geneid | 25 |
---|---|
ensemblid | ENSG00000097007.20 |
hgncid | 76 |
symbol | ABL1 |
name | ABL proto-oncogene 1, non-receptor tyrosine kinase |
refseq_nuc | NM_005157.6 |
refseq_prot | NP_005148.2 |
ensembl_nuc | ENST00000318560.6 |
ensembl_prot | ENSP00000323315.5 |
mane_status | MANE Select |
chr | chr9 |
start | 130835254 |
end | 130887675 |
strand | + |
ver | v1.2 |
region | chr9:130835254-130887675 |
region5000 | chr9:130830254-130892675 |
regionname0 | ABL1_chr9_130835254_130887675 |
regionname5000 | ABL1_chr9_130830254_130892675 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1130 | 265 | 85 | 61 | 81 | 8 | 28 | 59 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0002 | 0/0 | 1130 | 6 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0003 | 0/0 | 1130 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0004 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0005 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0006 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0007 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0008 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3393 | 133 | 31 | 38 | 48 | 5 | 11 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0002 | 1/1 | 3393 | 65 | 8 | 11 | 29 | 2 | 13 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0003 | 0/0 | 3393 | 28 | 21 | 5 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0004 | 0/0 | 3393 | 8 | 6 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0005 | 0/0 | 3393 | 6 | 3 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0006 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0007 | 0/0 | 3393 | 5 | 0 | 5 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0008 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0009 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0010 | 0/0 | 3393 | 3 | 0 | 1 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0011 | 0/0 | 3393 | 3 | 2 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0012 | 0/0 | 3393 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0013 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0014 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0015 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0016 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0017 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0018 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0019 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0020 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0021 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0022 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0023 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0024 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0025 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
c0026 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2189 | 145 | 13 | 36 | 68 | 5 | 22 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0002 | 0/0 | 2189 | 28 | 0 | 11 | 13 | 2 | 2 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0003 | 0/0 | 2189 | 19 | 18 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0004 | 0/0 | 2189 | 16 | 6 | 8 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0005 | 0/0 | 2189 | 11 | 7 | 3 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0006 | 0/0 | 2189 | 7 | 3 | 4 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0007 | 0/0 | 2189 | 6 | 5 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0008 | 0/0 | 2189 | 6 | 6 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0009 | 0/0 | 2189 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0010 | 0/0 | 2189 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0011 | 0/0 | 2189 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0012 | 0/0 | 2189 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0013 | 0/0 | 2189 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0014 | 0/0 | 2189 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0015 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0016 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0017 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0018 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0019 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0020 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0021 | 0/0 | 2189 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0022 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0023 | 0/0 | 2189 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0024 | 0/0 | 2189 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0025 | 0/0 | 2189 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0026 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0027 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0028 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0029 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0030 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0031 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0032 | 0/0 | 2189 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0033 | 0/0 | 2188 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0034 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0035 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0036 | 1/0 | 2186 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
t0037 | 0/0 | 2189 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3393 | 133 | 31 | 38 | 48 | 5 | 11 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002 | 1/1 | 3393 | 65 | 8 | 11 | 29 | 2 | 13 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0003 | 0/0 | 3393 | 28 | 21 | 5 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0004 | 0/0 | 3393 | 8 | 6 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0006 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0007 | 0/0 | 3393 | 5 | 0 | 5 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0008 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0009 | 0/0 | 3393 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0010 | 0/0 | 3393 | 3 | 0 | 1 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0011 | 0/0 | 3393 | 3 | 2 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0013 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0018 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0019 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0020 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0021 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0023 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0024 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0025 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0026 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0002c0005 | 0/0 | 3393 | 6 | 3 | 3 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0003c0012 | 0/0 | 3393 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0004c0014 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0005c0016 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0006c0017 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0007c0015 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0008c0022 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5581 | 76 | 8 | 23 | 35 | 3 | 7 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0002 | 0/0 | 5581 | 27 | 0 | 11 | 12 | 2 | 2 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0005 | 0/0 | 5581 | 2 | 1 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0007 | 0/0 | 5581 | 4 | 3 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0008 | 0/0 | 5581 | 6 | 6 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0009 | 0/0 | 5581 | 4 | 4 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0011 | 0/0 | 5581 | 3 | 3 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0012 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0013 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0015 | 0/0 | 5561 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0021 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0024 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0025 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0026 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0033 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0035 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0001t0037 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002t0001 | 0/1 | 5581 | 60 | 5 | 10 | 29 | 2 | 13 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002t0010 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002t0019 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002t0032 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0002t0036 | 1/0 | 5578 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0003t0003 | 0/0 | 5581 | 19 | 18 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0003t0004 | 0/0 | 5581 | 7 | 1 | 4 | 0 | 1 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0003t0016 | 0/0 | 5561 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0003t0020 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0004t0005 | 0/0 | 5581 | 6 | 4 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0004t0017 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0004t0022 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0006t0004 | 0/0 | 5581 | 5 | 5 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0007t0004 | 0/0 | 5581 | 4 | 0 | 4 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0007t0023 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0008t0013 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0008t0030 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0008t0031 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0009t0007 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0009t0034 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0010t0001 | 0/0 | 5581 | 3 | 0 | 1 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0011t0002 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0011t0014 | 0/0 | 5581 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0013t0027 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0018t0010 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0019t0001 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0020t0005 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0021t0001 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0023t0028 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0024t0001 | 0/0 | 5581 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0025t0018 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0001c0026t0029 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0002c0005t0005 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0002c0005t0006 | 0/0 | 5581 | 5 | 3 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0003c0012t0006 | 0/0 | 5581 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0004c0014t0009 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0005c0016t0001 | 0/0 | 5581 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0006c0017t0001 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0007c0015t0005 | 0/0 | 5581 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
a0008c0022t0001 | 0/0 | 5581 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | copy fasta | chr9 | 130830254 | 130892675 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0013g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0021g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0024g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0025g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0026g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0035g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0001t0037g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0019g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0032g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0002t0036g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0003t0020g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0004t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0006t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0006t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0006t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0006t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0006t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0007t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0007t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0007t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0007t0023g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0008t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0008t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0008t0031g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0009t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0009t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0009t0034g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0010t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0010t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0010t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0011t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0011t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0011t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0013t0027g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0018t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0019t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0020t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0021t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0023t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0024t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0025t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0001c0026t0029g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0002c0005t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0003c0012t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0003c0012t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0004c0014t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0005c0016t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0006c0017t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0007c0015t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
a0008c0022t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0001 | g0094 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0231 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | FIN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00639 | hp1 | a0002 | c0005 | t0005 | g0191 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01074 | hp2 | a0001 | c0007 | t0023 | g0002 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01081 | hp1 | a0001 | c0003 | t0004 | g0257 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01099 | hp1 | a0001 | c0007 | t0004 | g0246 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01106 | hp1 | a0001 | c0001 | t0024 | g0229 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01109 | hp2 | a0006 | c0017 | t0001 | g0111 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01167 | hp1 | a0001 | c0003 | t0003 | g0244 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01175 | hp1 | a0001 | c0003 | t0004 | g0256 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01255 | hp1 | a0001 | c0007 | t0004 | g0002 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01257 | hp1 | a0001 | c0002 | t0032 | g0113 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01257 | hp2 | a0001 | c0007 | t0004 | g0002 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01258 | hp2 | a0001 | c0007 | t0004 | g0202 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01361 | hp1 | a0001 | c0003 | t0004 | g0249 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01361 | hp2 | a0003 | c0012 | t0006 | g0014 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01433 | hp2 | a0002 | c0005 | t0006 | g0216 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01496 | hp1 | a0001 | c0004 | t0005 | g0027 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01496 | hp2 | a0001 | c0003 | t0004 | g0250 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01515 | hp2 | a0001 | c0003 | t0004 | g0255 | EUR | IBS | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01884 | hp1 | a0001 | c0002 | t0019 | g0048 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01884 | hp2 | a0001 | c0004 | t0005 | g0009 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0175 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01943 | hp2 | a0003 | c0012 | t0006 | g0215 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01993 | hp1 | a0001 | c0010 | t0001 | g0165 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02055 | hp1 | a0001 | c0002 | t0010 | g0044 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02055 | hp2 | a0001 | c0003 | t0004 | g0220 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02135 | hp1 | a0001 | c0021 | t0001 | g0050 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02145 | hp1 | a0001 | c0004 | t0022 | g0020 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0148 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02280 | hp1 | a0001 | c0008 | t0030 | g0040 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0222 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02300 | hp1 | a0001 | c0001 | t0033 | g0001 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02451 | hp1 | a0001 | c0003 | t0003 | g0210 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02615 | hp1 | a0002 | c0005 | t0006 | g0014 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02630 | hp1 | a0001 | c0008 | t0013 | g0036 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02630 | hp2 | a0001 | c0006 | t0004 | g0152 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02647 | hp1 | a0001 | c0006 | t0004 | g0173 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0206 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02717 | hp1 | a0001 | c0003 | t0016 | g0194 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02717 | hp2 | a0007 | c0015 | t0005 | g0201 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02723 | hp1 | a0001 | c0025 | t0018 | g0045 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02723 | hp2 | a0001 | c0006 | t0004 | g0151 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02738 | hp2 | a0001 | c0004 | t0005 | g0091 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02809 | hp1 | a0001 | c0009 | t0007 | g0177 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0043 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02818 | hp1 | a0001 | c0003 | t0003 | g0248 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02818 | hp2 | a0001 | c0004 | t0005 | g0107 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02897 | hp2 | a0001 | c0003 | t0003 | g0147 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0161 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0219 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02965 | hp1 | a0001 | c0003 | t0003 | g0192 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02970 | hp1 | a0001 | c0006 | t0004 | g0156 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02970 | hp2 | a0001 | c0003 | t0003 | g0243 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03041 | hp1 | a0001 | c0002 | t0010 | g0047 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0209 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0195 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03098 | hp2 | a0001 | c0020 | t0005 | g0133 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03130 | hp2 | a0001 | c0003 | t0003 | g0251 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0208 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03139 | hp2 | a0001 | c0003 | t0020 | g0221 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03195 | hp1 | a0001 | c0009 | t0034 | g0213 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03209 | hp1 | a0001 | c0011 | t0014 | g0039 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0024 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0149 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03225 | hp2 | a0001 | c0026 | t0029 | g0253 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03239 | hp1 | a0001 | c0024 | t0001 | g0090 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03239 | hp2 | a0001 | c0003 | t0004 | g0247 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03453 | hp1 | a0001 | c0018 | t0010 | g0046 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03492 | hp2 | a0001 | c0001 | t0037 | g0131 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0184 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | ESN | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0207 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03540 | hp2 | a0002 | c0005 | t0006 | g0245 | AFR | GWD | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03579 | hp2 | a0004 | c0014 | t0009 | g0037 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03654 | hp1 | a0001 | c0001 | t0025 | g0225 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03834 | hp2 | a0001 | c0019 | t0001 | g0129 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | BEB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | STU | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18522 | hp1 | a0001 | c0004 | t0005 | g0108 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18522 | hp2 | a0001 | c0011 | t0014 | g0218 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18963 | hp1 | a0001 | c0011 | t0002 | g0252 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19030 | hp1 | a0001 | c0003 | t0003 | g0130 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19030 | hp2 | a0001 | c0001 | t0035 | g0212 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19043 | hp2 | a0001 | c0003 | t0003 | g0162 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19066 | hp1 | a0001 | c0010 | t0001 | g0166 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19078 | hp1 | a0001 | c0010 | t0001 | g0172 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19085 | hp1 | a0001 | c0001 | t0021 | g0189 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19088 | hp1 | a0005 | c0016 | t0001 | g0157 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0138 | AFR | YRI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20129 | hp2 | a0001 | c0003 | t0003 | g0163 | AFR | ASW | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0114 | EUR | TSI | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | GIH | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01123 | hp1 | a0008 | c0022 | t0001 | g0011 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG01123 | hp2 | a0002 | c0005 | t0006 | g0214 | AMR | CLM | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02109 | hp1 | a0001 | c0006 | t0004 | g0055 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02109 | hp2 | a0001 | c0003 | t0003 | g0185 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02486 | hp1 | a0001 | c0009 | t0007 | g0145 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0178 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | ACB | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03471 | hp1 | a0001 | c0004 | t0005 | g0009 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG03471 | hp2 | a0001 | c0004 | t0017 | g0049 | AFR | MSL | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG06807 | hp1 | a0001 | c0008 | t0031 | g0038 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
HG06807 | hp2 | a0001 | c0023 | t0028 | g0059 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20300 | hp1 | a0002 | c0005 | t0006 | g0217 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
NA21309 | hp2 | a0001 | c0013 | t0027 | g0155 | AFR | LWK | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0119 | REF | REF | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0036 | g0254 | REF | REF | ABL1_chr9_130830254_130892675 | ABL1 | chr9 | 130830254 | 130892675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:130854112
|
G | A | 1 | a0003 | 2 | HG01361.hp2 HG01943.hp2 |
missense_variant | MODERATE | c.128G>A | p.Ser43Asn | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/11 | 321/5578 | 128/3393 | 43/1130 | chr9 | 130854112 | ||
chr9:130878562
|
G | A | 1 | a0004 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1418G>A | p.Arg473Gln | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/11 | 1611/5578 | 1418/3393 | 473/1130 | chr9 | 130878562 | ||
chr9:130884323
|
G | A | 1 | a0005 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.2033G>A | p.Gly678Asp | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2226/5578 | 2033/3393 | 678/1130 | chr9 | 130884323 | ||
chr9:130884325
|
T | G | 1 | a0006 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2035T>G | p.Ser679Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2228/5578 | 2035/3393 | 679/1130 | chr9 | 130884325 | ||
chr9:130884388
|
A | G | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2098A>G | p.Thr700Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2291/5578 | 2098/3393 | 700/1130 | chr9 | 130884388 | ||
chr9:130884719
|
C | T | 1 | a0008 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.2429C>T | p.Pro810Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2622/5578 | 2429/3393 | 810/1130 | chr9 | 130884719 | ||
chr9:130885205
|
C | T | 2 | a0002a0003 | 8 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
missense_variant | MODERATE | c.2915C>T | p.Ser972Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3108/5578 | 2915/3393 | 972/1130 | chr9 | 130885205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:130854967
|
G | A | 1 | a0001c0013 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.420G>A | p.Leu140Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/11 | 613/5578 | 420/3393 | 140/1130 | chr9 | 130854967 | ||
chr9:130862933
|
G | A | 2 | a0001c0008a0004c0014 | 4 | HG02280.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.720G>A | p.Thr240Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/11 | 913/5578 | 720/3393 | 240/1130 | chr9 | 130862933 | ||
chr9:130880141
|
A | G | 2 | a0001c0003a0001c0007 | 33 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(30): Show |
synonymous_variant | LOW | c.1497A>G | p.Glu499Glu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/11 | 1690/5578 | 1497/3393 | 499/1130 | chr9 | 130880141 | ||
chr9:130880156
|
C | T | 1 | a0001c0026 | 1 | HG03225.hp2 | splice_region_variant&synonymous_variant | LOW | c.1512C>T | p.Asp504Asp | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/11 | 1705/5578 | 1512/3393 | 504/1130 | chr9 | 130880156 | ||
chr9:130880663
|
C | T | 1 | a0001c0025 | 1 | HG02723.hp1 | splice_region_variant&synonymous_variant | LOW | c.1677C>T | p.Ser559Ser | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/11 | 1870/5578 | 1677/3393 | 559/1130 | chr9 | 130880663 | ||
chr9:130884159
|
G | A | 3 | a0002c0005a0003c0012a0007c0015 | 9 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(6): Show |
synonymous_variant | LOW | c.1869G>A | p.Glu623Glu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2062/5578 | 1869/3393 | 623/1130 | chr9 | 130884159 | ||
chr9:130884189
|
C | T | 1 | a0001c0011 | 3 | HG03209.hp1 NA18522.hp2 NA18963.hp1 |
synonymous_variant | LOW | c.1899C>T | p.Ala633Ala | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2092/5578 | 1899/3393 | 633/1130 | chr9 | 130884189 | ||
chr9:130884390
|
C | T | 1 | a0001c0024 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2100C>T | p.Thr700Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2293/5578 | 2100/3393 | 700/1130 | chr9 | 130884390 | ||
chr9:130884477
|
G | A | 1 | a0001c0018 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2187G>A | p.Thr729Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2380/5578 | 2187/3393 | 729/1130 | chr9 | 130884477 | ||
chr9:130884642
|
C | G | 4 | a0001c0003a0001c0006a0001c0007others(1): Show | 39 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
synonymous_variant | LOW | c.2352C>G | p.Pro784Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2545/5578 | 2352/3393 | 784/1130 | chr9 | 130884642 | ||
chr9:130885077
|
C | T | 1 | a0001c0021 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.2787C>T | p.Gly929Gly | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 2980/5578 | 2787/3393 | 929/1130 | chr9 | 130885077 | ||
chr9:130885206
|
G | A | 1 | a0001c0023 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2916G>A | p.Ser972Ser | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3109/5578 | 2916/3393 | 972/1130 | chr9 | 130885206 | ||
chr9:130885230
|
C | T | 4 | a0001c0004a0001c0007a0001c0020others(1): Show | 15 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(12): Show |
synonymous_variant | LOW | c.2940C>T | p.Pro980Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3133/5578 | 2940/3393 | 980/1130 | chr9 | 130885230 | ||
chr9:130885248
|
A | G | 1 | a0001c0010 | 3 | HG01993.hp1 NA19066.hp1 NA19078.hp1 |
synonymous_variant | LOW | c.2958A>G | p.Pro986Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3151/5578 | 2958/3393 | 986/1130 | chr9 | 130885248 | ||
chr9:130885281
|
G | A | 1 | a0001c0019 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.2991G>A | p.Pro997Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3184/5578 | 2991/3393 | 997/1130 | chr9 | 130885281 | ||
chr9:130885290
|
C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02809.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.3000C>T | p.Thr1000Thr | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3193/5578 | 3000/3393 | 1000/1130 | chr9 | 130885290 | ||
chr9:130885558
|
C | T | 1 | a0001c0020 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3268C>T | p.Leu1090Leu | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3461/5578 | 3268/3393 | 1090/1130 | chr9 | 130885558 | ||
chr9:130885614
|
A | G | 18 | a0001c0001a0001c0003a0001c0004others(15): Show | 204 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
synonymous_variant | LOW | c.3324A>G | p.Pro1108Pro | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 3517/5578 | 3324/3393 | 1108/1130 | chr9 | 130885614 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:130835296
|
C | T | 1 | a0001c0001t0037 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 151 | chr9 | 130835296 | |||||
chr9:130835335
|
G | GC | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(53): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
5_prime_UTR_variant | MODIFIER | c.-111dupC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 110 | INFO_REALIGN_3_PRIME | chr9 | 130835335 | ||||
chr9:130835348
|
GGGGCGCC others(12): Show |
G | 2 | a0001c0001t0015a0001c0003t0016 | 2 | HG02717.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-94_-76delGCCGGGGG others(11): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 76 | INFO_REALIGN_3_PRIME | chr9 | 130835348 | ||||
chr9:130835353
|
G | GC | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(46): Show | 265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
5_prime_UTR_variant | MODIFIER | c.-92dupC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 91 | INFO_REALIGN_3_PRIME | chr9 | 130835353 | ||||
chr9:130835353
|
G | GT | 4 | a0001c0001t0035a0001c0009t0034a0002c0005t0006others(1): Show | 9 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-93insT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 93 | chr9 | 130835353 | |||||
chr9:130835368
|
G | A | 7 | a0001c0001t0011a0001c0001t0012a0001c0002t0010others(4): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 79 | chr9 | 130835368 | |||||
chr9:130835377
|
C | A | 1 | a0001c0003t0020 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 70 | chr9 | 130835377 | |||||
chr9:130835377
|
C | T | 1 | a0001c0002t0032 | 1 | HG01257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | chr9 | 130835377 | ||||||
chr9:130835388
|
C | A | 1 | a0001c0001t0021 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 59 | chr9 | 130835388 | |||||
chr9:130835394
|
C | G | 2 | a0001c0001t0015a0001c0003t0016 | 2 | HG02717.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-53C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 53 | chr9 | 130835394 | |||||
chr9:130835417
|
T | C | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(53): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
5_prime_UTR_variant | MODIFIER | c.-30T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 30 | chr9 | 130835417 | |||||
chr9:130835432
|
T | TC | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(53): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
5_prime_UTR_variant | MODIFIER | c.-15_-14insC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/11 | 14 | chr9 | 130835432 | |||||
chr9:130885752
|
G | A | 3 | a0001c0001t0007a0001c0009t0007a0001c0009t0034 | 7 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 69 | chr9 | 130885752 | |||||
chr9:130885796
|
A | G | 1 | a0001c0002t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 113 | chr9 | 130885796 | |||||
chr9:130885820
|
G | C | 2 | a0001c0004t0017a0001c0004t0022 | 2 | HG02145.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*137G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 137 | chr9 | 130885820 | |||||
chr9:130885874
|
G | A | 1 | a0001c0007t0023 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 191 | chr9 | 130885874 | |||||
chr9:130886169
|
G | A | 2 | a0001c0001t0013a0001c0008t0013 | 2 | HG02630.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*486G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 486 | chr9 | 130886169 | |||||
chr9:130886202
|
C | T | 1 | a0001c0004t0022 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 519 | chr9 | 130886202 | |||||
chr9:130886229
|
C | T | 2 | a0001c0008t0030a0001c0008t0031 | 2 | HG02280.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 546 | chr9 | 130886229 | |||||
chr9:130886288
|
C | T | 3 | a0001c0003t0003a0001c0003t0016a0001c0003t0020 | 21 | HG01167.hp1 HG01891.hp2 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 605 | chr9 | 130886288 | |||||
chr9:130886496
|
T | C | 4 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(1): Show | 30 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*813T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 813 | chr9 | 130886496 | |||||
chr9:130886505
|
C | T | 1 | a0001c0008t0031 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 822 | chr9 | 130886505 | |||||
chr9:130886527
|
TGGAGGCA others(9): Show |
T | 1 | a0001c0026t0029 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853_*868delGGGACA others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 853 | INFO_REALIGN_3_PRIME | chr9 | 130886527 | ||||
chr9:130886605
|
G | C | 8 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(5): Show | 38 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*922G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 922 | chr9 | 130886605 | |||||
chr9:130886732
|
C | G | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1049 | chr9 | 130886732 | |||||
chr9:130886900
|
C | G | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1217C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1217 | chr9 | 130886900 | |||||
chr9:130887017
|
G | A | 1 | a0001c0013t0027 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1334 | chr9 | 130887017 | |||||
chr9:130887046
|
G | A | 4 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(1): Show | 30 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1363G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1363 | chr9 | 130887046 | |||||
chr9:130887107
|
C | T | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1424 | chr9 | 130887107 | |||||
chr9:130887113
|
C | T | 1 | a0001c0001t0025 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1430 | chr9 | 130887113 | |||||
chr9:130887128
|
C | G | 1 | a0001c0023t0028 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1445C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1445 | chr9 | 130887128 | |||||
chr9:130887128
|
C | T | 1 | a0001c0001t0024 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1445 | chr9 | 130887128 | |||||
chr9:130887166
|
A | G | 33 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(30): Show | 117 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1483A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1483 | chr9 | 130887166 | |||||
chr9:130887171
|
T | C | 18 | a0001c0001t0005a0001c0001t0011a0001c0003t0003others(15): Show | 63 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1488T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1488 | chr9 | 130887171 | |||||
chr9:130887203
|
G | A | 10 | a0001c0001t0011a0001c0003t0003a0001c0003t0004others(7): Show | 44 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1520G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1520 | chr9 | 130887203 | |||||
chr9:130887439
|
C | T | 8 | a0001c0003t0003a0001c0003t0004a0001c0003t0016others(5): Show | 39 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1756C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 11/11 | 1756 | chr9 | 130887439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:130835658
|
CCTCTT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 213 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.79+150_79+154delTC others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835658 | |||||
chr9:130835669
|
C | T | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+144C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835669 | ||||||
chr9:130835681
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+156G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835681 | ||||||
chr9:130835726
|
C | G | 1 | a0007c0015t0005g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+201C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835726 | ||||||
chr9:130835736
|
C | A | 3 | a0001c0007t0004g0002a0001c0007t0004g0202a0001c0007t0023g0002 | 4 | HG01074.hp2 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+211C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835736 | ||||||
chr9:130835751
|
T | TTTTCTC | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 186 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.79+228_79+233dupTT others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835751 | |||||
chr9:130835753
|
TTCTC | T | 3 | a0001c0003t0004g0255a0001c0003t0004g0256a0001c0003t0004g0257 | 3 | HG01081.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.79+236_79+239delCT others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130835753 | |||||
chr9:130835848
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.79+323A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835848 | ||||||
chr9:130835849
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.79+324C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835849 | ||||||
chr9:130835876
|
G | A | 64 | a0001c0001t0001g0211a0001c0001t0001g0224a0001c0001t0001g0227others(61): Show | 67 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.79+351G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835876 | ||||||
chr9:130835979
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0199 | 3 | HG02572.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.79+454C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835979 | ||||||
chr9:130835987
|
T | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0203a0001c0001t0002g0204others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+462T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130835987 | ||||||
chr9:130836016
|
A | G | 1 | a0007c0015t0005g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+491A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836016 | ||||||
chr9:130836108
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.79+583C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836108 | ||||||
chr9:130836163
|
G | A | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+638G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836163 | ||||||
chr9:130836194
|
G | A | 5 | a0001c0001t0008g0207a0001c0001t0008g0208a0001c0001t0008g0209others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+669G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836194 | ||||||
chr9:130836242
|
C | G | 1 | a0001c0008t0030g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79+717C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836242 | ||||||
chr9:130836465
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+940G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836465 | ||||||
chr9:130836482
|
G | C | 1 | a0001c0001t0007g0258 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+957G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836482 | ||||||
chr9:130836824
|
C | CA | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0005g0054others(5): Show | 8 | HG00673.hp2 HG02109.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+1321dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | |||||
chr9:130836824
|
CA | C | 16 | a0001c0001t0001g0193a0001c0001t0008g0197a0001c0001t0011g0004others(13): Show | 17 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+1321delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | |||||
chr9:130836824
|
CAAAA | C | 15 | a0001c0001t0035g0212a0001c0002t0001g0026a0001c0003t0003g0206others(12): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+1318_79+1321del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | |||||
chr9:130836824
|
CAAAAA | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(65): Show | 72 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.79+1317_79+1321del others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130836824 | |||||
chr9:130836843
|
A | G | 5 | a0001c0001t0008g0197a0001c0001t0015g0195a0001c0002t0001g0196others(2): Show | 5 | HG02486.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1318A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836843 | ||||||
chr9:130836854
|
A | G | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+1329A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836854 | ||||||
chr9:130836875
|
A | G | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+1350A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130836875 | ||||||
chr9:130837016
|
A | G | 2 | a0001c0003t0003g0206a0001c0003t0003g0210 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.79+1491A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837016 | ||||||
chr9:130837017
|
T | C | 86 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(83): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+1492T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837017 | ||||||
chr9:130837072
|
G | T | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+1547G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837072 | ||||||
chr9:130837340
|
G | A | 2 | a0001c0001t0008g0197a0001c0002t0001g0196 | 2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.79+1815G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837340 | ||||||
chr9:130837352
|
G | A | 2 | a0001c0001t0001g0058a0001c0002t0001g0057 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79+1827G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837352 | ||||||
chr9:130837414
|
T | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(84): Show | 91 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.79+1889T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837414 | ||||||
chr9:130837513
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+1988G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837513 | ||||||
chr9:130837549
|
CA | C | 66 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0224others(63): Show | 69 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.79+2038delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130837549 | |||||
chr9:130837813
|
C | G | 2 | a0001c0001t0026g0024a0001c0002t0001g0025 | 2 | HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.79+2288C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837813 | ||||||
chr9:130837914
|
T | C | 1 | a0001c0004t0005g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+2389T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130837914 | ||||||
chr9:130838056
|
A | G | 6 | a0001c0001t0008g0197a0001c0001t0015g0195a0001c0002t0001g0196others(3): Show | 6 | HG02486.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2531A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838056 | ||||||
chr9:130838065
|
A | G | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+2540A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838065 | ||||||
chr9:130838120
|
T | C | 87 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(84): Show | 91 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.79+2595T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838120 | ||||||
chr9:130838273
|
A | ATTGTGAC others(4): Show |
92 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(89): Show | 96 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.79+2749_79+2750ins others(11): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130838273 | |||||
chr9:130838311
|
A | G | 1 | a0001c0011t0002g0252 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.79+2786A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838311 | ||||||
chr9:130838529
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79+3004G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838529 | ||||||
chr9:130838576
|
TTTA | T | 86 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(83): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+3056_79+3058del others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130838576 | |||||
chr9:130838647
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+3122C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838647 | ||||||
chr9:130838669
|
A | G | 1 | a0001c0003t0003g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79+3144A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130838669 | ||||||
chr9:130839077
|
A | AT | 6 | a0001c0001t0001g0182a0001c0001t0015g0195a0001c0002t0001g0025others(3): Show | 6 | HG02717.hp1 HG03098.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+3568dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130839077 | |||||
chr9:130839078
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.79+3553T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839078 | ||||||
chr9:130839079
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.79+3554T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839079 | ||||||
chr9:130839127
|
G | T | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.79+3602G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839127 | ||||||
chr9:130839379
|
T | G | 53 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(50): Show | 56 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.79+3854T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839379 | ||||||
chr9:130839819
|
C | G | 86 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(83): Show | 90 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.79+4294C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839819 | ||||||
chr9:130839904
|
T | C | 93 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(90): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+4379T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839904 | ||||||
chr9:130839952
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.79+4427C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130839952 | ||||||
chr9:130840065
|
A | C | 1 | a0001c0002t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+4540A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840065 | ||||||
chr9:130840185
|
C | T | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+4660C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840185 | ||||||
chr9:130840203
|
C | T | 102 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0227others(99): Show | 107 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(104): Show |
intron_variant | MODIFIER | c.79+4678C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840203 | ||||||
chr9:130840242
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.79+4717A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840242 | ||||||
chr9:130840266
|
T | C | 9 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(6): Show | 9 | NA18945.hp1 NA18977.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+4741T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840266 | ||||||
chr9:130840314
|
G | A | 1 | a0001c0001t0011g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79+4789G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840314 | ||||||
chr9:130840322
|
T | C | 1 | a0001c0002t0001g0103 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.79+4797T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840322 | ||||||
chr9:130840349
|
A | G | 1 | a0001c0002t0001g0179 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.79+4824A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840349 | ||||||
chr9:130840410
|
C | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+4885C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840410 | ||||||
chr9:130840657
|
T | C | 2 | a0001c0003t0003g0243a0001c0003t0003g0244 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.79+5132T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840657 | ||||||
chr9:130840709
|
GGGTCTCA others(16): Show |
G | 2 | a0001c0001t0001g0053a0001c0002t0001g0052 | 2 | HG03927.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.79+5192_79+5214del others(23): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130840709 | |||||
chr9:130840758
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.79+5233A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840758 | ||||||
chr9:130840847
|
A | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+5322A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840847 | ||||||
chr9:130840877
|
T | A | 3 | a0001c0001t0015g0195a0001c0003t0016g0194a0001c0023t0028g0059 | 3 | HG02717.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.79+5352T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130840877 | ||||||
chr9:130841187
|
G | A | 1 | a0001c0003t0004g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.79+5662G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841187 | ||||||
chr9:130841223
|
C | G | 1 | a0001c0004t0005g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+5698C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841223 | ||||||
chr9:130841228
|
A | G | 9 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(6): Show | 9 | NA18945.hp1 NA18977.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+5703A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841228 | ||||||
chr9:130841248
|
C | T | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+5723C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841248 | ||||||
chr9:130841292
|
C | T | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+5767C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841292 | ||||||
chr9:130841307
|
C | G | 1 | a0001c0003t0004g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.79+5782C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841307 | ||||||
chr9:130841415
|
T | C | 93 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(90): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+5890T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841415 | ||||||
chr9:130841475
|
A | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79+5950A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841475 | ||||||
chr9:130841539
|
C | T | 2 | a0001c0001t0008g0178a0001c0009t0007g0177 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.79+6014C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841539 | ||||||
chr9:130841738
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.79+6213G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841738 | ||||||
chr9:130841822
|
G | A | 9 | a0001c0001t0035g0212a0001c0009t0034g0213a0002c0005t0006g0014others(6): Show | 9 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+6297G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841822 | ||||||
chr9:130841883
|
G | T | 1 | a0001c0003t0003g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79+6358G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841883 | ||||||
chr9:130841888
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0063 | 3 | HG02451.hp2 HG02523.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.79+6363T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841888 | ||||||
chr9:130841924
|
G | A | 4 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(1): Show | 5 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6399G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841924 | ||||||
chr9:130841936
|
T | TAGAG | 102 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(99): Show | 107 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.79+6422_79+6425dup others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130841936 | |||||
chr9:130841976
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.79+6451G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841976 | ||||||
chr9:130841998
|
C | A | 23 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(20): Show | 24 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+6473C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130841998 | ||||||
chr9:130842004
|
G | A | 87 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(84): Show | 91 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.79+6479G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842004 | ||||||
chr9:130842121
|
G | A | 2 | a0001c0004t0005g0107a0001c0004t0005g0108 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.79+6596G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842121 | ||||||
chr9:130842175
|
A | C | 1 | a0001c0002t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.79+6650A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842175 | ||||||
chr9:130842358
|
A | G | 5 | a0001c0008t0013g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6833A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842358 | ||||||
chr9:130842423
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.79+6898A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842423 | ||||||
chr9:130842494
|
C | T | 93 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(90): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+6969C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842494 | ||||||
chr9:130842774
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0021t0001g0050 | 4 | HG01934.hp1 HG02135.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+7249A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842774 | ||||||
chr9:130842818
|
T | G | 1 | a0001c0002t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+7293T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842818 | ||||||
chr9:130842855
|
G | T | 93 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(90): Show | 97 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+7330G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130842855 | ||||||
chr9:130843038
|
A | C | 1 | a0001c0002t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+7513A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843038 | ||||||
chr9:130843137
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79+7612A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843137 | ||||||
chr9:130843248
|
AC | A | 2 | a0001c0002t0001g0010a0001c0002t0001g0109 | 3 | HG01071.hp2 HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.79+7727delC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130843248 | |||||
chr9:130843254
|
G | A | 2 | a0001c0001t0035g0212a0001c0009t0034g0213 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79+7729G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843254 | ||||||
chr9:130843310
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.79+7785G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843310 | ||||||
chr9:130843869
|
T | A | 91 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(88): Show | 95 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+8344T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130843869 | ||||||
chr9:130844034
|
A | G | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+8509A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844034 | ||||||
chr9:130844135
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+8610G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844135 | ||||||
chr9:130844153
|
A | G | 91 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0224others(88): Show | 95 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+8628A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844153 | ||||||
chr9:130844159
|
T | C | 1 | a0001c0011t0014g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+8634T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844159 | ||||||
chr9:130844165
|
C | A | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+8640C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844165 | ||||||
chr9:130844257
|
G | A | 1 | a0001c0001t0009g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.79+8732G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844257 | ||||||
chr9:130844363
|
A | G | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+8838A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844363 | ||||||
chr9:130844491
|
AT | A | 111 | a0001c0001t0001g0019a0001c0001t0001g0102a0001c0001t0001g0110others(108): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.79+8978delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130844491 | |||||
chr9:130844491
|
ATT | A | 5 | a0001c0003t0004g0247a0001c0007t0004g0002a0001c0007t0004g0202others(2): Show | 6 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+8977_79+8978del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130844491 | |||||
chr9:130844795
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.80-9269C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130844795 | ||||||
chr9:130845014
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.80-9050C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845014 | ||||||
chr9:130845034
|
A | G | 5 | a0001c0008t0013g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-9030A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845034 | ||||||
chr9:130845477
|
G | T | 3 | a0001c0001t0001g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | HG01981.hp2 HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.80-8587G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845477 | ||||||
chr9:130845490
|
C | T | 64 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(61): Show | 67 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-8574C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845490 | ||||||
chr9:130845498
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG01981.hp1 HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.80-8566C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845498 | ||||||
chr9:130845589
|
C | T | 15 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-8475C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845589 | ||||||
chr9:130845601
|
C | T | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-8463C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845601 | ||||||
chr9:130845788
|
T | C | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-8276T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845788 | ||||||
chr9:130845859
|
T | TA | 65 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-8192dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130845859 | |||||
chr9:130845859
|
TA | T | 6 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-8192delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130845859 | |||||
chr9:130845891
|
C | G | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-8173C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845891 | ||||||
chr9:130845960
|
G | A | 1 | a0001c0003t0003g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.80-8104G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130845960 | ||||||
chr9:130846081
|
C | CTG | 17 | a0001c0001t0001g0058a0001c0001t0001g0093a0001c0001t0001g0122others(14): Show | 17 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-7956_80-7955dup others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846081
|
C | CTGTGTGT others(1): Show |
10 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0029others(7): Show | 10 | HG03209.hp1 NA18945.hp1 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-7962_80-7955dup others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846081
|
CTG | C | 4 | a0001c0001t0002g0186a0001c0003t0004g0247a0001c0004t0017g0049others(1): Show | 4 | HG03239.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-7956_80-7955del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846081
|
CTGTG | C | 65 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-7958_80-7955del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846081
|
CTGTGTG | C | 17 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-7960_80-7955del others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846081
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-7964_80-7955del others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846081 | |||||
chr9:130846095
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0002t0001g0010a0001c0002t0001g0109 | 3 | HG01071.hp2 HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.80-7954_80-7939del others(16): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130846095 | |||||
chr9:130846108
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.80-7956T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130846108 | ||||||
chr9:130846509
|
T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-7555T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130846509 | ||||||
chr9:130847022
|
A | G | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-7042A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847022 | ||||||
chr9:130847078
|
G | A | 2 | a0001c0001t0001g0053a0001c0002t0001g0052 | 2 | HG03927.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.80-6986G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847078 | ||||||
chr9:130847235
|
G | A | 1 | a0001c0008t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-6829G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847235 | ||||||
chr9:130847349
|
G | T | 15 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-6715G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847349 | ||||||
chr9:130847409
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.80-6655G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847409 | ||||||
chr9:130847566
|
A | G | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-6498A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847566 | ||||||
chr9:130847594
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80-6470C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847594 | ||||||
chr9:130847844
|
T | C | 1 | a0001c0024t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.80-6220T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847844 | ||||||
chr9:130847897
|
C | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.80-6167C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130847897 | ||||||
chr9:130848017
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-6047G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848017 | ||||||
chr9:130848075
|
C | A | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-5989C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848075 | ||||||
chr9:130848086
|
A | G | 1 | a0001c0002t0001g0103 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.80-5978A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848086 | ||||||
chr9:130848150
|
G | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-5914G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848150 | ||||||
chr9:130848151
|
A | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-5913A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848151 | ||||||
chr9:130848207
|
A | G | 56 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(53): Show | 59 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-5857A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848207 | ||||||
chr9:130848210
|
T | G | 2 | a0001c0002t0001g0065a0001c0019t0001g0129 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.80-5854T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848210 | ||||||
chr9:130848345
|
G | GA | 68 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 73 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.80-5697dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | |||||
chr9:130848345
|
G | GAA | 10 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0127others(7): Show | 10 | HG00621.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-5698_80-5697dup others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | |||||
chr9:130848345
|
GA | G | 60 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0239others(57): Show | 63 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-5697delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848345 | |||||
chr9:130848517
|
C | CA | 7 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0182others(4): Show | 8 | HG02572.hp1 HG02738.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-5528dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | |||||
chr9:130848517
|
CA | C | 77 | a0001c0001t0001g0080a0001c0001t0001g0124a0001c0001t0001g0211others(74): Show | 81 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-5528delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | |||||
chr9:130848517
|
CAA | C | 6 | a0001c0001t0002g0238a0001c0001t0007g0258a0001c0001t0007g0259others(3): Show | 6 | HG02027.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-5529_80-5528del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130848517 | |||||
chr9:130848529
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.80-5535A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848529 | ||||||
chr9:130848666
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.80-5398G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848666 | ||||||
chr9:130848677
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.80-5387C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848677 | ||||||
chr9:130848766
|
A | G | 3 | a0001c0008t0030g0040a0001c0008t0031g0038a0004c0014t0009g0037 | 3 | HG02280.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.80-5298A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848766 | ||||||
chr9:130848896
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.80-5168G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848896 | ||||||
chr9:130848985
|
A | G | 4 | a0001c0001t0001g0224a0001c0001t0002g0015a0001c0001t0002g0238others(1): Show | 5 | HG02027.hp1 NA18962.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-5079A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130848985 | ||||||
chr9:130849032
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-5032G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849032 | ||||||
chr9:130849071
|
T | C | 2 | a0001c0001t0001g0198a0001c0002t0001g0140 | 2 | NA18941.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.80-4993T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849071 | ||||||
chr9:130849244
|
G | A | 2 | a0001c0004t0005g0027a0001c0011t0014g0039 | 2 | HG01496.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80-4820G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849244 | ||||||
chr9:130849277
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.80-4787A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849277 | ||||||
chr9:130849528
|
G | T | 65 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(62): Show | 68 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4536G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849528 | ||||||
chr9:130849528
|
GT | G | 22 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.80-4527delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130849528 | |||||
chr9:130849529
|
T | G | 65 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(62): Show | 68 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4535T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849529 | ||||||
chr9:130849548
|
C | G | 3 | a0001c0001t0001g0180a0001c0002t0001g0137a0001c0002t0001g0171 | 3 | HG03017.hp1 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.80-4516C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849548 | ||||||
chr9:130849572
|
G | A | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-4492G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849572 | ||||||
chr9:130849637
|
A | G | 1 | a0001c0002t0001g0170 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.80-4427A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849637 | ||||||
chr9:130849771
|
C | A | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-4293C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130849771 | ||||||
chr9:130850086
|
C | G | 2 | a0001c0003t0003g0219a0001c0003t0020g0221 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.80-3978C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850086 | ||||||
chr9:130850125
|
A | G | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3939A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850125 | ||||||
chr9:130850362
|
C | CT | 66 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(63): Show | 69 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-3699dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130850362 | |||||
chr9:130850380
|
G | A | 66 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(63): Show | 69 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-3684G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850380 | ||||||
chr9:130850443
|
T | C | 88 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0227others(85): Show | 92 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.80-3621T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850443 | ||||||
chr9:130850505
|
G | A | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-3559G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850505 | ||||||
chr9:130850608
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-3456G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850608 | ||||||
chr9:130850650
|
G | A | 15 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-3414G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850650 | ||||||
chr9:130850670
|
C | A | 1 | a0001c0002t0001g0179 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80-3394C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850670 | ||||||
chr9:130850696
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-3368G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850696 | ||||||
chr9:130850796
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.80-3268C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850796 | ||||||
chr9:130850798
|
C | T | 2 | a0001c0001t0015g0195a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-3266C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850798 | ||||||
chr9:130850893
|
G | A | 1 | a0001c0025t0018g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-3171G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130850893 | ||||||
chr9:130850910
|
GTTTTTGT others(5): Show |
G | 33 | a0001c0001t0001g0068a0001c0001t0001g0102a0001c0001t0001g0224others(30): Show | 35 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-3152_80-3141del others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130850910 | |||||
chr9:130851025
|
G | A | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3039G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851025 | ||||||
chr9:130851072
|
C | T | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-2992C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851072 | ||||||
chr9:130851125
|
C | T | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-2939C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851125 | ||||||
chr9:130851382
|
T | C | 1 | a0001c0006t0004g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.80-2682T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851382 | ||||||
chr9:130851428
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.80-2636G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851428 | ||||||
chr9:130851569
|
A | T | 85 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(82): Show | 89 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.80-2495A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851569 | ||||||
chr9:130851607
|
T | G | 15 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-2457T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851607 | ||||||
chr9:130851766
|
C | CT | 6 | a0001c0001t0001g0019a0001c0001t0001g0169a0001c0001t0001g0182others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2280dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | |||||
chr9:130851766
|
CT | C | 77 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(74): Show | 81 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-2280delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | |||||
chr9:130851766
|
CTT | C | 16 | a0001c0001t0002g0226a0001c0001t0007g0258a0001c0001t0007g0259others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-2281_80-2280del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130851766 | |||||
chr9:130851869
|
A | C | 1 | a0001c0003t0003g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.80-2195A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851869 | ||||||
chr9:130851912
|
C | T | 15 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-2152C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851912 | ||||||
chr9:130851915
|
G | A | 21 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(18): Show | 22 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.80-2149G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130851915 | ||||||
chr9:130852066
|
T | A | 87 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(84): Show | 91 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(88): Show |
intron_variant | MODIFIER | c.80-1998T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852066 | ||||||
chr9:130852071
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.80-1993G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852071 | ||||||
chr9:130852100
|
A | C | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0035 | 3 | NA18945.hp1 NA18990.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.80-1964A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852100 | ||||||
chr9:130852106
|
A | T | 1 | a0001c0001t0008g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80-1958A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852106 | ||||||
chr9:130852272
|
C | T | 5 | a0001c0008t0013g0036a0001c0008t0030g0040a0001c0008t0031g0038others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1792C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852272 | ||||||
chr9:130852290
|
A | G | 14 | a0001c0001t0035g0212a0001c0003t0003g0175a0001c0003t0003g0219others(11): Show | 14 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-1774A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852290 | ||||||
chr9:130852470
|
A | G | 4 | a0001c0008t0030g0040a0001c0008t0031g0038a0001c0011t0014g0039others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1594A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852470 | ||||||
chr9:130852664
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0002t0001g0109others(2): Show | 5 | HG00639.hp1 HG01109.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1400G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852664 | ||||||
chr9:130852756
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-1308T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130852756 | ||||||
chr9:130852936
|
GGT | G | 16 | a0001c0001t0008g0056a0001c0001t0008g0197a0001c0001t0011g0004others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-1123_80-1122del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130852936 | |||||
chr9:130853015
|
C | T | 31 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0228others(28): Show | 33 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-1049C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853015 | ||||||
chr9:130853019
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.80-1045T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853019 | ||||||
chr9:130853170
|
C | CT | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 179 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.80-871dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | |||||
chr9:130853170
|
C | CTT | 35 | a0001c0001t0001g0058a0001c0001t0001g0182a0001c0001t0001g0227others(32): Show | 36 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.80-872_80-871dupTT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | |||||
chr9:130853170
|
C | CTTT | 15 | a0001c0001t0001g0224a0001c0001t0002g0023a0001c0001t0002g0235others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-873_80-871dupTT others(1): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 130853170 | |||||
chr9:130853175
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.80-889T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853175 | ||||||
chr9:130853176
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-888T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853176 | ||||||
chr9:130853387
|
G | A | 1 | a0001c0009t0007g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-677G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853387 | ||||||
chr9:130853389
|
T | C | 1 | a0001c0010t0001g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.80-675T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853389 | ||||||
chr9:130853424
|
G | A | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-640G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853424 | ||||||
chr9:130853503
|
C | T | 64 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0002g0013others(61): Show | 67 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.80-561C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853503 | ||||||
chr9:130853564
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.80-500G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853564 | ||||||
chr9:130853595
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0007g0018 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.80-469A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853595 | ||||||
chr9:130853704
|
C | T | 9 | a0001c0001t0001g0193a0001c0001t0002g0167a0001c0002t0001g0136others(6): Show | 9 | HG00558.hp1 HG01993.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-360C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853704 | ||||||
chr9:130853711
|
G | A | 1 | a0001c0003t0003g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80-353G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853711 | ||||||
chr9:130853889
|
G | C | 1 | a0001c0002t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.80-175G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 1/10 | chr9 | 130853889 | ||||||
chr9:130854361
|
A | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.253+124A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854361 | ||||||
chr9:130854386
|
G | A | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.253+149G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854386 | ||||||
chr9:130854488
|
C | T | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+251C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854488 | ||||||
chr9:130854507
|
A | G | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.253+270A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854507 | ||||||
chr9:130854507
|
A | T | 1 | a0001c0001t0008g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.253+270A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854507 | ||||||
chr9:130854751
|
G | A | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-50G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 2/10 | chr9 | 130854751 | ||||||
chr9:130855122
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.549+26T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855122 | ||||||
chr9:130855205
|
A | G | 1 | a0001c0010t0001g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.549+109A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855205 | ||||||
chr9:130855277
|
T | C | 2 | a0001c0001t0015g0195a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.549+181T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855277 | ||||||
chr9:130855398
|
C | T | 1 | a0001c0009t0007g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.549+302C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855398 | ||||||
chr9:130855405
|
TA | T | 105 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0239others(102): Show | 110 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(107): Show |
intron_variant | MODIFIER | c.549+317delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130855405 | |||||
chr9:130855444
|
G | A | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.549+348G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855444 | ||||||
chr9:130855469
|
C | T | 11 | a0001c0001t0008g0056a0001c0001t0011g0004a0001c0001t0011g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+373C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855469 | ||||||
chr9:130855797
|
T | C | 63 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0001g0239others(60): Show | 66 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.549+701T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855797 | ||||||
chr9:130855910
|
ATGTT | A | 11 | a0001c0001t0008g0056a0001c0001t0011g0004a0001c0001t0011g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+832_549+835del others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130855910 | |||||
chr9:130855979
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.549+883G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130855979 | ||||||
chr9:130856113
|
A | G | 11 | a0001c0001t0008g0056a0001c0001t0011g0004a0001c0001t0011g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+1017A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856113 | ||||||
chr9:130856145
|
A | G | 2 | a0001c0002t0001g0025a0001c0004t0022g0020 | 2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.549+1049A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856145 | ||||||
chr9:130856158
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.549+1062G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856158 | ||||||
chr9:130856181
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.549+1085C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856181 | ||||||
chr9:130856380
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.549+1284G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856380 | ||||||
chr9:130856461
|
A | G | 1 | a0001c0002t0019g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.549+1365A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856461 | ||||||
chr9:130856466
|
C | T | 2 | a0001c0001t0015g0195a0001c0023t0028g0059 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.549+1370C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856466 | ||||||
chr9:130856521
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.549+1425C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130856521 | ||||||
chr9:130857252
|
C | G | 1 | a0001c0008t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.549+2156C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857252 | ||||||
chr9:130857311
|
G | A | 28 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0002g0013others(25): Show | 30 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.549+2215G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857311 | ||||||
chr9:130857365
|
C | T | 27 | a0001c0001t0008g0178a0001c0001t0008g0207a0001c0001t0008g0208others(24): Show | 28 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.549+2269C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857365 | ||||||
chr9:130857537
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.549+2441G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857537 | ||||||
chr9:130857624
|
C | A | 1 | a0001c0001t0024g0229 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.549+2528C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857624 | ||||||
chr9:130857633
|
C | CT | 39 | a0001c0001t0008g0056a0001c0001t0008g0178a0001c0001t0008g0197others(36): Show | 40 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.549+2550dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130857633 | |||||
chr9:130857642
|
T | G | 10 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.549+2546T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857642 | ||||||
chr9:130857778
|
G | A | 1 | a0001c0003t0003g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.549+2682G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857778 | ||||||
chr9:130857851
|
G | A | 9 | a0001c0001t0001g0169a0001c0003t0003g0130a0001c0003t0003g0138others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+2755G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857851 | ||||||
chr9:130857933
|
C | G | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.549+2837C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130857933 | ||||||
chr9:130858015
|
T | G | 4 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(1): Show | 5 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+2919T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858015 | ||||||
chr9:130858574
|
A | G | 89 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0002g0013others(86): Show | 94 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(91): Show |
intron_variant | MODIFIER | c.549+3478A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858574 | ||||||
chr9:130858645
|
G | A | 2 | a0001c0003t0003g0243a0001c0003t0003g0244 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.549+3549G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858645 | ||||||
chr9:130858688
|
C | T | 79 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0002g0013others(76): Show | 83 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.549+3592C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858688 | ||||||
chr9:130858877
|
C | G | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549+3781C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858877 | ||||||
chr9:130858924
|
C | T | 11 | a0001c0001t0008g0056a0001c0001t0011g0004a0001c0001t0011g0043others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.549+3828C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858924 | ||||||
chr9:130858971
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(2): Show | 6 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-3792G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130858971 | ||||||
chr9:130859007
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-3756G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859007 | ||||||
chr9:130859386
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.550-3377C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859386 | ||||||
chr9:130859388
|
G | A | 3 | a0001c0001t0008g0197a0001c0002t0001g0196a0007c0015t0005g0201 | 3 | HG02486.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.550-3375G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859388 | ||||||
chr9:130859475
|
T | C | 4 | a0001c0008t0030g0040a0001c0008t0031g0038a0001c0023t0028g0059others(1): Show | 4 | HG02280.hp1 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-3288T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859475 | ||||||
chr9:130859525
|
G | A | 2 | a0001c0001t0035g0212a0001c0009t0034g0213 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.550-3238G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859525 | ||||||
chr9:130859668
|
CTTTCTTT others(13): Show |
C | 1 | a0001c0004t0022g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.550-3091_550-3072d others(22): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859668 | |||||
chr9:130859672
|
C | CT | 29 | a0001c0001t0001g0102a0001c0001t0001g0239a0001c0001t0002g0013others(26): Show | 31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.550-3088dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859672
|
CTTTCCTT others(3): Show |
C | 1 | a0001c0003t0003g0206 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-3087_550-3078d others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859672
|
CTTTCCTT others(4): Show |
C | 1 | a0001c0003t0003g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.550-3087_550-3077d others(13): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859672
|
CTTTCCTT others(6): Show |
C | 1 | a0001c0003t0004g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.550-3087_550-3075d others(15): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859672
|
CTTTCCTT others(7): Show |
C | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-3087_550-3074d others(16): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859672
|
CTTTCCTT others(9): Show |
C | 15 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(12): Show | 17 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.550-3087_550-3072d others(18): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859672 | |||||
chr9:130859675
|
TCC | T | 12 | a0001c0001t0035g0212a0001c0008t0013g0036a0001c0008t0030g0040others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-3087_550-3086d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859675 | ||||||
chr9:130859676
|
C | T | 41 | a0001c0001t0001g0169a0001c0001t0002g0203a0001c0001t0002g0234others(38): Show | 41 | HG01081.hp1 HG01167.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.550-3087C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859676 | ||||||
chr9:130859677
|
C | CT | 54 | a0001c0001t0001g0001a0001c0001t0001g0066a0001c0001t0001g0067others(51): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.550-3057dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | |||||
chr9:130859677
|
C | CTT | 9 | a0001c0001t0001g0096a0001c0001t0002g0235a0001c0002t0001g0160others(6): Show | 9 | HG01081.hp1 HG01175.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-3058_550-3057d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | |||||
chr9:130859677
|
C | CTTT | 18 | a0001c0001t0002g0234a0001c0001t0008g0178a0001c0001t0008g0207others(15): Show | 18 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.550-3059_550-3057d others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | |||||
chr9:130859677
|
C | T | 29 | a0001c0001t0001g0102a0001c0001t0001g0239a0001c0001t0002g0013others(26): Show | 31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.550-3086C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859677 | ||||||
chr9:130859677
|
CT | C | 15 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0002t0001g0025others(12): Show | 15 | HG02698.hp2 HG02818.hp2 HG03704.hp2 others(12): Show |
intron_variant | MODIFIER | c.550-3057delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | |||||
chr9:130859677
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.550-3068_550-3057d others(14): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130859677 | |||||
chr9:130859679
|
T | C | 12 | a0001c0001t0035g0212a0001c0008t0013g0036a0001c0008t0030g0040others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-3084T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859679 | ||||||
chr9:130859684
|
T | C | 2 | a0001c0002t0001g0196a0007c0015t0005g0201 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.550-3079T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859684 | ||||||
chr9:130859685
|
T | C | 2 | a0001c0001t0008g0197a0001c0023t0028g0059 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550-3078T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859685 | ||||||
chr9:130859687
|
T | C | 1 | a0001c0003t0003g0206 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-3076T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859687 | ||||||
chr9:130859688
|
T | C | 1 | a0001c0003t0003g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.550-3075T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859688 | ||||||
chr9:130859690
|
T | C | 1 | a0001c0003t0004g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.550-3073T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859690 | ||||||
chr9:130859691
|
T | C | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-3072T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859691 | ||||||
chr9:130859693
|
T | C | 16 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(13): Show | 18 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.550-3070T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859693 | ||||||
chr9:130859774
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.550-2989A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859774 | ||||||
chr9:130859779
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-2984C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859779 | ||||||
chr9:130859947
|
G | C | 1 | a0001c0001t0008g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.550-2816G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859947 | ||||||
chr9:130859959
|
G | A | 2 | a0001c0001t0002g0022a0001c0003t0003g0251 | 2 | HG02148.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.550-2804G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859959 | ||||||
chr9:130859963
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.550-2800G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859963 | ||||||
chr9:130859971
|
T | A | 1 | a0001c0002t0001g0164 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.550-2792T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130859971 | ||||||
chr9:130860082
|
C | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.550-2681C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860082 | ||||||
chr9:130860112
|
A | G | 3 | a0001c0001t0015g0195a0001c0008t0013g0036a0001c0020t0005g0133 | 3 | HG02630.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.550-2651A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860112 | ||||||
chr9:130860130
|
CT | C | 6 | a0001c0001t0001g0019a0001c0001t0007g0018a0001c0001t0009g0003others(3): Show | 7 | HG00735.hp1 HG01243.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-2632delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860130 | ||||||
chr9:130860177
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0154 | 2 | NA18977.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.550-2586G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860177 | ||||||
chr9:130860245
|
T | C | 14 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(11): Show | 14 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.550-2518T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860245 | ||||||
chr9:130860254
|
A | T | 4 | a0001c0003t0003g0219a0001c0003t0020g0221a0001c0004t0005g0027others(1): Show | 4 | HG01496.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2509A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860254 | ||||||
chr9:130860257
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(199): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.550-2506A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860257 | ||||||
chr9:130860355
|
A | C | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2408A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860355 | ||||||
chr9:130860394
|
A | G | 1 | a0001c0004t0005g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550-2369A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860394 | ||||||
chr9:130860426
|
C | T | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2337C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860426 | ||||||
chr9:130860599
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.550-2164T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860599 | ||||||
chr9:130860709
|
T | G | 1 | a0001c0001t0026g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.550-2054T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860709 | ||||||
chr9:130860729
|
A | G | 115 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0002g0013others(112): Show | 121 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(118): Show |
intron_variant | MODIFIER | c.550-2034A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860729 | ||||||
chr9:130860853
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG00621.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.550-1910G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860853 | ||||||
chr9:130860977
|
G | A | 1 | a0002c0005t0006g0214 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.550-1786G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860977 | ||||||
chr9:130860983
|
G | A | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1780G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130860983 | ||||||
chr9:130861009
|
T | C | 1 | a0001c0010t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.550-1754T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861009 | ||||||
chr9:130861142
|
C | T | 4 | a0001c0001t0012g0041a0001c0001t0012g0042a0001c0002t0001g0196others(1): Show | 4 | HG02615.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1621C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861142 | ||||||
chr9:130861224
|
TC | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-1538delC | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861224 | ||||||
chr9:130861324
|
A | G | 4 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1439A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861324 | ||||||
chr9:130861380
|
C | T | 3 | a0001c0001t0009g0003a0001c0001t0009g0016a0001c0001t0009g0017 | 4 | HG02965.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1383C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861380 | ||||||
chr9:130861390
|
T | C | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.550-1373T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861390 | ||||||
chr9:130861424
|
G | A | 1 | a0001c0003t0003g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.550-1339G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861424 | ||||||
chr9:130861471
|
A | C | 11 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0082others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-1292A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861471 | ||||||
chr9:130861583
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.550-1180A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861583 | ||||||
chr9:130861847
|
C | G | 1 | a0001c0003t0003g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.550-916C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861847 | ||||||
chr9:130861996
|
C | T | 5 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(2): Show | 6 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-767C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130861996 | ||||||
chr9:130862022
|
G | A | 1 | a0001c0003t0003g0162 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550-741G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862022 | ||||||
chr9:130862036
|
C | T | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.550-727C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862036 | ||||||
chr9:130862070
|
G | A | 12 | a0001c0001t0008g0056a0001c0001t0035g0212a0001c0004t0017g0049others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-693G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862070 | ||||||
chr9:130862098
|
C | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.550-665C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862098 | ||||||
chr9:130862132
|
A | G | 11 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0082others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-631A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862132 | ||||||
chr9:130862248
|
A | G | 8 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0002t0001g0025others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-515A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862248 | ||||||
chr9:130862262
|
G | A | 41 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0018others(38): Show | 43 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.550-501G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862262 | ||||||
chr9:130862419
|
T | C | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-344T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862419 | ||||||
chr9:130862474
|
G | A | 1 | a0001c0008t0013g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550-289G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862474 | ||||||
chr9:130862625
|
AAC | A | 9 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-135_550-134del others(2): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 130862625 | |||||
chr9:130862687
|
C | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-76C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862687 | ||||||
chr9:130862702
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.550-61A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 3/10 | chr9 | 130862702 | ||||||
chr9:130863051
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.822+16C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863051 | ||||||
chr9:130863145
|
C | T | 1 | a0001c0025t0018g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.822+110C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863145 | ||||||
chr9:130863222
|
C | T | 24 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0001g0193others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.822+187C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863222 | ||||||
chr9:130863237
|
A | G | 4 | a0001c0003t0003g0161a0001c0003t0003g0162a0001c0003t0003g0163others(1): Show | 4 | HG02717.hp1 HG02922.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+202A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863237 | ||||||
chr9:130863604
|
C | T | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.822+569C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863604 | ||||||
chr9:130863633
|
C | G | 4 | a0001c0008t0013g0036a0001c0008t0030g0040a0001c0008t0031g0038others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+598C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130863633 | ||||||
chr9:130864158
|
C | T | 1 | a0005c0016t0001g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.822+1123C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864158 | ||||||
chr9:130864223
|
C | T | 2 | a0001c0001t0011g0004a0001c0001t0011g0043 | 3 | HG02809.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.822+1188C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864223 | ||||||
chr9:130864224
|
C | G | 8 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0002t0001g0025others(5): Show | 9 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+1189C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864224 | ||||||
chr9:130864247
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.822+1212T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864247 | ||||||
chr9:130864348
|
G | T | 33 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(30): Show | 34 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.822+1313G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864348 | ||||||
chr9:130864394
|
G | A | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+1359G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864394 | ||||||
chr9:130864465
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.822+1430A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864465 | ||||||
chr9:130864591
|
C | G | 1 | a0001c0001t0021g0189 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.822+1556C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864591 | ||||||
chr9:130864744
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0067others(31): Show | 36 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.822+1709G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864744 | ||||||
chr9:130864862
|
C | G | 10 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(7): Show | 11 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.822+1827C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864862 | ||||||
chr9:130864879
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.822+1844T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864879 | ||||||
chr9:130864896
|
C | T | 4 | a0001c0008t0013g0036a0001c0008t0030g0040a0001c0008t0031g0038others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+1861C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864896 | ||||||
chr9:130864980
|
G | A | 2 | a0001c0001t0002g0230a0001c0002t0001g0026 | 2 | NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.822+1945G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130864980 | ||||||
chr9:130865002
|
T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+1967T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865002 | ||||||
chr9:130865230
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.822+2195G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865230 | ||||||
chr9:130865238
|
G | A | 2 | a0001c0001t0001g0134a0001c0002t0001g0160 | 2 | HG02074.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.822+2203G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865238 | ||||||
chr9:130865270
|
A | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+2235A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865270 | ||||||
chr9:130865327
|
G | A | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+2292G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865327 | ||||||
chr9:130865549
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.822+2514C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865549 | ||||||
chr9:130865576
|
G | A | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.822+2541G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865576 | ||||||
chr9:130865676
|
G | T | 2 | a0001c0001t0011g0004a0001c0001t0011g0043 | 3 | HG02809.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.822+2641G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865676 | ||||||
chr9:130865746
|
C | CA | 78 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0099others(75): Show | 81 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.822+2733dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | |||||
chr9:130865746
|
C | CAA | 14 | a0001c0001t0002g0167a0001c0001t0002g0223a0001c0001t0002g0235others(11): Show | 14 | HG01167.hp1 HG01175.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.822+2732_822+2733d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | |||||
chr9:130865746
|
CA | C | 11 | a0001c0001t0002g0205a0001c0001t0005g0054a0001c0001t0005g0105others(8): Show | 12 | HG01109.hp1 HG01256.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+2733delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130865746 | |||||
chr9:130865845
|
G | T | 1 | a0001c0002t0001g0028 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.822+2810G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865845 | ||||||
chr9:130865873
|
G | A | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+2838G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865873 | ||||||
chr9:130865908
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.822+2873C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865908 | ||||||
chr9:130865999
|
T | G | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+2964T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130865999 | ||||||
chr9:130866239
|
T | C | 60 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0008g0178others(57): Show | 62 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.822+3204T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866239 | ||||||
chr9:130866617
|
T | C | 6 | a0001c0002t0001g0025a0001c0002t0010g0044a0001c0002t0010g0047others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+3582T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866617 | ||||||
chr9:130866699
|
A | T | 2 | a0001c0001t0015g0195a0001c0011t0014g0218 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.822+3664A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866699 | ||||||
chr9:130866713
|
T | G | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+3678T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130866713 | ||||||
chr9:130867165
|
T | C | 15 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0258others(12): Show | 16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.822+4130T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867165 | ||||||
chr9:130867383
|
C | A | 1 | a0001c0001t0002g0230 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.822+4348C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867383 | ||||||
chr9:130867549
|
T | C | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+4514T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867549 | ||||||
chr9:130867648
|
T | C | 15 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0258others(12): Show | 16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.823-4481T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867648 | ||||||
chr9:130867712
|
G | T | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.823-4417G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130867712 | ||||||
chr9:130867937
|
G | GT | 83 | a0001c0001t0001g0102a0001c0001t0001g0224a0001c0001t0002g0013others(80): Show | 87 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.823-4179dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130867937 | |||||
chr9:130867937
|
G | GTT | 9 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-4180_823-4179d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130867937 | |||||
chr9:130868001
|
C | G | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-4128C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868001 | ||||||
chr9:130868029
|
G | A | 14 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0258others(11): Show | 15 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-4100G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868029 | ||||||
chr9:130868082
|
C | T | 16 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0258others(13): Show | 17 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-4047C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868082 | ||||||
chr9:130868149
|
A | G | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.823-3980A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868149 | ||||||
chr9:130868179
|
C | T | 23 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0002t0001g0064others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.823-3950C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868179 | ||||||
chr9:130868246
|
C | T | 3 | a0001c0001t0008g0056a0001c0001t0026g0024a0004c0014t0009g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-3883C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868246 | ||||||
chr9:130868267
|
G | A | 113 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(110): Show | 119 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-3862G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868267 | ||||||
chr9:130868306
|
G | T | 11 | a0001c0001t0035g0212a0001c0004t0017g0049a0001c0004t0022g0020others(8): Show | 11 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-3823G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868306 | ||||||
chr9:130868438
|
G | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3691G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868438 | ||||||
chr9:130868520
|
C | CT | 17 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0101others(14): Show | 18 | HG01109.hp1 HG01258.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-3588dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | |||||
chr9:130868520
|
CT | C | 48 | a0001c0001t0001g0066a0001c0001t0002g0231a0001c0001t0007g0018others(45): Show | 50 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.823-3588delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | |||||
chr9:130868520
|
CTTTTTTT others(3): Show |
C | 15 | a0001c0001t0035g0212a0001c0003t0003g0175a0001c0003t0003g0219others(12): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-3597_823-3588d others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130868520 | |||||
chr9:130868526
|
T | C | 1 | a0001c0001t0008g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-3603T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868526 | ||||||
chr9:130868527
|
T | C | 7 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-3602T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868527 | ||||||
chr9:130868541
|
T | C | 10 | a0001c0001t0001g0154a0001c0001t0011g0004a0001c0001t0011g0043others(7): Show | 11 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-3588T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868541 | ||||||
chr9:130868579
|
A | G | 2 | a0001c0001t0015g0195a0001c0011t0014g0218 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.823-3550A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868579 | ||||||
chr9:130868591
|
T | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-3538T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868591 | ||||||
chr9:130868605
|
C | T | 2 | a0001c0003t0003g0219a0001c0003t0020g0221 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.823-3524C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868605 | ||||||
chr9:130868644
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.823-3485C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868644 | ||||||
chr9:130868645
|
T | C | 114 | a0001c0001t0001g0169a0001c0001t0001g0224a0001c0001t0002g0013others(111): Show | 120 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(117): Show |
intron_variant | MODIFIER | c.823-3484T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868645 | ||||||
chr9:130868730
|
G | A | 1 | a0001c0010t0001g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.823-3399G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868730 | ||||||
chr9:130868833
|
C | T | 1 | a0001c0010t0001g0166 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.823-3296C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868833 | ||||||
chr9:130868845
|
G | T | 14 | a0001c0003t0003g0130a0001c0003t0003g0138a0001c0003t0003g0147others(11): Show | 14 | HG01167.hp1 HG02258.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-3284G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130868845 | ||||||
chr9:130869028
|
G | A | 15 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0001t0012g0041others(12): Show | 16 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-3101G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869028 | ||||||
chr9:130869040
|
G | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3089G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869040 | ||||||
chr9:130869051
|
C | T | 1 | a0001c0003t0003g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823-3078C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869051 | ||||||
chr9:130869099
|
G | A | 1 | a0001c0001t0009g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823-3030G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869099 | ||||||
chr9:130869116
|
G | A | 98 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(95): Show | 104 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(101): Show |
intron_variant | MODIFIER | c.823-3013G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869116 | ||||||
chr9:130869121
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.823-3008C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869121 | ||||||
chr9:130869123
|
C | T | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-3006C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869123 | ||||||
chr9:130869166
|
CA | C | 113 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(110): Show | 119 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.823-2952delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 130869166 | |||||
chr9:130869176
|
A | G | 1 | a0001c0011t0014g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.823-2953A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869176 | ||||||
chr9:130869275
|
C | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-2854C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869275 | ||||||
chr9:130869285
|
G | A | 98 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(95): Show | 104 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(101): Show |
intron_variant | MODIFIER | c.823-2844G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869285 | ||||||
chr9:130869337
|
C | T | 15 | a0001c0001t0035g0212a0001c0003t0003g0175a0001c0003t0003g0219others(12): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-2792C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869337 | ||||||
chr9:130869524
|
G | A | 81 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(78): Show | 86 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.823-2605G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869524 | ||||||
chr9:130869537
|
T | C | 9 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0002t0001g0025others(6): Show | 10 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-2592T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869537 | ||||||
chr9:130869814
|
T | C | 3 | a0001c0001t0008g0056a0001c0001t0026g0024a0004c0014t0009g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-2315T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130869814 | ||||||
chr9:130870053
|
G | A | 1 | a0001c0019t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.823-2076G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870053 | ||||||
chr9:130870100
|
A | G | 82 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(79): Show | 87 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.823-2029A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870100 | ||||||
chr9:130870172
|
C | A | 1 | a0001c0002t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823-1957C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870172 | ||||||
chr9:130870283
|
A | G | 9 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-1846A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870283 | ||||||
chr9:130870296
|
AT | A | 3 | a0001c0001t0008g0056a0001c0001t0026g0024a0004c0014t0009g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.823-1832delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870296 | ||||||
chr9:130870386
|
G | A | 1 | a0001c0007t0004g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.823-1743G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870386 | ||||||
chr9:130870478
|
C | T | 1 | a0002c0005t0006g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.823-1651C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870478 | ||||||
chr9:130870524
|
A | C | 1 | a0001c0023t0028g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823-1605A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870524 | ||||||
chr9:130870528
|
C | A | 8 | a0001c0001t0005g0054a0001c0002t0001g0106a0001c0004t0005g0009others(5): Show | 9 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.823-1601C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870528 | ||||||
chr9:130870544
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.823-1585G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870544 | ||||||
chr9:130870635
|
G | A | 2 | a0001c0001t0015g0195a0001c0011t0014g0218 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.823-1494G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870635 | ||||||
chr9:130870673
|
G | A | 51 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(48): Show | 54 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.823-1456G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870673 | ||||||
chr9:130870730
|
T | C | 93 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(90): Show | 99 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.823-1399T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870730 | ||||||
chr9:130870804
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.823-1325G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870804 | ||||||
chr9:130870983
|
G | A | 7 | a0001c0001t0012g0041a0001c0001t0012g0042a0001c0001t0013g0149others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-1146G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130870983 | ||||||
chr9:130871184
|
C | T | 5 | a0001c0006t0004g0055a0001c0006t0004g0151a0001c0006t0004g0152others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-945C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871184 | ||||||
chr9:130871198
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.823-931C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871198 | ||||||
chr9:130871395
|
G | A | 1 | a0001c0002t0001g0032 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.823-734G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871395 | ||||||
chr9:130871404
|
C | T | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-725C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871404 | ||||||
chr9:130871532
|
T | A | 1 | a0001c0002t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.823-597T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871532 | ||||||
chr9:130871570
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.823-559C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871570 | ||||||
chr9:130871778
|
T | C | 1 | a0001c0002t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823-351T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871778 | ||||||
chr9:130871915
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0001g0071others(7): Show | 11 | HG00280.hp2 HG00558.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-214G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130871915 | ||||||
chr9:130872027
|
C | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-102C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130872027 | ||||||
chr9:130872070
|
C | T | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-59C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 4/10 | chr9 | 130872070 | ||||||
chr9:130872275
|
G | A | 2 | a0001c0001t0012g0041a0001c0001t0012g0042 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.907+62G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872275 | ||||||
chr9:130872287
|
G | A | 12 | a0001c0001t0007g0018a0001c0001t0008g0178a0001c0001t0008g0197others(9): Show | 13 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.907+74G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872287 | ||||||
chr9:130872290
|
C | T | 2 | a0001c0001t0013g0149a0001c0008t0013g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.907+77C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872290 | ||||||
chr9:130872291
|
G | A | 5 | a0001c0001t0002g0074a0001c0001t0002g0223a0001c0001t0002g0232others(2): Show | 5 | NA18963.hp1 NA18971.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+78G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872291 | ||||||
chr9:130872311
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0190 | 2 | HG01256.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.907+98C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872311 | ||||||
chr9:130872336
|
C | T | 2 | a0001c0001t0013g0149a0001c0008t0013g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.907+123C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872336 | ||||||
chr9:130872337
|
G | A | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.907+124G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872337 | ||||||
chr9:130872347
|
C | T | 36 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(33): Show | 39 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.907+134C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872347 | ||||||
chr9:130872409
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.907+196G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872409 | ||||||
chr9:130872685
|
A | G | 3 | a0001c0001t0002g0230a0001c0002t0001g0026a0001c0002t0001g0034 | 3 | NA18977.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.908-175A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872685 | ||||||
chr9:130872696
|
A | G | 55 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(52): Show | 58 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.908-164A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872696 | ||||||
chr9:130872815
|
T | C | 7 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.908-45T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 5/10 | chr9 | 130872815 | ||||||
chr9:130873196
|
C | T | 3 | a0001c0001t0008g0056a0001c0001t0026g0024a0004c0014t0009g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+159C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873196 | ||||||
chr9:130873252
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1085+215C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873252 | ||||||
chr9:130873286
|
G | T | 3 | a0001c0001t0008g0056a0001c0001t0026g0024a0004c0014t0009g0037 | 3 | HG02572.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+249G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873286 | ||||||
chr9:130873418
|
G | A | 2 | a0001c0004t0005g0107a0001c0004t0005g0108 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1085+381G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873418 | ||||||
chr9:130873440
|
C | T | 1 | a0001c0001t0007g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1085+403C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873440 | ||||||
chr9:130873778
|
C | T | 2 | a0001c0001t0015g0195a0001c0011t0014g0218 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1085+741C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130873778 | ||||||
chr9:130874120
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1086-748C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874120 | ||||||
chr9:130874170
|
G | A | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1086-698G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874170 | ||||||
chr9:130874195
|
C | A | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086-673C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874195 | ||||||
chr9:130874362
|
C | A | 2 | a0001c0002t0001g0092a0001c0002t0001g0094 | 2 | HG00280.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1086-506C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874362 | ||||||
chr9:130874379
|
C | T | 30 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(27): Show | 32 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1086-489C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874379 | ||||||
chr9:130874461
|
C | T | 114 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(111): Show | 120 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(117): Show |
intron_variant | MODIFIER | c.1086-407C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874461 | ||||||
chr9:130874502
|
C | T | 1 | a0001c0001t0008g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1086-366C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874502 | ||||||
chr9:130874541
|
C | A | 2 | a0001c0001t0015g0195a0001c0011t0014g0218 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1086-327C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874541 | ||||||
chr9:130874594
|
G | C | 4 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(1): Show | 5 | HG01243.hp2 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086-274G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 6/10 | chr9 | 130874594 | ||||||
chr9:130875092
|
A | G | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1270+40A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875092 | ||||||
chr9:130875152
|
G | GT | 8 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1270+107dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875152 | |||||
chr9:130875163
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0153 | 2 | HG00323.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1270+111A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875163 | ||||||
chr9:130875165
|
G | A | 35 | a0001c0001t0007g0018a0001c0001t0009g0003a0001c0001t0009g0016others(32): Show | 37 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.1270+113G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875165 | ||||||
chr9:130875203
|
G | A | 2 | a0001c0001t0013g0149a0001c0008t0013g0036 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1270+151G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875203 | ||||||
chr9:130875220
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1270+168C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875220 | ||||||
chr9:130875244
|
C | T | 23 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0002t0001g0064others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1270+192C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875244 | ||||||
chr9:130875446
|
CT | C | 96 | a0001c0001t0001g0075a0001c0001t0001g0143a0001c0001t0001g0224others(93): Show | 102 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(99): Show |
intron_variant | MODIFIER | c.1270+410delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875446 | |||||
chr9:130875446
|
CTT | C | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+409_1270+410d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875446 | |||||
chr9:130875451
|
T | C | 15 | a0001c0001t0035g0212a0001c0003t0003g0175a0001c0003t0003g0219others(12): Show | 15 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1270+399T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875451 | ||||||
chr9:130875452
|
T | C | 94 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(91): Show | 100 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(97): Show |
intron_variant | MODIFIER | c.1270+400T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875452 | ||||||
chr9:130875536
|
C | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0203a0001c0001t0002g0204others(4): Show | 8 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270+484C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875536 | ||||||
chr9:130875596
|
G | A | 1 | a0001c0006t0004g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1270+544G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875596 | ||||||
chr9:130875641
|
A | G | 1 | a0001c0004t0017g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1270+589A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875641 | ||||||
chr9:130875846
|
C | T | 5 | a0001c0001t0013g0149a0001c0008t0013g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+794C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875846 | ||||||
chr9:130875931
|
G | A | 4 | a0001c0001t0008g0056a0001c0001t0011g0043a0001c0001t0026g0024others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+879G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130875931 | ||||||
chr9:130875987
|
CCGGCTAA others(21): Show |
C | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1270+939_1270+966d others(30): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130875987 | |||||
chr9:130876015
|
A | G | 18 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(15): Show | 18 | HG01123.hp2 HG01361.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+963A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876015 | ||||||
chr9:130876139
|
T | C | 29 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(26): Show | 31 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1270+1087T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876139 | ||||||
chr9:130876162
|
G | GT | 10 | a0001c0002t0001g0026a0001c0002t0001g0028a0001c0002t0001g0031others(7): Show | 10 | HG00642.hp1 HG02698.hp2 HG04199.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270+1119dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876162 | |||||
chr9:130876323
|
C | T | 1 | a0007c0015t0005g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1270+1271C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876323 | ||||||
chr9:130876353
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0099 | 3 | HG01934.hp1 HG02148.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1270+1301G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876353 | ||||||
chr9:130876411
|
C | CTTTTCT | 36 | a0001c0001t0007g0018a0001c0001t0007g0258a0001c0001t0007g0259others(33): Show | 38 | HG01123.hp2 HG01243.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1270+1363_1270+136 others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | |||||
chr9:130876411
|
C | CTTTTT | 38 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(35): Show | 40 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1270+1367_1270+137 others(9): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | |||||
chr9:130876411
|
C | CTTTTTT | 32 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(29): Show | 34 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1270+1366_1270+137 others(10): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | |||||
chr9:130876411
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1270+1364_1270+137 others(12): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876411 | |||||
chr9:130876585
|
A | AT | 9 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0106others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270+1540dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876585 | |||||
chr9:130876594
|
T | C | 24 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0007g0258others(21): Show | 25 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1270+1542T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876594 | ||||||
chr9:130876666
|
C | G | 1 | a0001c0001t0009g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1270+1614C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876666 | ||||||
chr9:130876701
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1270+1649G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876701 | ||||||
chr9:130876733
|
C | CT | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0019others(46): Show | 52 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1271-1659dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
C | CTTTTT | 25 | a0001c0003t0003g0138a0001c0003t0003g0147a0001c0003t0003g0148others(22): Show | 26 | HG01074.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1271-1663_1271-165 others(9): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
C | CTTTTTTT others(4): Show |
1 | a0001c0011t0014g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1271-1669_1271-165 others(15): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
CT | C | 21 | a0001c0001t0001g0193a0001c0001t0005g0054a0001c0001t0005g0105others(18): Show | 23 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1271-1659delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
CTT | C | 7 | a0001c0001t0001g0211a0001c0001t0007g0018a0001c0001t0008g0056others(4): Show | 8 | HG01243.hp2 HG02572.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1271-1660_1271-165 others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
CTTTT | C | 6 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-1662_1271-165 others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876733
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1271-1668_1271-165 others(14): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876733 | |||||
chr9:130876738
|
T | C | 1 | a0001c0018t0010g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1271-1677T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876738 | ||||||
chr9:130876746
|
TTTTTTTT others(1055): Show |
T | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-1658_1271-597 others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876746 | |||||
chr9:130876775
|
C | T | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-1640C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876775 | ||||||
chr9:130876782
|
GCTGGAGT others(1063): Show |
G | 25 | a0001c0003t0003g0138a0001c0003t0003g0147a0001c0003t0003g0148others(22): Show | 26 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1271-1617_1271-548 others(3): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130876782 | |||||
chr9:130876798
|
A | G | 1 | a0001c0001t0007g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1271-1617A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876798 | ||||||
chr9:130876798
|
A | T | 2 | a0001c0003t0003g0243a0001c0003t0003g0244 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1617A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876798 | ||||||
chr9:130876805
|
C | T | 2 | a0001c0003t0003g0243a0001c0003t0003g0244 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1610C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876805 | ||||||
chr9:130876806
|
A | G | 2 | a0001c0003t0003g0243a0001c0003t0003g0244 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1271-1609A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876806 | ||||||
chr9:130876871
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1271-1544A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876871 | ||||||
chr9:130876877
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1271-1538T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876877 | ||||||
chr9:130876966
|
G | C | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1271-1449G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130876966 | ||||||
chr9:130877175
|
A | T | 5 | a0001c0001t0013g0149a0001c0008t0013g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1240A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877175 | ||||||
chr9:130877182
|
A | G | 5 | a0001c0001t0013g0149a0001c0008t0013g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1233A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877182 | ||||||
chr9:130877188
|
T | A | 1 | a0001c0001t0007g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1271-1227T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877188 | ||||||
chr9:130877214
|
T | A | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-1201T>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877214 | ||||||
chr9:130877224
|
G | A | 41 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(38): Show | 44 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.1271-1191G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877224 | ||||||
chr9:130877362
|
A | G | 1 | a0001c0004t0017g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1271-1053A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877362 | ||||||
chr9:130877559
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-856C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877559 | ||||||
chr9:130877560
|
A | AGGGGGGG others(23): Show |
1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-852_1271-851i others(32): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877560 | |||||
chr9:130877564
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-851T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877564 | ||||||
chr9:130877565
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-850C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877565 | ||||||
chr9:130877566
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-849T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877566 | ||||||
chr9:130877568
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-847A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877568 | ||||||
chr9:130877569
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-846A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877569 | ||||||
chr9:130877570
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-845A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877570 | ||||||
chr9:130877571
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1271-844C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877571 | ||||||
chr9:130877603
|
G | A | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-812G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877603 | ||||||
chr9:130877607
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG00621.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1271-808A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877607 | ||||||
chr9:130877726
|
C | T | 60 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(57): Show | 64 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1271-689C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877726 | ||||||
chr9:130877727
|
G | C | 6 | a0001c0001t0007g0018a0001c0006t0004g0055a0001c0006t0004g0151others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-688G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877727 | ||||||
chr9:130877808
|
A | AT | 11 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0002t0001g0183others(8): Show | 12 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1271-591dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877808 | |||||
chr9:130877808
|
ATTT | A | 34 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(31): Show | 37 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1271-593_1271-591d others(5): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877808 | |||||
chr9:130877828
|
ATG | A | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-586_1271-585d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877828 | ||||||
chr9:130877831
|
G | C | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-584G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877831 | ||||||
chr9:130877831
|
G | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0011t0014g0218others(1): Show | 5 | HG02809.hp2 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-584G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877831 | ||||||
chr9:130877838
|
G | A | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-577G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877838 | ||||||
chr9:130877846
|
A | G | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-569A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877846 | ||||||
chr9:130877852
|
C | G | 6 | a0001c0003t0003g0130a0001c0003t0003g0185a0001c0003t0003g0222others(3): Show | 6 | HG01081.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271-563C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877852 | ||||||
chr9:130877961
|
T | C | 118 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(115): Show | 124 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1271-454T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877961 | ||||||
chr9:130877973
|
C | T | 1 | a0001c0001t0009g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1271-442C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130877973 | ||||||
chr9:130877979
|
ATT | A | 60 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(57): Show | 64 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1271-430_1271-429d others(4): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 130877979 | |||||
chr9:130878011
|
C | T | 1 | a0001c0003t0003g0148 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1271-404C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878011 | ||||||
chr9:130878022
|
C | G | 66 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(63): Show | 70 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1271-393C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878022 | ||||||
chr9:130878060
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1271-355G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878060 | ||||||
chr9:130878065
|
G | A | 1 | a0001c0001t0008g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1271-350G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878065 | ||||||
chr9:130878097
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1271-318G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878097 | ||||||
chr9:130878131
|
A | T | 5 | a0001c0001t0013g0149a0001c0008t0013g0036a0001c0008t0030g0040others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-284A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878131 | ||||||
chr9:130878147
|
C | T | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-268C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878147 | ||||||
chr9:130878148
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1271-267G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 7/10 | chr9 | 130878148 | ||||||
chr9:130878593
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0085 | 2 | NA18941.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1423+26C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878593 | ||||||
chr9:130878645
|
A | G | 32 | a0001c0003t0003g0130a0001c0003t0003g0138a0001c0003t0003g0147others(29): Show | 33 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1423+78A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878645 | ||||||
chr9:130878712
|
C | A | 45 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0011g0004others(42): Show | 48 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1423+145C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878712 | ||||||
chr9:130878768
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0070others(4): Show | 8 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423+201G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878768 | ||||||
chr9:130878769
|
C | G | 2 | a0001c0002t0001g0119a0001c0002t0001g0190 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1423+202C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878769 | ||||||
chr9:130878833
|
T | C | 106 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(103): Show | 112 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(109): Show |
intron_variant | MODIFIER | c.1423+266T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878833 | ||||||
chr9:130878871
|
G | A | 1 | a0001c0001t0007g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1423+304G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878871 | ||||||
chr9:130878874
|
A | AT | 32 | a0001c0001t0001g0012a0001c0001t0001g0124a0001c0001t0001g0125others(29): Show | 34 | HG01175.hp1 HG01496.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1423+327dupT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 130878874 | |||||
chr9:130878874
|
AT | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0063others(25): Show | 29 | HG01074.hp1 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1423+327delT | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 130878874 | |||||
chr9:130878939
|
G | A | 41 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(38): Show | 44 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1423+372G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130878939 | ||||||
chr9:130879034
|
C | T | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+467C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879034 | ||||||
chr9:130879035
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1423+468G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879035 | ||||||
chr9:130879038
|
C | T | 1 | a0001c0003t0004g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1423+471C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879038 | ||||||
chr9:130879089
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0043a0001c0011t0014g0218others(1): Show | 5 | HG02809.hp2 HG03225.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+522C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879089 | ||||||
chr9:130879137
|
A | G | 1 | a0001c0001t0008g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1423+570A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879137 | ||||||
chr9:130879157
|
G | A | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423+590G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879157 | ||||||
chr9:130879199
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1423+632G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879199 | ||||||
chr9:130879398
|
G | A | 11 | a0001c0001t0007g0018a0001c0001t0007g0258a0001c0001t0007g0259others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-670G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879398 | ||||||
chr9:130879481
|
G | A | 5 | a0001c0001t0007g0258a0001c0001t0007g0259a0001c0001t0007g0260others(2): Show | 5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1424-587G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879481 | ||||||
chr9:130879668
|
T | C | 11 | a0001c0001t0007g0018a0001c0001t0007g0258a0001c0001t0007g0259others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-400T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879668 | ||||||
chr9:130879718
|
A | T | 5 | a0001c0001t0008g0178a0001c0001t0008g0197a0001c0001t0008g0207others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1424-350A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879718 | ||||||
chr9:130879895
|
T | G | 33 | a0001c0003t0003g0130a0001c0003t0003g0138a0001c0003t0003g0147others(30): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1424-173T>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879895 | ||||||
chr9:130879906
|
A | G | 11 | a0001c0001t0007g0018a0001c0001t0007g0258a0001c0001t0007g0259others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1424-162A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 8/10 | chr9 | 130879906 | ||||||
chr9:130880163
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG00558.hp1 | splice_region_variant&intron_variant | LOW | c.1513+6G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880163 | ||||||
chr9:130880249
|
A | C | 9 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0004t0005g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1513+92A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880249 | ||||||
chr9:130880300
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1513+143G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880300 | ||||||
chr9:130880367
|
T | C | 119 | a0001c0001t0001g0224a0001c0001t0002g0013a0001c0001t0002g0015others(116): Show | 125 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.1514-133T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880367 | ||||||
chr9:130880374
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1514-126G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 9/10 | chr9 | 130880374 | ||||||
chr9:130880732
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1678+68C>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880732 | ||||||
chr9:130880742
|
C | T | 1 | a0001c0001t0015g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1678+78C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880742 | ||||||
chr9:130880793
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0143 | 2 | NA18963.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1678+129A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880793 | ||||||
chr9:130880843
|
A | G | 1 | a0001c0011t0014g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1678+179A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880843 | ||||||
chr9:130880960
|
C | T | 7 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0004t0005g0009others(4): Show | 8 | HG01109.hp1 HG01884.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+296C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130880960 | ||||||
chr9:130881083
|
C | T | 8 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0004t0005g0009others(5): Show | 9 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+419C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881083 | ||||||
chr9:130881249
|
CTCTGT | C | 3 | a0001c0001t0015g0195a0001c0009t0007g0145a0001c0009t0007g0177 | 3 | HG02486.hp1 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1678+589_1678+593d others(7): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881249 | |||||
chr9:130881323
|
T | C | 8 | a0001c0001t0008g0056a0001c0001t0008g0178a0001c0001t0008g0197others(5): Show | 8 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+659T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881323 | ||||||
chr9:130881340
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1678+676C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881340 | ||||||
chr9:130881406
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1678+742T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881406 | ||||||
chr9:130881449
|
C | A | 6 | a0002c0005t0006g0014a0002c0005t0006g0214a0002c0005t0006g0217others(3): Show | 6 | HG01123.hp2 HG01361.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+785C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881449 | ||||||
chr9:130881501
|
G | T | 8 | a0001c0006t0004g0151a0002c0005t0006g0014a0002c0005t0006g0214others(5): Show | 8 | HG01123.hp2 HG01361.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+837G>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881501 | ||||||
chr9:130881568
|
A | C | 1 | a0001c0001t0009g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1678+904A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881568 | ||||||
chr9:130881569
|
T | C | 5 | a0001c0006t0004g0055a0001c0006t0004g0151a0001c0006t0004g0152others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+905T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881569 | ||||||
chr9:130881670
|
C | T | 8 | a0002c0005t0005g0191a0002c0005t0006g0014a0002c0005t0006g0214others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1006C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881670 | ||||||
chr9:130881693
|
G | A | 61 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0008g0056others(58): Show | 64 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.1678+1029G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881693 | ||||||
chr9:130881715
|
C | T | 114 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0021others(111): Show | 120 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.1678+1051C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881715 | ||||||
chr9:130881765
|
A | G | 9 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0004t0005g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+1101A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881765 | ||||||
chr9:130881773
|
C | T | 1 | a0001c0001t0005g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1678+1109C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881773 | ||||||
chr9:130881855
|
T | TTTTC | 109 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0021others(106): Show | 115 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.1678+1194_1678+119 others(8): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881855 | |||||
chr9:130881877
|
T | TA | 31 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0001t0008g0056others(28): Show | 33 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1678+1223dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881877 | |||||
chr9:130881877
|
TA | T | 5 | a0001c0006t0004g0055a0001c0006t0004g0151a0001c0006t0004g0152others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1223delA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881877 | |||||
chr9:130881886
|
AAC | A | 33 | a0001c0003t0003g0130a0001c0003t0003g0138a0001c0003t0003g0147others(30): Show | 34 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1678+1224_1678+122 others(6): Show |
ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130881886 | |||||
chr9:130881888
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1678+1224C>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881888 | ||||||
chr9:130881935
|
G | A | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+1271G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881935 | ||||||
chr9:130881949
|
G | A | 1 | a0001c0001t0001g0008 | 2 | HG01934.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1678+1285G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130881949 | ||||||
chr9:130882134
|
G | A | 1 | a0001c0024t0001g0090 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1678+1470G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882134 | ||||||
chr9:130882239
|
G | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0174 | 2 | HG00408.hp1 HG00423.hp1 |
intron_variant | MODIFIER | c.1678+1575G>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882239 | ||||||
chr9:130882308
|
G | A | 42 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0021others(39): Show | 45 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1678+1644G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882308 | ||||||
chr9:130882356
|
A | C | 5 | a0001c0006t0004g0055a0001c0006t0004g0151a0001c0006t0004g0152others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-1613A>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882356 | ||||||
chr9:130882398
|
G | A | 42 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0021others(39): Show | 45 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1679-1571G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882398 | ||||||
chr9:130882504
|
T | C | 9 | a0002c0005t0005g0191a0002c0005t0006g0014a0002c0005t0006g0214others(6): Show | 9 | HG00639.hp1 HG01123.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1679-1465T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882504 | ||||||
chr9:130882734
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1679-1235T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882734 | ||||||
chr9:130882777
|
G | A | 1 | a0001c0026t0029g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-1192G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882777 | ||||||
chr9:130882791
|
C | T | 1 | a0001c0008t0031g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1679-1178C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882791 | ||||||
chr9:130882850
|
A | T | 1 | a0001c0001t0002g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1679-1119A>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130882850 | ||||||
chr9:130883061
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-908G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883061 | ||||||
chr9:130883324
|
C | T | 9 | a0001c0001t0005g0054a0001c0001t0005g0105a0001c0004t0005g0009others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1679-645C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883324 | ||||||
chr9:130883429
|
G | A | 1 | a0003c0012t0006g0215 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1679-540G>A | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883429 | ||||||
chr9:130883451
|
C | T | 117 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0021others(114): Show | 123 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.1679-518C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883451 | ||||||
chr9:130883495
|
C | CA | 54 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0125others(51): Show | 57 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1679-459dupA | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 130883495 | |||||
chr9:130883649
|
C | T | 1 | a0001c0004t0005g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1679-320C>T | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883649 | ||||||
chr9:130883716
|
A | G | 1 | a0001c0001t0008g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1679-253A>G | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883716 | ||||||
chr9:130883850
|
T | C | 1 | a0001c0001t0013g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1679-119T>C | ABL1 | ENSG00000097007.20 | transcript | ENST00000318560.6 | protein_coding | 10/10 | chr9 | 130883850 |