|
AT | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(187): Show | 196 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.156+4464delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541650 | |||||
chr22:20541751
|
ACAATTAC others(14): Show |
A | 1 | a0002c0014t0001g0191 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.156+4549_156+4569d others(23): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541751 | |||||
chr22:20541870
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.156+4666G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541870 | ||||||
chr22:20541884
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+4680G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541884 | ||||||
chr22:20541934
|
C | T | 16 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(13): Show | 16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+4730C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541934 | ||||||
chr22:20542275
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.156+5071A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542275 | ||||||
chr22:20542406
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+5202G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542406 | ||||||
chr22:20542613
|
T | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+5409T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542613 | ||||||
chr22:20542639
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(158): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.156+5435G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542639 | ||||||
chr22:20542694
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.156+5490T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542694 | ||||||
chr22:20542739
|
C | G | 2 | a0001c0002t0002g0238a0001c0002t0002g0262 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.156+5535C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542739 | ||||||
chr22:20542780
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+5576C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542780 | ||||||
chr22:20542945
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+5741T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542945 | ||||||
chr22:20543035
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.156+5831G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543035 | ||||||
chr22:20543110
|
TTTGTGTG others(12): Show |
T | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.156+5908_156+5926d others(21): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543110 | |||||
chr22:20543111
|
T | TTG | 9 | a0001c0001t0001g0169a0001c0001t0001g0296a0001c0001t0001g0312others(6): Show | 9 | HG00280.hp2 HG02165.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+5947_156+5948d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
T | TTGTG | 23 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0113others(20): Show | 23 | HG00621.hp1 HG02074.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.156+5945_156+5948d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
T | TTGTGTG | 37 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(34): Show | 39 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.156+5943_156+5948d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
T | TTGTGTGT others(1): Show |
9 | a0001c0002t0002g0006a0001c0002t0002g0195a0001c0002t0002g0242others(6): Show | 10 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5941_156+5948d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
T | TTGTGTGT others(3): Show |
1 | a0001c0002t0002g0237 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.156+5939_156+5948d others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTG | T | 10 | a0001c0001t0001g0063a0001c0004t0001g0141a0001c0004t0001g0142others(7): Show | 11 | HG01261.hp2 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+5945_156+5948d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTG | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0107a0001c0001t0001g0110 | 3 | HG03834.hp1 HG04184.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.156+5943_156+5948d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(5): Show |
T | 1 | a0002c0003t0001g0150 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.156+5937_156+5948d others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(7): Show |
T | 10 | a0001c0001t0001g0278a0001c0001t0006g0283a0001c0001t0006g0286others(7): Show | 10 | HG01255.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5935_156+5948d others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(9): Show |
T | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(7): Show | 10 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5933_156+5948d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(11): Show |
T | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0206others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+5931_156+5948d others(20): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(13): Show |
T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(164): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.156+5929_156+5948d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0001g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.156+5927_156+5948d others(24): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543111
|
TTGTGTGT others(19): Show |
T | 1 | a0001c0001t0001g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.156+5923_156+5948d others(28): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | |||||
chr22:20543142
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.156+5938T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543142 | ||||||
chr22:20543202
|
C | CT | 6 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0307others(3): Show | 7 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+6024dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CT | C | 12 | a0001c0001t0001g0107a0001c0001t0001g0295a0001c0001t0001g0296others(9): Show | 13 | HG00741.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.156+6024delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTT | C | 18 | a0001c0001t0001g0319a0001c0004t0001g0141a0001c0004t0001g0142others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+6023_156+6024d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTT | C | 39 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(36): Show | 40 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.156+6022_156+6024d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTT | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0059others(11): Show | 14 | HG00558.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+6021_156+6024d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTTT | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.156+6020_156+6024d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTTTT | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0094others(3): Show | 6 | HG01256.hp2 HG01346.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+6019_156+6024d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0285others(7): Show | 10 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+6017_156+6024d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0278a0001c0002t0002g0216a0001c0002t0002g0220others(3): Show | 6 | HG01255.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+6015_156+6024d others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543202
|
CTTTTTTT others(4): Show |
C | 59 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(56): Show | 62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.156+6014_156+6024d others(13): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | |||||
chr22:20543272
|
C | T | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+6068C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543272 | ||||||
chr22:20543359
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.156+6155C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543359 | ||||||
chr22:20543559
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(275): Show | 288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.156+6355C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543559 | ||||||
chr22:20543561
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.156+6357T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543561 | ||||||
chr22:20543596
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+6392C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543596 | ||||||
chr22:20543597
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+6393G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543597 | ||||||
chr22:20543627
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(177): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.156+6423G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543627 | ||||||
chr22:20543718
|
C | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.156+6514C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543718 | ||||||
chr22:20543833
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.156+6629T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543833 | ||||||
chr22:20543853
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(8): Show | 12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+6649C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543853 | ||||||
chr22:20543870
|
T | G | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+6666T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543870 | ||||||
chr22:20544036
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.156+6832T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544036 | ||||||
chr22:20544115
|
G | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.156+6911G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544115 | ||||||
chr22:20544120
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+6916T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544120 | ||||||
chr22:20544221
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156+7017C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544221 | ||||||
chr22:20544388
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.157-7048G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544388 | ||||||
chr22:20544394
|
G | A | 1 | a0001c0001t0001g0001 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.157-7042G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544394 | ||||||
chr22:20544403
|
C | T | 5 | a0001c0002t0002g0216a0001c0002t0002g0219a0001c0002t0002g0220others(2): Show | 5 | HG00544.hp2 NA18941.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-7033C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544403 | ||||||
chr22:20544470
|
C | A | 1 | a0003c0012t0001g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157-6966C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544470 | ||||||
chr22:20544528
|
G | A | 11 | a0001c0001t0001g0296a0001c0004t0001g0141a0001c0004t0001g0142others(8): Show | 11 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-6908G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544528 | ||||||
chr22:20544632
|
C | T | 1 | a0001c0002t0002g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.157-6804C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544632 | ||||||
chr22:20544669
|
A | C | 60 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0002t0002g0006others(57): Show | 63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.157-6767A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544669 | ||||||
chr22:20544729
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157-6707T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544729 | ||||||
chr22:20544870
|
TA | T | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-6563delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20544870 | |||||
chr22:20544899
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-6537G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544899 | ||||||
chr22:20544967
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-6469G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544967 | ||||||
chr22:20545029
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(191): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-6407G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545029 | ||||||
chr22:20545076
|
A | G | 12 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(9): Show | 13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-6360A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545076 | ||||||
chr22:20545347
|
C | T | 63 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(60): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.157-6089C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545347 | ||||||
chr22:20545418
|
G | A | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.157-6018G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545418 | ||||||
chr22:20545473
|
C | CA | 12 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(9): Show | 13 | HG02135.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-5943dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | |||||
chr22:20545473
|
C | CAAAAA | 47 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(44): Show | 50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-5947_157-5943d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | |||||
chr22:20545473
|
C | CAAAAAA | 11 | a0001c0002t0002g0194a0001c0002t0002g0225a0001c0002t0002g0229others(8): Show | 11 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-5948_157-5943d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | |||||
chr22:20545473
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(195): Show | 204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.157-5943delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | |||||
chr22:20545568
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.157-5868C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545568 | ||||||
chr22:20545674
|
T | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157-5762T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545674 | ||||||
chr22:20545684
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.157-5752G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545684 | ||||||
chr22:20545689
|
T | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.157-5747T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545689 | ||||||
chr22:20545704
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.157-5732G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545704 | ||||||
chr22:20545787
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(191): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-5649T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545787 | ||||||
chr22:20546044
|
G | A | 1 | a0002c0003t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157-5392G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546044 | ||||||
chr22:20546189
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157-5247T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546189 | ||||||
chr22:20546290
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(164): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.157-5146G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546290 | ||||||
chr22:20546322
|
A | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-5114A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546322 | ||||||
chr22:20546379
|
G | A | 1 | a0003c0012t0001g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157-5057G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546379 | ||||||
chr22:20546493
|
T | G | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-4943T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546493 | ||||||
chr22:20546502
|
G | GT | 90 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0025others(87): Show | 94 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.157-4926dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546502 | |||||
chr22:20546502
|
G | GTT | 22 | a0001c0001t0001g0035a0001c0001t0001g0136a0001c0001t0001g0137others(19): Show | 22 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-4927_157-4926d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546502 | |||||
chr22:20546511
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.157-4925G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546511 | ||||||
chr22:20546642
|
G | A | 1 | a0001c0004t0001g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-4794G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546642 | ||||||
chr22:20546657
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-4779C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546657 | ||||||
chr22:20546714
|
C | T | 1 | a0001c0002t0002g0008 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.157-4722C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546714 | ||||||
chr22:20546757
|
C | CA | 3 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143 | 3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.157-4678dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546757 | |||||
chr22:20546789
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-4647C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546789 | ||||||
chr22:20547063
|
CAT | C | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.157-4372_157-4371d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547063 | ||||||
chr22:20547133
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.157-4303A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547133 | ||||||
chr22:20547228
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.157-4208T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547228 | ||||||
chr22:20547235
|
C | T | 1 | a0001c0002t0002g0008 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.157-4201C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547235 | ||||||
chr22:20547333
|
G | A | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-4103G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547333 | ||||||
chr22:20547363
|
T | C | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(8): Show | 12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-4073T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547363 | ||||||
chr22:20547409
|
G | C | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.157-4027G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547409 | ||||||
chr22:20547410
|
A | G | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-4026A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547410 | ||||||
chr22:20547500
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0084 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.157-3936A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547500 | ||||||
chr22:20547511
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-3925G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547511 | ||||||
chr22:20547519
|
C | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(262): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.157-3917C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547519 | ||||||
chr22:20547628
|
G | GCTAACAC others(13): Show |
1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157-3805_157-3786d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20547628 | |||||
chr22:20547692
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-3744C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547692 | ||||||
chr22:20547748
|
G | A | 1 | a0001c0004t0001g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-3688G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547748 | ||||||
chr22:20547754
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | NA18971.hp2 NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.157-3682C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547754 | ||||||
chr22:20547769
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.157-3667A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547769 | ||||||
chr22:20547830
|
A | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0193a0001c0001t0001g0201others(5): Show | 9 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.157-3606A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547830 | ||||||
chr22:20547978
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-3458C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547978 | ||||||
chr22:20548152
|
TTTTTTTG | T | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.157-3265_157-3259d others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20548152 | |||||
chr22:20548231
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0067 | 3 | HG02040.hp1 NA18747.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.157-3205G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548231 | ||||||
chr22:20548585
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-2851C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548585 | ||||||
chr22:20548693
|
T | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-2743T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548693 | ||||||
chr22:20549123
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(191): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-2313C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549123 | ||||||
chr22:20549152
|
T | C | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.157-2284T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549152 | ||||||
chr22:20549154
|
G | A | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.157-2282G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549154 | ||||||
chr22:20549230
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-2206T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549230 | ||||||
chr22:20549231
|
G | A | 3 | a0001c0001t0001g0294a0004c0009t0001g0213a0004c0009t0001g0214 | 3 | HG01258.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.157-2205G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549231 | ||||||
chr22:20549409
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-2027G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549409 | ||||||
chr22:20549495
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.157-1941T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549495 | ||||||
chr22:20549576
|
C | G | 74 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(71): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.157-1860C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549576 | ||||||
chr22:20549744
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0047others(2): Show | 5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-1692C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549744 | ||||||
chr22:20549768
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.157-1668G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549768 | ||||||
chr22:20549786
|
G | C | 74 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(71): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.157-1650G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549786 | ||||||
chr22:20549977
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0106 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.157-1459A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549977 | ||||||
chr22:20550389
|
G | A | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157-1047G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550389 | ||||||
chr22:20550584
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-852C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550584 | ||||||
chr22:20550742
|
G | A | 1 | a0002c0003t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.157-694G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550742 | ||||||
chr22:20550775
|
T | G | 12 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(9): Show | 13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-661T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550775 | ||||||
chr22:20550795
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-641A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550795 | ||||||
chr22:20550801
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(323): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.157-635T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550801 | ||||||
chr22:20550918
|
T | C | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-518T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550918 | ||||||
chr22:20550922
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157-514G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550922 | ||||||
chr22:20550945
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-491C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550945 | ||||||
chr22:20551280
|
C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0193a0001c0001t0001g0202others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-156C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551280 | ||||||
chr22:20551288
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.157-148G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551288 | ||||||
chr22:20551333
|
A | G | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-103A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551333 | ||||||
chr22:20551335
|
G | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 12 | HG00408.hp2 HG00423.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-101G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551335 | ||||||
chr22:20551359
|
C | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-77C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551359 | ||||||
chr22:20551623
|
A | C | 1 | a0014c0013t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.208+136A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551623 | ||||||
chr22:20551664
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208+177C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551664 | ||||||
chr22:20551732
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0114a0011c0019t0001g0091 | 3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.208+245A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551732 | ||||||
chr22:20551765
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.208+278C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551765 | ||||||
chr22:20552055
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.208+568A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552055 | ||||||
chr22:20552079
|
C | T | 1 | a0001c0002t0002g0246 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.208+592C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552079 | ||||||
chr22:20552080
|
G | A | 11 | a0001c0001t0001g0132a0001c0001t0003g0003a0001c0001t0003g0015others(8): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+593G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552080 | ||||||
chr22:20552096
|
C | G | 1 | a0001c0002t0002g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+609C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552096 | ||||||
chr22:20552167
|
C | T | 11 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0312others(8): Show | 12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+680C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552167 | ||||||
chr22:20552185
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.208+698C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552185 | ||||||
chr22:20552190
|
G | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208+703G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552190 | ||||||
chr22:20552509
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.209-636G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552509 | ||||||
chr22:20552661
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.209-484C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552661 | ||||||
chr22:20552713
|
A | G | 2 | a0008c0007t0001g0281a0008c0007t0001g0282 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.209-432A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552713 | ||||||
chr22:20552838
|
T | C | 2 | a0001c0002t0002g0242a0001c0002t0002g0243 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.209-307T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552838 | ||||||
chr22:20552933
|
A | G | 1 | a0001c0002t0002g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.209-212A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552933 | ||||||
chr22:20553016
|
T | C | 135 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(132): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.209-129T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20553016 | ||||||
chr22:20553119
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-26G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20553119 | ||||||
chr22:20553294
|
G | A | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.238+120G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553294 | ||||||
chr22:20553363
|
CTG | C | 10 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0208others(7): Show | 10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+192_238+193del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr22 | 20553363 | |||||
chr22:20553432
|
C | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.238+258C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553432 | ||||||
chr22:20553729
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+555G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553729 | ||||||
chr22:20553778
|
T | C | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.238+604T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553778 | ||||||
chr22:20553825
|
C | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG01081.hp1 HG01256.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.238+651C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553825 | ||||||
chr22:20553828
|
G | A | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.238+654G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553828 | ||||||
chr22:20553959
|
C | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.238+785C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553959 | ||||||
chr22:20553965
|
T | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.238+791T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553965 | ||||||
chr22:20554066
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.239-870C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554066 | ||||||
chr22:20554228
|
C | T | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.239-708C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554228 | ||||||
chr22:20554276
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.239-660T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554276 | ||||||
chr22:20554415
|
A | C | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.239-521A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554415 | ||||||
chr22:20554445
|
A | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.239-491A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554445 | ||||||
chr22:20554449
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-487G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554449 | ||||||
chr22:20554526
|
C | T | 1 | a0001c0002t0002g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.239-410C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554526 | ||||||
chr22:20554581
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0312 | 2 | HG02165.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-355G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554581 | ||||||
chr22:20554640
|
G | A | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239-296G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554640 | ||||||
chr22:20554700
|
T | A | 2 | a0002c0003t0001g0154a0013c0015t0011g0179 | 2 | NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.239-236T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554700 | ||||||
chr22:20554706
|
T | C | 135 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(132): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.239-230T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554706 | ||||||
chr22:20554844
|
C | T | 1 | a0001c0002t0002g0224 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.239-92C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554844 | ||||||
chr22:20554864
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.239-72C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554864 | ||||||
chr22:20554919
|
C | T | 11 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0323others(8): Show | 11 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-17C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554919 | ||||||
chr22:20555161
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0079a0001c0001t0001g0084others(2): Show | 5 | HG02074.hp2 HG02155.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+13C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555161 | ||||||
chr22:20555202
|
A | G | 1 | a0007c0008t0002g0217 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.451+54A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555202 | ||||||
chr22:20555239
|
A | G | 1 | a0002c0003t0001g0174 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.451+91A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555239 | ||||||
chr22:20555257
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+109G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555257 | ||||||
chr22:20555354
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+206C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555354 | ||||||
chr22:20555387
|
G | C | 45 | a0001c0001t0001g0169a0001c0023t0001g0183a0002c0003t0001g0004others(42): Show | 46 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.451+239G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555387 | ||||||
chr22:20555744
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG01081.hp1 HG01256.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+596C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555744 | ||||||
chr22:20555746
|
G | T | 46 | a0001c0001t0001g0169a0001c0001t0001g0319a0001c0023t0001g0183others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.451+598G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555746 | ||||||
chr22:20555753
|
G | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(7): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+605G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555753 | ||||||
chr22:20555790
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0307 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.451+642C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555790 | ||||||
chr22:20555804
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.451+656C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555804 | ||||||
chr22:20555878
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451+730C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555878 | ||||||
chr22:20555906
|
A | G | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+758A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555906 | ||||||
chr22:20555933
|
G | C | 2 | a0002c0003t0001g0159a0002c0003t0001g0180 | 2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.451+785G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555933 | ||||||
chr22:20555934
|
G | A | 60 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+786G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555934 | ||||||
chr22:20555960
|
C | T | 1 | a0001c0002t0002g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.451+812C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555960 | ||||||
chr22:20555977
|
C | T | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.451+829C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555977 | ||||||
chr22:20556012
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.451+864C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556012 | ||||||
chr22:20556034
|
C | T | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+886C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556034 | ||||||
chr22:20556195
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1047C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556195 | ||||||
chr22:20556302
|
G | GT | 54 | a0001c0001t0001g0014a0001c0001t0001g0090a0001c0001t0001g0228others(51): Show | 57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.451+1170dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | |||||
chr22:20556302
|
G | GTT | 11 | a0001c0001t0001g0236a0001c0002t0002g0194a0001c0002t0002g0219others(8): Show | 11 | HG00423.hp2 HG02135.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+1169_451+1170d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | |||||
chr22:20556302
|
GT | G | 86 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0037others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.451+1170delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | |||||
chr22:20556396
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+1248A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556396 | ||||||
chr22:20556466
|
A | G | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+1318A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556466 | ||||||
chr22:20556478
|
T | G | 1 | a0002c0003t0001g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.451+1330T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556478 | ||||||
chr22:20556546
|
C | T | 61 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(58): Show | 64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.451+1398C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556546 | ||||||
chr22:20556579
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.451+1431C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556579 | ||||||
chr22:20556596
|
A | G | 134 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(131): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.451+1448A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556596 | ||||||
chr22:20556673
|
C | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+1525C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556673 | ||||||
chr22:20556793
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.451+1645A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556793 | ||||||
chr22:20556962
|
T | C | 1 | a0001c0002t0002g0263 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.451+1814T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556962 | ||||||
chr22:20557094
|
A | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.451+1946A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557094 | ||||||
chr22:20557270
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.451+2122G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557270 | ||||||
chr22:20557386
|
T | G | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2238T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557386 | ||||||
chr22:20557390
|
C | G | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+2242C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557390 | ||||||
chr22:20557469
|
A | C | 73 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(70): Show | 77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.451+2321A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557469 | ||||||
chr22:20557742
|
G | A | 1 | a0001c0002t0002g0274 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.451+2594G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557742 | ||||||
chr22:20557881
|
C | T | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.451+2733C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557881 | ||||||
chr22:20557888
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+2740C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557888 | ||||||
chr22:20557922
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01070.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.451+2774C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557922 | ||||||
chr22:20557966
|
C | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.451+2818C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557966 | ||||||
chr22:20557967
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+2819G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557967 | ||||||
chr22:20557996
|
C | T | 1 | a0003c0012t0001g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.451+2848C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557996 | ||||||
chr22:20558116
|
GAA | G | 5 | a0001c0004t0001g0144a0001c0004t0001g0145a0001c0004t0001g0146others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+2972_451+2973d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20558116 | |||||
chr22:20558341
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.451+3193G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558341 | ||||||
chr22:20558506
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0193a0001c0001t0001g0202others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+3358A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558506 | ||||||
chr22:20558555
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0088others(2): Show | 6 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+3407A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558555 | ||||||
chr22:20558592
|
T | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+3444T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558592 | ||||||
chr22:20558683
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+3535A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558683 | ||||||
chr22:20558708
|
G | A | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+3560G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558708 | ||||||
chr22:20558725
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+3577T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558725 | ||||||
chr22:20558799
|
G | A | 1 | a0001c0002t0002g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.451+3651G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558799 | ||||||
chr22:20558920
|
A | G | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+3772A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558920 | ||||||
chr22:20559048
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.451+3900C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559048 | ||||||
chr22:20559064
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+3916G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559064 | ||||||
chr22:20559223
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+4075A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559223 | ||||||
chr22:20559241
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.451+4093C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559241 | ||||||
chr22:20559262
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.451+4114G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559262 | ||||||
chr22:20559345
|
TAGAAGCT others(8): Show |
T | 2 | a0001c0002t0002g0238a0001c0002t0002g0262 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.451+4202_451+4216d others(17): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20559345 | |||||
chr22:20559470
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.451+4322G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559470 | ||||||
chr22:20559558
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.451+4410A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559558 | ||||||
chr22:20559591
|
G | A | 46 | a0001c0001t0001g0169a0001c0001t0001g0319a0001c0023t0001g0183others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.451+4443G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559591 | ||||||
chr22:20559659
|
C | T | 1 | a0002c0003t0001g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.451+4511C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559659 | ||||||
chr22:20559785
|
C | G | 1 | a0001c0001t0001g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451+4637C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559785 | ||||||
chr22:20559929
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-4521G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559929 | ||||||
chr22:20560261
|
C | CTATTAT | 60 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0002t0002g0006others(57): Show | 63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.452-4171_452-4166d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20560261 | |||||
chr22:20560340
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.452-4110C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560340 | ||||||
chr22:20560372
|
C | G | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452-4078C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560372 | ||||||
chr22:20560402
|
C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0006t0001g0135others(1): Show | 4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4048C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560402 | ||||||
chr22:20560411
|
C | T | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452-4039C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560411 | ||||||
chr22:20560412
|
G | A | 59 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0002t0002g0006others(56): Show | 62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-4038G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560412 | ||||||
chr22:20560421
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.452-4029C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560421 | ||||||
chr22:20560453
|
C | T | 1 | a0001c0002t0002g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.452-3997C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560453 | ||||||
chr22:20560454
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.452-3996G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560454 | ||||||
chr22:20560470
|
G | A | 60 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0107others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-3980G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560470 | ||||||
chr22:20560474
|
A | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0059others(22): Show | 25 | HG00558.hp2 HG01261.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.452-3976A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560474 | ||||||
chr22:20560484
|
C | T | 2 | a0002c0003t0001g0151a0002c0003t0001g0152 | 2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.452-3966C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560484 | ||||||
chr22:20560509
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.452-3941C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560509 | ||||||
chr22:20560528
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.452-3922G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560528 | ||||||
chr22:20560558
|
T | C | 1 | a0001c0002t0002g0273 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.452-3892T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560558 | ||||||
chr22:20560671
|
C | T | 60 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-3779C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560671 | ||||||
chr22:20560776
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.452-3674G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560776 | ||||||
chr22:20561101
|
A | G | 1 | a0002c0003t0001g0158 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.452-3349A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561101 | ||||||
chr22:20561241
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0315 | 2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452-3209C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561241 | ||||||
chr22:20561248
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(4): Show | 8 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-3202C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561248 | ||||||
chr22:20561330
|
C | G | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-3120C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561330 | ||||||
chr22:20561344
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-3106C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561344 | ||||||
chr22:20561345
|
G | A | 1 | a0002c0003t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.452-3105G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561345 | ||||||
chr22:20561388
|
C | T | 58 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 59 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.452-3062C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561388 | ||||||
chr22:20561435
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.452-3015G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561435 | ||||||
chr22:20561452
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0009g0089 | 3 | HG02809.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.452-2998G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561452 | ||||||
chr22:20561505
|
T | C | 3 | a0001c0004t0001g0145a0001c0004t0001g0146a0001c0004t0001g0148 | 3 | HG02615.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.452-2945T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561505 | ||||||
chr22:20561549
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.452-2901T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561549 | ||||||
chr22:20561572
|
A | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-2878A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561572 | ||||||
chr22:20561702
|
C | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-2748C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561702 | ||||||
chr22:20561703
|
G | A | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-2747G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561703 | ||||||
chr22:20561941
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | NA18943.hp1 NA18950.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-2509T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561941 | ||||||
chr22:20561944
|
T | C | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-2506T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561944 | ||||||
chr22:20561986
|
CTCAA | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.452-2456_452-2453d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20561986 | |||||
chr22:20561996
|
C | T | 1 | a0001c0002t0002g0250 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.452-2454C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561996 | ||||||
chr22:20562046
|
A | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-2404A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562046 | ||||||
chr22:20562230
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-2220G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562230 | ||||||
chr22:20562333
|
A | G | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.452-2117A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562333 | ||||||
chr22:20562380
|
A | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-2070A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562380 | ||||||
chr22:20562407
|
CAG | C | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-2040_452-2039d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20562407 | |||||
chr22:20562465
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.452-1985A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562465 | ||||||
chr22:20562545
|
C | T | 11 | a0001c0001t0001g0132a0001c0001t0003g0003a0001c0001t0003g0015others(8): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-1905C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562545 | ||||||
chr22:20562586
|
G | C | 1 | a0001c0002t0002g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.452-1864G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562586 | ||||||
chr22:20562641
|
C | G | 1 | a0001c0002t0002g0244 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.452-1809C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562641 | ||||||
chr22:20562682
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.452-1768G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562682 | ||||||
chr22:20562780
|
A | G | 123 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(120): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.452-1670A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562780 | ||||||
chr22:20562863
|
C | T | 1 | a0002c0003t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.452-1587C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562863 | ||||||
chr22:20563017
|
C | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-1433C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563017 | ||||||
chr22:20563035
|
C | CA | 6 | a0001c0001t0001g0102a0001c0001t0001g0278a0001c0001t0005g0292others(3): Show | 6 | HG01255.hp1 HG01346.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-1403dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20563035 | |||||
chr22:20563035
|
CA | C | 71 | a0001c0001t0001g0104a0001c0001t0001g0122a0001c0001t0001g0228others(68): Show | 75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.452-1403delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20563035 | |||||
chr22:20563118
|
A | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.452-1332A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563118 | ||||||
chr22:20563143
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.452-1307A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563143 | ||||||
chr22:20563240
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-1210A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563240 | ||||||
chr22:20563241
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0005g0292a0001c0001t0005g0293 | 3 | HG01346.hp1 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.452-1209T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563241 | ||||||
chr22:20563397
|
A | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-1053A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563397 | ||||||
chr22:20563544
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.452-906C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563544 | ||||||
chr22:20563544
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0114others(1): Show | 4 | HG01099.hp1 HG01516.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-906C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563544 | ||||||
chr22:20563775
|
C | T | 2 | a0004c0009t0001g0213a0004c0009t0001g0214 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.452-675C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563775 | ||||||
chr22:20563965
|
C | T | 1 | a0002c0003t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.452-485C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563965 | ||||||
chr22:20564117
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.452-333C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564117 | ||||||
chr22:20564175
|
C | T | 1 | a0001c0001t0013g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.452-275C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564175 | ||||||
chr22:20564198
|
C | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-252C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564198 | ||||||
chr22:20564228
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-222T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564228 | ||||||
chr22:20564231
|
T | G | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-219T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564231 | ||||||
chr22:20564240
|
A | G | 2 | a0005c0011t0001g0139a0005c0011t0001g0140 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.452-210A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564240 | ||||||
chr22:20564343
|
C | T | 1 | a0001c0002t0002g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.452-107C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564343 | ||||||
chr22:20564778
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.690+90G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20564778 | ||||||
chr22:20564880
|
C | T | 1 | a0014c0013t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.690+192C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20564880 | ||||||
chr22:20565019
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.690+331A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565019 | ||||||
chr22:20565085
|
G | A | 1 | a0002c0003t0001g0156 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.690+397G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565085 | ||||||
chr22:20565089
|
C | T | 1 | a0003c0005t0010g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+401C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565089 | ||||||
chr22:20565090
|
G | A | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.690+402G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565090 | ||||||
chr22:20565109
|
T | C | 168 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(165): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.690+421T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565109 | ||||||
chr22:20565117
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.690+429C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565117 | ||||||
chr22:20565148
|
A | G | 1 | a0001c0001t0005g0292 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690+460A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565148 | ||||||
chr22:20565159
|
G | A | 11 | a0001c0001t0001g0234a0001c0002t0002g0226a0001c0002t0002g0227others(8): Show | 11 | HG00621.hp2 HG02056.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.690+471G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565159 | ||||||
chr22:20565430
|
T | G | 2 | a0001c0002t0002g0216a0001c0002t0002g0220 | 2 | NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.690+742T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565430 | ||||||
chr22:20565468
|
C | T | 46 | a0001c0001t0001g0169a0001c0001t0001g0319a0001c0023t0001g0183others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.690+780C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565468 | ||||||
chr22:20565709
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-758C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565709 | ||||||
chr22:20565709
|
C | T | 1 | a0001c0001t0005g0293 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.691-758C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565709 | ||||||
chr22:20565757
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-710C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565757 | ||||||
chr22:20565896
|
C | CCCAGGCA others(11): Show |
2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.691-568_691-551dup others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20565896 | |||||
chr22:20565912
|
G | C | 51 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.691-555G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565912 | ||||||
chr22:20565922
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.691-545G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565922 | ||||||
chr22:20566030
|
C | CT | 79 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(76): Show | 81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.691-417dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | |||||
chr22:20566030
|
CT | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0071others(17): Show | 22 | HG02083.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-417delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | |||||
chr22:20566030
|
CTT | C | 11 | a0001c0001t0001g0312a0001c0001t0005g0292a0001c0001t0005g0293others(8): Show | 12 | HG01346.hp1 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-418_691-417del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | |||||
chr22:20566030
|
CTTTT | C | 60 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.691-420_691-417del others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | |||||
chr22:20566101
|
G | A | 2 | a0001c0001t0001g0206a0003c0005t0001g0265 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.691-366G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566101 | ||||||
chr22:20566149
|
C | A | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.691-318C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566149 | ||||||
chr22:20566284
|
C | T | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.691-183C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566284 | ||||||
chr22:20566339
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.691-128C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566339 | ||||||
chr22:20566407
|
A | G | 2 | a0001c0002t0002g0238a0001c0002t0002g0262 | 2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.691-60A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566407 | ||||||
chr22:20566415
|
G | A | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-52G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566415 | ||||||
chr22:20566969
|
C | T | 1 | a0002c0003t0001g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1041+152C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20566969 | ||||||
chr22:20567035
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1041+218A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567035 | ||||||
chr22:20567052
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1041+235A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567052 | ||||||
chr22:20567068
|
G | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1041+251G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567068 | ||||||
chr22:20567168
|
G | A | 8 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(5): Show | 9 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+351G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567168 | ||||||
chr22:20567436
|
C | G | 9 | a0001c0002t0002g0006a0001c0002t0002g0008a0001c0002t0002g0240others(6): Show | 11 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1041+619C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567436 | ||||||
chr22:20567499
|
G | C | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041+682G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567499 | ||||||
chr22:20567585
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1041+768G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567585 | ||||||
chr22:20567606
|
G | T | 123 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(120): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1041+789G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567606 | ||||||
chr22:20567672
|
A | C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1042-849A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567672 | ||||||
chr22:20567869
|
T | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0296a0002c0003t0001g0009others(6): Show | 10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-652T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567869 | ||||||
chr22:20567943
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1042-578G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567943 | ||||||
chr22:20568029
|
T | C | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1042-492T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568029 | ||||||
chr22:20568183
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0013g0288 | 2 | HG01952.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1042-338C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568183 | ||||||
chr22:20568231
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1042-290G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568231 | ||||||
chr22:20568273
|
T | TGTG | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1042-247_1042-245d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr22 | 20568273 | |||||
chr22:20568289
|
G | C | 1 | a0001c0002t0002g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1042-232G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568289 | ||||||
chr22:20568409
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1042-112G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568409 | ||||||
chr22:20568438
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0315 | 2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-83A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568438 | ||||||
chr22:20568923
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1152+292T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568923 | ||||||
chr22:20568932
|
G | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0236 | 2 | NA18939.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1152+301G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568932 | ||||||
chr22:20568960
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1152+329C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568960 | ||||||
chr22:20569074
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1152+443C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569074 | ||||||
chr22:20569419
|
G | A | 1 | a0002c0003t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1152+788G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569419 | ||||||
chr22:20569459
|
C | T | 1 | a0001c0002t0002g0259 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1152+828C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569459 | ||||||
chr22:20569460
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1152+829G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569460 | ||||||
chr22:20569583
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1152+952G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569583 | ||||||
chr22:20569635
|
TGAG | T | 14 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(11): Show | 14 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+1009_1152+101 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20569635 | |||||
chr22:20569741
|
A | G | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1152+1110A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569741 | ||||||
chr22:20569872
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+1241G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569872 | ||||||
chr22:20570066
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0205a0001c0001t0001g0266 | 4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1435C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570066 | ||||||
chr22:20570087
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1152+1456C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570087 | ||||||
chr22:20570088
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0002g0040 | 2 | HG02300.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1152+1457G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570088 | ||||||
chr22:20570192
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1152+1561T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570192 | ||||||
chr22:20570224
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+1593C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570224 | ||||||
chr22:20570269
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0307 | 3 | HG02818.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1152+1638G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570269 | ||||||
chr22:20570304
|
T | G | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1152+1673T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570304 | ||||||
chr22:20570315
|
G | A | 1 | a0001c0002t0004g0016 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1152+1684G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570315 | ||||||
chr22:20570318
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1152+1687C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570318 | ||||||
chr22:20570333
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0205a0001c0001t0001g0266 | 4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1702G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570333 | ||||||
chr22:20570393
|
CT | C | 84 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1152+1778delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570393 | |||||
chr22:20570414
|
C | T | 2 | a0001c0002t0002g0194a0001c0002t0002g0264 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1152+1783C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570414 | ||||||
chr22:20570494
|
C | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0284 | 2 | HG00741.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1152+1863C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570494 | ||||||
chr22:20570526
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0006t0001g0135others(1): Show | 4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+1895G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570526 | ||||||
chr22:20570614
|
C | A | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+1983C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570614 | ||||||
chr22:20570652
|
A | C | 1 | a0001c0002t0002g0008 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1152+2021A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570652 | ||||||
chr22:20570726
|
T | TTTTC | 14 | a0001c0002t0002g0195a0001c0002t0002g0216a0001c0002t0002g0219others(11): Show | 14 | HG00408.hp1 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+2115_1152+211 others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570726 | |||||
chr22:20570726
|
T | TTTTCTTT others(1): Show |
15 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(12): Show | 15 | HG00140.hp2 HG00621.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1152+2111_1152+211 others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570726 | |||||
chr22:20570746
|
C | CTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0306others(3): Show | 7 | HG01109.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2144_1152+214 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
C | CTTTTTTT others(5): Show |
1 | a0002c0003t0001g0299 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1152+2134_1152+214 others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CT | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1152+2145delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTT | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0051others(9): Show | 12 | HG00733.hp1 HG01070.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+2144_1152+214 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTT | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | HG00741.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2143_1152+214 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTTTTTT others(3): Show |
C | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1152+2136_1152+214 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0005g0293 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1152+2135_1152+214 others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0061a0001c0001t0005g0292 | 2 | HG02698.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+2134_1152+214 others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+2133_1152+214 others(17): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570746
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1152+2130_1152+214 others(20): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | |||||
chr22:20570747
|
T | TTTC | 50 | a0001c0001t0001g0200a0001c0001t0001g0234a0001c0001t0001g0236others(47): Show | 53 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | |||||
chr22:20570747
|
T | TTTCTTTC | 27 | a0001c0001t0001g0169a0002c0003t0001g0004a0002c0003t0001g0151others(24): Show | 28 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(11): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | |||||
chr22:20570747
|
T | TTTCTTTC others(4): Show |
1 | a0001c0023t0001g0183 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1152+2118_1152+211 others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | |||||
chr22:20570748
|
T | TTCTTTCT others(3): Show |
1 | a0002c0003t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1152+2118_1152+211 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570748 | |||||
chr22:20570749
|
T | TCTTTCTT others(2): Show |
4 | a0001c0001t0001g0107a0002c0003t0001g0164a0002c0003t0001g0166others(1): Show | 4 | HG00280.hp2 HG00735.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(13): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570749 | ||||||
chr22:20570750
|
T | C | 16 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(13): Show | 16 | HG00140.hp2 HG01069.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1152+2119T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570750 | ||||||
chr22:20570751
|
T | C | 38 | a0001c0001t0001g0169a0001c0004t0001g0144a0001c0004t0001g0145others(35): Show | 39 | HG00438.hp2 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1152+2120T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570751 | ||||||
chr22:20570753
|
T | C | 2 | a0001c0001t0001g0319a0002c0003t0001g0166 | 2 | HG00099.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1152+2122T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570753 | ||||||
chr22:20570754
|
T | C | 1 | a0002c0003t0001g0172 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1152+2123T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570754 | ||||||
chr22:20570755
|
T | C | 2 | a0002c0003t0001g0171a0002c0003t0001g0173 | 2 | HG00733.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1152+2124T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570755 | ||||||
chr22:20570757
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1152+2126T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570757 | ||||||
chr22:20570773
|
T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1152+2145_1152+214 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570773 | |||||
chr22:20570814
|
G | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1152+2183G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570814 | ||||||
chr22:20570830
|
A | G | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1152+2199A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570830 | ||||||
chr22:20570850
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1152+2219C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570850 | ||||||
chr22:20570917
|
A | G | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+2286A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570917 | ||||||
chr22:20571060
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1152+2429G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571060 | ||||||
chr22:20571067
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+2436C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571067 | ||||||
chr22:20571102
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1152+2471A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571102 | ||||||
chr22:20571275
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1152+2644A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571275 | ||||||
chr22:20571337
|
C | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1152+2706C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571337 | ||||||
chr22:20571347
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1152+2716G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571347 | ||||||
chr22:20571373
|
C | T | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+2742C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571373 | ||||||
chr22:20571428
|
C | T | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+2797C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571428 | ||||||
chr22:20571473
|
G | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1152+2842G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571473 | ||||||
chr22:20571658
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+3027C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571658 | ||||||
chr22:20572008
|
G | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(317): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1153-3105G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572008 | ||||||
chr22:20572214
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1153-2899A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572214 | ||||||
chr22:20572272
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0278others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1153-2841G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572272 | ||||||
chr22:20572338
|
G | A | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-2775G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572338 | ||||||
chr22:20572517
|
T | G | 2 | a0004c0009t0001g0213a0004c0009t0001g0214 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1153-2596T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572517 | ||||||
chr22:20572526
|
C | T | 62 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(59): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1153-2587C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572526 | ||||||
chr22:20572601
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1153-2512C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572601 | ||||||
chr22:20572637
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1153-2476A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572637 | ||||||
chr22:20572639
|
G | GC | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1153-2473dupC | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20572639 | |||||
chr22:20572739
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-2374C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572739 | ||||||
chr22:20572786
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1153-2327G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572786 | ||||||
chr22:20572812
|
C | T | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-2301C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572812 | ||||||
chr22:20572839
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-2274C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572839 | ||||||
chr22:20572966
|
C | CT | 73 | a0001c0001t0001g0125a0001c0001t0001g0136a0001c0001t0001g0137others(70): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1153-2130dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20572966 | |||||
chr22:20572971
|
T | TC | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-2142_1153-214 others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572971 | ||||||
chr22:20573046
|
G | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-2067G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573046 | ||||||
chr22:20573092
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-2021C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573092 | ||||||
chr22:20573247
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1153-1866C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573247 | ||||||
chr22:20573256
|
C | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1857C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573256 | ||||||
chr22:20573326
|
G | A | 9 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0001g0208others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1153-1787G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573326 | ||||||
chr22:20573388
|
G | A | 59 | a0001c0001t0001g0234a0001c0002t0002g0006a0001c0002t0002g0007others(56): Show | 62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1725G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573388 | ||||||
chr22:20573429
|
T | C | 63 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(60): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1153-1684T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573429 | ||||||
chr22:20573515
|
G | A | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1598G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573515 | ||||||
chr22:20573711
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-1402C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573711 | ||||||
chr22:20573717
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1153-1396T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573717 | ||||||
chr22:20573753
|
T | G | 1 | a0002c0003t0001g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1153-1360T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573753 | ||||||
chr22:20573830
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1153-1283C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573830 | ||||||
chr22:20573843
|
C | T | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-1270C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573843 | ||||||
chr22:20573878
|
C | T | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-1235C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573878 | ||||||
chr22:20573947
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1153-1166C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573947 | ||||||
chr22:20573979
|
G | A | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1134G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573979 | ||||||
chr22:20574271
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-842A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574271 | ||||||
chr22:20574278
|
A | G | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-835A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574278 | ||||||
chr22:20574284
|
G | A | 1 | a0001c0002t0002g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1153-829G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574284 | ||||||
chr22:20574330
|
G | A | 2 | a0005c0011t0001g0139a0005c0011t0001g0140 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1153-783G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574330 | ||||||
chr22:20574401
|
T | G | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-712T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574401 | ||||||
chr22:20574497
|
T | C | 3 | a0001c0001t0001g0278a0006c0010t0001g0277a0006c0010t0001g0279 | 3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1153-616T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574497 | ||||||
chr22:20574522
|
C | T | 127 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(124): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1153-591C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574522 | ||||||
chr22:20574604
|
G | T | 3 | a0001c0002t0002g0225a0001c0002t0002g0260a0001c0002t0002g0263 | 3 | NA18955.hp2 NA18957.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1153-509G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574604 | ||||||
chr22:20574661
|
C | T | 5 | a0001c0002t0002g0226a0001c0002t0002g0227a0001c0002t0002g0252others(2): Show | 5 | HG00621.hp2 HG02071.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-452C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574661 | ||||||
chr22:20574690
|
T | G | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-423T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574690 | ||||||
chr22:20574787
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1153-326C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574787 | ||||||
chr22:20574797
|
T | C | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1153-316T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574797 | ||||||
chr22:20574808
|
T | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0192others(11): Show | 17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1153-305T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574808 | ||||||
chr22:20574999
|
C | G | 163 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0107others(160): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1153-114C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574999 | ||||||
chr22:20575055
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1153-58C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20575055 | ||||||
chr22:20575368
|
CT | C | 17 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0193others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1272+151delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575368 | |||||
chr22:20575469
|
G | A | 1 | a0014c0013t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1272+237G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575469 | ||||||
chr22:20575495
|
C | A | 151 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(148): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1272+263C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575495 | ||||||
chr22:20575593
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1272+361C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575593 | ||||||
chr22:20575627
|
C | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1272+395C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575627 | ||||||
chr22:20575637
|
C | T | 51 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1272+405C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575637 | ||||||
chr22:20575688
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1272+456A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575688 | ||||||
chr22:20575692
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1272+460C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575692 | ||||||
chr22:20575705
|
C | T | 1 | a0001c0002t0002g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1272+473C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575705 | ||||||
chr22:20575721
|
AT | A | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+495delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575721 | |||||
chr22:20575768
|
CA | C | 125 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(122): Show | 129 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1272+546delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575768 | |||||
chr22:20575778
|
A | C | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+546A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575778 | ||||||
chr22:20575788
|
C | T | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+556C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575788 | ||||||
chr22:20576055
|
CT | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(5): Show | 9 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+827delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20576055 | |||||
chr22:20576253
|
T | C | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+1021T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576253 | ||||||
chr22:20576329
|
G | A | 2 | a0003c0005t0001g0313a0003c0012t0001g0314 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1272+1097G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576329 | ||||||
chr22:20576433
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1201C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576433 | ||||||
chr22:20576691
|
TGGG | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1272+1462_1272+146 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20576691 | |||||
chr22:20576704
|
T | G | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1472T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576704 | ||||||
chr22:20576807
|
T | C | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1575T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576807 | ||||||
chr22:20576836
|
G | C | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1604G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576836 | ||||||
chr22:20576891
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1659G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576891 | ||||||
chr22:20576929
|
G | T | 1 | a0001c0001t0007g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1272+1697G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576929 | ||||||
chr22:20577015
|
T | C | 2 | a0004c0009t0001g0213a0004c0009t0001g0214 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1272+1783T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577015 | ||||||
chr22:20577111
|
C | T | 1 | a0001c0002t0002g0194 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1272+1879C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577111 | ||||||
chr22:20577170
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1938G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577170 | ||||||
chr22:20577203
|
T | G | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+1971T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577203 | ||||||
chr22:20577257
|
G | A | 11 | a0001c0002t0002g0006a0001c0002t0002g0008a0001c0002t0002g0223others(8): Show | 13 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+2025G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577257 | ||||||
chr22:20577456
|
C | T | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1272+2224C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577456 | ||||||
chr22:20577726
|
C | G | 1 | a0002c0003t0001g0178 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1272+2494C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577726 | ||||||
chr22:20577823
|
G | A | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+2591G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577823 | ||||||
chr22:20577876
|
T | A | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1272+2644T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577876 | ||||||
chr22:20577880
|
G | A | 1 | a0001c0001t0005g0292 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1272+2648G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577880 | ||||||
chr22:20577936
|
T | A | 1 | a0001c0002t0002g0224 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272+2704T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577936 | ||||||
chr22:20577951
|
T | G | 8 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(5): Show | 9 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+2719T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577951 | ||||||
chr22:20577955
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1272+2723G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577955 | ||||||
chr22:20577992
|
C | T | 167 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(164): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1272+2760C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577992 | ||||||
chr22:20578028
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+2796G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578028 | ||||||
chr22:20578053
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1272+2821T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578053 | ||||||
chr22:20578167
|
C | T | 1 | a0001c0001t0005g0293 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1272+2935C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578167 | ||||||
chr22:20578171
|
C | T | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+2939C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578171 | ||||||
chr22:20578176
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1272+2944C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578176 | ||||||
chr22:20578271
|
A | G | 1 | a0009c0024t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+3039A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578271 | ||||||
chr22:20578354
|
C | A | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1272+3122C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578354 | ||||||
chr22:20578393
|
C | A | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+3161C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578393 | ||||||
chr22:20578425
|
C | T | 66 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+3193C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578425 | ||||||
chr22:20578426
|
C | G | 128 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(125): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1272+3194C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578426 | ||||||
chr22:20578606
|
G | A | 1 | a0001c0002t0002g0224 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272+3374G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578606 | ||||||
chr22:20578676
|
CAG | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272+3445_1272+344 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578676 | ||||||
chr22:20578825
|
A | G | 2 | a0005c0011t0001g0139a0005c0011t0001g0140 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1272+3593A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578825 | ||||||
chr22:20578910
|
CCT | C | 57 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 58 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1272+3681_1272+368 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20578910 | |||||
chr22:20578922
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1273-3689C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578922 | ||||||
chr22:20578949
|
G | A | 1 | a0003c0005t0002g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1273-3662G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578949 | ||||||
chr22:20579149
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1273-3462C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579149 | ||||||
chr22:20579381
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1273-3230C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579381 | ||||||
chr22:20579448
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0013g0288 | 2 | HG01952.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1273-3163C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579448 | ||||||
chr22:20579497
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0306a0001c0001t0001g0308others(1): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-3114C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579497 | ||||||
chr22:20579536
|
C | T | 1 | a0001c0001t0002g0291 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-3075C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579536 | ||||||
chr22:20579614
|
T | C | 67 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(64): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273-2997T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579614 | ||||||
chr22:20579753
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1273-2858C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579753 | ||||||
chr22:20579757
|
C | G | 1 | a0001c0001t0002g0291 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-2854C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579757 | ||||||
chr22:20579952
|
T | A | 67 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(64): Show | 70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273-2659T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579952 | ||||||
chr22:20580124
|
C | T | 7 | a0002c0003t0001g0009a0002c0003t0001g0297a0002c0003t0001g0298others(4): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1273-2487C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580124 | ||||||
chr22:20580221
|
C | T | 10 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(7): Show | 10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1273-2390C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580221 | ||||||
chr22:20580338
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1273-2273C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580338 | ||||||
chr22:20580476
|
AG | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0047others(2): Show | 5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-2133delG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20580476 | |||||
chr22:20580685
|
T | G | 64 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0236others(61): Show | 67 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1273-1926T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580685 | ||||||
chr22:20580722
|
C | T | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-1889C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580722 | ||||||
chr22:20580897
|
G | A | 1 | a0001c0001t0001g0001 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1273-1714G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580897 | ||||||
chr22:20580942
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1273-1669G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580942 | ||||||
chr22:20580986
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1273-1625G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580986 | ||||||
chr22:20581089
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(286): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1273-1522A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581089 | ||||||
chr22:20581105
|
G | A | 6 | a0002c0003t0001g0297a0002c0003t0001g0298a0002c0003t0001g0299others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273-1506G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581105 | ||||||
chr22:20581159
|
C | T | 1 | a0002c0003t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1273-1452C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581159 | ||||||
chr22:20581253
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0025t0001g0087 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1273-1358G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581253 | ||||||
chr22:20581386
|
A | C | 48 | a0001c0001t0001g0120a0001c0001t0001g0169a0001c0001t0001g0289others(45): Show | 49 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1273-1225A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581386 | ||||||
chr22:20581398
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1273-1213G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581398 | ||||||
chr22:20581430
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1273-1181G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581430 | ||||||
chr22:20581444
|
G | A | 126 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(123): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1273-1167G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581444 | ||||||
chr22:20581659
|
G | A | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0280others(9): Show | 12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-952G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581659 | ||||||
chr22:20581805
|
G | C | 1 | a0001c0001t0001g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1273-806G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581805 | ||||||
chr22:20581840
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1273-771C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581840 | ||||||
chr22:20581920
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1273-691C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581920 | ||||||
chr22:20582047
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0278a0001c0001t0001g0280others(26): Show | 30 | HG00741.hp2 HG01109.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1273-564C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582047 | ||||||
chr22:20582228
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1273-383G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582228 | ||||||
chr22:20582411
|
G | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG02257.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1273-200G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582411 | ||||||
chr22:20582533
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1273-78T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582533 | ||||||
chr22:20582534
|
G | A | 3 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143 | 3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1273-77G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582534 | ||||||
chr22:20582565
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1273-46C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582565 | ||||||
chr22:20582586
|
G | A | 6 | a0001c0004t0001g0144a0001c0004t0001g0146a0001c0004t0001g0147others(3): Show | 6 | HG02723.hp1 HG02895.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273-25G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582586 | ||||||
chr22:20582764
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1409+17G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/17 | chr22 | 20582764 | ||||||
chr22:20583314
|
C | T | 60 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1673-16C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 12/17 | chr22 | 20583314 | ||||||
chr22:20583406
|
CACAGCCC others(8): Show |
C | 1 | a0013c0015t0011g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1736+14_1736+28del others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583406 | ||||||
chr22:20583893
|
G | A | 63 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008others(60): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737-466G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583893 | ||||||
chr22:20583940
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1737-419A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583940 | ||||||
chr22:20584090
|
A | G | 64 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737-269A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20584090 | ||||||
chr22:20584175
|
G | C | 1 | a0002c0003t0001g0318 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1737-184G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20584175 | ||||||
chr22:20584485
|
T | C | 66 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0001t0001g0316others(63): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1803+60T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584485 | ||||||
chr22:20584488
|
T | C | 201 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(198): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1803+63T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584488 | ||||||
chr22:20584836
|
G | A | 64 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1804-19G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584836 | ||||||
chr22:20585321
|
C | A | 63 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008others(60): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2131+54C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585321 | ||||||
chr22:20585330
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2131+63C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585330 | ||||||
chr22:20585344
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2131+77A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585344 | ||||||
chr22:20585345
|
G | C | 1 | a0002c0003t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2131+78G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585345 | ||||||
chr22:20585422
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2131+155C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585422 | ||||||
chr22:20585468
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0002g0040 | 2 | HG02300.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2131+201A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585468 | ||||||
chr22:20585524
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2132-204T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585524 | ||||||
chr22:20585562
|
CCAGGCTT others(19): Show |
C | 1 | a0013c0015t0011g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2132-165_2132-140d others(28): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585562 | ||||||
chr22:20585921
|
T | C | 164 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0048others(161): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.2230+95T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585921 | ||||||
chr22:20585923
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(2): Show | 5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2230+97C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585923 | ||||||
chr22:20585979
|
A | G | 64 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.2230+153A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585979 | ||||||
chr22:20585985
|
C | G | 127 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(124): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2230+159C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585985 | ||||||
chr22:20586004
|
C | T | 63 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008others(60): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2230+178C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586004 | ||||||
chr22:20586044
|
C | T | 2 | a0001c0004t0001g0144a0001c0004t0001g0147 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2230+218C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586044 | ||||||
chr22:20586190
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0304a0001c0001t0001g0305others(5): Show | 9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2230+364G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586190 | ||||||
chr22:20586223
|
A | T | 1 | a0013c0015t0011g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2231-345A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586223 | ||||||
chr22:20586278
|
C | CCAGAGCT others(9): Show |
1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2231-257_2231-242d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr22 | 20586278 | |||||
chr22:20586278
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CCAGAGCT others(9): Show |
C | 9 | a0001c0001t0001g0278a0001c0001t0009g0089a0001c0002t0002g0255others(6): Show | 9 | HG01192.hp2 HG01255.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2231-257_2231-242d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr22 | 20586278 | |||||
chr22:20586430
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C | T | 1 | a0001c0001t0001g0042 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2231-138C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586430 | ||||||
chr22:20586474
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G | A | 1 | a0001c0002t0002g0226 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2231-94G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586474 | ||||||
chr22:20586507
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G | A | 63 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0063others(60): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.2231-61G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586507 | ||||||
chr22:20586529
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G | A | 1 | a0011c0019t0001g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2231-39G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586529 | ||||||
chr22:20586535
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C | T | 11 | a0001c0001t0001g0132a0001c0001t0003g0003a0001c0001t0003g0015others(8): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2231-33C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586535 |