geneid | 81 |
---|---|
ensemblid | ENSG00000130402.14 |
hgncid | 166 |
symbol | ACTN4 |
name | actinin alpha 4 |
refseq_nuc | NM_004924.6 |
refseq_prot | NP_004915.2 |
ensembl_nuc | ENST00000252699.7 |
ensembl_prot | ENSP00000252699.2 |
mane_status | MANE Select |
chr | chr19 |
start | 38647649 |
end | 38731589 |
strand | + |
ver | v1.2 |
region | chr19:38647649-38731589 |
region5000 | chr19:38642649-38736589 |
regionname0 | ACTN4_chr19_38647649_38731589 |
regionname5000 | ACTN4_chr19_38642649_38736589 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 911 | 307 | 70 | 65 | 116 | 16 | 38 | 82 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0002 | 0/0 | 911 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0003 | 0/0 | 911 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0004 | 0/0 | 911 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0005 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2736 | 144 | 38 | 23 | 63 | 4 | 15 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0002 | 0/1 | 2736 | 94 | 16 | 16 | 46 | 4 | 11 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0003 | 0/0 | 2736 | 22 | 5 | 11 | 0 | 2 | 4 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0004 | 0/0 | 2736 | 21 | 3 | 5 | 4 | 3 | 6 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0005 | 0/0 | 2736 | 10 | 0 | 8 | 0 | 2 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0006 | 0/0 | 2736 | 3 | 0 | 2 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0007 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0008 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0009 | 0/0 | 2736 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0010 | 0/0 | 2736 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0011 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0012 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0013 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0014 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0015 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0016 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0017 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0018 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0019 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
c0020 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2255 | 85 | 18 | 13 | 38 | 5 | 10 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0002 | 1/0 | 2255 | 81 | 19 | 14 | 39 | 4 | 4 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0003 | 0/0 | 2245 | 19 | 6 | 8 | 0 | 2 | 3 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0004 | 0/0 | 2255 | 18 | 0 | 0 | 15 | 0 | 3 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0005 | 0/0 | 2255 | 18 | 3 | 6 | 4 | 2 | 3 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0006 | 0/0 | 2256 | 7 | 0 | 0 | 1 | 0 | 6 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0007 | 0/0 | 2256 | 7 | 0 | 1 | 6 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0008 | 0/0 | 2254 | 5 | 0 | 4 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0009 | 0/0 | 2246 | 5 | 1 | 2 | 0 | 0 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0010 | 0/0 | 2254 | 5 | 0 | 4 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0011 | 0/0 | 2255 | 4 | 4 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0012 | 0/0 | 2255 | 4 | 4 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0013 | 0/0 | 2254 | 4 | 0 | 1 | 0 | 1 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0014 | 0/0 | 2256 | 3 | 2 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0015 | 0/0 | 2256 | 3 | 0 | 1 | 2 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0016 | 0/0 | 2255 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0017 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0018 | 0/0 | 2254 | 2 | 0 | 1 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0019 | 0/0 | 2256 | 2 | 1 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0020 | 0/0 | 2255 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0021 | 0/0 | 2255 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0022 | 0/0 | 2255 | 2 | 0 | 0 | 0 | 0 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0023 | 0/0 | 2251 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0024 | 0/0 | 2254 | 2 | 0 | 1 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0025 | 0/0 | 2257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0026 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0027 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0028 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0029 | 0/0 | 2215 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0030 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0031 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0032 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0033 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0034 | 0/0 | 2255 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0035 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0036 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0037 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0038 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0039 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0040 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0041 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0042 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0043 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0044 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0045 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0046 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0047 | 0/0 | 2251 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0048 | 0/0 | 2255 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0049 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0050 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0051 | 0/0 | 2246 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
t0052 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2736 | 144 | 38 | 23 | 63 | 4 | 15 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002 | 0/1 | 2736 | 94 | 16 | 16 | 46 | 4 | 11 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0003 | 0/0 | 2736 | 22 | 5 | 11 | 0 | 2 | 4 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0004 | 0/0 | 2736 | 21 | 3 | 5 | 4 | 3 | 6 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005 | 0/0 | 2736 | 10 | 0 | 8 | 0 | 2 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0006 | 0/0 | 2736 | 3 | 0 | 2 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0007 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0010 | 0/0 | 2736 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0011 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0012 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0013 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0014 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0015 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0016 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0017 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0020 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0002c0008 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0003c0009 | 0/0 | 2736 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0004c0019 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0005c0018 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4990 | 3 | 2 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0002 | 1/0 | 4990 | 78 | 17 | 14 | 38 | 4 | 4 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0004 | 0/0 | 4990 | 17 | 0 | 0 | 15 | 0 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0006 | 0/0 | 4991 | 7 | 0 | 0 | 1 | 0 | 6 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0010 | 0/0 | 4989 | 5 | 0 | 4 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0011 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0014 | 0/0 | 4991 | 3 | 2 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0015 | 0/0 | 4991 | 3 | 0 | 1 | 2 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0016 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0017 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0019 | 0/0 | 4991 | 2 | 1 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0020 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0021 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0022 | 0/0 | 4990 | 2 | 0 | 0 | 0 | 0 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0023 | 0/0 | 4986 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0024 | 0/0 | 4989 | 2 | 0 | 1 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0025 | 0/0 | 4992 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0026 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0029 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0030 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0032 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0036 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0038 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0039 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0043 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0044 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0001t0049 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0001 | 0/1 | 4990 | 74 | 10 | 12 | 37 | 4 | 10 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0005 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0007 | 0/0 | 4991 | 7 | 0 | 1 | 6 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0012 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0031 | 0/0 | 4991 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0033 | 0/0 | 4991 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0034 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0035 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0040 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0041 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0042 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0045 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0002t0050 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0003t0003 | 0/0 | 4980 | 16 | 4 | 8 | 0 | 2 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0003t0009 | 0/0 | 4981 | 5 | 1 | 2 | 0 | 0 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0003t0051 | 0/0 | 4981 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0004t0005 | 0/0 | 4990 | 16 | 3 | 4 | 4 | 2 | 3 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0004t0013 | 0/0 | 4989 | 4 | 0 | 1 | 0 | 1 | 2 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0004t0048 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005t0001 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005t0008 | 0/0 | 4989 | 5 | 0 | 4 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005t0018 | 0/0 | 4989 | 2 | 0 | 1 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005t0027 | 0/0 | 4989 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0005t0028 | 0/0 | 4988 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0006t0005 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0006t0046 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0006t0047 | 0/0 | 4986 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0007t0001 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0010t0001 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0011t0012 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0012t0003 | 0/0 | 4980 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0013t0003 | 0/0 | 4980 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0014t0003 | 0/0 | 4980 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0015t0004 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0016t0037 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0017t0002 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0001c0020t0001 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0002c0008t0011 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0003c0009t0002 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0004c0019t0052 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
a0005c0018t0001 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | copy fasta | chr19 | 38642649 | 38736589 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0010g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0015g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0016g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0017g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0017g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0019g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0019g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0021g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0022g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0022g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0023g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0023g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0024g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0025g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0026g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0029g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0030g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0032g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0036g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0038g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0039g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0043g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0044g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0001t0049g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0012g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0031g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0033g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0034g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0035g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0040g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0041g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0042g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0045g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0002t0050g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0009g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0009g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0003t0051g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0013g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0013g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0013g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0013g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0004t0048g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0008g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0008g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0018g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0018g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0027g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0005t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0006t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0006t0046g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0006t0047g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0007t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0010t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0010t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0011t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0012t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0013t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0014t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0015t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0016t0037g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0017t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0001c0020t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0002c0008t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0002c0008t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0002c0008t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0003c0009t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0003c0009t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0004c0019t0052g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
a0005c0018t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | GBR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0026 | EUR | GBR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0034 | EUR | GBR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00140 | hp2 | a0001 | c0005 | t0018 | g0308 | EUR | GBR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00280 | hp1 | a0001 | c0005 | t0008 | g0004 | EUR | FIN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00280 | hp2 | a0001 | c0004 | t0005 | g0095 | EUR | FIN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0191 | EUR | FIN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0117 | EUR | FIN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00558 | hp2 | a0001 | c0002 | t0007 | g0217 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00639 | hp2 | a0001 | c0003 | t0003 | g0185 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00642 | hp1 | a0001 | c0001 | t0036 | g0268 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00733 | hp1 | a0001 | c0004 | t0005 | g0227 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00735 | hp1 | a0001 | c0003 | t0009 | g0176 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00735 | hp2 | a0001 | c0003 | t0009 | g0182 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00738 | hp1 | a0001 | c0004 | t0005 | g0232 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00741 | hp1 | a0001 | c0003 | t0003 | g0213 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG00741 | hp2 | a0001 | c0001 | t0015 | g0140 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01069 | hp1 | a0001 | c0001 | t0024 | g0092 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01069 | hp2 | a0001 | c0005 | t0008 | g0004 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01071 | hp2 | a0001 | c0003 | t0003 | g0094 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01081 | hp1 | a0001 | c0003 | t0003 | g0177 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01099 | hp1 | a0001 | c0004 | t0005 | g0230 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01106 | hp1 | a0001 | c0003 | t0051 | g0189 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01109 | hp1 | a0001 | c0002 | t0040 | g0203 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01109 | hp2 | a0001 | c0003 | t0003 | g0179 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01168 | hp1 | a0001 | c0003 | t0003 | g0180 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01168 | hp2 | a0001 | c0005 | t0008 | g0001 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01169 | hp1 | a0001 | c0005 | t0028 | g0001 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01175 | hp1 | a0001 | c0005 | t0027 | g0306 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0087 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01243 | hp2 | a0001 | c0005 | t0018 | g0307 | AMR | PUR | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01256 | hp2 | a0001 | c0005 | t0008 | g0077 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01257 | hp1 | a0001 | c0001 | t0029 | g0084 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01433 | hp2 | a0001 | c0005 | t0001 | g0304 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01496 | hp2 | a0004 | c0019 | t0052 | g0031 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01515 | hp2 | a0001 | c0004 | t0013 | g0228 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0030 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01517 | hp2 | a0001 | c0004 | t0005 | g0229 | EUR | IBS | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01884 | hp1 | a0001 | c0001 | t0026 | g0287 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01891 | hp2 | a0001 | c0011 | t0012 | g0291 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01934 | hp1 | a0001 | c0002 | t0031 | g0046 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01952 | hp1 | a0001 | c0002 | t0007 | g0219 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01952 | hp2 | a0001 | c0001 | t0032 | g0155 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01975 | hp1 | a0001 | c0004 | t0005 | g0222 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01978 | hp1 | a0001 | c0001 | t0010 | g0211 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0142 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01981 | hp1 | a0001 | c0005 | t0008 | g0305 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01981 | hp2 | a0001 | c0002 | t0005 | g0054 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02004 | hp2 | a0001 | c0006 | t0005 | g0237 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02015 | hp2 | a0001 | c0001 | t0038 | g0158 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02027 | hp2 | a0001 | c0002 | t0050 | g0069 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02055 | hp1 | a0003 | c0009 | t0002 | g0208 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02055 | hp2 | a0001 | c0001 | t0019 | g0299 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02071 | hp1 | a0001 | c0001 | t0019 | g0297 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02135 | hp1 | a0001 | c0001 | t0014 | g0120 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02135 | hp2 | a0001 | c0004 | t0005 | g0225 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | CDX | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CDX | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02257 | hp1 | a0001 | c0002 | t0012 | g0301 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02257 | hp2 | a0001 | c0001 | t0014 | g0168 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02273 | hp2 | a0001 | c0001 | t0010 | g0082 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0286 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02293 | hp1 | a0001 | c0006 | t0047 | g0239 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02293 | hp2 | a0001 | c0001 | t0010 | g0078 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0089 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02451 | hp2 | a0001 | c0003 | t0003 | g0090 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02602 | hp2 | a0001 | c0003 | t0009 | g0183 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02622 | hp1 | a0001 | c0001 | t0023 | g0310 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02630 | hp1 | a0001 | c0001 | t0030 | g0294 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02647 | hp1 | a0005 | c0018 | t0001 | g0201 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0195 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0188 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02723 | hp2 | a0001 | c0001 | t0023 | g0309 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02735 | hp1 | a0001 | c0001 | t0022 | g0198 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0298 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0254 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02809 | hp2 | a0001 | c0002 | t0042 | g0290 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0288 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02896 | hp1 | a0001 | c0007 | t0001 | g0204 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02896 | hp2 | a0001 | c0001 | t0043 | g0295 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02897 | hp1 | a0001 | c0007 | t0001 | g0202 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02965 | hp1 | a0002 | c0008 | t0011 | g0278 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02970 | hp1 | a0001 | c0001 | t0016 | g0302 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0284 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02976 | hp2 | a0001 | c0013 | t0003 | g0187 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03017 | hp1 | a0001 | c0004 | t0013 | g0235 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0242 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03041 | hp2 | a0001 | c0003 | t0003 | g0194 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03098 | hp1 | a0001 | c0002 | t0033 | g0300 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03139 | hp1 | a0001 | c0001 | t0049 | g0076 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03139 | hp2 | a0002 | c0008 | t0011 | g0279 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03209 | hp2 | a0001 | c0001 | t0021 | g0196 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03453 | hp1 | a0001 | c0002 | t0012 | g0003 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03453 | hp2 | a0001 | c0007 | t0001 | g0200 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03490 | hp2 | a0001 | c0003 | t0009 | g0192 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03491 | hp2 | a0001 | c0004 | t0005 | g0233 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0274 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0277 | AFR | ESN | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0169 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0303 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0221 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03704 | hp2 | a0001 | c0001 | t0044 | g0259 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03710 | hp1 | a0001 | c0004 | t0013 | g0236 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03710 | hp2 | a0001 | c0001 | t0022 | g0199 | SAS | PJL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03831 | hp1 | a0001 | c0003 | t0003 | g0184 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0253 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03927 | hp1 | a0001 | c0003 | t0003 | g0178 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0252 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03942 | hp2 | a0001 | c0014 | t0003 | g0193 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04115 | hp1 | a0001 | c0004 | t0048 | g0223 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04115 | hp2 | a0001 | c0002 | t0034 | g0045 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0250 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | BEB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04199 | hp2 | a0001 | c0004 | t0005 | g0243 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04228 | hp1 | a0001 | c0015 | t0004 | g0247 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18522 | hp1 | a0001 | c0012 | t0003 | g0190 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18522 | hp2 | a0001 | c0004 | t0005 | g0240 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | CHB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18747 | hp2 | a0001 | c0002 | t0007 | g0214 | EAS | CHB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18939 | hp2 | a0001 | c0004 | t0005 | g0244 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18942 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18953 | hp2 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18961 | hp2 | a0001 | c0001 | t0015 | g0124 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18966 | hp2 | a0001 | c0006 | t0046 | g0238 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18970 | hp2 | a0001 | c0001 | t0039 | g0108 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18981 | hp1 | a0001 | c0004 | t0005 | g0231 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18986 | hp1 | a0001 | c0002 | t0007 | g0023 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19000 | hp1 | a0001 | c0002 | t0041 | g0007 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19000 | hp2 | a0001 | c0002 | t0007 | g0220 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19002 | hp1 | a0001 | c0016 | t0037 | g0165 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19010 | hp1 | a0001 | c0004 | t0005 | g0246 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19011 | hp1 | a0001 | c0002 | t0035 | g0050 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19030 | hp2 | a0001 | c0004 | t0005 | g0224 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19043 | hp1 | a0001 | c0002 | t0045 | g0186 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19070 | hp1 | a0001 | c0002 | t0007 | g0216 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19079 | hp2 | a0001 | c0017 | t0002 | g0121 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19083 | hp2 | a0001 | c0001 | t0024 | g0098 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19087 | hp1 | a0001 | c0002 | t0007 | g0215 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA19240 | hp2 | a0001 | c0002 | t0012 | g0003 | AFR | YRI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ASW | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20129 | hp2 | a0001 | c0001 | t0020 | g0269 | AFR | ASW | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20805 | hp1 | a0001 | c0020 | t0001 | g0234 | EUR | TSI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20805 | hp2 | a0001 | c0003 | t0003 | g0088 | EUR | TSI | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20905 | hp1 | a0001 | c0004 | t0005 | g0245 | SAS | GIH | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | GIH | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG01123 | hp2 | a0001 | c0004 | t0013 | g0241 | AMR | CLM | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02486 | hp2 | a0001 | c0003 | t0009 | g0181 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG02559 | hp2 | a0001 | c0010 | t0001 | g0292 | AFR | ACB | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03471 | hp1 | a0001 | c0010 | t0001 | g0134 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | MSL | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20300 | hp1 | a0001 | c0001 | t0021 | g0083 | AFR | USA | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA20300 | hp2 | a0002 | c0008 | t0011 | g0280 | AFR | USA | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0281 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
NA21309 | hp2 | a0003 | c0009 | t0002 | g0130 | AFR | LWK | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0038 | REF | REF | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0141 | REF | REF | ACTN4_chr19_38642649_38736589 | ACTN4 | chr19 | 38642649 | 38736589 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:38706095
|
C | T | 1 | a0002 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.536C>T | p.Pro179Leu | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/21 | 633/4990 | 536/2736 | 179/911 | chr19 | 38706095 | ||
chr19:38728009
|
G | A | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.2401G>A | p.Val801Met | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/21 | 2498/4990 | 2401/2736 | 801/911 | chr19 | 38728009 | ||
chr19:38729325
|
G | A | 1 | a0005 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2629G>A | p.Glu877Lys | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 2726/4990 | 2629/2736 | 877/911 | chr19 | 38729325 | ||
chr19:38729366
|
C | A | 1 | a0003 | 2 | HG02055.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.2670C>A | p.Asp890Glu | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 2767/4990 | 2670/2736 | 890/911 | chr19 | 38729366 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:38700683
|
C | T | 1 | a0001c0005 | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
synonymous_variant | LOW | c.246C>T | p.Leu82Leu | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 2/21 | 343/4990 | 246/2736 | 82/911 | chr19 | 38700683 | ||
chr19:38701021
|
G | A | 1 | a0001c0011 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.297G>A | p.Pro99Pro | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/21 | 394/4990 | 297/2736 | 99/911 | chr19 | 38701021 | ||
chr19:38706096
|
G | A | 4 | a0001c0003a0001c0012a0001c0013others(1): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
synonymous_variant | LOW | c.537G>A | p.Pro179Pro | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/21 | 634/4990 | 537/2736 | 179/911 | chr19 | 38706096 | ||
chr19:38706105
|
C | T | 7 | a0001c0002a0001c0007a0001c0010others(4): Show | 103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
synonymous_variant | LOW | c.546C>T | p.Asn182Asn | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/21 | 643/4990 | 546/2736 | 182/911 | chr19 | 38706105 | ||
chr19:38717151
|
G | A | 1 | a0001c0006 | 3 | HG02004.hp2 HG02293.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.978G>A | p.Gln326Gln | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/21 | 1075/4990 | 978/2736 | 326/911 | chr19 | 38717151 | ||
chr19:38718001
|
C | A | 1 | a0001c0012 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1218C>A | p.Arg406Arg | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/21 | 1315/4990 | 1218/2736 | 406/911 | chr19 | 38718001 | ||
chr19:38723996
|
G | A | 2 | a0001c0007a0005c0018 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1611G>A | p.Ala537Ala | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 14/21 | 1708/4990 | 1611/2736 | 537/911 | chr19 | 38723996 | ||
chr19:38724234
|
C | T | 1 | a0001c0010 | 2 | HG02559.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1770C>T | p.Ile590Ile | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 15/21 | 1867/4990 | 1770/2736 | 590/911 | chr19 | 38724234 | ||
chr19:38724312
|
G | T | 1 | a0001c0014 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1848G>T | p.Pro616Pro | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 15/21 | 1945/4990 | 1848/2736 | 616/911 | chr19 | 38724312 | ||
chr19:38724457
|
C | T | 1 | a0001c0020 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1902C>T | p.Asp634Asp | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/21 | 1999/4990 | 1902/2736 | 634/911 | chr19 | 38724457 | ||
chr19:38724532
|
T | C | 2 | a0001c0004a0001c0006 | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
synonymous_variant | LOW | c.1977T>C | p.Asn659Asn | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/21 | 2074/4990 | 1977/2736 | 659/911 | chr19 | 38724532 | ||
chr19:38725864
|
C | G | 1 | a0001c0017 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.2151C>G | p.Ala717Ala | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/21 | 2248/4990 | 2151/2736 | 717/911 | chr19 | 38725864 | ||
chr19:38727082
|
G | A | 1 | a0001c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2316G>A | p.Ala772Ala | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/21 | 2413/4990 | 2316/2736 | 772/911 | chr19 | 38727082 | ||
chr19:38728008
|
C | T | 1 | a0001c0016 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.2400C>T | p.Asp800Asp | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/21 | 2497/4990 | 2400/2736 | 800/911 | chr19 | 38728008 | ||
chr19:38729140
|
T | C | 6 | a0001c0003a0001c0004a0001c0006others(3): Show | 49 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
synonymous_variant | LOW | c.2563T>C | p.Leu855Leu | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 20/21 | 2660/4990 | 2563/2736 | 855/911 | chr19 | 38729140 | ||
chr19:38729384
|
C | T | 1 | a0001c0015 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.2688C>T | p.Leu896Leu | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 2785/4990 | 2688/2736 | 896/911 | chr19 | 38729384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:38647654
|
A | G | 1 | a0004c0019t0052 | 1 | HG01496.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/21 | 92 | chr19 | 38647654 | |||||
chr19:38729463
|
C | T | 1 | a0001c0003t0051 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 31 | chr19 | 38729463 | |||||
chr19:38729616
|
G | T | 1 | a0001c0002t0050 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 184 | chr19 | 38729616 | |||||
chr19:38729640
|
C | G | 1 | a0001c0001t0049 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 208 | chr19 | 38729640 | |||||
chr19:38729780
|
T | C | 1 | a0001c0001t0016 | 2 | HG02970.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 348 | chr19 | 38729780 | |||||
chr19:38730068
|
G | A | 7 | a0001c0001t0017a0001c0001t0025a0001c0001t0026others(4): Show | 13 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*636G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 636 | chr19 | 38730068 | |||||
chr19:38730086
|
GAACCAAA others(33): Show |
G | 1 | a0001c0001t0029 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671_*710delGGAAAA others(34): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 671 | INFO_REALIGN_3_PRIME | chr19 | 38730086 | ||||
chr19:38730090
|
C | CA | 10 | a0001c0001t0006a0001c0001t0011a0001c0001t0014others(7): Show | 22 | HG01884.hp1 HG01934.hp1 HG02135.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*670dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 671 | INFO_REALIGN_3_PRIME | chr19 | 38730090 | ||||
chr19:38730090
|
CA | C | 9 | a0001c0001t0024a0001c0002t0005a0001c0004t0005others(6): Show | 28 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*670delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 670 | INFO_REALIGN_3_PRIME | chr19 | 38730090 | ||||
chr19:38730130
|
C | CA | 13 | a0001c0001t0015a0001c0001t0019a0001c0001t0025others(10): Show | 35 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*712dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 713 | INFO_REALIGN_3_PRIME | chr19 | 38730130 | ||||
chr19:38730130
|
CA | C | 10 | a0001c0001t0010a0001c0001t0011a0001c0001t0016others(7): Show | 22 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*712delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 712 | INFO_REALIGN_3_PRIME | chr19 | 38730130 | ||||
chr19:38730154
|
C | A | 1 | a0001c0002t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 722 | chr19 | 38730154 | |||||
chr19:38730158
|
A | G | 1 | a0001c0004t0048 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 726 | chr19 | 38730158 | |||||
chr19:38730168
|
AAAAG | A | 2 | a0001c0001t0023a0001c0006t0047 | 3 | HG02293.hp1 HG02622.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*743_*746delAGAA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 743 | INFO_REALIGN_3_PRIME | chr19 | 38730168 | ||||
chr19:38730256
|
A | G | 1 | a0001c0001t0022 | 2 | HG02735.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*824A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 824 | chr19 | 38730256 | |||||
chr19:38730261
|
T | G | 1 | a0001c0002t0035 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 829 | chr19 | 38730261 | |||||
chr19:38730297
|
C | A | 1 | a0001c0003t0051 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 865 | chr19 | 38730297 | |||||
chr19:38730317
|
C | T | 1 | a0001c0001t0043 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 885 | chr19 | 38730317 | |||||
chr19:38730334
|
G | A | 1 | a0001c0001t0043 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*902G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 902 | chr19 | 38730334 | |||||
chr19:38730341
|
C | T | 1 | a0001c0002t0042 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 909 | chr19 | 38730341 | |||||
chr19:38730344
|
C | T | 1 | a0001c0001t0043 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 912 | chr19 | 38730344 | |||||
chr19:38730543
|
T | G | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0019others(6): Show | 34 | HG00140.hp2 HG00642.hp1 HG01243.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1111T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1111 | chr19 | 38730543 | |||||
chr19:38730549
|
T | A | 3 | a0001c0005t0008a0001c0005t0027a0001c0005t0028 | 7 | HG00280.hp1 HG01069.hp2 HG01168.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1117T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1117 | chr19 | 38730549 | |||||
chr19:38730655
|
A | G | 56 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(53): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*1223A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1223 | chr19 | 38730655 | |||||
chr19:38730680
|
A | G | 1 | a0001c0002t0041 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1248A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1248 | chr19 | 38730680 | |||||
chr19:38730688
|
G | A | 2 | a0001c0001t0020a0001c0001t0036 | 3 | HG00642.hp1 HG03516.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1256G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1256 | chr19 | 38730688 | |||||
chr19:38730724
|
T | G | 1 | a0001c0001t0030 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1292 | chr19 | 38730724 | |||||
chr19:38730884
|
G | A | 1 | a0001c0001t0023 | 2 | HG02622.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1452 | chr19 | 38730884 | |||||
chr19:38730920
|
C | T | 3 | a0001c0002t0012a0001c0002t0033a0001c0011t0012 | 5 | HG01891.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1488 | chr19 | 38730920 | |||||
chr19:38730921
|
G | A | 1 | a0001c0001t0038 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1489G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1489 | chr19 | 38730921 | |||||
chr19:38730931
|
GCCTGAGC others(25): Show |
G | 1 | a0001c0001t0026 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1504_*1535delAGCC others(28): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1504 | INFO_REALIGN_3_PRIME | chr19 | 38730931 | ||||
chr19:38731075
|
CCCATGCC others(3): Show |
C | 6 | a0001c0003t0003a0001c0003t0009a0001c0003t0051others(3): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1651_*1660delCCAC others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1651 | INFO_REALIGN_3_PRIME | chr19 | 38731075 | ||||
chr19:38731090
|
G | A | 1 | a0001c0002t0035 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1658 | chr19 | 38731090 | |||||
chr19:38731141
|
G | A | 1 | a0001c0002t0040 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1709G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1709 | chr19 | 38731141 | |||||
chr19:38731182
|
G | A | 1 | a0001c0001t0032 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1750G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1750 | chr19 | 38731182 | |||||
chr19:38731218
|
G | A | 1 | a0001c0001t0036 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1786G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1786 | chr19 | 38731218 | |||||
chr19:38731251
|
T | C | 1 | a0001c0006t0046 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1819T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1819 | chr19 | 38731251 | |||||
chr19:38731307
|
A | T | 28 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(25): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1875A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1875 | chr19 | 38731307 | |||||
chr19:38731349
|
C | T | 1 | a0001c0002t0007 | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1917C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1917 | chr19 | 38731349 | |||||
chr19:38731428
|
G | A | 1 | a0001c0005t0027 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 1996 | chr19 | 38731428 | |||||
chr19:38731468
|
G | A | 1 | a0001c0001t0039 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 2036 | chr19 | 38731468 | |||||
chr19:38731572
|
T | TA | 1 | a0001c0002t0007 | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2141dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 21/21 | 2142 | INFO_REALIGN_3_PRIME | chr19 | 38731572 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:38647968
|
T | C | 71 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.162+61T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38647968 | ||||||
chr19:38648031
|
T | C | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.162+124T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648031 | ||||||
chr19:38648162
|
T | C | 3 | a0001c0005t0008g0001a0001c0005t0008g0077a0001c0005t0028g0001 | 3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.162+255T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648162 | ||||||
chr19:38648251
|
G | T | 2 | a0001c0001t0023g0309a0001c0001t0023g0310 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.162+344G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648251 | ||||||
chr19:38648308
|
A | G | 171 | a0001c0001t0002g0248a0001c0001t0002g0296a0001c0001t0004g0221others(168): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.162+401A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648308 | ||||||
chr19:38648359
|
G | A | 1 | a0001c0001t0010g0078 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.162+452G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648359 | ||||||
chr19:38648377
|
G | A | 7 | a0001c0002t0001g0218a0001c0002t0007g0214a0001c0002t0007g0215others(4): Show | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+470G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648377 | ||||||
chr19:38648624
|
G | T | 1 | a0001c0002t0001g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.162+717G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648624 | ||||||
chr19:38648690
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01891.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+783G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648690 | ||||||
chr19:38648766
|
G | A | 1 | a0001c0001t0004g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.162+859G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648766 | ||||||
chr19:38648777
|
G | A | 2 | a0001c0004t0005g0222a0001c0004t0048g0223 | 2 | HG01975.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.162+870G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38648777 | ||||||
chr19:38649121
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+1214C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649121 | ||||||
chr19:38649183
|
G | T | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.162+1276G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649183 | ||||||
chr19:38649186
|
C | CG | 25 | a0001c0001t0001g0205a0001c0001t0002g0081a0001c0001t0002g0206others(22): Show | 25 | HG00423.hp1 HG00741.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+1287dupG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38649186 | |||||
chr19:38649225
|
G | C | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+1318G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649225 | ||||||
chr19:38649255
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162+1348C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649255 | ||||||
chr19:38649263
|
C | G | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+1356C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649263 | ||||||
chr19:38649272
|
T | G | 1 | a0001c0001t0010g0082 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162+1365T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649272 | ||||||
chr19:38649272
|
TG | T | 27 | a0001c0001t0043g0295a0001c0002t0001g0075a0001c0002t0001g0226others(24): Show | 27 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.162+1374delG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38649272 | |||||
chr19:38649332
|
TAAAG | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+1430_162+1433d others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38649332 | |||||
chr19:38649347
|
G | A | 25 | a0001c0002t0001g0226a0001c0004t0005g0222a0001c0004t0005g0224others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+1440G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649347 | ||||||
chr19:38649363
|
T | G | 2 | a0001c0001t0021g0083a0001c0015t0004g0247 | 2 | HG04228.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162+1456T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649363 | ||||||
chr19:38649447
|
A | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+1540A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649447 | ||||||
chr19:38649617
|
G | A | 1 | a0001c0001t0029g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+1710G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649617 | ||||||
chr19:38649883
|
G | A | 1 | a0001c0002t0007g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.162+1976G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649883 | ||||||
chr19:38649972
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.162+2065T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38649972 | ||||||
chr19:38650109
|
G | A | 24 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(21): Show | 24 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+2202G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38650109 | ||||||
chr19:38650284
|
C | T | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+2377C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38650284 | ||||||
chr19:38650737
|
G | GTTGT | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+2853_162+2856d others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38650737 | |||||
chr19:38650822
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.162+2915G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38650822 | ||||||
chr19:38650828
|
C | T | 1 | a0001c0004t0005g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.162+2921C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38650828 | ||||||
chr19:38651119
|
G | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+3212G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651119 | ||||||
chr19:38651167
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+3260A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651167 | ||||||
chr19:38651273
|
G | A | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.162+3366G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651273 | ||||||
chr19:38651334
|
C | T | 25 | a0001c0002t0001g0226a0001c0004t0005g0222a0001c0004t0005g0224others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+3427C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651334 | ||||||
chr19:38651449
|
A | G | 1 | a0001c0002t0001g0064 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.162+3542A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651449 | ||||||
chr19:38651569
|
G | A | 3 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089 | 3 | HG01243.hp1 HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.162+3662G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651569 | ||||||
chr19:38651689
|
C | T | 204 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(201): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.162+3782C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651689 | ||||||
chr19:38651710
|
T | C | 1 | a0001c0002t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.162+3803T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651710 | ||||||
chr19:38651722
|
GT | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+3823delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38651722 | |||||
chr19:38651751
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.162+3844T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651751 | ||||||
chr19:38651876
|
C | T | 1 | a0001c0001t0016g0303 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+3969C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651876 | ||||||
chr19:38651890
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162+3983C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38651890 | ||||||
chr19:38652048
|
G | A | 24 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(21): Show | 24 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.162+4141G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652048 | ||||||
chr19:38652050
|
A | G | 5 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+4143A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652050 | ||||||
chr19:38652185
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+4278G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652185 | ||||||
chr19:38652251
|
T | C | 1 | a0001c0002t0001g0027 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162+4344T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652251 | ||||||
chr19:38652288
|
G | A | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+4381G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652288 | ||||||
chr19:38652499
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+4592A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652499 | ||||||
chr19:38652591
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+4684T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652591 | ||||||
chr19:38652649
|
G | A | 37 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.162+4742G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652649 | ||||||
chr19:38652915
|
G | A | 1 | a0001c0004t0005g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+5008G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38652915 | ||||||
chr19:38653001
|
G | T | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162+5094G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653001 | ||||||
chr19:38653085
|
C | CA | 61 | a0001c0001t0002g0091a0001c0001t0002g0093a0001c0001t0011g0281others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.162+5195dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38653085 | |||||
chr19:38653085
|
C | CAA | 92 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.162+5194_162+5195d others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38653085 | |||||
chr19:38653209
|
GCGCCCTT others(3): Show |
G | 1 | a0001c0001t0006g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.162+5304_162+5313d others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38653209 | |||||
chr19:38653244
|
G | A | 83 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+5337G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653244 | ||||||
chr19:38653343
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+5436T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653343 | ||||||
chr19:38653363
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+5456G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653363 | ||||||
chr19:38653367
|
T | C | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+5460T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653367 | ||||||
chr19:38653397
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+5490C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653397 | ||||||
chr19:38653413
|
TA | T | 20 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0173others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+5522delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38653413 | |||||
chr19:38653527
|
A | G | 92 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.162+5620A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653527 | ||||||
chr19:38653549
|
A | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+5642A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653549 | ||||||
chr19:38653604
|
C | T | 86 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.162+5697C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38653604 | ||||||
chr19:38654074
|
C | A | 201 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(198): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.162+6167C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654074 | ||||||
chr19:38654078
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+6171G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654078 | ||||||
chr19:38654096
|
TC | T | 25 | a0001c0002t0001g0226a0001c0004t0005g0222a0001c0004t0005g0224others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+6190delC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654096 | ||||||
chr19:38654261
|
C | T | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.162+6354C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654261 | ||||||
chr19:38654286
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+6379G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654286 | ||||||
chr19:38654298
|
A | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+6391A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654298 | ||||||
chr19:38654479
|
T | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+6572T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654479 | ||||||
chr19:38654495
|
G | A | 1 | a0001c0004t0005g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+6588G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654495 | ||||||
chr19:38654518
|
C | A | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+6611C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654518 | ||||||
chr19:38654540
|
C | A | 1 | a0001c0002t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.162+6633C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654540 | ||||||
chr19:38654561
|
C | CA | 45 | a0001c0001t0002g0097a0001c0001t0002g0099a0001c0001t0004g0221others(42): Show | 46 | HG00323.hp1 HG00642.hp1 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.162+6670dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38654561 | |||||
chr19:38654561
|
C | CAA | 26 | a0001c0002t0001g0062a0001c0002t0045g0186a0001c0003t0003g0087others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+6669_162+6670d others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38654561 | |||||
chr19:38654561
|
CA | C | 28 | a0001c0001t0001g0170a0001c0001t0022g0198a0001c0001t0022g0199others(25): Show | 28 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.162+6670delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38654561 | |||||
chr19:38654709
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+6802G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654709 | ||||||
chr19:38654740
|
G | A | 3 | a0001c0005t0008g0001a0001c0005t0008g0077a0001c0005t0028g0001 | 3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.162+6833G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654740 | ||||||
chr19:38654927
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.162+7020G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654927 | ||||||
chr19:38654937
|
G | A | 25 | a0001c0002t0001g0226a0001c0004t0005g0222a0001c0004t0005g0224others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+7030G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38654937 | ||||||
chr19:38655164
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+7257G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655164 | ||||||
chr19:38655212
|
A | G | 5 | a0001c0001t0002g0212a0001c0001t0014g0168a0001c0001t0014g0169others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+7305A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655212 | ||||||
chr19:38655279
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+7372G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655279 | ||||||
chr19:38655298
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+7391G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655298 | ||||||
chr19:38655322
|
C | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+7415C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655322 | ||||||
chr19:38655352
|
G | C | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162+7445G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655352 | ||||||
chr19:38655477
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+7570C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655477 | ||||||
chr19:38655807
|
C | T | 1 | a0001c0004t0005g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.162+7900C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655807 | ||||||
chr19:38655853
|
T | C | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+7946T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655853 | ||||||
chr19:38655895
|
C | T | 3 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089 | 3 | HG01243.hp1 HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.162+7988C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655895 | ||||||
chr19:38655969
|
A | C | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+8062A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38655969 | ||||||
chr19:38656104
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+8197G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656104 | ||||||
chr19:38656140
|
G | C | 83 | a0001c0001t0043g0295a0001c0002t0001g0005a0001c0002t0001g0006others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+8233G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656140 | ||||||
chr19:38656247
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162+8340G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656247 | ||||||
chr19:38656384
|
T | A | 5 | a0001c0001t0006g0250a0001c0001t0006g0251a0001c0001t0006g0252others(2): Show | 5 | HG02738.hp2 HG03669.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+8477T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656384 | ||||||
chr19:38656458
|
T | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+8551T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656458 | ||||||
chr19:38656478
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+8571T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656478 | ||||||
chr19:38656780
|
T | G | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+8873T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656780 | ||||||
chr19:38656786
|
C | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+8879C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656786 | ||||||
chr19:38656851
|
C | T | 2 | a0001c0002t0012g0003a0001c0002t0012g0301 | 3 | HG02257.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.162+8944C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656851 | ||||||
chr19:38656870
|
G | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0034others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+8963G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656870 | ||||||
chr19:38656986
|
T | C | 30 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(27): Show | 30 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.162+9079T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38656986 | ||||||
chr19:38657146
|
AT | A | 25 | a0001c0001t0029g0084a0001c0002t0001g0226a0001c0004t0005g0222others(22): Show | 25 | HG00733.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.162+9253delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38657146 | |||||
chr19:38657380
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.162+9473C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657380 | ||||||
chr19:38657384
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.162+9477C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657384 | ||||||
chr19:38657408
|
G | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+9501G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657408 | ||||||
chr19:38657409
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+9502C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657409 | ||||||
chr19:38657430
|
A | G | 3 | a0001c0001t0002g0164a0001c0001t0002g0166a0001c0016t0037g0165 | 3 | HG02132.hp1 NA19002.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.162+9523A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657430 | ||||||
chr19:38657463
|
A | G | 98 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.162+9556A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657463 | ||||||
chr19:38657586
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.162+9679G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657586 | ||||||
chr19:38657634
|
TTTTC | T | 4 | a0001c0002t0001g0218a0001c0002t0007g0023a0001c0002t0007g0219others(1): Show | 4 | HG01952.hp1 NA18986.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+9739_162+9742d others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38657634 | |||||
chr19:38657642
|
C | A | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+9735C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657642 | ||||||
chr19:38657821
|
A | G | 6 | a0001c0005t0001g0304a0001c0005t0008g0004a0001c0005t0008g0305others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+9914A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657821 | ||||||
chr19:38657868
|
C | T | 1 | a0001c0001t0011g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162+9961C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657868 | ||||||
chr19:38657917
|
A | G | 3 | a0001c0001t0010g0078a0001c0001t0010g0082a0001c0001t0010g0211 | 3 | HG01978.hp1 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.162+10010A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657917 | ||||||
chr19:38657973
|
A | G | 1 | a0001c0004t0005g0244 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.162+10066A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38657973 | ||||||
chr19:38658080
|
G | C | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+10173G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658080 | ||||||
chr19:38658286
|
G | A | 1 | a0001c0002t0001g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.162+10379G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658286 | ||||||
chr19:38658294
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+10387C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658294 | ||||||
chr19:38658409
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+10502A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658409 | ||||||
chr19:38658434
|
C | A | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+10527C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658434 | ||||||
chr19:38658436
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+10529A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658436 | ||||||
chr19:38658437
|
C | A | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+10530C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658437 | ||||||
chr19:38658582
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+10675G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658582 | ||||||
chr19:38658626
|
T | G | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+10719T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658626 | ||||||
chr19:38658668
|
A | C | 1 | a0001c0002t0007g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.162+10761A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658668 | ||||||
chr19:38658801
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+10894A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658801 | ||||||
chr19:38658923
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+11016A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658923 | ||||||
chr19:38658997
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162+11090G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38658997 | ||||||
chr19:38659033
|
C | T | 1 | a0001c0004t0005g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162+11126C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659033 | ||||||
chr19:38659065
|
C | CTTTCTTT others(3): Show |
1 | a0001c0001t0004g0272 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.162+11161_162+1116 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTCTTT others(2): Show |
26 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(23): Show | 26 | HG00642.hp1 HG02040.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+11161_162+1116 others(13): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTCTTT others(3): Show |
2 | a0001c0001t0006g0254a0001c0002t0001g0270 | 2 | HG02738.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.162+11161_162+1116 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(2): Show |
18 | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0002t0001g0036others(15): Show | 18 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.162+11163_162+1117 others(13): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(3): Show |
110 | a0001c0001t0001g0170a0001c0001t0002g0296a0001c0001t0004g0271others(107): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.162+11162_162+1117 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(4): Show |
42 | a0001c0001t0011g0281a0001c0001t0021g0083a0001c0001t0030g0294others(39): Show | 42 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.162+11161_162+1117 others(15): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.162+11160_162+1117 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0021g0196a0001c0001t0049g0076a0001c0002t0001g0060 | 3 | HG03139.hp1 HG03209.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.162+11159_162+1117 others(17): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+11171_162+1117 others(18): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659065
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0042g0290 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162+11171_162+1117 others(19): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659065 | |||||
chr19:38659216
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.162+11309C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659216 | ||||||
chr19:38659493
|
T | A | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+11586T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659493 | ||||||
chr19:38659559
|
A | G | 32 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(29): Show | 33 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.162+11652A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659559 | ||||||
chr19:38659595
|
A | G | 88 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.162+11688A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659595 | ||||||
chr19:38659690
|
A | G | 2 | a0001c0001t0002g0210a0001c0001t0002g0248 | 2 | HG00639.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.162+11783A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659690 | ||||||
chr19:38659763
|
C | A | 4 | a0001c0002t0001g0032a0001c0002t0001g0038a0001c0002t0001g0039others(1): Show | 4 | HG01981.hp2 HG04199.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+11856C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659763 | ||||||
chr19:38659845
|
A | G | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.162+11938A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659845 | ||||||
chr19:38659864
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+11957T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659864 | ||||||
chr19:38659921
|
C | CT | 121 | a0001c0001t0001g0170a0001c0001t0002g0099a0001c0001t0002g0163others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.162+12030dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659921 | |||||
chr19:38659921
|
C | CTT | 80 | a0001c0001t0006g0249a0001c0002t0001g0005a0001c0002t0001g0006others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.162+12029_162+1203 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38659921 | |||||
chr19:38659982
|
G | T | 208 | a0001c0001t0001g0170a0001c0001t0002g0296a0001c0001t0004g0221others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.162+12075G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38659982 | ||||||
chr19:38660051
|
T | G | 1 | a0001c0001t0016g0303 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+12144T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660051 | ||||||
chr19:38660142
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+12235C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660142 | ||||||
chr19:38660282
|
A | G | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+12375A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660282 | ||||||
chr19:38660301
|
G | C | 1 | a0001c0001t0002g0102 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.162+12394G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660301 | ||||||
chr19:38660301
|
G | T | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162+12394G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660301 | ||||||
chr19:38660323
|
T | G | 4 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(1): Show | 5 | HG01891.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+12416T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660323 | ||||||
chr19:38660394
|
G | T | 92 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.162+12487G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660394 | ||||||
chr19:38660542
|
C | T | 27 | a0001c0001t0002g0296a0001c0002t0001g0226a0001c0004t0005g0095others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.162+12635C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660542 | ||||||
chr19:38660735
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+12828T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660735 | ||||||
chr19:38660923
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+13016C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660923 | ||||||
chr19:38660954
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+13047A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38660954 | ||||||
chr19:38660981
|
AAG | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+13080_162+1308 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38660981 | |||||
chr19:38661063
|
C | G | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+13156C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661063 | ||||||
chr19:38661078
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+13171G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661078 | ||||||
chr19:38661225
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+13318G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661225 | ||||||
chr19:38661290
|
C | A | 1 | a0001c0002t0001g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.162+13383C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661290 | ||||||
chr19:38661364
|
G | C | 207 | a0001c0001t0001g0170a0001c0001t0004g0221a0001c0001t0004g0255others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.162+13457G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661364 | ||||||
chr19:38661489
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+13582C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661489 | ||||||
chr19:38661754
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0005g0054 | 2 | HG01981.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.162+13847G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661754 | ||||||
chr19:38661813
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+13906C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661813 | ||||||
chr19:38661890
|
T | G | 32 | a0001c0001t0002g0296a0001c0002t0001g0226a0001c0002t0040g0203others(29): Show | 32 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+13983T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661890 | ||||||
chr19:38661915
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162+14008G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38661915 | ||||||
chr19:38662103
|
C | G | 27 | a0001c0002t0001g0062a0001c0002t0045g0186a0001c0003t0003g0087others(24): Show | 27 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.162+14196C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662103 | ||||||
chr19:38662268
|
T | C | 209 | a0001c0001t0001g0170a0001c0001t0002g0296a0001c0001t0004g0221others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.162+14361T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662268 | ||||||
chr19:38662376
|
C | CTGA | 5 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+14474_162+1447 others(7): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38662376 | |||||
chr19:38662376
|
C | G | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162+14469C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662376 | ||||||
chr19:38662398
|
C | T | 6 | a0001c0001t0002g0162a0001c0002t0040g0203a0001c0007t0001g0200others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+14491C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662398 | ||||||
chr19:38662404
|
G | A | 92 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.162+14497G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662404 | ||||||
chr19:38662428
|
T | C | 23 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(20): Show | 23 | HG02015.hp1 HG02040.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.162+14521T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662428 | ||||||
chr19:38662519
|
T | C | 6 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(3): Show | 6 | HG02523.hp1 NA18942.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+14612T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662519 | ||||||
chr19:38662548
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.162+14641G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662548 | ||||||
chr19:38662557
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+14650G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662557 | ||||||
chr19:38662561
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.162+14654G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662561 | ||||||
chr19:38662625
|
A | G | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+14718A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662625 | ||||||
chr19:38662667
|
T | A | 26 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+14760T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662667 | ||||||
chr19:38662671
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.162+14764G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662671 | ||||||
chr19:38662740
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.162+14833C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662740 | ||||||
chr19:38662890
|
T | C | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+14983T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38662890 | ||||||
chr19:38662909
|
G | GT | 36 | a0001c0001t0002g0093a0001c0001t0006g0249a0001c0001t0049g0076others(33): Show | 37 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+15017dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38662909 | |||||
chr19:38663067
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+15160G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663067 | ||||||
chr19:38663099
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.162+15192C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663099 | ||||||
chr19:38663112
|
T | C | 1 | a0001c0001t0039g0108 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.162+15205T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663112 | ||||||
chr19:38663202
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+15295C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663202 | ||||||
chr19:38663237
|
T | G | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+15330T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663237 | ||||||
chr19:38663306
|
A | G | 1 | a0001c0001t0004g0267 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.162+15399A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663306 | ||||||
chr19:38663350
|
G | C | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+15443G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663350 | ||||||
chr19:38663352
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+15445C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663352 | ||||||
chr19:38663411
|
G | A | 2 | a0001c0002t0007g0219a0001c0002t0007g0220 | 2 | HG01952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.162+15504G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663411 | ||||||
chr19:38663439
|
A | G | 2 | a0001c0002t0012g0003a0001c0002t0012g0301 | 3 | HG02257.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.162+15532A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663439 | ||||||
chr19:38663634
|
C | T | 1 | a0001c0001t0029g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+15727C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38663634 | ||||||
chr19:38664046
|
G | A | 1 | a0001c0002t0033g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.162+16139G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664046 | ||||||
chr19:38664056
|
C | A | 1 | a0001c0001t0002g0162 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.162+16149C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664056 | ||||||
chr19:38664102
|
G | A | 1 | a0001c0002t0007g0215 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.162+16195G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664102 | ||||||
chr19:38664117
|
C | A | 1 | a0001c0002t0001g0074 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.162+16210C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664117 | ||||||
chr19:38664141
|
C | G | 1 | a0001c0003t0003g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.162+16234C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664141 | ||||||
chr19:38664285
|
T | G | 4 | a0001c0001t0011g0281a0002c0008t0011g0278a0002c0008t0011g0279others(1): Show | 4 | HG02965.hp1 HG03139.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+16378T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664285 | ||||||
chr19:38664420
|
C | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+16513C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664420 | ||||||
chr19:38664714
|
G | C | 1 | a0001c0001t0006g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.162+16807G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38664714 | ||||||
chr19:38665028
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+17121G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665028 | ||||||
chr19:38665031
|
G | A | 1 | a0001c0002t0001g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.162+17124G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665031 | ||||||
chr19:38665062
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+17155C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665062 | ||||||
chr19:38665086
|
A | T | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+17179A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665086 | ||||||
chr19:38665128
|
A | C | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+17221A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665128 | ||||||
chr19:38665240
|
G | A | 93 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.162+17333G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665240 | ||||||
chr19:38665363
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0050g0069 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.162+17456T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665363 | ||||||
chr19:38665368
|
C | T | 3 | a0001c0001t0020g0269a0001c0001t0020g0277a0001c0001t0036g0268 | 3 | HG00642.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+17461C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665368 | ||||||
chr19:38665464
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162+17557A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665464 | ||||||
chr19:38665498
|
C | T | 29 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(26): Show | 30 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.162+17591C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665498 | ||||||
chr19:38665534
|
A | T | 1 | a0001c0001t0020g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.162+17627A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665534 | ||||||
chr19:38665742
|
A | G | 24 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(21): Show | 24 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.162+17835A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665742 | ||||||
chr19:38665841
|
C | T | 117 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.162+17934C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665841 | ||||||
chr19:38665860
|
G | C | 2 | a0001c0002t0001g0008a0001c0002t0050g0069 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.162+17953G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665860 | ||||||
chr19:38665873
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+17966C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665873 | ||||||
chr19:38665949
|
G | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+18042G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38665949 | ||||||
chr19:38666014
|
A | C | 1 | a0001c0004t0005g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162+18107A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666014 | ||||||
chr19:38666015
|
T | C | 1 | a0001c0001t0022g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.162+18108T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666015 | ||||||
chr19:38666107
|
G | T | 9 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(6): Show | 9 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+18200G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666107 | ||||||
chr19:38666166
|
C | T | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+18259C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666166 | ||||||
chr19:38666223
|
T | TC | 46 | a0001c0001t0030g0294a0001c0002t0001g0025a0001c0002t0001g0026others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.162+18323dupC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38666223 | |||||
chr19:38666223
|
TC | T | 22 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(19): Show | 22 | HG02015.hp1 HG02040.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.162+18323delC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38666223 | |||||
chr19:38666238
|
A | G | 1 | a0001c0003t0003g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162+18331A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666238 | ||||||
chr19:38666449
|
G | C | 1 | a0001c0002t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.162+18542G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666449 | ||||||
chr19:38666620
|
G | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+18713G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666620 | ||||||
chr19:38666635
|
A | G | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+18728A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666635 | ||||||
chr19:38666840
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+18933C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666840 | ||||||
chr19:38666959
|
C | T | 28 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0002t0001g0226others(25): Show | 28 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.162+19052C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666959 | ||||||
chr19:38666988
|
A | G | 1 | a0001c0005t0027g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+19081A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38666988 | ||||||
chr19:38667091
|
A | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+19184A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667091 | ||||||
chr19:38667205
|
C | G | 1 | a0001c0001t0016g0302 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.162+19298C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667205 | ||||||
chr19:38667211
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.162+19304A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667211 | ||||||
chr19:38667273
|
C | T | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+19366C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667273 | ||||||
chr19:38667313
|
G | T | 2 | a0001c0001t0014g0168a0001c0001t0014g0169 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.162+19406G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667313 | ||||||
chr19:38667432
|
A | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+19525A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667432 | ||||||
chr19:38667469
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.162+19562T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667469 | ||||||
chr19:38667541
|
T | G | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+19634T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38667541 | ||||||
chr19:38667706
|
C | CA | 105 | a0001c0001t0002g0101a0001c0001t0002g0104a0001c0001t0002g0105others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.162+19814dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38667706 | |||||
chr19:38667706
|
C | CAA | 11 | a0001c0001t0001g0170a0001c0001t0006g0249a0001c0002t0001g0005others(8): Show | 11 | HG00438.hp2 HG01433.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+19813_162+1981 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38667706 | |||||
chr19:38668289
|
A | G | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+20382A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668289 | ||||||
chr19:38668304
|
C | A | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+20397C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668304 | ||||||
chr19:38668385
|
A | C | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+20478A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668385 | ||||||
chr19:38668501
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+20594C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668501 | ||||||
chr19:38668553
|
G | A | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+20646G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668553 | ||||||
chr19:38668638
|
G | A | 207 | a0001c0001t0001g0170a0001c0001t0004g0221a0001c0001t0004g0255others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.162+20731G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668638 | ||||||
chr19:38668672
|
G | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+20765G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668672 | ||||||
chr19:38668684
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0021g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.162+20790_162+2080 others(19): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38668684 | |||||
chr19:38668685
|
AAAAAAAG | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+20792_162+2079 others(11): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38668685 | |||||
chr19:38668694
|
A | G | 3 | a0001c0005t0008g0001a0001c0005t0008g0077a0001c0005t0028g0001 | 3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.162+20787A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668694 | ||||||
chr19:38668743
|
C | CAG | 98 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.162+20837_162+2083 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38668743 | |||||
chr19:38668772
|
G | A | 1 | a0001c0004t0005g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.162+20865G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668772 | ||||||
chr19:38668795
|
G | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+20888G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668795 | ||||||
chr19:38668896
|
C | G | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+20989C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668896 | ||||||
chr19:38668934
|
T | G | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+21027T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668934 | ||||||
chr19:38668941
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+21034T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668941 | ||||||
chr19:38668960
|
C | T | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+21053C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38668960 | ||||||
chr19:38669025
|
C | T | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+21118C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669025 | ||||||
chr19:38669026
|
G | T | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+21119G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669026 | ||||||
chr19:38669046
|
G | A | 4 | a0001c0003t0003g0179a0001c0003t0003g0180a0001c0003t0003g0213others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+21139G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669046 | ||||||
chr19:38669089
|
C | T | 85 | a0001c0001t0001g0170a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.162+21182C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669089 | ||||||
chr19:38669154
|
T | C | 7 | a0001c0003t0003g0177a0001c0003t0003g0179a0001c0003t0003g0180others(4): Show | 7 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+21247T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669154 | ||||||
chr19:38669211
|
T | C | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+21304T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669211 | ||||||
chr19:38669275
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.162+21368C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669275 | ||||||
chr19:38669277
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.162+21370C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669277 | ||||||
chr19:38669313
|
CT | C | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+21408delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38669313 | |||||
chr19:38669414
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+21507G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669414 | ||||||
chr19:38669451
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+21544A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669451 | ||||||
chr19:38669497
|
C | T | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+21590C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669497 | ||||||
chr19:38669626
|
C | T | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.162+21719C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669626 | ||||||
chr19:38669683
|
A | G | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162+21776A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669683 | ||||||
chr19:38669758
|
G | A | 1 | a0001c0002t0045g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162+21851G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669758 | ||||||
chr19:38669768
|
C | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+21861C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669768 | ||||||
chr19:38669779
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+21872G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38669779 | ||||||
chr19:38670039
|
G | A | 3 | a0001c0001t0020g0269a0001c0001t0020g0277a0001c0001t0036g0268 | 3 | HG00642.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+22132G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670039 | ||||||
chr19:38670059
|
G | A | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162+22152G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670059 | ||||||
chr19:38670095
|
A | C | 1 | a0001c0001t0006g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.162+22188A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670095 | ||||||
chr19:38670214
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+22307G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670214 | ||||||
chr19:38670407
|
G | C | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+22500G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670407 | ||||||
chr19:38670545
|
G | A | 2 | a0001c0003t0003g0178a0001c0014t0003g0193 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.162+22638G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670545 | ||||||
chr19:38670614
|
A | T | 1 | a0001c0002t0001g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.162+22707A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670614 | ||||||
chr19:38670667
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162+22760G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670667 | ||||||
chr19:38670706
|
C | T | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+22799C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670706 | ||||||
chr19:38670798
|
T | C | 123 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(120): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.162+22891T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670798 | ||||||
chr19:38670921
|
T | TA | 9 | a0001c0001t0002g0112a0001c0001t0006g0298a0001c0002t0001g0009others(6): Show | 9 | HG00438.hp2 HG01106.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+23031dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38670921 | |||||
chr19:38670921
|
TAAAA | T | 11 | a0001c0001t0001g0086a0001c0001t0002g0002a0001c0001t0002g0093others(8): Show | 12 | HG00438.hp1 HG01978.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+23028_162+2303 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38670921 | |||||
chr19:38670932
|
A | AC | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+23025_162+2302 others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38670932 | ||||||
chr19:38671007
|
A | G | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+23100A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671007 | ||||||
chr19:38671014
|
T | C | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+23107T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671014 | ||||||
chr19:38671194
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+23287G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671194 | ||||||
chr19:38671211
|
C | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+23304C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671211 | ||||||
chr19:38671280
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162+23373C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671280 | ||||||
chr19:38671359
|
A | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+23452A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671359 | ||||||
chr19:38671559
|
T | C | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+23652T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671559 | ||||||
chr19:38671590
|
A | C | 208 | a0001c0001t0001g0170a0001c0001t0004g0221a0001c0001t0004g0255others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.162+23683A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671590 | ||||||
chr19:38671602
|
A | G | 1 | a0001c0001t0004g0273 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.162+23695A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671602 | ||||||
chr19:38671694
|
A | AT | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+23793dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38671694 | |||||
chr19:38671762
|
G | A | 7 | a0001c0002t0001g0218a0001c0002t0007g0214a0001c0002t0007g0215others(4): Show | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+23855G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671762 | ||||||
chr19:38671777
|
AGTCT | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+23876_162+2387 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38671777 | |||||
chr19:38671795
|
C | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+23888C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671795 | ||||||
chr19:38671871
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+23964A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38671871 | ||||||
chr19:38672160
|
C | A | 26 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+24253C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672160 | ||||||
chr19:38672201
|
C | T | 1 | a0001c0003t0009g0183 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.162+24294C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672201 | ||||||
chr19:38672238
|
C | CT | 185 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0002g0210others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.162+24351dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38672238 | |||||
chr19:38672238
|
C | CTT | 11 | a0001c0002t0001g0042a0001c0002t0001g0060a0001c0002t0007g0023others(8): Show | 11 | HG01123.hp2 HG01358.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+24350_162+2435 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38672238 | |||||
chr19:38672272
|
T | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+24365T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672272 | ||||||
chr19:38672279
|
C | T | 1 | a0001c0003t0009g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.162+24372C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672279 | ||||||
chr19:38672334
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.162+24427A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672334 | ||||||
chr19:38672365
|
T | C | 204 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(201): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.162+24458T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672365 | ||||||
chr19:38672426
|
A | T | 1 | a0001c0015t0004g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162+24519A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672426 | ||||||
chr19:38672487
|
C | T | 1 | a0001c0004t0005g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.162+24580C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672487 | ||||||
chr19:38672533
|
A | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+24626A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672533 | ||||||
chr19:38672544
|
G | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+24637G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672544 | ||||||
chr19:38672557
|
A | G | 26 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+24650A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672557 | ||||||
chr19:38672803
|
A | C | 176 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.162+24896A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672803 | ||||||
chr19:38672868
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+24961C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672868 | ||||||
chr19:38672925
|
T | C | 3 | a0001c0001t0010g0078a0001c0001t0010g0082a0001c0001t0010g0211 | 3 | HG01978.hp1 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.162+25018T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38672925 | ||||||
chr19:38672943
|
C | CT | 69 | a0001c0001t0002g0099a0001c0001t0002g0163a0001c0001t0002g0166others(66): Show | 70 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.162+25054dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38672943 | |||||
chr19:38673239
|
G | A | 1 | a0001c0004t0005g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+25332G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673239 | ||||||
chr19:38673329
|
T | C | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+25422T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673329 | ||||||
chr19:38673370
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25463T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673370 | ||||||
chr19:38673439
|
TTTTATAT others(25): Show |
T | 10 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+25534_162+2556 others(36): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673439 | |||||
chr19:38673441
|
T | A | 10 | a0001c0001t0030g0294a0001c0005t0001g0304a0001c0005t0008g0001others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+25534T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673441 | ||||||
chr19:38673442
|
T | TATATATA others(47): Show |
74 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.162+25567_162+2556 others(58): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673442 | |||||
chr19:38673443
|
A | ATATATAT others(25): Show |
2 | a0001c0001t0020g0277a0001c0001t0021g0196 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.162+25568_162+2559 others(36): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673443 | |||||
chr19:38673443
|
A | ATATATAT others(115): Show |
2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.162+25568_162+2556 others(126): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673443 | |||||
chr19:38673444
|
T | TATATATA others(45): Show |
2 | a0001c0002t0001g0044a0001c0002t0001g0053 | 2 | HG01106.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.162+25567_162+2556 others(56): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673444 | |||||
chr19:38673456
|
C | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25549C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673456 | ||||||
chr19:38673456
|
C | CATATATA others(3): Show |
4 | a0001c0001t0002g0107a0001c0001t0002g0153a0001c0001t0002g0154others(1): Show | 4 | HG00099.hp1 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+25568_162+2557 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673456 | |||||
chr19:38673456
|
C | CATATATA others(45): Show |
3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01891.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+25569_162+2562 others(56): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673456 | |||||
chr19:38673456
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.162+25559_162+2558 others(26): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673456 | |||||
chr19:38673463
|
A | ATT | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25558_162+2555 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673463 | |||||
chr19:38673466
|
T | C | 1 | a0001c0001t0002g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.162+25559T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673466 | ||||||
chr19:38673466
|
T | TATATATA others(3): Show |
2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25567_162+2556 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673466 | |||||
chr19:38673469
|
A | ATATATGA others(43): Show |
4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+25567_162+2556 others(54): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673469 | |||||
chr19:38673475
|
T | A | 14 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+25568T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673475 | ||||||
chr19:38673475
|
TTA | T | 11 | a0001c0001t0002g0002a0001c0001t0002g0093a0001c0001t0002g0110others(8): Show | 12 | HG00438.hp1 HG01978.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+25578_162+2557 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673475 | |||||
chr19:38673476
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25569T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673476 | ||||||
chr19:38673477
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.162+25580_162+2559 others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673477 | |||||
chr19:38673479
|
A | T | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+25572A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673479 | ||||||
chr19:38673485
|
A | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25578A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673485 | ||||||
chr19:38673487
|
T | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25580T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673487 | ||||||
chr19:38673488
|
C | CATATATA others(33): Show |
22 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(19): Show | 22 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.162+25619_162+2562 others(44): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673488 | |||||
chr19:38673488
|
C | CATATATA others(33): Show |
2 | a0001c0002t0001g0226a0001c0004t0005g0243 | 2 | HG01943.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.162+25591_162+2559 others(44): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673488 | |||||
chr19:38673488
|
C | T | 7 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0040g0203others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+25581C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673488 | ||||||
chr19:38673495
|
A | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25588A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673495 | ||||||
chr19:38673497
|
T | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25590T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673497 | ||||||
chr19:38673498
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25591T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673498 | ||||||
chr19:38673507
|
G | T | 7 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0040g0203others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+25600G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673507 | ||||||
chr19:38673508
|
A | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25601A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673508 | ||||||
chr19:38673508
|
A | T | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25601A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673508 | ||||||
chr19:38673508
|
AATATATA others(43): Show |
A | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+25629_162+2567 others(54): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673508 | |||||
chr19:38673511
|
ATATATT | A | 79 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.162+25610_162+2561 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673511 | |||||
chr19:38673514
|
T | TATATATT others(21): Show |
1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+25609_162+2561 others(32): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673514 | |||||
chr19:38673515
|
A | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25608A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673515 | ||||||
chr19:38673517
|
T | A | 2 | a0001c0001t0043g0295a0001c0002t0001g0276 | 2 | HG02155.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.162+25610T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673517 | ||||||
chr19:38673517
|
T | TTATATAT others(73): Show |
2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162+25628_162+2562 others(84): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673517 | |||||
chr19:38673517
|
T | TTATATTC others(55): Show |
1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162+25615_162+2561 others(66): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673517 | |||||
chr19:38673518
|
T | C | 2 | a0001c0002t0001g0052a0001c0002t0001g0059 | 2 | HG00733.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.162+25611T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673518 | ||||||
chr19:38673528
|
C | CATATATA others(13): Show |
1 | a0001c0001t0002g0113 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.162+25649_162+2566 others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673528 | |||||
chr19:38673528
|
C | T | 2 | a0001c0002t0001g0052a0001c0002t0001g0059 | 2 | HG00733.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.162+25621C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673528 | ||||||
chr19:38673533
|
ATACT | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25629_162+2563 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673533 | |||||
chr19:38673536
|
C | T | 87 | a0001c0001t0043g0295a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.162+25629C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673536 | ||||||
chr19:38673538
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25631T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673538 | ||||||
chr19:38673538
|
TATATATA others(33): Show |
T | 1 | a0001c0001t0020g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162+25649_162+2568 others(44): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673538 | |||||
chr19:38673546
|
T | C | 4 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0062others(1): Show | 4 | HG00733.hp2 HG01123.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+25639T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673546 | ||||||
chr19:38673547
|
T | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25640T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673547 | ||||||
chr19:38673551
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.162+25644A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673551 | ||||||
chr19:38673556
|
C | T | 11 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0062others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+25649C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673556 | ||||||
chr19:38673558
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25651T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673558 | ||||||
chr19:38673558
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0020g0277a0001c0001t0036g0268 | 2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.162+25681_162+2570 others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673558 | |||||
chr19:38673564
|
T | A | 4 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0062others(1): Show | 4 | HG00733.hp2 HG01123.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+25657T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673564 | ||||||
chr19:38673565
|
ATT | A | 4 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0062others(1): Show | 4 | HG00733.hp2 HG01123.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+25660_162+2566 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673565 | |||||
chr19:38673566
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25659T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673566 | ||||||
chr19:38673567
|
T | TTATATAA others(1): Show |
81 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.162+25666_162+2566 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673567 | |||||
chr19:38673568
|
T | C | 2 | a0001c0001t0021g0196a0001c0001t0043g0295 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.162+25661T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673568 | ||||||
chr19:38673577
|
T | G | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+25670T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673577 | ||||||
chr19:38673577
|
TCA | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25671_162+2567 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673577 | ||||||
chr19:38673578
|
C | A | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+25671C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673578 | ||||||
chr19:38673578
|
C | T | 4 | a0001c0001t0021g0196a0001c0001t0043g0295a0001c0002t0001g0274others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+25671C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673578 | ||||||
chr19:38673586
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25679T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673586 | ||||||
chr19:38673587
|
T | G | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25680T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673587 | ||||||
chr19:38673588
|
T | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25681T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673588 | ||||||
chr19:38673588
|
T | C | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+25681T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673588 | ||||||
chr19:38673597
|
T | G | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+25690T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673597 | ||||||
chr19:38673598
|
C | A | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.162+25691C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673598 | ||||||
chr19:38673598
|
C | T | 9 | a0001c0001t0043g0295a0001c0002t0001g0274a0001c0002t0001g0275others(6): Show | 9 | HG01109.hp1 HG01175.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+25691C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673598 | ||||||
chr19:38673601
|
A | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+25694A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673601 | ||||||
chr19:38673601
|
ATATATTC others(116): Show |
A | 1 | a0001c0005t0027g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+25695_162+2581 others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673601 | ||||||
chr19:38673604
|
T | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25697T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673604 | ||||||
chr19:38673608
|
C | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+25701C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673608 | ||||||
chr19:38673611
|
T | A | 9 | a0001c0001t0021g0196a0001c0001t0043g0295a0001c0002t0001g0274others(6): Show | 9 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+25704T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673611 | ||||||
chr19:38673616
|
T | C | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25709T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673616 | ||||||
chr19:38673618
|
T | C | 8 | a0001c0001t0021g0196a0001c0002t0001g0274a0001c0002t0001g0275others(5): Show | 8 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+25711T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673618 | ||||||
chr19:38673627
|
T | TTA | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25720_162+2572 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673627 | ||||||
chr19:38673628
|
C | T | 4 | a0001c0001t0021g0196a0001c0001t0043g0295a0001c0002t0001g0274others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+25721C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673628 | ||||||
chr19:38673628
|
CAT | C | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.162+25728_162+2572 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673628 | |||||
chr19:38673636
|
T | C | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25729T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673636 | ||||||
chr19:38673636
|
T | TTTATATA others(20): Show |
19 | a0001c0001t0002g0099a0001c0001t0002g0102a0001c0001t0002g0109others(16): Show | 19 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+25783_162+2580 others(31): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673636 | |||||
chr19:38673636
|
TTTATATA others(20): Show |
T | 3 | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0001t0038g0158 | 3 | HG02015.hp2 HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162+25783_162+2580 others(31): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673636 | |||||
chr19:38673638
|
T | C | 8 | a0001c0001t0021g0196a0001c0002t0001g0274a0001c0002t0001g0275others(5): Show | 8 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+25731T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673638 | ||||||
chr19:38673647
|
T | TCA | 3 | a0001c0001t0021g0196a0001c0002t0001g0274a0001c0002t0001g0275 | 3 | HG03209.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25740_162+2574 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673647 | ||||||
chr19:38673647
|
T | TCATATAT others(5): Show |
2 | a0001c0001t0021g0083a0001c0001t0049g0076 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.162+25740_162+2574 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673647 | ||||||
chr19:38673647
|
TTATATAT others(3): Show |
T | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.162+25749_162+2575 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673647 | |||||
chr19:38673649
|
A | T | 5 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076others(2): Show | 5 | HG03139.hp1 HG03209.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25742A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673649 | ||||||
chr19:38673651
|
AT | A | 31 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(28): Show | 32 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+25745delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673651 | ||||||
chr19:38673651
|
ATATTTAT others(2): Show |
A | 84 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.162+25745_162+2575 others(13): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673651 | ||||||
chr19:38673651
|
ATATTTAT others(66): Show |
A | 19 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(16): Show | 20 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+25745_162+2581 others(77): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673651 | ||||||
chr19:38673652
|
T | A | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+25745T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673652 | ||||||
chr19:38673653
|
A | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+25746A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673653 | ||||||
chr19:38673654
|
TTTATATA others(29): Show |
T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25759_162+2579 others(40): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673654 | |||||
chr19:38673656
|
TATATATA others(3): Show |
T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+25750_162+2575 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673656 | ||||||
chr19:38673657
|
ATATATAT others(10): Show |
A | 30 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(27): Show | 31 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.162+25759_162+2577 others(21): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673657 | |||||
chr19:38673662
|
T | A | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.162+25755T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673662 | ||||||
chr19:38673662
|
TA | T | 84 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.162+25756delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673662 | ||||||
chr19:38673663
|
A | C | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.162+25756A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673663 | ||||||
chr19:38673663
|
ATTATATA others(11): Show |
A | 1 | a0001c0003t0003g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162+25768_162+2578 others(22): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673663 | |||||
chr19:38673665
|
T | TC | 6 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0043g0295others(3): Show | 6 | HG02896.hp2 HG03139.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+25758_162+2575 others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673665 | ||||||
chr19:38673666
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0152 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.162+25784_162+2581 others(39): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673666 | |||||
chr19:38673666
|
ATATATAT others(1): Show |
A | 5 | a0001c0001t0002g0212a0001c0001t0014g0168a0001c0001t0014g0169others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25775_162+2578 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673666 | |||||
chr19:38673676
|
A | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.162+25769A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673676 | ||||||
chr19:38673681
|
T | TA | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00642.hp2 HG01891.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+25774_162+2577 others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673681 | ||||||
chr19:38673682
|
T | A | 5 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076others(2): Show | 5 | HG03139.hp1 HG03209.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25775T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673682 | ||||||
chr19:38673684
|
A | T | 5 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076others(2): Show | 5 | HG03139.hp1 HG03209.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25777A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673684 | ||||||
chr19:38673689
|
T | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25782T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673689 | ||||||
chr19:38673689
|
T | C | 86 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.162+25782T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673689 | ||||||
chr19:38673690
|
A | AT | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+25785dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673690 | |||||
chr19:38673690
|
A | T | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25783A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673690 | ||||||
chr19:38673693
|
ATATATAT others(1): Show |
A | 29 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0212others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.162+25810_162+2581 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673693 | |||||
chr19:38673701
|
T | TA | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+25794_162+2579 others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673701 | ||||||
chr19:38673705
|
AT | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25799delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673705 | ||||||
chr19:38673714
|
T | C | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+25807T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673714 | ||||||
chr19:38673716
|
T | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25809T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673716 | ||||||
chr19:38673717
|
T | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25810T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673717 | ||||||
chr19:38673717
|
TTATATAT others(1): Show |
T | 82 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.162+25811_162+2581 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673717 | ||||||
chr19:38673719
|
A | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25812A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673719 | ||||||
chr19:38673726
|
C | T | 26 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.162+25819C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673726 | ||||||
chr19:38673729
|
A | T | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25822A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673729 | ||||||
chr19:38673737
|
TTATATAT others(3): Show |
T | 1 | a0001c0002t0001g0027 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162+25840_162+2584 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673737 | |||||
chr19:38673743
|
ATTTATAT others(5): Show |
A | 6 | a0001c0002t0001g0008a0001c0002t0001g0056a0001c0002t0001g0057others(3): Show | 6 | HG00438.hp2 HG00597.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+25848_162+2585 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673743 | |||||
chr19:38673746
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25839T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673746 | ||||||
chr19:38673747
|
A | T | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25840A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673747 | ||||||
chr19:38673753
|
ATT | A | 78 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0009others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+25850_162+2585 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673753 | |||||
chr19:38673754
|
T | C | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162+25847T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673754 | ||||||
chr19:38673755
|
T | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0274a0001c0002t0001g0275 | 3 | HG01261.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+25848T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673755 | ||||||
chr19:38673757
|
T | A | 10 | a0001c0001t0002g0248a0001c0001t0019g0299a0001c0001t0022g0198others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+25850T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673757 | ||||||
chr19:38673784
|
A | AT | 12 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0105others(9): Show | 12 | HG01261.hp2 HG01952.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+25897dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673784 | |||||
chr19:38673784
|
A | T | 1 | a0001c0004t0048g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.162+25877A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673784 | ||||||
chr19:38673784
|
AT | A | 27 | a0001c0001t0004g0258a0001c0001t0004g0260a0001c0001t0004g0261others(24): Show | 28 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.162+25897delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673784 | |||||
chr19:38673784
|
ATT | A | 86 | a0001c0001t0030g0294a0001c0002t0001g0005a0001c0002t0001g0006others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.162+25896_162+2589 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38673784 | |||||
chr19:38673788
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.162+25881T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673788 | ||||||
chr19:38673824
|
C | T | 87 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.162+25917C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673824 | ||||||
chr19:38673844
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+25937G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38673844 | ||||||
chr19:38674012
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.162+26105C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674012 | ||||||
chr19:38674032
|
G | A | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162+26125G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674032 | ||||||
chr19:38674037
|
C | G | 1 | a0001c0004t0005g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.162+26130C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674037 | ||||||
chr19:38674075
|
C | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+26168C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674075 | ||||||
chr19:38674109
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+26202G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674109 | ||||||
chr19:38674133
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+26226G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674133 | ||||||
chr19:38674166
|
G | GT | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162+26259_162+2626 others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674166 | ||||||
chr19:38674280
|
A | G | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-26320A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674280 | ||||||
chr19:38674348
|
T | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-26252T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674348 | ||||||
chr19:38674419
|
C | T | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.163-26181C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674419 | ||||||
chr19:38674422
|
G | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-26178G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674422 | ||||||
chr19:38674423
|
C | G | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-26177C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674423 | ||||||
chr19:38674478
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.163-26122G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674478 | ||||||
chr19:38674589
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-26011G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674589 | ||||||
chr19:38674735
|
T | C | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-25865T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674735 | ||||||
chr19:38674767
|
C | T | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-25833C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674767 | ||||||
chr19:38674797
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-25803C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674797 | ||||||
chr19:38674875
|
G | A | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.163-25725G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38674875 | ||||||
chr19:38675025
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163-25575G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675025 | ||||||
chr19:38675110
|
A | G | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163-25490A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675110 | ||||||
chr19:38675197
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-25403G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675197 | ||||||
chr19:38675213
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-25387C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675213 | ||||||
chr19:38675660
|
T | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-24940T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675660 | ||||||
chr19:38675800
|
C | T | 2 | a0001c0001t0004g0266a0001c0001t0006g0249 | 2 | NA18955.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.163-24800C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675800 | ||||||
chr19:38675960
|
C | T | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-24640C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675960 | ||||||
chr19:38675976
|
C | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-24624C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38675976 | ||||||
chr19:38676139
|
C | CG | 26 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-24460dupG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38676139 | |||||
chr19:38676232
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.163-24368G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676232 | ||||||
chr19:38676412
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-24188G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676412 | ||||||
chr19:38676475
|
C | G | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-24125C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676475 | ||||||
chr19:38676501
|
G | T | 24 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(21): Show | 24 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-24099G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676501 | ||||||
chr19:38676649
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-23951C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676649 | ||||||
chr19:38676720
|
A | G | 176 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.163-23880A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676720 | ||||||
chr19:38676929
|
T | C | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-23671T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676929 | ||||||
chr19:38676990
|
C | T | 2 | a0001c0003t0003g0194a0001c0003t0003g0195 | 2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.163-23610C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38676990 | ||||||
chr19:38677098
|
G | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-23502G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677098 | ||||||
chr19:38677109
|
C | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-23491C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677109 | ||||||
chr19:38677120
|
T | C | 92 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(89): Show | 93 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.163-23480T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677120 | ||||||
chr19:38677168
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.163-23432C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677168 | ||||||
chr19:38677195
|
CCAT | C | 7 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(4): Show | 7 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-23402_163-2340 others(7): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38677195 | |||||
chr19:38677350
|
A | G | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-23250A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677350 | ||||||
chr19:38677370
|
AACAG | A | 84 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-23224_163-2322 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38677370 | |||||
chr19:38677474
|
G | A | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.163-23126G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677474 | ||||||
chr19:38677580
|
C | T | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-23020C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677580 | ||||||
chr19:38677611
|
A | AGCTGACC others(12): Show |
203 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(200): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.163-22988_163-2298 others(23): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38677611 | |||||
chr19:38677678
|
G | A | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-22922G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677678 | ||||||
chr19:38677765
|
G | A | 5 | a0001c0001t0006g0250a0001c0001t0006g0251a0001c0001t0006g0252others(2): Show | 5 | HG02738.hp2 HG03669.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-22835G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677765 | ||||||
chr19:38677875
|
C | T | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.163-22725C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677875 | ||||||
chr19:38677955
|
G | A | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.163-22645G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38677955 | ||||||
chr19:38678214
|
A | G | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-22386A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678214 | ||||||
chr19:38678273
|
C | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-22327C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678273 | ||||||
chr19:38678328
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-22272G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678328 | ||||||
chr19:38678635
|
C | T | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.163-21965C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678635 | ||||||
chr19:38678708
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-21892C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678708 | ||||||
chr19:38678715
|
C | T | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-21885C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38678715 | ||||||
chr19:38679102
|
A | G | 1 | a0001c0001t0002g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163-21498A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679102 | ||||||
chr19:38679125
|
C | G | 3 | a0001c0001t0004g0265a0001c0001t0004g0266a0001c0001t0006g0249 | 3 | NA18955.hp2 NA18970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.163-21475C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679125 | ||||||
chr19:38679211
|
C | T | 2 | a0001c0004t0005g0240a0001c0004t0005g0242 | 2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.163-21389C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679211 | ||||||
chr19:38679294
|
T | C | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-21306T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679294 | ||||||
chr19:38679324
|
G | A | 4 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(1): Show | 5 | HG01891.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-21276G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679324 | ||||||
chr19:38679389
|
C | T | 30 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(27): Show | 31 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.163-21211C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679389 | ||||||
chr19:38679528
|
C | G | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163-21072C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679528 | ||||||
chr19:38679545
|
G | A | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.163-21055G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679545 | ||||||
chr19:38679562
|
G | GGTGTGTG others(5): Show |
1 | a0001c0005t0008g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.163-21033_163-2103 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679562 | |||||
chr19:38679562
|
G | GGTGTGTG others(7): Show |
2 | a0001c0005t0008g0001a0001c0005t0028g0001 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.163-21033_163-2103 others(18): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679562 | |||||
chr19:38679568
|
C | CGT | 35 | a0001c0001t0001g0205a0001c0001t0002g0126a0001c0001t0002g0151others(32): Show | 35 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.163-21001_163-2100 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGT | 3 | a0001c0002t0001g0036a0001c0002t0001g0042a0001c0010t0001g0292 | 3 | HG01358.hp1 HG02559.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.163-21003_163-2100 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGT | 4 | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0001t0049g0076others(1): Show | 4 | HG01081.hp2 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-21005_163-2100 others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(1): Show |
12 | a0001c0001t0019g0299a0001c0001t0043g0295a0001c0002t0001g0033others(9): Show | 12 | HG00738.hp2 HG01981.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-21007_163-2100 others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(3): Show |
39 | a0001c0001t0017g0284a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.163-21009_163-2100 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(5): Show |
41 | a0001c0001t0004g0258a0001c0001t0006g0250a0001c0001t0006g0251others(38): Show | 41 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.163-21011_163-2100 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(7): Show |
28 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(25): Show | 29 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.163-21013_163-2100 others(18): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(9): Show |
5 | a0001c0001t0004g0261a0001c0001t0004g0266a0001c0002t0001g0022others(2): Show | 5 | HG00423.hp1 HG04228.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-21015_163-2100 others(20): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | CGTGTGTG others(11): Show |
2 | a0001c0001t0006g0249a0001c0005t0018g0308 | 2 | HG00140.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.163-21017_163-2100 others(22): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
C | T | 3 | a0001c0005t0008g0001a0001c0005t0008g0077a0001c0005t0028g0001 | 3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.163-21032C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679568 | ||||||
chr19:38679568
|
CGT | C | 35 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0001t0014g0168others(32): Show | 35 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.163-21001_163-2100 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679568
|
CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-21009_163-2100 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679568 | |||||
chr19:38679623
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.163-20977G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679623 | ||||||
chr19:38679833
|
A | G | 87 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.163-20767A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38679833 | ||||||
chr19:38679859
|
G | GA | 31 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(28): Show | 32 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-20734dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38679859 | |||||
chr19:38680059
|
T | C | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-20541T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680059 | ||||||
chr19:38680212
|
G | GT | 34 | a0001c0001t0001g0086a0001c0001t0001g0205a0001c0001t0002g0081others(31): Show | 34 | HG00438.hp1 HG00558.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.163-20355dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
G | GTT | 21 | a0001c0001t0002g0105a0001c0001t0002g0122a0001c0001t0002g0123others(18): Show | 21 | HG00423.hp2 HG00597.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.163-20356_163-2035 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
G | GTTT | 7 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0002g0125others(4): Show | 7 | HG01952.hp2 HG02523.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-20357_163-2035 others(7): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GT | G | 18 | a0001c0001t0001g0170a0001c0001t0002g0114a0001c0001t0002g0131others(15): Show | 18 | HG01175.hp1 HG01243.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-20355delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0004t0005g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-20364_163-2035 others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(4): Show |
G | 30 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0002t0001g0226others(27): Show | 30 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.163-20365_163-2035 others(15): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0004t0005g0233a0001c0007t0001g0204 | 2 | HG02896.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.163-20366_163-2035 others(16): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(6): Show |
G | 31 | a0001c0002t0001g0051a0001c0002t0001g0055a0001c0002t0012g0003others(28): Show | 32 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-20367_163-2035 others(17): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(7): Show |
G | 85 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.163-20368_163-2035 others(18): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680212
|
GTTTTTTT others(8): Show |
G | 4 | a0001c0001t0016g0302a0001c0001t0016g0303a0001c0002t0001g0013others(1): Show | 4 | HG02970.hp1 HG03579.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-20369_163-2035 others(19): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680212 | |||||
chr19:38680220
|
T | G | 1 | a0001c0001t0025g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163-20380T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680220 | ||||||
chr19:38680222
|
T | G | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-20378T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680222 | ||||||
chr19:38680225
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.163-20375T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680225 | ||||||
chr19:38680226
|
T | G | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-20374T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680226 | ||||||
chr19:38680229
|
T | G | 2 | a0001c0002t0001g0051a0001c0002t0001g0055 | 2 | HG02602.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.163-20371T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680229 | ||||||
chr19:38680230
|
T | G | 84 | a0001c0001t0043g0295a0001c0002t0001g0005a0001c0002t0001g0006others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-20370T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680230 | ||||||
chr19:38680231
|
T | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0218 | 2 | NA18986.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.163-20369T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680231 | ||||||
chr19:38680234
|
T | G | 3 | a0001c0001t0021g0196a0001c0001t0043g0295a0001c0001t0049g0076 | 3 | HG02896.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163-20366T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680234 | ||||||
chr19:38680249
|
G | T | 2 | a0001c0005t0008g0001a0001c0005t0028g0001 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.163-20351G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680249 | ||||||
chr19:38680268
|
G | A | 84 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-20332G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680268 | ||||||
chr19:38680464
|
A | G | 33 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0002t0001g0226others(30): Show | 33 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-20136A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680464 | ||||||
chr19:38680513
|
GA | G | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.163-20085delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38680513 | |||||
chr19:38680605
|
C | T | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.163-19995C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680605 | ||||||
chr19:38680799
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-19801C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680799 | ||||||
chr19:38680853
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-19747C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680853 | ||||||
chr19:38680924
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-19676G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680924 | ||||||
chr19:38680952
|
C | A | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.163-19648C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38680952 | ||||||
chr19:38681094
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.163-19506C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681094 | ||||||
chr19:38681129
|
G | GA | 65 | a0001c0001t0002g0079a0001c0001t0002g0081a0001c0001t0002g0126others(62): Show | 65 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.163-19447dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38681129 | |||||
chr19:38681129
|
G | GAA | 10 | a0001c0001t0020g0277a0001c0001t0036g0268a0001c0002t0001g0034others(7): Show | 10 | HG00140.hp1 HG00642.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-19448_163-1944 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38681129 | |||||
chr19:38681129
|
GA | G | 52 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0257others(49): Show | 52 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-19447delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38681129 | |||||
chr19:38681129
|
GAA | G | 11 | a0001c0002t0001g0027a0001c0002t0012g0003a0001c0002t0012g0301others(8): Show | 12 | HG01261.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-19448_163-1944 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38681129 | |||||
chr19:38681129
|
GAAA | G | 24 | a0001c0002t0001g0226a0001c0004t0005g0095a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-19449_163-1944 others(7): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38681129 | |||||
chr19:38681305
|
C | T | 1 | a0001c0010t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.163-19295C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681305 | ||||||
chr19:38681359
|
C | T | 20 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.163-19241C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681359 | ||||||
chr19:38681402
|
G | C | 34 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.163-19198G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681402 | ||||||
chr19:38681413
|
C | G | 6 | a0001c0001t0016g0303a0001c0002t0040g0203a0001c0007t0001g0200others(3): Show | 6 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-19187C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681413 | ||||||
chr19:38681580
|
A | G | 33 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0002t0001g0226others(30): Show | 33 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-19020A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681580 | ||||||
chr19:38681594
|
C | T | 7 | a0001c0004t0005g0095a0001c0004t0005g0227a0001c0004t0005g0230others(4): Show | 7 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-19006C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681594 | ||||||
chr19:38681598
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.163-19002C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681598 | ||||||
chr19:38681651
|
C | T | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163-18949C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681651 | ||||||
chr19:38681664
|
C | A | 20 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(17): Show | 20 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.163-18936C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681664 | ||||||
chr19:38681694
|
G | C | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163-18906G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681694 | ||||||
chr19:38681765
|
G | A | 16 | a0001c0001t0002g0097a0001c0001t0002g0104a0001c0001t0002g0105others(13): Show | 16 | HG01169.hp2 HG01943.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-18835G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681765 | ||||||
chr19:38681866
|
T | C | 2 | a0001c0003t0003g0179a0001c0003t0003g0180 | 2 | HG01109.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.163-18734T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681866 | ||||||
chr19:38681869
|
T | C | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-18731T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38681869 | ||||||
chr19:38682316
|
G | A | 1 | a0001c0001t0020g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.163-18284G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682316 | ||||||
chr19:38682365
|
A | G | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-18235A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682365 | ||||||
chr19:38682662
|
T | C | 1 | a0001c0002t0001g0014 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.163-17938T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682662 | ||||||
chr19:38682846
|
A | C | 89 | a0001c0001t0002g0162a0001c0002t0001g0005a0001c0002t0001g0006others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.163-17754A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682846 | ||||||
chr19:38682893
|
C | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-17707C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682893 | ||||||
chr19:38682915
|
C | T | 1 | a0001c0003t0009g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163-17685C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38682915 | ||||||
chr19:38683005
|
T | C | 36 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0001t0021g0083others(33): Show | 36 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-17595T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683005 | ||||||
chr19:38683088
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-17512T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683088 | ||||||
chr19:38683234
|
C | G | 1 | a0001c0003t0003g0178 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-17366C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683234 | ||||||
chr19:38683342
|
G | A | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163-17258G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683342 | ||||||
chr19:38683457
|
C | T | 5 | a0001c0002t0001g0226a0001c0004t0005g0222a0001c0004t0005g0243others(2): Show | 5 | HG01943.hp2 HG01975.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-17143C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683457 | ||||||
chr19:38683554
|
C | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-17046C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683554 | ||||||
chr19:38683571
|
A | G | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.163-17029A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683571 | ||||||
chr19:38683692
|
G | A | 270 | a0001c0001t0001g0086a0001c0001t0001g0170a0001c0001t0001g0205others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.163-16908G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683692 | ||||||
chr19:38683760
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-16840G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683760 | ||||||
chr19:38683761
|
A | G | 309 | a0001c0001t0001g0086a0001c0001t0001g0170a0001c0001t0001g0205others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.163-16839A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683761 | ||||||
chr19:38683857
|
C | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163-16743C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683857 | ||||||
chr19:38683886
|
A | C | 10 | a0001c0001t0004g0271a0001c0001t0006g0298a0001c0004t0005g0225others(7): Show | 10 | HG02004.hp2 HG02135.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-16714A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38683886 | ||||||
chr19:38684029
|
C | A | 58 | a0001c0001t0001g0170a0001c0001t0001g0205a0001c0001t0011g0281others(55): Show | 58 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.163-16571C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684029 | ||||||
chr19:38684075
|
G | A | 5 | a0001c0001t0002g0212a0001c0001t0014g0168a0001c0001t0014g0169others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-16525G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684075 | ||||||
chr19:38684161
|
G | A | 5 | a0001c0002t0001g0043a0001c0002t0001g0058a0001c0002t0001g0071others(2): Show | 5 | HG00558.hp2 HG01433.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-16439G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684161 | ||||||
chr19:38684276
|
G | A | 6 | a0001c0005t0001g0304a0001c0005t0008g0004a0001c0005t0008g0305others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-16324G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684276 | ||||||
chr19:38684445
|
C | G | 1 | a0001c0003t0003g0094 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.163-16155C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684445 | ||||||
chr19:38684666
|
G | A | 1 | a0001c0003t0003g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-15934G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684666 | ||||||
chr19:38684836
|
G | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-15764G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684836 | ||||||
chr19:38684977
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-15623C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38684977 | ||||||
chr19:38685049
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.163-15551G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685049 | ||||||
chr19:38685155
|
G | A | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-15445G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685155 | ||||||
chr19:38685166
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0010g0103 | 2 | NA18942.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.163-15434G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685166 | ||||||
chr19:38685317
|
C | T | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-15283C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685317 | ||||||
chr19:38685446
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-15154C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685446 | ||||||
chr19:38685527
|
A | G | 1 | a0001c0003t0009g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.163-15073A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685527 | ||||||
chr19:38685538
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-15062G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685538 | ||||||
chr19:38685654
|
C | A | 8 | a0001c0002t0001g0218a0001c0002t0007g0023a0001c0002t0007g0214others(5): Show | 8 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-14946C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685654 | ||||||
chr19:38685655
|
G | A | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-14945G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685655 | ||||||
chr19:38685825
|
G | A | 7 | a0001c0002t0001g0218a0001c0002t0007g0023a0001c0002t0007g0214others(4): Show | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-14775G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685825 | ||||||
chr19:38685898
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.163-14702C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38685898 | ||||||
chr19:38686224
|
C | T | 13 | a0001c0001t0002g0107a0001c0001t0002g0153a0001c0001t0002g0154others(10): Show | 14 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-14376C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38686224 | ||||||
chr19:38686551
|
G | A | 1 | a0001c0002t0033g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163-14049G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38686551 | ||||||
chr19:38686802
|
G | C | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-13798G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38686802 | ||||||
chr19:38686965
|
C | CT | 87 | a0001c0001t0019g0299a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.163-13619dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38686965 | |||||
chr19:38686965
|
CT | C | 27 | a0001c0001t0002g0162a0001c0001t0002g0173a0001c0001t0004g0257others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-13619delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38686965 | |||||
chr19:38686970
|
T | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-13630T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38686970 | ||||||
chr19:38687181
|
C | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-13419C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38687181 | ||||||
chr19:38687225
|
GC | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-13368delC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38687225 | |||||
chr19:38687225
|
GCC | G | 10 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-13369_163-1336 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38687225 | |||||
chr19:38687253
|
G | C | 1 | a0001c0001t0002g0145 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.163-13347G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38687253 | ||||||
chr19:38687726
|
A | G | 1 | a0001c0002t0001g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.163-12874A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38687726 | ||||||
chr19:38687841
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-12759G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38687841 | ||||||
chr19:38687977
|
TCTACAAA others(67): Show |
T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-12587_163-1251 others(78): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38687977 | |||||
chr19:38688270
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-12330C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688270 | ||||||
chr19:38688319
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-12281C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688319 | ||||||
chr19:38688390
|
C | CA | 62 | a0001c0001t0001g0205a0001c0001t0002g0080a0001c0001t0002g0102others(59): Show | 63 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.163-12189dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688390
|
C | CAA | 24 | a0001c0001t0002g0156a0001c0002t0001g0019a0001c0002t0001g0057others(21): Show | 24 | HG00323.hp1 HG00558.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-12190_163-1218 others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688390
|
C | CAAA | 66 | a0001c0001t0002g0152a0001c0001t0016g0302a0001c0001t0016g0303others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-12191_163-1218 others(7): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688390
|
C | CAAAA | 26 | a0001c0001t0011g0281a0001c0001t0025g0286a0001c0001t0026g0287others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.163-12192_163-1218 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688390
|
C | CAAAAA | 7 | a0001c0002t0001g0036a0001c0002t0001g0270a0001c0005t0001g0304others(4): Show | 7 | HG01175.hp1 HG01243.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-12193_163-1218 others(9): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688390
|
CAAAA | C | 21 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(18): Show | 21 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-12192_163-1218 others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688390 | |||||
chr19:38688426
|
C | T | 1 | a0001c0001t0021g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.163-12174C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688426 | ||||||
chr19:38688442
|
G | A | 1 | a0001c0002t0040g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.163-12158G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688442 | ||||||
chr19:38688452
|
T | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-12148T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688452 | ||||||
chr19:38688502
|
G | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-12098G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688502 | ||||||
chr19:38688611
|
C | T | 1 | a0001c0002t0045g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-11989C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688611 | ||||||
chr19:38688631
|
G | A | 94 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.163-11969G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688631 | ||||||
chr19:38688639
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-11961A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688639 | ||||||
chr19:38688642
|
G | T | 1 | a0001c0002t0001g0010 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.163-11958G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688642 | ||||||
chr19:38688702
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-11898G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688702 | ||||||
chr19:38688732
|
C | CA | 64 | a0001c0001t0002g0166a0001c0001t0004g0221a0001c0001t0004g0255others(61): Show | 65 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.163-11859dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38688732 | |||||
chr19:38688840
|
C | T | 1 | a0001c0003t0003g0089 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.163-11760C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38688840 | ||||||
chr19:38689199
|
T | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-11401T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689199 | ||||||
chr19:38689250
|
A | G | 23 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(20): Show | 23 | HG02015.hp1 HG02040.hp2 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.163-11350A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689250 | ||||||
chr19:38689294
|
A | G | 119 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.163-11306A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689294 | ||||||
chr19:38689537
|
G | A | 1 | a0001c0002t0007g0215 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.163-11063G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689537 | ||||||
chr19:38689546
|
A | G | 3 | a0001c0002t0001g0020a0001c0002t0001g0075a0001c0002t0041g0007 | 3 | NA18942.hp1 NA18957.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.163-11054A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689546 | ||||||
chr19:38689573
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-11027C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689573 | ||||||
chr19:38689705
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-10895G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689705 | ||||||
chr19:38689818
|
C | T | 95 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.163-10782C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689818 | ||||||
chr19:38689834
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-10766C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689834 | ||||||
chr19:38689884
|
A | G | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-10716A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689884 | ||||||
chr19:38689917
|
G | A | 2 | a0001c0002t0001g0005a0001c0002t0001g0071 | 2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.163-10683G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38689917 | ||||||
chr19:38690448
|
T | C | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163-10152T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690448 | ||||||
chr19:38690605
|
T | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9995T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690605 | ||||||
chr19:38690640
|
G | A | 2 | a0001c0004t0005g0229a0001c0004t0013g0228 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.163-9960G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690640 | ||||||
chr19:38690674
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9926C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690674 | ||||||
chr19:38690729
|
T | G | 27 | a0001c0001t0002g0085a0001c0002t0001g0038a0001c0002t0005g0054others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-9871T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690729 | ||||||
chr19:38690768
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.163-9832C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690768 | ||||||
chr19:38690849
|
A | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-9751A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38690849 | ||||||
chr19:38691051
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9549G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691051 | ||||||
chr19:38691137
|
C | T | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-9463C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691137 | ||||||
chr19:38691138
|
G | A | 52 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(49): Show | 54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.163-9462G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691138 | ||||||
chr19:38691269
|
G | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-9331G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691269 | ||||||
chr19:38691272
|
A | G | 207 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.163-9328A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691272 | ||||||
chr19:38691332
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9268C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691332 | ||||||
chr19:38691337
|
G | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-9263G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691337 | ||||||
chr19:38691401
|
C | CA | 29 | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0002t0001g0218others(26): Show | 29 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.163-9186dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38691401 | |||||
chr19:38691413
|
AAC | A | 7 | a0001c0002t0001g0020a0001c0002t0001g0040a0001c0002t0040g0203others(4): Show | 7 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-9185_163-9184d others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38691413 | |||||
chr19:38691414
|
AC | A | 65 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.163-9185delC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691414 | ||||||
chr19:38691415
|
C | A | 24 | a0001c0001t0001g0170a0001c0002t0001g0009a0001c0002t0001g0013others(21): Show | 24 | HG00558.hp2 HG01106.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9185C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691415 | ||||||
chr19:38691417
|
A | C | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.163-9183A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691417 | ||||||
chr19:38691420
|
A | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9180A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691420 | ||||||
chr19:38691423
|
A | C | 6 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(3): Show | 6 | NA18940.hp1 NA18994.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-9177A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691423 | ||||||
chr19:38691424
|
C | A | 39 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(36): Show | 39 | HG00280.hp2 HG00558.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-9176C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691424 | ||||||
chr19:38691425
|
A | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-9175A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691425 | ||||||
chr19:38691427
|
A | G | 1 | a0004c0019t0052g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.163-9173A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691427 | ||||||
chr19:38691485
|
G | A | 2 | a0001c0004t0013g0235a0001c0004t0013g0236 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.163-9115G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691485 | ||||||
chr19:38691640
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163-8960C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691640 | ||||||
chr19:38691660
|
T | C | 2 | a0001c0004t0005g0222a0001c0004t0048g0223 | 2 | HG01975.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.163-8940T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691660 | ||||||
chr19:38691700
|
C | T | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-8900C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691700 | ||||||
chr19:38691869
|
CTCCAACC others(15): Show |
C | 1 | a0001c0001t0002g0162 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163-8730_163-8709d others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691869 | ||||||
chr19:38691880
|
C | T | 1 | a0001c0001t0004g0261 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.163-8720C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691880 | ||||||
chr19:38691925
|
C | T | 76 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.163-8675C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38691925 | ||||||
chr19:38692052
|
T | A | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-8548T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692052 | ||||||
chr19:38692074
|
A | G | 5 | a0001c0001t0001g0170a0001c0001t0017g0284a0001c0001t0017g0288others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-8526A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692074 | ||||||
chr19:38692098
|
A | G | 1 | a0001c0004t0005g0244 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163-8502A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692098 | ||||||
chr19:38692216
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163-8384G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692216 | ||||||
chr19:38692259
|
T | C | 31 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(28): Show | 31 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.163-8341T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692259 | ||||||
chr19:38692568
|
G | GGCCTAA | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.163-8030_163-8029i others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38692568 | |||||
chr19:38692571
|
T | C | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.163-8029T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692571 | ||||||
chr19:38692790
|
A | G | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-7810A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692790 | ||||||
chr19:38692874
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-7726C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692874 | ||||||
chr19:38692908
|
G | T | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163-7692G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692908 | ||||||
chr19:38692944
|
A | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-7656A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38692944 | ||||||
chr19:38693078
|
T | C | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-7522T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693078 | ||||||
chr19:38693089
|
G | A | 5 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0260others(2): Show | 5 | HG02040.hp2 HG02071.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-7511G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693089 | ||||||
chr19:38693106
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-7494G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693106 | ||||||
chr19:38693121
|
C | T | 3 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0001g0292 | 3 | HG02559.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.163-7479C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693121 | ||||||
chr19:38693139
|
G | A | 26 | a0001c0002t0045g0186a0001c0003t0003g0087a0001c0003t0003g0088others(23): Show | 26 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-7461G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693139 | ||||||
chr19:38693162
|
G | T | 2 | a0001c0001t0002g0091a0001c0001t0024g0092 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-7438G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693162 | ||||||
chr19:38693262
|
G | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-7338G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693262 | ||||||
chr19:38693526
|
C | T | 88 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.163-7074C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693526 | ||||||
chr19:38693530
|
T | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-7070T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693530 | ||||||
chr19:38693567
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-7033G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693567 | ||||||
chr19:38693720
|
C | T | 22 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(19): Show | 22 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.163-6880C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693720 | ||||||
chr19:38693878
|
G | C | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-6722G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693878 | ||||||
chr19:38693949
|
C | G | 2 | a0001c0002t0001g0218a0001c0002t0007g0023 | 2 | NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.163-6651C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38693949 | ||||||
chr19:38694000
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-6600G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694000 | ||||||
chr19:38694029
|
C | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-6571C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694029 | ||||||
chr19:38694066
|
T | G | 1 | a0001c0001t0020g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.163-6534T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694066 | ||||||
chr19:38694155
|
C | T | 1 | a0005c0018t0001g0201 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.163-6445C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694155 | ||||||
chr19:38694171
|
G | A | 73 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.163-6429G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694171 | ||||||
chr19:38694182
|
T | G | 204 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(201): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.163-6418T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694182 | ||||||
chr19:38694219
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-6381C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694219 | ||||||
chr19:38694264
|
C | CT | 31 | a0001c0002t0001g0283a0001c0002t0012g0003a0001c0002t0012g0301others(28): Show | 32 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-6323dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38694264 | |||||
chr19:38694322
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-6278C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694322 | ||||||
chr19:38694635
|
G | A | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-5965G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694635 | ||||||
chr19:38694704
|
A | G | 1 | a0001c0004t0005g0244 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163-5896A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694704 | ||||||
chr19:38694740
|
T | TA | 310 | a0001c0001t0001g0086a0001c0001t0001g0170a0001c0001t0001g0205others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.163-5859dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38694740 | |||||
chr19:38694816
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.163-5784G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694816 | ||||||
chr19:38694879
|
C | CG | 27 | a0001c0001t0002g0132a0001c0001t0002g0166a0001c0002t0001g0021others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.163-5714dupG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38694879 | |||||
chr19:38694917
|
G | C | 207 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.163-5683G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694917 | ||||||
chr19:38694973
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.163-5627C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38694973 | ||||||
chr19:38695114
|
A | G | 1 | a0001c0001t0004g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-5486A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695114 | ||||||
chr19:38695135
|
A | T | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-5465A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695135 | ||||||
chr19:38695182
|
A | G | 1 | a0001c0001t0004g0285 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.163-5418A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695182 | ||||||
chr19:38695302
|
C | T | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-5298C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695302 | ||||||
chr19:38695472
|
C | A | 7 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0057others(4): Show | 7 | HG00438.hp2 HG01123.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-5128C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695472 | ||||||
chr19:38695503
|
GGGGA | G | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-5094_163-5091d others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38695503 | |||||
chr19:38695546
|
C | G | 1 | a0001c0002t0001g0283 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-5054C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695546 | ||||||
chr19:38695589
|
T | C | 208 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.163-5011T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695589 | ||||||
chr19:38695676
|
G | A | 2 | a0001c0001t0004g0271a0001c0001t0006g0298 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.163-4924G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695676 | ||||||
chr19:38695709
|
A | G | 1 | a0001c0001t0020g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.163-4891A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695709 | ||||||
chr19:38695828
|
C | T | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-4772C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695828 | ||||||
chr19:38695835
|
TGCCCCCC others(1): Show |
T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-4764_163-4757d others(10): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695835 | ||||||
chr19:38695849
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-4751G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695849 | ||||||
chr19:38695973
|
G | A | 84 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-4627G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38695973 | ||||||
chr19:38696125
|
G | T | 1 | a0001c0001t0002g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163-4475G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696125 | ||||||
chr19:38696173
|
G | A | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.163-4427G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696173 | ||||||
chr19:38696310
|
A | G | 119 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.163-4290A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696310 | ||||||
chr19:38696351
|
G | A | 1 | a0001c0003t0003g0089 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.163-4249G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696351 | ||||||
chr19:38696354
|
G | C | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.163-4246G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696354 | ||||||
chr19:38696364
|
C | A | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-4236C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696364 | ||||||
chr19:38696472
|
C | G | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-4128C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696472 | ||||||
chr19:38696473
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-4127C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696473 | ||||||
chr19:38696528
|
A | C | 1 | a0001c0001t0039g0108 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.163-4072A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696528 | ||||||
chr19:38696735
|
A | T | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-3865A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696735 | ||||||
chr19:38696745
|
A | G | 202 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(199): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.163-3855A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696745 | ||||||
chr19:38696765
|
G | A | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-3835G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696765 | ||||||
chr19:38696779
|
T | A | 2 | a0001c0001t0020g0269a0001c0001t0036g0268 | 2 | HG00642.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3821T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696779 | ||||||
chr19:38696839
|
A | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-3761A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696839 | ||||||
chr19:38696977
|
C | G | 5 | a0001c0001t0002g0212a0001c0001t0014g0168a0001c0001t0014g0169others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-3623C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38696977 | ||||||
chr19:38697083
|
G | T | 6 | a0001c0003t0003g0090a0001c0003t0003g0188a0001c0003t0003g0194others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3517G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697083 | ||||||
chr19:38697106
|
AAGCCAG | A | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-3490_163-3485d others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38697106 | |||||
chr19:38697158
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-3442C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697158 | ||||||
chr19:38697424
|
C | G | 207 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.163-3176C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697424 | ||||||
chr19:38697472
|
G | A | 95 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.163-3128G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697472 | ||||||
chr19:38697509
|
A | G | 51 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(48): Show | 53 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.163-3091A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697509 | ||||||
chr19:38697536
|
T | C | 1 | a0001c0014t0003g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.163-3064T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697536 | ||||||
chr19:38697596
|
G | T | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-3004G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697596 | ||||||
chr19:38697661
|
G | A | 26 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(23): Show | 26 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-2939G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697661 | ||||||
chr19:38697676
|
C | T | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2924C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697676 | ||||||
chr19:38697818
|
T | A | 7 | a0001c0001t0002g0091a0001c0001t0002g0143a0001c0001t0002g0144others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-2782T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697818 | ||||||
chr19:38697842
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0042g0290 | 2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.163-2758G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697842 | ||||||
chr19:38697956
|
C | T | 1 | a0001c0004t0005g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-2644C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38697956 | ||||||
chr19:38698060
|
G | T | 1 | a0001c0002t0001g0068 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.163-2540G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698060 | ||||||
chr19:38698091
|
C | T | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2509C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698091 | ||||||
chr19:38698242
|
C | T | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.163-2358C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698242 | ||||||
chr19:38698289
|
G | A | 3 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276 | 3 | HG02155.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-2311G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698289 | ||||||
chr19:38698649
|
C | T | 1 | a0001c0004t0005g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-1951C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698649 | ||||||
chr19:38698727
|
A | G | 1 | a0001c0004t0005g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.163-1873A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698727 | ||||||
chr19:38698902
|
G | A | 1 | a0001c0004t0005g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-1698G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38698902 | ||||||
chr19:38699051
|
G | A | 1 | a0001c0003t0003g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.163-1549G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699051 | ||||||
chr19:38699106
|
T | C | 172 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(169): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.163-1494T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699106 | ||||||
chr19:38699255
|
C | T | 48 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(45): Show | 48 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-1345C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699255 | ||||||
chr19:38699295
|
G | T | 1 | a0001c0002t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-1305G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699295 | ||||||
chr19:38699321
|
G | A | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-1279G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699321 | ||||||
chr19:38699339
|
C | G | 1 | a0001c0001t0002g0113 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.163-1261C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699339 | ||||||
chr19:38699442
|
C | G | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163-1158C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699442 | ||||||
chr19:38699492
|
C | T | 1 | a0001c0004t0005g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.163-1108C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699492 | ||||||
chr19:38699627
|
C | T | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-973C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699627 | ||||||
chr19:38699679
|
C | G | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-921C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699679 | ||||||
chr19:38699719
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.163-881C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699719 | ||||||
chr19:38699728
|
C | T | 1 | a0001c0004t0005g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-872C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699728 | ||||||
chr19:38699734
|
GACAGAGC others(17): Show |
G | 1 | a0001c0002t0001g0197 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-864_163-841del others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38699734 | |||||
chr19:38699754
|
C | CA | 66 | a0001c0001t0002g0129a0001c0001t0004g0221a0001c0001t0004g0255others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.163-833dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr19 | 38699754 | |||||
chr19:38699791
|
A | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-809A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699791 | ||||||
chr19:38699823
|
A | G | 25 | a0001c0002t0001g0040a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-777A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699823 | ||||||
chr19:38699948
|
C | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-652C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38699948 | ||||||
chr19:38700074
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-526G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38700074 | ||||||
chr19:38700231
|
C | T | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-369C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38700231 | ||||||
chr19:38700262
|
G | A | 1 | a0001c0004t0005g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-338G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 1/20 | chr19 | 38700262 | ||||||
chr19:38700743
|
G | C | 207 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(204): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.277+29G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 2/20 | chr19 | 38700743 | ||||||
chr19:38700904
|
G | A | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.278-98G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 2/20 | chr19 | 38700904 | ||||||
chr19:38701224
|
C | T | 1 | a0001c0004t0005g0230 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.397+103C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701224 | ||||||
chr19:38701328
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.397+207C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701328 | ||||||
chr19:38701373
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+252G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701373 | ||||||
chr19:38701382
|
G | A | 4 | a0001c0001t0002g0097a0001c0001t0002g0146a0001c0001t0002g0147others(1): Show | 4 | HG01943.hp1 HG01975.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+261G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701382 | ||||||
chr19:38701492
|
G | C | 2 | a0003c0009t0002g0130a0003c0009t0002g0208 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.397+371G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701492 | ||||||
chr19:38701524
|
C | T | 1 | a0001c0001t0006g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.397+403C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701524 | ||||||
chr19:38701580
|
G | A | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.397+459G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701580 | ||||||
chr19:38701642
|
C | G | 1 | a0001c0006t0047g0239 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.397+521C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701642 | ||||||
chr19:38701686
|
C | G | 1 | a0001c0001t0002g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.397+565C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701686 | ||||||
chr19:38701807
|
C | T | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.397+686C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38701807 | ||||||
chr19:38702007
|
C | T | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+886C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702007 | ||||||
chr19:38702072
|
C | T | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+951C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702072 | ||||||
chr19:38702237
|
T | C | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.397+1116T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702237 | ||||||
chr19:38702289
|
T | C | 4 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(1): Show | 5 | HG01891.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1168T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702289 | ||||||
chr19:38702395
|
C | T | 1 | a0001c0002t0042g0290 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.397+1274C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702395 | ||||||
chr19:38702554
|
C | T | 1 | a0005c0018t0001g0201 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.397+1433C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702554 | ||||||
chr19:38702576
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.397+1455G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702576 | ||||||
chr19:38702701
|
G | A | 5 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+1580G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702701 | ||||||
chr19:38702782
|
C | G | 1 | a0001c0002t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.397+1661C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702782 | ||||||
chr19:38702827
|
C | G | 1 | a0001c0001t0021g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.397+1706C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38702827 | ||||||
chr19:38703050
|
C | T | 12 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.398-1884C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703050 | ||||||
chr19:38703236
|
A | AT | 76 | a0001c0001t0001g0205a0001c0002t0001g0005a0001c0002t0001g0006others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.398-1679dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 38703236 | |||||
chr19:38703236
|
A | ATT | 6 | a0001c0002t0001g0022a0001c0002t0001g0042a0001c0002t0001g0064others(3): Show | 6 | HG01358.hp1 HG01934.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.398-1680_398-1679d others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 38703236 | |||||
chr19:38703236
|
AT | A | 38 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0172others(35): Show | 38 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.398-1679delT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 38703236 | |||||
chr19:38703236
|
ATT | A | 45 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(42): Show | 46 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-1680_398-1679d others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 38703236 | |||||
chr19:38703405
|
A | AT | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.398-1525dupT | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr19 | 38703405 | |||||
chr19:38703476
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.398-1458G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703476 | ||||||
chr19:38703530
|
C | A | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-1404C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703530 | ||||||
chr19:38703542
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.398-1392G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703542 | ||||||
chr19:38703775
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.398-1159A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703775 | ||||||
chr19:38703854
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.398-1080C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703854 | ||||||
chr19:38703959
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.398-975C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38703959 | ||||||
chr19:38704033
|
C | A | 1 | a0001c0001t0004g0262 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.398-901C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704033 | ||||||
chr19:38704184
|
G | A | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-750G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704184 | ||||||
chr19:38704312
|
A | C | 1 | a0001c0003t0009g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.398-622A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704312 | ||||||
chr19:38704375
|
C | T | 19 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(16): Show | 20 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.398-559C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704375 | ||||||
chr19:38704443
|
C | G | 101 | a0001c0001t0017g0284a0001c0002t0001g0005a0001c0002t0001g0006others(98): Show | 102 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.398-491C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704443 | ||||||
chr19:38704474
|
A | G | 1 | a0001c0002t0001g0197 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.398-460A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704474 | ||||||
chr19:38704527
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.398-407G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704527 | ||||||
chr19:38704547
|
G | A | 7 | a0001c0002t0045g0186a0001c0003t0003g0090a0001c0003t0003g0188others(4): Show | 7 | HG02451.hp2 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.398-387G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704547 | ||||||
chr19:38704614
|
A | C | 1 | a0001c0001t0004g0272 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.398-320A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704614 | ||||||
chr19:38704644
|
G | C | 5 | a0001c0002t0001g0033a0001c0002t0001g0036a0001c0002t0001g0072others(2): Show | 5 | HG02523.hp2 HG03669.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-290G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704644 | ||||||
chr19:38704662
|
AGGAG | A | 90 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.398-271_398-268del others(4): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704662 | ||||||
chr19:38704674
|
T | G | 102 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.398-260T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704674 | ||||||
chr19:38704681
|
G | C | 2 | a0001c0002t0001g0040a0001c0002t0001g0064 | 2 | NA18981.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.398-253G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704681 | ||||||
chr19:38704918
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.398-16C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 3/20 | chr19 | 38704918 | ||||||
chr19:38705045
|
G | A | 1 | a0001c0005t0001g0304 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.484+25G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705045 | ||||||
chr19:38705095
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.484+75C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705095 | ||||||
chr19:38705107
|
C | G | 8 | a0001c0001t0004g0261a0001c0002t0007g0023a0001c0002t0007g0214others(5): Show | 8 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.484+87C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705107 | ||||||
chr19:38705155
|
G | A | 2 | a0001c0004t0005g0095a0001c0004t0005g0227 | 2 | HG00280.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.484+135G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705155 | ||||||
chr19:38705385
|
C | G | 1 | a0001c0001t0010g0142 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.484+365C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705385 | ||||||
chr19:38705445
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.484+425A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705445 | ||||||
chr19:38705567
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.485-477C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705567 | ||||||
chr19:38705584
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.485-460G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705584 | ||||||
chr19:38705613
|
C | T | 19 | a0001c0001t0002g0099a0001c0001t0002g0102a0001c0001t0002g0109others(16): Show | 19 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.485-431C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705613 | ||||||
chr19:38705675
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-369C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705675 | ||||||
chr19:38705688
|
C | T | 173 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(170): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.485-356C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705688 | ||||||
chr19:38705801
|
C | T | 13 | a0001c0001t0004g0255a0001c0001t0004g0256a0001c0001t0004g0257others(10): Show | 13 | HG02040.hp2 HG02071.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.485-243C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705801 | ||||||
chr19:38705856
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0010g0103a0001c0001t0024g0098 | 3 | NA18942.hp2 NA18952.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.485-188G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705856 | ||||||
chr19:38705891
|
C | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.485-153C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38705891 | ||||||
chr19:38706030
|
T | A | 1 | a0001c0001t0002g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-14T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 4/20 | chr19 | 38706030 | ||||||
chr19:38706181
|
C | A | 2 | a0001c0002t0001g0033a0001c0002t0034g0045 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+50C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706181 | ||||||
chr19:38706462
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+331A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706462 | ||||||
chr19:38706670
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+539C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706670 | ||||||
chr19:38706862
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+731C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706862 | ||||||
chr19:38706887
|
C | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+756C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706887 | ||||||
chr19:38706912
|
C | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+781C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706912 | ||||||
chr19:38706945
|
A | G | 208 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.572+814A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706945 | ||||||
chr19:38706992
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.572+861G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38706992 | ||||||
chr19:38707089
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+958A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707089 | ||||||
chr19:38707133
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.573-984G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707133 | ||||||
chr19:38707197
|
T | G | 1 | a0001c0003t0003g0094 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.573-920T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707197 | ||||||
chr19:38707207
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.573-910A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707207 | ||||||
chr19:38707314
|
T | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.573-803T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707314 | ||||||
chr19:38707342
|
C | T | 1 | a0001c0002t0035g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.573-775C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707342 | ||||||
chr19:38707344
|
C | T | 20 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.573-773C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707344 | ||||||
chr19:38707420
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573-697A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707420 | ||||||
chr19:38707512
|
G | A | 1 | a0001c0002t0007g0215 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.573-605G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707512 | ||||||
chr19:38707513
|
A | G | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.573-604A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707513 | ||||||
chr19:38707581
|
G | C | 4 | a0001c0007t0001g0200a0001c0007t0001g0202a0001c0007t0001g0204others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-536G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707581 | ||||||
chr19:38707592
|
G | T | 1 | a0001c0001t0006g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.573-525G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707592 | ||||||
chr19:38707625
|
G | A | 5 | a0001c0001t0006g0250a0001c0001t0006g0251a0001c0001t0006g0252others(2): Show | 5 | HG02738.hp2 HG03669.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-492G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707625 | ||||||
chr19:38707680
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.573-437A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707680 | ||||||
chr19:38707735
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.573-382G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707735 | ||||||
chr19:38707844
|
C | T | 1 | a0001c0001t0006g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.573-273C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38707844 | ||||||
chr19:38708060
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573-57C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 5/20 | chr19 | 38708060 | ||||||
chr19:38708334
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+139C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708334 | ||||||
chr19:38708350
|
G | A | 3 | a0001c0001t0022g0198a0001c0001t0022g0199a0001c0002t0001g0029 | 3 | HG01099.hp2 HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.651+155G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708350 | ||||||
chr19:38708364
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.651+169G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708364 | ||||||
chr19:38708402
|
T | G | 2 | a0001c0002t0001g0058a0001c0002t0001g0063 | 2 | NA18962.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.651+207T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708402 | ||||||
chr19:38708422
|
C | T | 1 | a0001c0001t0010g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.651+227C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708422 | ||||||
chr19:38708651
|
G | C | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.651+456G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708651 | ||||||
chr19:38708699
|
C | A | 1 | a0001c0015t0004g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.651+504C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708699 | ||||||
chr19:38708747
|
T | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.651+552T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708747 | ||||||
chr19:38708776
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.651+581C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708776 | ||||||
chr19:38708781
|
G | A | 2 | a0001c0003t0003g0191a0001c0004t0005g0232 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.651+586G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708781 | ||||||
chr19:38708875
|
A | G | 2 | a0001c0005t0018g0307a0001c0005t0018g0308 | 2 | HG00140.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.652-520A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708875 | ||||||
chr19:38708981
|
T | C | 209 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.652-414T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38708981 | ||||||
chr19:38709008
|
G | T | 1 | a0001c0002t0007g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.652-387G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709008 | ||||||
chr19:38709106
|
AG | A | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-286delG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr19 | 38709106 | |||||
chr19:38709178
|
G | A | 1 | a0001c0001t0004g0272 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.652-217G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709178 | ||||||
chr19:38709196
|
G | A | 10 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-199G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709196 | ||||||
chr19:38709233
|
C | G | 2 | a0001c0001t0002g0206a0001c0001t0002g0209 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.652-162C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709233 | ||||||
chr19:38709340
|
G | T | 20 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-55G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709340 | ||||||
chr19:38709358
|
G | A | 20 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-37G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709358 | ||||||
chr19:38709361
|
G | T | 20 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-34G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 6/20 | chr19 | 38709361 | ||||||
chr19:38709517
|
A | G | 1 | a0001c0005t0018g0308 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.733+41A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709517 | ||||||
chr19:38709611
|
G | A | 1 | a0001c0001t0021g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733+135G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709611 | ||||||
chr19:38709711
|
G | A | 2 | a0003c0009t0002g0130a0003c0009t0002g0208 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.733+235G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709711 | ||||||
chr19:38709739
|
C | G | 1 | a0001c0010t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733+263C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709739 | ||||||
chr19:38709762
|
A | T | 1 | a0001c0001t0004g0261 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.733+286A>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709762 | ||||||
chr19:38709858
|
A | G | 3 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276 | 3 | HG02155.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+382A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38709858 | ||||||
chr19:38710203
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.734-54C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 7/20 | chr19 | 38710203 | ||||||
chr19:38710383
|
C | T | 2 | a0001c0003t0003g0178a0001c0014t0003g0193 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.819+41C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38710383 | ||||||
chr19:38710634
|
C | G | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+292C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38710634 | ||||||
chr19:38710830
|
C | T | 1 | a0001c0001t0011g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+488C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38710830 | ||||||
chr19:38710848
|
C | T | 102 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.819+506C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38710848 | ||||||
chr19:38711132
|
G | C | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+790G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711132 | ||||||
chr19:38711141
|
C | T | 102 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.819+799C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711141 | ||||||
chr19:38711167
|
C | T | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819+825C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711167 | ||||||
chr19:38711176
|
T | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+834T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711176 | ||||||
chr19:38711240
|
C | G | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.819+898C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711240 | ||||||
chr19:38711416
|
C | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+1074C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711416 | ||||||
chr19:38711431
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+1089G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711431 | ||||||
chr19:38711544
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+1202G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711544 | ||||||
chr19:38711568
|
C | G | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.819+1226C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711568 | ||||||
chr19:38711670
|
G | C | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.819+1328G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711670 | ||||||
chr19:38711690
|
C | T | 2 | a0001c0001t0019g0299a0001c0001t0030g0294 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.819+1348C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711690 | ||||||
chr19:38711701
|
G | A | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+1359G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711701 | ||||||
chr19:38711843
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.819+1501G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711843 | ||||||
chr19:38711862
|
G | A | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.819+1520G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711862 | ||||||
chr19:38711869
|
C | T | 1 | a0001c0005t0001g0304 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.819+1527C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711869 | ||||||
chr19:38711977
|
C | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.819+1635C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38711977 | ||||||
chr19:38712070
|
C | T | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819+1728C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712070 | ||||||
chr19:38712112
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.819+1770C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712112 | ||||||
chr19:38712156
|
G | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.819+1814G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712156 | ||||||
chr19:38712246
|
A | AG | 25 | a0001c0001t0006g0253a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+1912dupG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 38712246 | |||||
chr19:38712248
|
G | C | 102 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.819+1906G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712248 | ||||||
chr19:38712253
|
G | T | 1 | a0001c0001t0011g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+1911G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712253 | ||||||
chr19:38712257
|
G | A | 90 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.819+1915G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712257 | ||||||
chr19:38712407
|
G | A | 1 | a0001c0001t0024g0098 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.820-2062G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712407 | ||||||
chr19:38712587
|
G | A | 1 | a0001c0003t0003g0089 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.820-1882G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712587 | ||||||
chr19:38712622
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.820-1847G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712622 | ||||||
chr19:38712814
|
A | G | 1 | a0001c0004t0005g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.820-1655A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712814 | ||||||
chr19:38712851
|
G | A | 1 | a0001c0002t0007g0219 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.820-1618G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712851 | ||||||
chr19:38712885
|
G | T | 5 | a0001c0001t0006g0250a0001c0001t0006g0251a0001c0001t0006g0252others(2): Show | 5 | HG02738.hp2 HG03669.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-1584G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712885 | ||||||
chr19:38712949
|
CTGGCCCC others(15): Show |
C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.820-1516_820-1495d others(24): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 38712949 | |||||
chr19:38712964
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.820-1505G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38712964 | ||||||
chr19:38713110
|
C | G | 1 | a0001c0002t0005g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.820-1359C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713110 | ||||||
chr19:38713176
|
C | G | 1 | a0001c0002t0001g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.820-1293C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713176 | ||||||
chr19:38713257
|
C | T | 1 | a0001c0015t0004g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.820-1212C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713257 | ||||||
chr19:38713332
|
C | G | 1 | a0001c0001t0022g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.820-1137C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713332 | ||||||
chr19:38713342
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.820-1127G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713342 | ||||||
chr19:38713566
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820-903C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713566 | ||||||
chr19:38713588
|
C | T | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.820-881C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713588 | ||||||
chr19:38713589
|
G | A | 1 | a0001c0002t0035g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.820-880G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713589 | ||||||
chr19:38713597
|
G | A | 4 | a0001c0003t0003g0179a0001c0003t0003g0180a0001c0003t0003g0213others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-872G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713597 | ||||||
chr19:38713803
|
TCCCCGTG others(4): Show |
T | 30 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(27): Show | 30 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.820-661_820-651del others(11): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr19 | 38713803 | |||||
chr19:38713942
|
C | T | 3 | a0001c0001t0002g0091a0001c0001t0024g0092a0001c0001t0030g0294 | 3 | HG01069.hp1 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.820-527C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38713942 | ||||||
chr19:38714054
|
G | C | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-415G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714054 | ||||||
chr19:38714205
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.820-264C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714205 | ||||||
chr19:38714206
|
G | A | 96 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.820-263G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714206 | ||||||
chr19:38714242
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.820-227G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714242 | ||||||
chr19:38714271
|
G | A | 2 | a0001c0002t0001g0282a0001c0002t0001g0283 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.820-198G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714271 | ||||||
chr19:38714321
|
G | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.820-148G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714321 | ||||||
chr19:38714341
|
T | A | 4 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-128T>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714341 | ||||||
chr19:38714375
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0036a0001c0002t0001g0038others(4): Show | 7 | HG01981.hp2 HG02523.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-94C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714375 | ||||||
chr19:38714437
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.820-32C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 8/20 | chr19 | 38714437 | ||||||
chr19:38714626
|
C | A | 1 | a0001c0002t0005g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.912+65C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714626 | ||||||
chr19:38714714
|
C | T | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.912+153C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714714 | ||||||
chr19:38714869
|
G | A | 2 | a0001c0003t0003g0087a0001c0003t0003g0089 | 2 | HG01243.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.912+308G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714869 | ||||||
chr19:38714874
|
A | G | 1 | a0001c0002t0001g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.912+313A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714874 | ||||||
chr19:38714895
|
G | T | 6 | a0001c0002t0007g0023a0001c0002t0007g0214a0001c0002t0007g0216others(3): Show | 6 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+334G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714895 | ||||||
chr19:38714911
|
T | G | 1 | a0001c0005t0027g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.912+350T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714911 | ||||||
chr19:38714967
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.912+406G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714967 | ||||||
chr19:38714973
|
C | T | 76 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.912+412C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38714973 | ||||||
chr19:38715162
|
C | T | 1 | a0001c0002t0007g0215 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.912+601C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715162 | ||||||
chr19:38715212
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.912+651G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715212 | ||||||
chr19:38715294
|
C | T | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.912+733C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715294 | ||||||
chr19:38715439
|
G | A | 1 | a0002c0008t0011g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.912+878G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715439 | ||||||
chr19:38715612
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.912+1051G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715612 | ||||||
chr19:38715648
|
C | T | 96 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.912+1087C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715648 | ||||||
chr19:38715989
|
C | T | 6 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(3): Show | 7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.913-1097C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38715989 | ||||||
chr19:38716046
|
C | T | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.913-1040C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716046 | ||||||
chr19:38716594
|
G | A | 31 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(28): Show | 32 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.913-492G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716594 | ||||||
chr19:38716597
|
G | A | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.913-489G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716597 | ||||||
chr19:38716630
|
A | C | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-456A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716630 | ||||||
chr19:38716643
|
G | A | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.913-443G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716643 | ||||||
chr19:38716689
|
C | T | 96 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.913-397C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716689 | ||||||
chr19:38716858
|
CAA | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.913-227_913-226del others(2): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 9/20 | chr19 | 38716858 | ||||||
chr19:38717378
|
G | T | 1 | a0001c0001t0015g0124 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1143+62G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/20 | chr19 | 38717378 | ||||||
chr19:38717573
|
G | C | 9 | a0001c0005t0001g0304a0001c0005t0008g0001a0001c0005t0008g0004others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1143+257G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/20 | chr19 | 38717573 | ||||||
chr19:38717588
|
G | C | 1 | a0001c0002t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1143+272G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/20 | chr19 | 38717588 | ||||||
chr19:38717623
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1144-304G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/20 | chr19 | 38717623 | ||||||
chr19:38717644
|
C | T | 1 | a0001c0003t0009g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1144-283C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 10/20 | chr19 | 38717644 | ||||||
chr19:38718155
|
C | T | 27 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076others(24): Show | 27 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+81C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718155 | ||||||
chr19:38718646
|
G | A | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+572G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718646 | ||||||
chr19:38718647
|
A | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1291+573A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718647 | ||||||
chr19:38718757
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0159 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1291+683G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718757 | ||||||
chr19:38718833
|
G | A | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1291+759G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718833 | ||||||
chr19:38718920
|
C | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1291+846C>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718920 | ||||||
chr19:38718923
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1291+849G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718923 | ||||||
chr19:38718995
|
C | G | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.1291+921C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38718995 | ||||||
chr19:38719110
|
G | A | 1 | a0001c0006t0005g0237 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1291+1036G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719110 | ||||||
chr19:38719165
|
C | T | 5 | a0001c0002t0040g0203a0001c0007t0001g0200a0001c0007t0001g0202others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+1091C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719165 | ||||||
chr19:38719245
|
C | T | 1 | a0001c0003t0003g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+1171C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719245 | ||||||
chr19:38719248
|
C | G | 209 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1291+1174C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719248 | ||||||
chr19:38719301
|
G | A | 3 | a0001c0005t0008g0001a0001c0005t0008g0077a0001c0005t0028g0001 | 3 | HG01168.hp2 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1291+1227G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719301 | ||||||
chr19:38719352
|
C | G | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.1291+1278C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719352 | ||||||
chr19:38719363
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1291+1289G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719363 | ||||||
chr19:38719373
|
G | A | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1291+1299G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719373 | ||||||
chr19:38719513
|
A | G | 1 | a0001c0002t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1291+1439A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719513 | ||||||
chr19:38719583
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1291+1509G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719583 | ||||||
chr19:38719586
|
C | T | 2 | a0001c0003t0009g0182a0001c0003t0009g0183 | 2 | HG00735.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1291+1512C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719586 | ||||||
chr19:38719666
|
G | A | 4 | a0001c0001t0017g0284a0001c0001t0017g0288a0001c0001t0025g0286others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1592G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719666 | ||||||
chr19:38719827
|
G | A | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1292-1711G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719827 | ||||||
chr19:38719908
|
G | A | 7 | a0001c0002t0007g0023a0001c0002t0007g0214a0001c0002t0007g0215others(4): Show | 7 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-1630G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719908 | ||||||
chr19:38719941
|
C | T | 1 | a0001c0002t0031g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1292-1597C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719941 | ||||||
chr19:38719953
|
G | A | 49 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1292-1585G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38719953 | ||||||
chr19:38720033
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1292-1505C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720033 | ||||||
chr19:38720093
|
C | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1292-1445C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720093 | ||||||
chr19:38720124
|
C | T | 1 | a0001c0004t0005g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1292-1414C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720124 | ||||||
chr19:38720168
|
C | G | 1 | a0001c0003t0003g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1292-1370C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720168 | ||||||
chr19:38720261
|
C | T | 3 | a0001c0001t0021g0083a0001c0001t0021g0196a0001c0001t0049g0076 | 3 | HG03139.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1292-1277C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720261 | ||||||
chr19:38720320
|
C | T | 5 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0061others(2): Show | 5 | HG00438.hp2 HG01952.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-1218C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720320 | ||||||
chr19:38720321
|
A | G | 209 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1292-1217A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720321 | ||||||
chr19:38720370
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1292-1168G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720370 | ||||||
chr19:38720483
|
G | A | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1292-1055G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720483 | ||||||
chr19:38720689
|
G | A | 3 | a0001c0003t0009g0182a0001c0003t0009g0183a0001c0003t0009g0192 | 3 | HG00735.hp2 HG02602.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1292-849G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720689 | ||||||
chr19:38720714
|
G | T | 3 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0070 | 3 | HG00544.hp2 HG02080.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1292-824G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720714 | ||||||
chr19:38720912
|
T | C | 1 | a0001c0002t0035g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1292-626T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38720912 | ||||||
chr19:38721085
|
C | T | 1 | a0001c0003t0003g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1292-453C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38721085 | ||||||
chr19:38721180
|
G | A | 6 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-358G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38721180 | ||||||
chr19:38721310
|
G | A | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1292-228G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38721310 | ||||||
chr19:38721412
|
T | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1292-126T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 11/20 | chr19 | 38721412 | ||||||
chr19:38721729
|
C | T | 1 | a0001c0001t0021g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1442+41C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38721729 | ||||||
chr19:38721752
|
C | T | 25 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(22): Show | 25 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1442+64C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38721752 | ||||||
chr19:38721753
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1442+65G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38721753 | ||||||
chr19:38721760
|
C | T | 32 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(29): Show | 32 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.1442+72C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38721760 | ||||||
chr19:38722155
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1442+467G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722155 | ||||||
chr19:38722219
|
C | T | 96 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1442+531C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722219 | ||||||
chr19:38722477
|
AG | A | 75 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1442+791delG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr19 | 38722477 | |||||
chr19:38722547
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1442+859A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722547 | ||||||
chr19:38722568
|
G | A | 4 | a0001c0002t0012g0003a0001c0002t0012g0301a0001c0002t0033g0300others(1): Show | 5 | HG01891.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442+880G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722568 | ||||||
chr19:38722602
|
C | T | 1 | a0001c0004t0005g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1442+914C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722602 | ||||||
chr19:38722604
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1442+916G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722604 | ||||||
chr19:38722612
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1442+924A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722612 | ||||||
chr19:38722616
|
C | T | 21 | a0001c0001t0011g0281a0001c0001t0016g0302a0001c0001t0016g0303others(18): Show | 22 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1442+928C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722616 | ||||||
chr19:38722918
|
G | A | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.1443-696G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722918 | ||||||
chr19:38722963
|
G | A | 1 | a0001c0015t0004g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1443-651G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38722963 | ||||||
chr19:38723016
|
C | G | 1 | a0001c0005t0001g0304 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1443-598C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38723016 | ||||||
chr19:38723211
|
C | T | 6 | a0001c0002t0007g0023a0001c0002t0007g0214a0001c0002t0007g0216others(3): Show | 6 | HG00558.hp2 HG01952.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1443-403C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38723211 | ||||||
chr19:38723255
|
C | T | 2 | a0003c0009t0002g0130a0003c0009t0002g0208 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1443-359C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38723255 | ||||||
chr19:38723262
|
G | T | 3 | a0001c0001t0017g0288a0001c0001t0025g0286a0001c0001t0026g0287 | 3 | HG01884.hp1 HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1443-352G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 12/20 | chr19 | 38723262 | ||||||
chr19:38723771
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1551+49C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 13/20 | chr19 | 38723771 | ||||||
chr19:38724090
|
C | T | 1 | a0001c0001t0023g0310 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1692+13C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 14/20 | chr19 | 38724090 | ||||||
chr19:38724693
|
C | T | 96 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2010+128C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724693 | ||||||
chr19:38724741
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2010+176C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724741 | ||||||
chr19:38724753
|
C | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2010+188C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724753 | ||||||
chr19:38724899
|
C | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2010+334C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724899 | ||||||
chr19:38724968
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2010+403A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724968 | ||||||
chr19:38724974
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2010+409G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38724974 | ||||||
chr19:38725084
|
ATTAC | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2010+522_2010+525d others(6): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr19 | 38725084 | |||||
chr19:38725144
|
C | G | 1 | a0001c0001t0020g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2010+579C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725144 | ||||||
chr19:38725302
|
T | C | 1 | a0001c0001t0030g0294 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2011-422T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725302 | ||||||
chr19:38725396
|
C | T | 3 | a0002c0008t0011g0278a0002c0008t0011g0279a0002c0008t0011g0280 | 3 | HG02965.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2011-328C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725396 | ||||||
chr19:38725439
|
C | G | 1 | a0001c0001t0011g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2011-285C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725439 | ||||||
chr19:38725551
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2011-173G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725551 | ||||||
chr19:38725563
|
T | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2011-161T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725563 | ||||||
chr19:38725574
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2011-150G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725574 | ||||||
chr19:38725580
|
C | T | 1 | a0001c0001t0049g0076 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2011-144C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725580 | ||||||
chr19:38725608
|
C | T | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2011-116C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725608 | ||||||
chr19:38725628
|
G | A | 1 | a0001c0001t0019g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2011-96G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725628 | ||||||
chr19:38725650
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2011-74G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 16/20 | chr19 | 38725650 | ||||||
chr19:38726287
|
C | CA | 14 | a0001c0001t0002g0152a0001c0001t0002g0174a0001c0001t0002g0207others(11): Show | 14 | HG01106.hp1 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2190+402dupA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr19 | 38726287 | |||||
chr19:38726287
|
CA | C | 21 | a0001c0001t0002g0131a0001c0001t0002g0149a0001c0001t0002g0153others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.2190+402delA | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr19 | 38726287 | |||||
chr19:38726527
|
C | T | 1 | a0001c0001t0043g0295 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2191-430C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726527 | ||||||
chr19:38726651
|
T | C | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2191-306T>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726651 | ||||||
chr19:38726652
|
C | T | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2191-305C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726652 | ||||||
chr19:38726867
|
G | A | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2191-90G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726867 | ||||||
chr19:38726882
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2191-75A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726882 | ||||||
chr19:38726952
|
C | T | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
splice_region_variant&intron_variant | LOW | c.2191-5C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 17/20 | chr19 | 38726952 | ||||||
chr19:38727253
|
G | C | 1 | a0001c0005t0008g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2337+150G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727253 | ||||||
chr19:38727318
|
A | G | 3 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0218 | 3 | NA18986.hp2 NA19007.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2337+215A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727318 | ||||||
chr19:38727400
|
C | G | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2337+297C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727400 | ||||||
chr19:38727402
|
G | C | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2337+299G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727402 | ||||||
chr19:38727539
|
G | T | 31 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(28): Show | 31 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.2338-407G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727539 | ||||||
chr19:38727542
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2338-404G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727542 | ||||||
chr19:38727569
|
G | A | 2 | a0001c0001t0022g0198a0001c0001t0022g0199 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2338-377G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727569 | ||||||
chr19:38727570
|
C | T | 1 | a0001c0001t0006g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2338-376C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727570 | ||||||
chr19:38727627
|
A | AC | 30 | a0001c0001t0002g0127a0001c0001t0002g0163a0001c0001t0002g0207others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2338-309dupC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr19 | 38727627 | |||||
chr19:38727635
|
C | G | 1 | a0001c0002t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2338-311C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727635 | ||||||
chr19:38727636
|
C | G | 1 | a0001c0002t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2338-310C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727636 | ||||||
chr19:38727637
|
CG | C | 67 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.2338-308delG | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727637 | ||||||
chr19:38727638
|
G | C | 33 | a0001c0001t0006g0251a0001c0001t0006g0252a0001c0001t0006g0253others(30): Show | 33 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2338-308G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727638 | ||||||
chr19:38727744
|
G | T | 5 | a0001c0001t0006g0250a0001c0001t0006g0251a0001c0001t0006g0252others(2): Show | 5 | HG02738.hp2 HG03669.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-202G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727744 | ||||||
chr19:38727754
|
A | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2338-192A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727754 | ||||||
chr19:38727755
|
A | C | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2338-191A>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727755 | ||||||
chr19:38727776
|
C | G | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2338-170C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727776 | ||||||
chr19:38727777
|
G | C | 1 | a0001c0001t0004g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2338-169G>C | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 18/20 | chr19 | 38727777 | ||||||
chr19:38728054
|
A | G | 25 | a0001c0002t0001g0293a0001c0004t0005g0095a0001c0004t0005g0222others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2418+28A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728054 | ||||||
chr19:38728187
|
CCTGGTCT others(3): Show |
C | 1 | a0001c0001t0002g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2418+162_2418+171d others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728187 | ||||||
chr19:38728256
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2418+230C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728256 | ||||||
chr19:38728410
|
G | GCTC | 9 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0009g0183others(6): Show | 9 | HG01975.hp1 HG02602.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2418+422_2418+424d others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
G | GCTCCTC | 29 | a0001c0002t0001g0044a0001c0002t0001g0073a0001c0002t0012g0003others(26): Show | 30 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2418+419_2418+424d others(8): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
G | GCTCCTCC others(2): Show |
3 | a0001c0002t0001g0043a0001c0002t0001g0274a0001c0004t0005g0233 | 3 | HG01433.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2418+416_2418+424d others(11): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
G | GCTCCTCC others(5): Show |
23 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0034others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.2418+413_2418+424d others(14): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
G | GCTCCTCC others(8): Show |
2 | a0001c0002t0001g0029a0001c0002t0001g0062 | 2 | HG01099.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.2418+410_2418+424d others(17): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
G | GCTCCTCC others(14): Show |
1 | a0001c0001t0014g0120 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2418+404_2418+424d others(23): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
GCTC | G | 7 | a0001c0001t0002g0110a0001c0001t0002g0153a0001c0001t0017g0288others(4): Show | 7 | HG01516.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2418+422_2418+424d others(5): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
GCTCCTCC others(2): Show |
G | 39 | a0001c0001t0004g0221a0001c0001t0004g0255a0001c0001t0004g0256others(36): Show | 39 | HG00642.hp1 HG02015.hp1 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.2418+416_2418+424d others(11): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
GCTCCTCC others(8): Show |
G | 2 | a0001c0001t0016g0302a0001c0001t0016g0303 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2418+410_2418+424d others(17): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728410
|
GCTCCTCC others(14): Show |
G | 19 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(16): Show | 19 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2418+404_2418+424d others(23): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728410 | |||||
chr19:38728448
|
T | TC | 9 | a0001c0001t0002g0157a0001c0001t0002g0163a0001c0001t0002g0296others(6): Show | 9 | HG00597.hp2 HG01884.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2418+429dupC | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728448 | |||||
chr19:38728448
|
T | TCCTCCTC others(3): Show |
1 | a0001c0002t0001g0027 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2418+424_2418+425i others(12): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728448 | |||||
chr19:38728448
|
T | TCCTCCTC others(6): Show |
4 | a0001c0001t0002g0207a0001c0002t0001g0040a0001c0002t0001g0048others(1): Show | 4 | HG03491.hp1 NA18981.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.2418+424_2418+425i others(15): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728448 | |||||
chr19:38728449
|
C | CCTCCTCC others(25): Show |
1 | a0001c0002t0001g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2418+424_2418+425i others(34): Show |
ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr19 | 38728449 | |||||
chr19:38728469
|
A | G | 1 | a0001c0001t0014g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2418+443A>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728469 | ||||||
chr19:38728484
|
T | G | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2418+458T>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728484 | ||||||
chr19:38728494
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2418+468C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728494 | ||||||
chr19:38728628
|
C | G | 1 | a0001c0002t0001g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2419-368C>G | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728628 | ||||||
chr19:38728634
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0034others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2419-362C>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728634 | ||||||
chr19:38728692
|
G | A | 2 | a0001c0001t0004g0272a0001c0001t0004g0273 | 2 | HG02015.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2419-304G>A | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728692 | ||||||
chr19:38728920
|
G | T | 24 | a0001c0004t0005g0095a0001c0004t0005g0222a0001c0004t0005g0224others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2419-76G>T | ACTN4 | ENSG00000130402.14 | transcript | ENST00000252699.7 | protein_coding | 19/20 | chr19 | 38728920 |