geneid | 558 |
---|---|
ensemblid | ENSG00000167601.12 |
hgncid | 905 |
symbol | AXL |
name | AXL receptor tyrosine kinase |
refseq_nuc | NM_021913.5 |
refseq_prot | NP_068713.2 |
ensembl_nuc | ENST00000301178.9 |
ensembl_prot | ENSP00000301178.3 |
mane_status | MANE Select |
chr | chr19 |
start | 41219223 |
end | 41261766 |
strand | + |
ver | v1.2 |
region | chr19:41219223-41261766 |
region5000 | chr19:41214223-41266766 |
regionname0 | AXL_chr19_41219223_41261766 |
regionname5000 | AXL_chr19_41214223_41266766 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 894 | 304 | 90 | 60 | 108 | 10 | 34 | 78 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002 | 0/0 | 894 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0003 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0005 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0006 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0007 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0008 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2685 | 293 | 80 | 60 | 107 | 10 | 34 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0002 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0003 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0004 | 0/0 | 2685 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0005 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0006 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0007 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0008 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0009 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0010 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0011 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0012 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0013 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
c0014 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2033 | 32 | 2 | 7 | 20 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0002 | 0/0 | 2027 | 28 | 5 | 7 | 14 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0003 | 0/0 | 2027 | 20 | 3 | 1 | 15 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0004 | 0/0 | 2022 | 20 | 11 | 0 | 8 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0005 | 0/0 | 2034 | 19 | 0 | 4 | 9 | 1 | 5 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0006 | 0/1 | 2033 | 18 | 3 | 2 | 7 | 1 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0007 | 0/0 | 2034 | 15 | 0 | 5 | 7 | 1 | 2 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0008 | 0/0 | 2022 | 12 | 7 | 0 | 4 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0009 | 0/0 | 2040 | 12 | 10 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0010 | 0/0 | 2037 | 8 | 0 | 3 | 1 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0011 | 0/0 | 2039 | 8 | 3 | 2 | 2 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0012 | 0/0 | 2040 | 8 | 0 | 2 | 2 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0013 | 0/0 | 2028 | 6 | 1 | 1 | 4 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0014 | 0/0 | 2033 | 6 | 1 | 3 | 1 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0015 | 0/0 | 2028 | 6 | 1 | 0 | 4 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0016 | 0/0 | 2035 | 5 | 0 | 1 | 3 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0017 | 0/0 | 2041 | 5 | 2 | 0 | 1 | 0 | 2 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0018 | 0/0 | 2042 | 5 | 4 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0019 | 0/0 | 2043 | 5 | 2 | 2 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0020 | 0/0 | 2033 | 5 | 1 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0021 | 0/0 | 2022 | 4 | 0 | 4 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0022 | 0/0 | 2038 | 4 | 0 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0023 | 0/0 | 2039 | 4 | 3 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0024 | 0/0 | 2035 | 4 | 1 | 3 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0025 | 0/0 | 2042 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0026 | 0/0 | 2034 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0027 | 0/0 | 2037 | 3 | 1 | 1 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0028 | 0/0 | 2038 | 3 | 1 | 0 | 1 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0029 | 0/0 | 2041 | 3 | 2 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0030 | 0/0 | 2043 | 3 | 2 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0031 | 0/0 | 2046 | 3 | 2 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0032 | 0/0 | 2022 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0033 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0034 | 0/0 | 2053 | 2 | 1 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0035 | 0/0 | 2033 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0036 | 0/0 | 2056 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0037 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0038 | 0/0 | 2021 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0039 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0040 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0041 | 0/0 | 2033 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0042 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0043 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0044 | 0/0 | 2051 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0045 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0046 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0047 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0048 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0049 | 0/0 | 2021 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0050 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0051 | 0/0 | 2027 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0052 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0053 | 0/0 | 2047 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0054 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0055 | 0/0 | 2049 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0056 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0057 | 0/0 | 2053 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
t0058 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0010 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2685 | 293 | 80 | 60 | 107 | 10 | 34 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0002 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0003 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0007 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0011 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0013 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002c0004 | 0/0 | 2685 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002c0010 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0003c0005 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0004c0006 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0005c0012 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0006c0008 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0007c0009 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0008c0014 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4717 | 30 | 1 | 7 | 19 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0002 | 0/0 | 4711 | 28 | 5 | 7 | 14 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0003 | 0/0 | 4711 | 20 | 3 | 1 | 15 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0004 | 0/0 | 4706 | 20 | 11 | 0 | 8 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0005 | 0/0 | 4718 | 16 | 0 | 4 | 6 | 1 | 5 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0006 | 0/1 | 4717 | 17 | 3 | 2 | 6 | 1 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0007 | 0/0 | 4718 | 13 | 0 | 4 | 6 | 1 | 2 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0008 | 0/0 | 4706 | 12 | 7 | 0 | 4 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0009 | 0/0 | 4724 | 7 | 5 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0010 | 0/0 | 4721 | 8 | 0 | 3 | 1 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0011 | 0/0 | 4723 | 7 | 2 | 2 | 2 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0012 | 0/0 | 4724 | 8 | 0 | 2 | 2 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0013 | 0/0 | 4712 | 6 | 1 | 1 | 4 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0014 | 0/0 | 4717 | 5 | 1 | 2 | 1 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0015 | 0/0 | 4712 | 5 | 1 | 0 | 3 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0016 | 0/0 | 4719 | 5 | 0 | 1 | 3 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0017 | 0/0 | 4725 | 5 | 2 | 0 | 1 | 0 | 2 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0018 | 0/0 | 4726 | 5 | 4 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0019 | 0/0 | 4727 | 5 | 2 | 2 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0020 | 0/0 | 4717 | 5 | 1 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0021 | 0/0 | 4706 | 4 | 0 | 4 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0022 | 0/0 | 4722 | 4 | 0 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0023 | 0/0 | 4723 | 2 | 1 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0024 | 0/0 | 4719 | 4 | 1 | 3 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0025 | 0/0 | 4726 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0026 | 0/0 | 4718 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0027 | 0/0 | 4721 | 3 | 1 | 1 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0028 | 0/0 | 4722 | 3 | 1 | 0 | 1 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0029 | 0/0 | 4725 | 2 | 1 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0030 | 0/0 | 4727 | 3 | 2 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0031 | 0/0 | 4730 | 3 | 2 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0032 | 0/0 | 4706 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0033 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0034 | 0/0 | 4737 | 2 | 1 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0035 | 0/0 | 4717 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0036 | 0/0 | 4740 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0037 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0038 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0039 | 0/0 | 4707 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0040 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0041 | 0/0 | 4717 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0042 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0043 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0045 | 0/0 | 4718 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0046 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0047 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0048 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0049 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0050 | 0/0 | 4707 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0051 | 0/0 | 4711 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0052 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0053 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0054 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0055 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0056 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0057 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0001t0058 | 0/0 | 4739 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0002t0009 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0002t0023 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0002t0029 | 0/0 | 4725 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0003t0009 | 0/0 | 4724 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0007t0001 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0011t0011 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0001c0013t0044 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002c0004t0005 | 0/0 | 4718 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002c0004t0007 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0002c0010t0005 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0003c0005t0006 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0004c0006t0015 | 0/0 | 4712 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0005c0012t0007 | 0/0 | 4718 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0006c0008t0014 | 0/0 | 4717 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0007c0009t0033 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
a0008c0014t0001 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | copy fasta | chr19 | 41214223 | 41266766 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0010 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0023g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0023g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0029g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0033g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0034g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0034g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0035g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0035g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0036g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0036g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0037g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0038g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0039g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0040g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0041g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0043g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0045g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0046g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0047g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0048g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0049g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0050g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0051g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0052g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0053g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0054g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0055g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0056g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0057g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0058g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0023g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0029g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0011t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0013t0044g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0010t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0003c0005t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0004c0006t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0005c0012t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0006c0008t0014g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0007c0009t0033g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0008c0014t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | GBR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0088 | EUR | GBR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0199 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0207 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0090 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00423 | hp1 | a0001 | c0001 | t0015 | g0184 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00423 | hp2 | a0001 | c0001 | t0015 | g0187 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0253 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0089 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00642 | hp1 | a0001 | c0001 | t0014 | g0049 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00642 | hp2 | a0001 | c0001 | t0058 | g0013 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0075 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00735 | hp1 | a0001 | c0001 | t0020 | g0196 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00735 | hp2 | a0001 | c0001 | t0013 | g0062 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00738 | hp1 | a0001 | c0001 | t0034 | g0110 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00738 | hp2 | a0001 | c0001 | t0057 | g0013 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01070 | hp2 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01071 | hp2 | a0001 | c0001 | t0023 | g0028 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0135 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01081 | hp1 | a0001 | c0001 | t0030 | g0258 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01081 | hp2 | a0001 | c0001 | t0022 | g0097 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01099 | hp1 | a0001 | c0001 | t0027 | g0255 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01109 | hp1 | a0001 | c0001 | t0024 | g0200 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01109 | hp2 | a0001 | c0001 | t0024 | g0005 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01167 | hp2 | a0001 | c0001 | t0021 | g0042 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0122 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01169 | hp1 | a0001 | c0001 | t0022 | g0120 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01169 | hp2 | a0001 | c0001 | t0021 | g0044 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01192 | hp2 | a0001 | c0001 | t0022 | g0096 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0108 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0109 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01256 | hp1 | a0001 | c0001 | t0011 | g0221 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01257 | hp1 | a0001 | c0001 | t0024 | g0206 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01346 | hp2 | a0001 | c0001 | t0020 | g0276 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0224 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01361 | hp1 | a0001 | c0001 | t0021 | g0279 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01433 | hp2 | a0005 | c0012 | t0007 | g0095 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01496 | hp1 | a0001 | c0001 | t0012 | g0157 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01496 | hp2 | a0001 | c0001 | t0045 | g0074 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01515 | hp1 | a0001 | c0001 | t0016 | g0130 | EUR | IBS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01515 | hp2 | a0001 | c0001 | t0014 | g0065 | EUR | IBS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01884 | hp1 | a0007 | c0009 | t0033 | g0278 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01884 | hp2 | a0001 | c0001 | t0030 | g0219 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01928 | hp1 | a0001 | c0001 | t0021 | g0043 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0188 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01952 | hp2 | a0001 | c0001 | t0016 | g0041 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0203 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02040 | hp1 | a0001 | c0001 | t0027 | g0205 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02055 | hp2 | a0001 | c0002 | t0009 | g0282 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0256 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02071 | hp2 | a0001 | c0001 | t0016 | g0077 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02083 | hp1 | a0001 | c0001 | t0012 | g0027 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02129 | hp1 | a0001 | c0001 | t0035 | g0189 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02129 | hp2 | a0001 | c0001 | t0015 | g0286 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02135 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0094 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02145 | hp1 | a0001 | c0003 | t0009 | g0019 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02145 | hp2 | a0001 | c0001 | t0019 | g0114 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02155 | hp1 | a0001 | c0001 | t0050 | g0257 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02155 | hp2 | a0001 | c0001 | t0026 | g0248 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02257 | hp1 | a0001 | c0001 | t0025 | g0171 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0115 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0030 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0070 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02280 | hp2 | a0001 | c0001 | t0055 | g0156 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02293 | hp1 | a0001 | c0001 | t0014 | g0048 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02523 | hp2 | a0001 | c0001 | t0014 | g0064 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0217 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02615 | hp1 | a0001 | c0001 | t0031 | g0155 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02622 | hp1 | a0001 | c0002 | t0029 | g0233 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02622 | hp2 | a0001 | c0001 | t0019 | g0117 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0288 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02630 | hp2 | a0001 | c0001 | t0030 | g0211 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0225 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02683 | hp1 | a0001 | c0001 | t0038 | g0076 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02683 | hp2 | a0001 | c0001 | t0049 | g0190 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0092 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0127 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02723 | hp2 | a0008 | c0014 | t0001 | g0138 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0249 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0059 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0175 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0174 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02809 | hp1 | a0001 | c0002 | t0023 | g0284 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02809 | hp2 | a0001 | c0001 | t0034 | g0034 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02818 | hp1 | a0001 | c0003 | t0009 | g0018 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0210 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02886 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0209 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02896 | hp1 | a0001 | c0001 | t0032 | g0163 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02896 | hp2 | a0001 | c0001 | t0037 | g0031 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02897 | hp2 | a0001 | c0001 | t0032 | g0164 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02922 | hp1 | a0001 | c0013 | t0044 | g0063 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02965 | hp2 | a0001 | c0001 | t0025 | g0230 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02970 | hp1 | a0001 | c0001 | t0018 | g0116 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02976 | hp2 | a0001 | c0001 | t0036 | g0216 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0231 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03041 | hp1 | a0001 | c0001 | t0054 | g0159 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0142 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03098 | hp2 | a0001 | c0001 | t0013 | g0140 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03130 | hp1 | a0001 | c0001 | t0027 | g0168 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03130 | hp2 | a0001 | c0001 | t0036 | g0215 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03139 | hp1 | a0001 | c0001 | t0047 | g0277 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03139 | hp2 | a0001 | c0001 | t0056 | g0229 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03195 | hp2 | a0001 | c0001 | t0043 | g0015 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03225 | hp1 | a0001 | c0001 | t0048 | g0112 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0123 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03486 | hp2 | a0001 | c0001 | t0046 | g0106 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03490 | hp1 | a0001 | c0001 | t0012 | g0191 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03491 | hp1 | a0001 | c0001 | t0031 | g0232 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03492 | hp1 | a0001 | c0001 | t0012 | g0192 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0274 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03516 | hp1 | a0001 | c0002 | t0023 | g0283 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03516 | hp2 | a0001 | c0003 | t0009 | g0006 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03540 | hp1 | a0001 | c0003 | t0009 | g0006 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0103 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03669 | hp1 | a0001 | c0001 | t0029 | g0193 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0201 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0266 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03710 | hp2 | a0001 | c0001 | t0020 | g0272 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03834 | hp1 | a0001 | c0001 | t0017 | g0026 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03834 | hp2 | a0001 | c0001 | t0019 | g0029 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03942 | hp1 | a0001 | c0001 | t0011 | g0270 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0177 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0023 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04199 | hp1 | a0001 | c0001 | t0022 | g0098 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04199 | hp2 | a0001 | c0001 | t0028 | g0202 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0024 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0125 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18906 | hp1 | a0001 | c0001 | t0025 | g0167 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0101 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18943 | hp1 | a0001 | c0001 | t0039 | g0008 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18943 | hp2 | a0001 | c0001 | t0035 | g0246 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18946 | hp2 | a0001 | c0001 | t0013 | g0107 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18950 | hp2 | a0001 | c0001 | t0051 | g0179 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18957 | hp1 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18959 | hp1 | a0002 | c0010 | t0005 | g0121 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18968 | hp1 | a0002 | c0004 | t0007 | g0104 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18968 | hp2 | a0001 | c0001 | t0028 | g0238 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18970 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18971 | hp1 | a0002 | c0004 | t0005 | g0226 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18971 | hp2 | a0003 | c0005 | t0006 | g0239 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18975 | hp1 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0093 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18981 | hp1 | a0004 | c0006 | t0015 | g0247 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18984 | hp2 | a0001 | c0001 | t0026 | g0261 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18990 | hp2 | a0002 | c0004 | t0005 | g0227 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18995 | hp2 | a0001 | c0001 | t0016 | g0054 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18997 | hp1 | a0001 | c0001 | t0013 | g0051 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19010 | hp1 | a0001 | c0001 | t0026 | g0245 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19030 | hp1 | a0001 | c0001 | t0053 | g0005 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19043 | hp1 | a0001 | c0011 | t0011 | g0260 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19043 | hp2 | a0001 | c0001 | t0052 | g0267 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19060 | hp2 | a0001 | c0007 | t0001 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19079 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19081 | hp1 | a0001 | c0001 | t0040 | g0066 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19082 | hp1 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19091 | hp1 | a0001 | c0001 | t0012 | g0198 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20129 | hp1 | a0001 | c0001 | t0023 | g0102 | AFR | ASW | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0100 | AFR | ASW | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20752 | hp1 | a0001 | c0001 | t0041 | g0073 | EUR | TSI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0273 | SAS | GIH | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20905 | hp2 | a0001 | c0001 | t0010 | g0084 | SAS | GIH | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01123 | hp2 | a0006 | c0008 | t0014 | g0047 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02486 | hp1 | a0001 | c0001 | t0031 | g0005 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02486 | hp2 | a0001 | c0001 | t0033 | g0124 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02559 | hp1 | a0001 | c0001 | t0020 | g0195 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0137 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0158 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20300 | hp2 | a0001 | c0001 | t0015 | g0166 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0214 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA21309 | hp2 | a0001 | c0001 | t0025 | g0173 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0250 | REF | REF | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0010 | REF | REF | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219445
|
C | T | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.53C>T | p.Ala18Val | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | 223/4717 | 53/2685 | 18/894 | chr19 | 41219445 | ||
chr19:41220693
|
G | A | 1 | a0003 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.143G>A | p.Arg48Gln | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/20 | 313/4717 | 143/2685 | 48/894 | chr19 | 41220693 | ||
chr19:41221919
|
T | C | 1 | a0004 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.449T>C | p.Val150Ala | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/20 | 619/4717 | 449/2685 | 150/894 | chr19 | 41221919 | ||
chr19:41238005
|
C | T | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.845C>T | p.Pro282Leu | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1015/4717 | 845/2685 | 282/894 | chr19 | 41238005 | ||
chr19:41242913
|
G | T | 1 | a0002 | 4 | NA18959.hp1 NA18968.hp1 NA18971.hp1 others(1): Show |
missense_variant | MODERATE | c.1343G>T | p.Trp448Leu | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/20 | 1513/4717 | 1343/2685 | 448/894 | chr19 | 41242913 | ||
chr19:41253609
|
C | T | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1937C>T | p.Thr646Ile | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/20 | 2107/4717 | 1937/2685 | 646/894 | chr19 | 41253609 | ||
chr19:41257584
|
G | A | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2288G>A | p.Arg763His | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/20 | 2458/4717 | 2288/2685 | 763/894 | chr19 | 41257584 | ||
chr19:41259633
|
A | C | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2414A>C | p.Asn805Thr | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2584/4717 | 2414/2685 | 805/894 | chr19 | 41259633 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41221905
|
C | T | 1 | a0001c0013 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.435C>T | p.Pro145Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/20 | 605/4717 | 435/2685 | 145/894 | chr19 | 41221905 | ||
chr19:41238024
|
C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.864C>T | p.Ser288Ser | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1034/4717 | 864/2685 | 288/894 | chr19 | 41238024 | ||
chr19:41238144
|
G | A | 1 | a0001c0007 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.984G>A | p.Thr328Thr | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1154/4717 | 984/2685 | 328/894 | chr19 | 41238144 | ||
chr19:41242986
|
C | T | 1 | a0002c0010 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1416C>T | p.Val472Val | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/20 | 1586/4717 | 1416/2685 | 472/894 | chr19 | 41242986 | ||
chr19:41259670
|
C | T | 1 | a0001c0003 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.2451C>T | p.Asp817Asp | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2621/4717 | 2451/2685 | 817/894 | chr19 | 41259670 | ||
chr19:41259712
|
T | C | 1 | a0001c0002 | 4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.2493T>C | p.Pro831Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2663/4717 | 2493/2685 | 831/894 | chr19 | 41259712 | ||
chr19:41259847
|
C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2628C>T | p.Pro876Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2798/4717 | 2628/2685 | 876/894 | chr19 | 41259847 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219353
|
C | T | 1 | a0001c0001t0032 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-40C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | chr19 | 41219353 | ||||||
chr19:41219366
|
A | G | 37 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(34): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-27A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | 27 | chr19 | 41219366 | |||||
chr19:41259953
|
C | T | 1 | a0001c0001t0046 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 49 | chr19 | 41259953 | |||||
chr19:41259975
|
C | A | 2 | a0001c0001t0037a0001c0001t0047 | 2 | HG02896.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 71 | chr19 | 41259975 | |||||
chr19:41259992
|
C | T | 1 | a0001c0001t0045 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 88 | chr19 | 41259992 | |||||
chr19:41260272
|
T | C | 1 | a0001c0001t0032 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 368 | chr19 | 41260272 | |||||
chr19:41260298
|
C | CT | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0026others(5): Show | 38 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*425dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTT | 2 | a0001c0001t0016a0001c0001t0024 | 9 | HG01109.hp1 HG01109.hp2 HG01257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*424_*425dupTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTT | 2 | a0001c0001t0010a0001c0001t0027 | 11 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*425dupTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTT | 2 | a0001c0001t0022a0001c0001t0028 | 7 | HG01081.hp2 HG01169.hp1 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*425dupTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTT | 5 | a0001c0001t0011a0001c0001t0023a0001c0001t0052others(2): Show | 13 | HG01071.hp2 HG01074.hp2 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*420_*425dupTTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT | 4 | a0001c0001t0009a0001c0001t0012a0001c0002t0009others(1): Show | 20 | HG00639.hp1 HG01496.hp1 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*425dupTTTTTT others(1): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(1): Show |
3 | a0001c0001t0017a0001c0001t0029a0001c0002t0029 | 8 | HG02622.hp1 HG02735.hp2 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*418_*425dupTTTTTT others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(2): Show |
2 | a0001c0001t0018a0001c0001t0025 | 9 | HG02257.hp1 HG02258.hp1 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*425dupTTTTTT others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0019a0001c0001t0030 | 8 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*416_*425dupTTTTTT others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415_*425dupTTTTTT others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0031a0001c0001t0033a0007c0009t0033 | 5 | HG01884.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*425dupTTTTTT others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0053 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412_*425dupTTTTTT others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411_*425dupTTTTTT others(9): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0043a0001c0001t0055 | 2 | HG02280.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*410_*425dupTTTTTT others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(11): Show |
1 | a0001c0013t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408_*425dupTTTTTT others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0056 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*407_*425dupTTTTTT others(13): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0034a0001c0001t0057 | 3 | HG00738.hp1 HG00738.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406_*425dupTTTTTT others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0058 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404_*425dupTTTTTT others(16): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0036 | 2 | HG02976.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*425dupTTTTTT others(17): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTT | C | 3 | a0001c0001t0013a0001c0001t0015a0004c0006t0015 | 12 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*425delTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 421 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTTT | C | 3 | a0001c0001t0002a0001c0001t0003a0001c0001t0051 | 49 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*420_*425delTTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 420 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0039a0001c0001t0050 | 2 | HG02155.hp1 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416_*425delTTTTTT others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 416 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0004a0001c0001t0008a0001c0001t0021others(1): Show | 39 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*425delTTTTTT others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 415 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0038a0001c0001t0049 | 2 | HG02683.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*414_*425delTTTTTT others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 414 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260298
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0037a0001c0001t0047a0001c0001t0048 | 3 | HG02896.hp2 HG03139.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*411_*425delTTTTTT others(9): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 411 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | ||||
chr19:41260380
|
C | T | 1 | a0001c0001t0041 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 476 | chr19 | 41260380 | |||||
chr19:41260473
|
G | A | 1 | a0001c0001t0021 | 4 | HG01167.hp2 HG01169.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 569 | chr19 | 41260473 | |||||
chr19:41260853
|
T | C | 1 | a0001c0001t0047 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 949 | chr19 | 41260853 | |||||
chr19:41260890
|
G | A | 1 | a0001c0001t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 986 | chr19 | 41260890 | |||||
chr19:41261043
|
A | G | 1 | a0001c0001t0051 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1139A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1139 | chr19 | 41261043 | |||||
chr19:41261073
|
G | C | 3 | a0001c0001t0014a0001c0001t0020a0006c0008t0014 | 11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1169 | chr19 | 41261073 | |||||
chr19:41261077
|
C | T | 1 | a0001c0001t0052 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1173C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1173 | chr19 | 41261077 | |||||
chr19:41261085
|
C | T | 2 | a0001c0001t0056a0001c0013t0044 | 2 | HG02922.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1181C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1181 | chr19 | 41261085 | |||||
chr19:41261138
|
G | A | 1 | a0001c0001t0037 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1234 | chr19 | 41261138 | |||||
chr19:41261390
|
C | T | 7 | a0001c0001t0004a0001c0001t0008a0001c0001t0021others(4): Show | 45 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1486 | chr19 | 41261390 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219505
|
G | A | 5 | a0001c0001t0008g0017a0001c0001t0018g0020a0001c0003t0009g0006others(2): Show | 6 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+28G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219505 | ||||||
chr19:41219625
|
GAC | G | 5 | a0001c0001t0008g0017a0001c0001t0018g0020a0001c0003t0009g0006others(2): Show | 6 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+152_85+153delCA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41219625 | |||||
chr19:41219846
|
C | T | 1 | a0001c0001t0032g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.85+369C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219846 | ||||||
chr19:41219847
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0150a0001c0001t0002g0003others(164): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.85+370A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219847 | ||||||
chr19:41219849
|
T | C | 165 | a0001c0001t0001g0150a0001c0001t0002g0003a0001c0001t0002g0136others(162): Show | 168 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.85+372T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219849 | ||||||
chr19:41219852
|
G | C | 1 | a0001c0001t0005g0133 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.85+375G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219852 | ||||||
chr19:41219885
|
G | C | 163 | a0001c0001t0001g0150a0001c0001t0002g0003a0001c0001t0002g0136others(160): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.85+408G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219885 | ||||||
chr19:41219931
|
C | A | 1 | a0001c0001t0004g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+454C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219931 | ||||||
chr19:41219933
|
C | A | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+456C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219933 | ||||||
chr19:41220027
|
C | A | 3 | a0001c0001t0002g0136a0001c0001t0011g0135a0001c0001t0024g0137 | 3 | HG01074.hp2 HG01358.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.85+550C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220027 | ||||||
chr19:41220068
|
GTCTC | G | 10 | a0001c0001t0002g0269a0001c0001t0004g0271a0001c0001t0005g0275others(7): Show | 10 | HG00597.hp2 HG01346.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.86-558_86-555delCT others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220068 | |||||
chr19:41220093
|
C | G | 1 | a0001c0001t0009g0030 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.86-543C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220093 | ||||||
chr19:41220124
|
C | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01070.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-512C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220124 | ||||||
chr19:41220228
|
GCCACCAC others(15): Show |
G | 60 | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0001t0002g0240others(57): Show | 64 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.86-391_86-370delCC others(20): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220228 | |||||
chr19:41220242
|
CTCCCCCC others(11): Show |
C | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.86-392_86-375delCC others(16): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220242 | |||||
chr19:41220262
|
A | C | 84 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0194others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.86-374A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220262 | ||||||
chr19:41220448
|
T | C | 3 | a0001c0001t0042g0015a0001c0001t0043g0015a0007c0009t0033g0278 | 3 | HG01884.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.86-188T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220448 | ||||||
chr19:41220548
|
C | T | 3 | a0001c0001t0002g0228a0002c0004t0005g0226a0002c0004t0005g0227 | 3 | NA18964.hp2 NA18971.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.86-88C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220548 | ||||||
chr19:41220549
|
G | A | 6 | a0001c0001t0003g0113a0001c0001t0003g0118a0001c0001t0018g0115others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-87G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220549 | ||||||
chr19:41220573
|
T | C | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.86-63T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220573 | ||||||
chr19:41221074
|
C | T | 2 | a0001c0001t0006g0128a0001c0001t0048g0112 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.309-72C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/19 | chr19 | 41221074 | ||||||
chr19:41221131
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.309-15C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/19 | chr19 | 41221131 | ||||||
chr19:41221292
|
C | T | 40 | a0001c0001t0002g0220a0001c0001t0002g0222a0001c0001t0002g0269others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.409+46C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221292 | ||||||
chr19:41221326
|
GGGTCAA | G | 40 | a0001c0001t0002g0220a0001c0001t0002g0222a0001c0001t0002g0269others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.409+87_409+92delGG others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 41221326 | |||||
chr19:41221552
|
G | A | 1 | a0001c0001t0037g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.409+306G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221552 | ||||||
chr19:41221563
|
G | T | 1 | a0001c0001t0020g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.409+317G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221563 | ||||||
chr19:41221587
|
C | A | 11 | a0001c0001t0003g0113a0001c0001t0003g0118a0001c0001t0003g0172others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.410-293C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221587 | ||||||
chr19:41221724
|
T | C | 11 | a0001c0001t0003g0113a0001c0001t0003g0118a0001c0001t0003g0172others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.410-156T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221724 | ||||||
chr19:41221864
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.410-16C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221864 | ||||||
chr19:41222202
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.586+146T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222202 | ||||||
chr19:41222269
|
T | G | 2 | a0001c0001t0003g0033a0001c0001t0003g0119 | 2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.586+213T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222269 | ||||||
chr19:41222306
|
G | GTC | 10 | a0001c0001t0002g0269a0001c0001t0004g0271a0001c0001t0005g0275others(7): Show | 10 | HG00597.hp2 HG01346.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+260_586+261dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41222306 | |||||
chr19:41222330
|
C | T | 3 | a0001c0001t0003g0172a0001c0001t0006g0128a0001c0001t0048g0112 | 3 | HG02615.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.586+274C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222330 | ||||||
chr19:41222483
|
C | T | 1 | a0001c0001t0004g0265 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.586+427C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222483 | ||||||
chr19:41222530
|
C | T | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0034g0110 | 3 | HG00738.hp1 HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.586+474C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222530 | ||||||
chr19:41222548
|
G | T | 1 | a0001c0001t0013g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.586+492G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222548 | ||||||
chr19:41222550
|
G | C | 15 | a0001c0001t0008g0004a0001c0001t0008g0007a0001c0001t0008g0017others(12): Show | 19 | HG02145.hp1 HG02258.hp2 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.586+494G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222550 | ||||||
chr19:41222634
|
T | C | 41 | a0001c0001t0002g0220a0001c0001t0002g0222a0001c0001t0002g0269others(38): Show | 41 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.586+578T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222634 | ||||||
chr19:41222688
|
C | T | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+632C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222688 | ||||||
chr19:41222722
|
C | T | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.586+666C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222722 | ||||||
chr19:41222740
|
A | C | 1 | a0001c0001t0002g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586+684A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222740 | ||||||
chr19:41222798
|
C | T | 20 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0271others(17): Show | 20 | HG01346.hp2 HG02129.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.586+742C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222798 | ||||||
chr19:41222855
|
G | A | 8 | a0001c0001t0008g0004a0001c0001t0008g0007a0001c0001t0009g0141others(5): Show | 11 | HG02258.hp2 HG02809.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+799G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222855 | ||||||
chr19:41222860
|
T | C | 180 | a0001c0001t0001g0035a0001c0001t0002g0003a0001c0001t0002g0144others(177): Show | 187 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.586+804T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222860 | ||||||
chr19:41222884
|
C | A | 6 | a0001c0001t0001g0035a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | NA18944.hp1 NA18986.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+828C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222884 | ||||||
chr19:41222910
|
GA | G | 95 | a0001c0001t0001g0035a0001c0001t0001g0105a0001c0001t0002g0003others(92): Show | 98 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.586+869delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41222910 | |||||
chr19:41222960
|
C | A | 2 | a0001c0001t0012g0231a0001c0001t0031g0232 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.586+904C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222960 | ||||||
chr19:41223032
|
C | T | 1 | a0002c0004t0007g0104 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.586+976C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223032 | ||||||
chr19:41223164
|
GGGCATCT others(3): Show |
G | 3 | a0001c0001t0042g0015a0001c0001t0043g0015a0007c0009t0033g0278 | 3 | HG01884.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.586+1110_586+1119d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223164 | |||||
chr19:41223269
|
T | G | 1 | a0001c0001t0013g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.586+1213T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223269 | ||||||
chr19:41223486
|
C | T | 4 | a0001c0001t0004g0169a0001c0001t0025g0167a0001c0001t0027g0168others(1): Show | 4 | HG02486.hp2 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+1430C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223486 | ||||||
chr19:41223600
|
T | C | 120 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0035others(117): Show | 127 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.586+1544T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223600 | ||||||
chr19:41223606
|
G | A | 1 | a0001c0001t0007g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586+1550G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223606 | ||||||
chr19:41223808
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0013g0062a0001c0001t0015g0174 | 3 | HG00735.hp2 HG02738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.586+1752G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223808 | ||||||
chr19:41223902
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.586+1846C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223902 | ||||||
chr19:41223969
|
G | GGT | 6 | a0001c0001t0005g0204a0001c0001t0005g0275a0001c0001t0006g0128others(3): Show | 6 | HG03225.hp1 HG03239.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1933_586+1934d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | |||||
chr19:41223969
|
G | GGTGT | 6 | a0001c0001t0011g0210a0001c0001t0011g0217a0001c0001t0025g0230others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1931_586+1934d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | |||||
chr19:41223969
|
GGT | G | 63 | a0001c0001t0002g0220a0001c0001t0003g0118a0001c0001t0004g0134others(60): Show | 67 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.586+1933_586+1934d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | |||||
chr19:41224046
|
T | C | 1 | a0001c0001t0007g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+1990T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224046 | ||||||
chr19:41224066
|
G | A | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.586+2010G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224066 | ||||||
chr19:41224108
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0009g0285a0001c0001t0018g0115others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+2052G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224108 | ||||||
chr19:41224114
|
T | C | 2 | a0001c0001t0010g0122a0001c0001t0022g0120 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.586+2058T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224114 | ||||||
chr19:41224707
|
G | T | 1 | a0001c0001t0019g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.586+2651G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224707 | ||||||
chr19:41224734
|
G | A | 1 | a0001c0001t0011g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.586+2678G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224734 | ||||||
chr19:41224753
|
G | T | 2 | a0001c0001t0008g0008a0001c0001t0039g0008 | 2 | NA18943.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.586+2697G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224753 | ||||||
chr19:41224788
|
C | CTG | 57 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0002g0228others(54): Show | 58 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.586+2752_586+2753d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | |||||
chr19:41224788
|
C | CTGTG | 4 | a0001c0001t0017g0101a0001c0001t0017g0103a0001c0001t0023g0102others(1): Show | 4 | HG02896.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+2750_586+2753d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | |||||
chr19:41224788
|
CTG | C | 9 | a0001c0001t0006g0128a0001c0001t0018g0115a0001c0001t0018g0116others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+2752_586+2753d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | |||||
chr19:41224888
|
G | A | 1 | a0001c0001t0046g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.586+2832G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224888 | ||||||
chr19:41225002
|
T | G | 19 | a0001c0001t0004g0134a0001c0001t0004g0139a0001c0001t0004g0152others(16): Show | 22 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.586+2946T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225002 | ||||||
chr19:41225067
|
G | A | 19 | a0001c0001t0004g0134a0001c0001t0004g0139a0001c0001t0004g0152others(16): Show | 22 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.586+3011G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225067 | ||||||
chr19:41225080
|
T | C | 9 | a0001c0001t0006g0128a0001c0001t0018g0115a0001c0001t0018g0116others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+3024T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225080 | ||||||
chr19:41225270
|
A | G | 10 | a0001c0001t0001g0132a0001c0001t0014g0064a0001c0001t0014g0065others(7): Show | 10 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+3214A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225270 | ||||||
chr19:41225700
|
G | A | 1 | a0007c0009t0033g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.586+3644G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225700 | ||||||
chr19:41225844
|
T | G | 70 | a0001c0001t0001g0067a0001c0001t0002g0197a0001c0001t0002g0222others(67): Show | 72 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.586+3788T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225844 | ||||||
chr19:41225961
|
G | A | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.586+3905G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225961 | ||||||
chr19:41225971
|
G | A | 9 | a0001c0001t0006g0128a0001c0001t0018g0115a0001c0001t0018g0116others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+3915G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225971 | ||||||
chr19:41226011
|
G | T | 2 | a0001c0001t0015g0166a0001c0011t0011g0260 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.586+3955G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226011 | ||||||
chr19:41226067
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+4011G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226067 | ||||||
chr19:41226097
|
A | G | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+4041A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226097 | ||||||
chr19:41226123
|
G | A | 1 | a0001c0001t0055g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586+4067G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226123 | ||||||
chr19:41226191
|
G | T | 2 | a0001c0001t0005g0275a0001c0001t0006g0274 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.586+4135G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226191 | ||||||
chr19:41226463
|
T | C | 1 | a0001c0001t0006g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.586+4407T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226463 | ||||||
chr19:41226474
|
G | T | 1 | a0001c0002t0023g0283 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+4418G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226474 | ||||||
chr19:41226518
|
T | C | 173 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(170): Show | 185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.587-4449T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226518 | ||||||
chr19:41226585
|
C | T | 1 | a0001c0001t0026g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.587-4382C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226585 | ||||||
chr19:41226705
|
C | G | 18 | a0001c0001t0001g0132a0001c0001t0014g0064a0001c0001t0014g0065others(15): Show | 18 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.587-4262C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226705 | ||||||
chr19:41226783
|
G | T | 10 | a0001c0001t0001g0132a0001c0001t0014g0064a0001c0001t0014g0065others(7): Show | 10 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-4184G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226783 | ||||||
chr19:41226822
|
C | G | 160 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0002g0003others(157): Show | 171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.587-4145C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226822 | ||||||
chr19:41226826
|
T | A | 2 | a0001c0001t0003g0033a0001c0001t0003g0119 | 2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.587-4141T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226826 | ||||||
chr19:41227240
|
G | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(164): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.587-3727G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227240 | ||||||
chr19:41227450
|
A | G | 17 | a0001c0001t0001g0132a0001c0001t0014g0064a0001c0001t0014g0065others(14): Show | 17 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.587-3517A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227450 | ||||||
chr19:41227454
|
G | A | 1 | a0001c0001t0007g0053 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587-3513G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227454 | ||||||
chr19:41227462
|
G | A | 1 | a0001c0001t0033g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.587-3505G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227462 | ||||||
chr19:41227488
|
C | CT | 23 | a0001c0001t0001g0035a0001c0001t0001g0132a0001c0001t0005g0208others(20): Show | 23 | HG00735.hp1 HG01192.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.587-3463dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41227488 | |||||
chr19:41227488
|
CT | C | 77 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(74): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.587-3463delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41227488 | |||||
chr19:41227548
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0150a0001c0001t0005g0254 | 3 | HG02056.hp1 NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.587-3419C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227548 | ||||||
chr19:41227725
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.587-3242G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227725 | ||||||
chr19:41227911
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.587-3056G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227911 | ||||||
chr19:41227918
|
G | A | 1 | a0001c0001t0041g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.587-3049G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227918 | ||||||
chr19:41227923
|
G | A | 1 | a0001c0001t0018g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.587-3044G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227923 | ||||||
chr19:41228110
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-2857G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228110 | ||||||
chr19:41228146
|
G | A | 3 | a0001c0001t0012g0157a0001c0001t0056g0229a0001c0013t0044g0063 | 3 | HG01496.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.587-2821G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228146 | ||||||
chr19:41228154
|
C | T | 171 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(168): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.587-2813C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228154 | ||||||
chr19:41228190
|
T | C | 1 | a0001c0001t0004g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587-2777T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228190 | ||||||
chr19:41228585
|
C | G | 107 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(104): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.587-2382C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228585 | ||||||
chr19:41228586
|
G | A | 3 | a0001c0001t0005g0175a0001c0001t0005g0249a0001c0001t0007g0125 | 3 | HG02735.hp1 HG02738.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.587-2381G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228586 | ||||||
chr19:41228632
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.587-2335G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228632 | ||||||
chr19:41228655
|
T | C | 177 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(174): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-2312T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228655 | ||||||
chr19:41228675
|
C | T | 3 | a0001c0001t0013g0140a0001c0001t0025g0171a0001c0001t0031g0155 | 3 | HG02257.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.587-2292C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228675 | ||||||
chr19:41228761
|
C | T | 146 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(143): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.587-2206C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228761 | ||||||
chr19:41228940
|
G | T | 175 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(172): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.587-2027G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228940 | ||||||
chr19:41228947
|
CT | C | 8 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0100others(5): Show | 8 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-2016delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228947 | |||||
chr19:41228953
|
TTTC | T | 8 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0100others(5): Show | 8 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-2011_587-2009d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228953 | |||||
chr19:41228956
|
C | CT | 118 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(115): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.587-2001dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228956 | |||||
chr19:41228956
|
C | CTT | 43 | a0001c0001t0003g0280a0001c0001t0004g0265a0001c0001t0005g0178others(40): Show | 43 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.587-2002_587-2001d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228956 | |||||
chr19:41229010
|
C | T | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.587-1957C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229010 | ||||||
chr19:41229053
|
T | G | 177 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(174): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-1914T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229053 | ||||||
chr19:41229210
|
T | C | 177 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(174): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-1757T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229210 | ||||||
chr19:41229239
|
G | A | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-1728G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229239 | ||||||
chr19:41229305
|
C | T | 1 | a0001c0001t0007g0093 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.587-1662C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229305 | ||||||
chr19:41229347
|
T | C | 1 | a0001c0001t0005g0254 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-1620T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229347 | ||||||
chr19:41229412
|
G | T | 1 | a0001c0001t0004g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.587-1555G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229412 | ||||||
chr19:41229466
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.587-1501C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229466 | ||||||
chr19:41229531
|
C | T | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1436C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229531 | ||||||
chr19:41229553
|
C | G | 8 | a0001c0001t0006g0160a0001c0001t0011g0210a0001c0001t0011g0217others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-1414C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229553 | ||||||
chr19:41229751
|
A | T | 11 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(8): Show | 12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-1216A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229751 | ||||||
chr19:41229769
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.587-1198C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229769 | ||||||
chr19:41229887
|
G | A | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-1080G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229887 | ||||||
chr19:41229937
|
A | G | 6 | a0001c0001t0009g0141a0001c0001t0009g0142a0001c0001t0009g0143others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1030A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229937 | ||||||
chr19:41229983
|
G | A | 1 | a0001c0001t0020g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.587-984G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229983 | ||||||
chr19:41230100
|
G | C | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.587-867G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230100 | ||||||
chr19:41230114
|
TGTGTGTG others(7): Show |
T | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-845_587-832del others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230114 | |||||
chr19:41230136
|
T | G | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-831T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230136 | ||||||
chr19:41230137
|
G | C | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-830G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230137 | ||||||
chr19:41230142
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.587-825G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230142 | ||||||
chr19:41230145
|
G | C | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-822G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230145 | ||||||
chr19:41230147
|
G | GTCTGTTT others(3): Show |
1 | a0001c0001t0013g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.587-813_587-812ins others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230147 | |||||
chr19:41230149
|
C | CTGTT | 134 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(131): Show | 145 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.587-816_587-813dup others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230149 | |||||
chr19:41230149
|
C | T | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-818C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230149 | ||||||
chr19:41230153
|
TTC | T | 6 | a0001c0001t0011g0210a0001c0001t0011g0217a0001c0001t0025g0230others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-812_587-811del others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230153 | |||||
chr19:41230159
|
G | T | 6 | a0001c0001t0011g0210a0001c0001t0011g0217a0001c0001t0025g0230others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-808G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230159 | ||||||
chr19:41230257
|
A | C | 1 | a0001c0001t0003g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.587-710A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230257 | ||||||
chr19:41230264
|
G | A | 13 | a0001c0001t0004g0134a0001c0001t0004g0139a0001c0001t0004g0152others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.587-703G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230264 | ||||||
chr19:41230321
|
A | ATG | 14 | a0001c0001t0004g0134a0001c0001t0004g0139a0001c0001t0004g0152others(11): Show | 14 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.587-630_587-629dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230321 | |||||
chr19:41230485
|
T | G | 15 | a0001c0001t0004g0134a0001c0001t0004g0139a0001c0001t0004g0152others(12): Show | 15 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-482T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230485 | ||||||
chr19:41230517
|
T | C | 48 | a0001c0001t0003g0280a0001c0001t0004g0134a0001c0001t0004g0139others(45): Show | 48 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.587-450T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230517 | ||||||
chr19:41230548
|
G | C | 48 | a0001c0001t0003g0280a0001c0001t0004g0134a0001c0001t0004g0139others(45): Show | 48 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.587-419G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230548 | ||||||
chr19:41230592
|
G | T | 1 | a0001c0001t0010g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.587-375G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230592 | ||||||
chr19:41230756
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0002g0151a0001c0001t0002g0240others(15): Show | 22 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.587-211G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230756 | ||||||
chr19:41230828
|
A | C | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.587-139A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230828 | ||||||
chr19:41230911
|
C | T | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-56C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230911 | ||||||
chr19:41230930
|
C | T | 3 | a0001c0001t0024g0005a0001c0001t0031g0005a0001c0001t0053g0005 | 3 | HG01109.hp2 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.587-37C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230930 | ||||||
chr19:41231101
|
G | C | 1 | a0001c0001t0055g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.667+54G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231101 | ||||||
chr19:41231103
|
G | T | 1 | a0001c0001t0010g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.667+56G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231103 | ||||||
chr19:41231112
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+65G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231112 | ||||||
chr19:41231112
|
G | T | 1 | a0001c0001t0015g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.667+65G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231112 | ||||||
chr19:41231424
|
G | T | 39 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(36): Show | 40 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.783+126G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231424 | ||||||
chr19:41231439
|
C | T | 10 | a0001c0001t0001g0099a0001c0001t0010g0012a0001c0001t0010g0122others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+141C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231439 | ||||||
chr19:41231505
|
C | T | 10 | a0001c0001t0001g0099a0001c0001t0010g0012a0001c0001t0010g0122others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+207C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231505 | ||||||
chr19:41231509
|
G | A | 3 | a0001c0001t0007g0075a0001c0001t0007g0126a0001c0001t0045g0074 | 3 | HG00733.hp1 HG01175.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.783+211G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231509 | ||||||
chr19:41231538
|
T | C | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.783+240T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231538 | ||||||
chr19:41231583
|
G | T | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+285G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231583 | ||||||
chr19:41231584
|
T | G | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+286T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231584 | ||||||
chr19:41231585
|
G | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+287G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231585 | ||||||
chr19:41231616
|
A | T | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+318A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231616 | ||||||
chr19:41231620
|
C | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+322C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231620 | ||||||
chr19:41231625
|
G | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+327G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231625 | ||||||
chr19:41231639
|
A | C | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+341A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231639 | ||||||
chr19:41231653
|
G | A | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.783+355G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231653 | ||||||
chr19:41231655
|
G | A | 1 | a0001c0001t0049g0190 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.783+357G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231655 | ||||||
chr19:41231798
|
G | A | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+500G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231798 | ||||||
chr19:41231859
|
G | A | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.783+561G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231859 | ||||||
chr19:41231918
|
C | A | 1 | a0002c0010t0005g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.783+620C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231918 | ||||||
chr19:41231926
|
CA | C | 145 | a0001c0001t0001g0016a0001c0001t0001g0131a0001c0001t0001g0132others(142): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.783+640delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231926 | |||||
chr19:41231939
|
G | A | 3 | a0001c0001t0004g0139a0001c0001t0004g0212a0001c0001t0004g0213 | 3 | HG02572.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.783+641G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231939 | ||||||
chr19:41231940
|
A | C | 3 | a0001c0001t0004g0139a0001c0001t0004g0212a0001c0001t0004g0213 | 3 | HG02572.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.783+642A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231940 | ||||||
chr19:41231943
|
C | CA | 9 | a0001c0001t0014g0064a0001c0001t0018g0115a0001c0001t0018g0116others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.783+647dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231943 | |||||
chr19:41231945
|
A | AAC | 21 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0006g0128others(18): Show | 22 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.783+647_783+648ins others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231945 | ||||||
chr19:41231945
|
AC | A | 3 | a0001c0001t0003g0052a0001c0001t0014g0065a0001c0001t0015g0174 | 3 | HG01515.hp2 HG02738.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.783+648delC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231945 | ||||||
chr19:41231946
|
C | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(91): Show | 105 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.783+648C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231946 | ||||||
chr19:41231947
|
A | C | 7 | a0001c0001t0002g0244a0001c0001t0032g0163a0001c0001t0032g0164others(4): Show | 8 | HG02145.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+649A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231947 | ||||||
chr19:41231948
|
A | C | 4 | a0001c0001t0004g0162a0001c0001t0008g0004a0001c0001t0008g0007others(1): Show | 7 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+650A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231948 | ||||||
chr19:41231949
|
C | A | 95 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(92): Show | 106 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.783+651C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231949 | ||||||
chr19:41231949
|
C | CAA | 33 | a0001c0001t0003g0280a0001c0001t0009g0030a0001c0001t0009g0225others(30): Show | 33 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.783+658_783+659dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231949 | |||||
chr19:41231949
|
C | CAAA | 34 | a0001c0001t0004g0014a0001c0001t0004g0152a0001c0001t0004g0153others(31): Show | 35 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.783+657_783+659dup others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231949 | |||||
chr19:41231951
|
A | C | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+653A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231951 | ||||||
chr19:41232091
|
A | G | 178 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(175): Show | 190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.783+793A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232091 | ||||||
chr19:41232307
|
C | T | 72 | a0001c0001t0003g0280a0001c0001t0004g0014a0001c0001t0004g0134others(69): Show | 73 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.783+1009C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232307 | ||||||
chr19:41232547
|
C | T | 6 | a0001c0001t0009g0141a0001c0001t0009g0142a0001c0001t0009g0143others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+1249C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232547 | ||||||
chr19:41232619
|
G | A | 1 | a0001c0001t0012g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.783+1321G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232619 | ||||||
chr19:41232628
|
A | G | 177 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(174): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.783+1330A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232628 | ||||||
chr19:41232811
|
C | T | 72 | a0001c0001t0003g0280a0001c0001t0004g0014a0001c0001t0004g0134others(69): Show | 73 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.783+1513C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232811 | ||||||
chr19:41232948
|
C | T | 2 | a0001c0001t0015g0166a0001c0011t0011g0260 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.783+1650C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232948 | ||||||
chr19:41233149
|
C | T | 11 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(8): Show | 12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.783+1851C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233149 | ||||||
chr19:41233162
|
G | A | 1 | a0001c0001t0027g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.783+1864G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233162 | ||||||
chr19:41233164
|
A | G | 1 | a0001c0001t0027g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.783+1866A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233164 | ||||||
chr19:41233275
|
G | C | 104 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(101): Show | 115 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.783+1977G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233275 | ||||||
chr19:41233278
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.783+1980C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233278 | ||||||
chr19:41233281
|
C | T | 1 | a0001c0001t0005g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.783+1983C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233281 | ||||||
chr19:41233349
|
T | C | 177 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(174): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.783+2051T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233349 | ||||||
chr19:41233492
|
G | A | 3 | a0001c0001t0032g0163a0001c0001t0032g0164a0001c0001t0032g0288 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.783+2194G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233492 | ||||||
chr19:41233629
|
G | C | 94 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(91): Show | 104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.783+2331G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233629 | ||||||
chr19:41233669
|
C | T | 6 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0007g0075others(3): Show | 6 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+2371C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233669 | ||||||
chr19:41233706
|
C | T | 1 | a0001c0001t0031g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.783+2408C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233706 | ||||||
chr19:41233929
|
A | C | 38 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(35): Show | 39 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.783+2631A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233929 | ||||||
chr19:41234015
|
C | T | 1 | a0001c0001t0009g0225 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.783+2717C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234015 | ||||||
chr19:41234097
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.783+2799C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234097 | ||||||
chr19:41234459
|
A | T | 1 | a0001c0001t0007g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.783+3161A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234459 | ||||||
chr19:41234686
|
T | G | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | NA18986.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.784-3258T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234686 | ||||||
chr19:41234734
|
A | G | 29 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0006g0128others(26): Show | 30 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.784-3210A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234734 | ||||||
chr19:41234930
|
G | T | 1 | a0001c0001t0017g0103 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784-3014G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234930 | ||||||
chr19:41234973
|
G | A | 2 | a0001c0001t0011g0270a0001c0001t0028g0202 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.784-2971G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234973 | ||||||
chr19:41234990
|
T | C | 178 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(175): Show | 190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.784-2954T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234990 | ||||||
chr19:41235113
|
G | A | 1 | a0001c0001t0038g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.784-2831G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235113 | ||||||
chr19:41235207
|
C | T | 32 | a0001c0001t0003g0280a0001c0001t0009g0030a0001c0001t0010g0094others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-2737C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235207 | ||||||
chr19:41235351
|
CAAAT | C | 3 | a0001c0001t0009g0141a0001c0001t0009g0142a0001c0001t0009g0285 | 3 | HG01891.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.784-2575_784-2572d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235351 | |||||
chr19:41235369
|
A | AATAG | 31 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0060others(28): Show | 32 | HG01109.hp1 HG01123.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-2535_784-2532d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0009g0143 | 2 | HG03195.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.784-2575A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235369 | ||||||
chr19:41235369
|
AATAG | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0129a0001c0001t0005g0088others(24): Show | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.784-2535_784-2532d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
AATAGATA others(1): Show |
A | 5 | a0001c0001t0006g0188a0001c0001t0016g0041a0001c0001t0025g0167others(2): Show | 5 | HG01928.hp2 HG01952.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2539_784-2532d others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
AATAGATA others(5): Show |
A | 5 | a0001c0001t0012g0157a0001c0001t0056g0229a0001c0003t0009g0006others(2): Show | 6 | HG01496.hp1 HG02145.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-2543_784-2532d others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
AATAGATA others(9): Show |
A | 15 | a0001c0001t0004g0162a0001c0001t0006g0160a0001c0001t0008g0004others(12): Show | 18 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.784-2547_784-2532d others(18): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
AATAGATA others(13): Show |
A | 100 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0003g0280others(97): Show | 102 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.784-2551_784-2532d others(22): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235369
|
AATAGATA others(17): Show |
A | 61 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(58): Show | 67 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-2555_784-2532d others(26): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | |||||
chr19:41235385
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2559G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235385 | ||||||
chr19:41235389
|
G | A | 14 | a0001c0001t0004g0162a0001c0001t0006g0160a0001c0001t0008g0004others(11): Show | 17 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-2555G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235389 | ||||||
chr19:41235393
|
G | A | 101 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0003g0280others(98): Show | 103 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.784-2551G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235393 | ||||||
chr19:41235397
|
G | A | 61 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(58): Show | 67 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-2547G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235397 | ||||||
chr19:41235435
|
A | G | 1 | a0001c0001t0014g0049 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.784-2509A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235435 | ||||||
chr19:41235461
|
A | G | 1 | a0001c0001t0004g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.784-2483A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235461 | ||||||
chr19:41235466
|
G | A | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-2478G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235466 | ||||||
chr19:41235635
|
T | C | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2309T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235635 | ||||||
chr19:41235652
|
G | A | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.784-2292G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235652 | ||||||
chr19:41235899
|
A | T | 9 | a0001c0001t0001g0058a0001c0001t0001g0083a0001c0001t0001g0150others(6): Show | 9 | HG02056.hp1 HG02698.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2045A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235899 | ||||||
chr19:41235963
|
G | A | 2 | a0001c0001t0010g0123a0001c0001t0024g0137 | 2 | HG02559.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.784-1981G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235963 | ||||||
chr19:41236052
|
C | T | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1892C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236052 | ||||||
chr19:41236067
|
A | G | 2 | a0001c0001t0009g0030a0001c0001t0023g0028 | 2 | HG01071.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.784-1877A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236067 | ||||||
chr19:41236204
|
A | C | 1 | a0001c0001t0003g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.784-1740A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236204 | ||||||
chr19:41236206
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-1738G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236206 | ||||||
chr19:41236238
|
CAGA | C | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1701_784-1699d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236238 | |||||
chr19:41236331
|
T | TA | 75 | a0001c0001t0001g0083a0001c0001t0003g0072a0001c0001t0003g0280others(72): Show | 76 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.784-1592dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | |||||
chr19:41236331
|
T | TAA | 61 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(58): Show | 68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.784-1593_784-1592d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | |||||
chr19:41236331
|
T | TAAA | 7 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0185others(4): Show | 7 | HG02055.hp1 HG02056.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-1594_784-1592d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | |||||
chr19:41236331
|
TA | T | 7 | a0001c0001t0001g0131a0001c0001t0004g0162a0001c0001t0008g0004others(4): Show | 10 | HG01070.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.784-1592delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | |||||
chr19:41236386
|
C | T | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-1558C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236386 | ||||||
chr19:41236403
|
G | A | 62 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(59): Show | 68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.784-1541G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236403 | ||||||
chr19:41236498
|
A | G | 1 | a0001c0001t0020g0203 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784-1446A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236498 | ||||||
chr19:41236627
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1317G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236627 | ||||||
chr19:41236685
|
A | G | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1259A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236685 | ||||||
chr19:41236786
|
GA | G | 144 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(141): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.784-1143delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236786 | |||||
chr19:41236786
|
GAA | G | 24 | a0001c0001t0001g0099a0001c0001t0003g0072a0001c0001t0004g0162others(21): Show | 28 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.784-1144_784-1143d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236786 | |||||
chr19:41236871
|
G | A | 1 | a0001c0001t0046g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-1073G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236871 | ||||||
chr19:41236880
|
G | T | 1 | a0001c0001t0028g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.784-1064G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236880 | ||||||
chr19:41237024
|
G | A | 46 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(43): Show | 48 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.784-920G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237024 | ||||||
chr19:41237093
|
C | T | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-851C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237093 | ||||||
chr19:41237112
|
G | C | 2 | a0001c0001t0004g0134a0001c0001t0004g0152 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784-832G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237112 | ||||||
chr19:41237115
|
C | A | 1 | a0001c0001t0012g0198 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.784-829C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237115 | ||||||
chr19:41237239
|
A | G | 1 | a0005c0012t0007g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.784-705A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237239 | ||||||
chr19:41237344
|
G | A | 41 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(38): Show | 42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.784-600G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237344 | ||||||
chr19:41237387
|
C | T | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-557C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237387 | ||||||
chr19:41237477
|
C | T | 2 | a0001c0001t0004g0139a0001c0001t0004g0213 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.784-467C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237477 | ||||||
chr19:41237549
|
C | A | 50 | a0001c0001t0001g0099a0001c0001t0003g0280a0001c0001t0006g0128others(47): Show | 51 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.784-395C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237549 | ||||||
chr19:41237549
|
C | T | 2 | a0001c0001t0015g0166a0001c0011t0011g0260 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.784-395C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237549 | ||||||
chr19:41237601
|
C | G | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-343C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237601 | ||||||
chr19:41237671
|
C | T | 4 | a0001c0001t0004g0162a0001c0001t0008g0004a0001c0001t0008g0007others(1): Show | 7 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-273C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237671 | ||||||
chr19:41238178
|
C | T | 1 | a0007c0009t0033g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.994+24C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238178 | ||||||
chr19:41238196
|
G | A | 1 | a0001c0001t0008g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.994+42G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238196 | ||||||
chr19:41238196
|
G | T | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+42G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238196 | ||||||
chr19:41238324
|
T | C | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.995-146T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238324 | ||||||
chr19:41238450
|
C | A | 3 | a0001c0001t0013g0140a0001c0001t0025g0171a0001c0001t0031g0155 | 3 | HG02257.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.995-20C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238450 | ||||||
chr19:41238926
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(63): Show | 75 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1135-238C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 8/19 | chr19 | 41238926 | ||||||
chr19:41239104
|
G | A | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135-60G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 8/19 | chr19 | 41239104 | ||||||
chr19:41239376
|
C | G | 4 | a0001c0001t0006g0160a0001c0003t0009g0006a0001c0003t0009g0018others(1): Show | 5 | HG02145.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285+62C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239376 | ||||||
chr19:41239468
|
C | CCCTCACT others(18): Show |
1 | a0001c0001t0004g0265 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1285+164_1285+188d others(27): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr19 | 41239468 | |||||
chr19:41239509
|
C | T | 67 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(64): Show | 76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1286-185C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239509 | ||||||
chr19:41239535
|
G | A | 45 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(42): Show | 47 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1286-159G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239535 | ||||||
chr19:41239570
|
TTCACTCC others(18): Show |
T | 40 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(37): Show | 41 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1286-111_1286-87de others(26): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr19 | 41239570 | |||||
chr19:41239634
|
C | T | 1 | a0001c0001t0030g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1286-60C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239634 | ||||||
chr19:41239635
|
G | A | 4 | a0001c0001t0006g0160a0001c0003t0009g0006a0001c0003t0009g0018others(1): Show | 5 | HG02145.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286-59G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239635 | ||||||
chr19:41239806
|
C | A | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1312+86C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239806 | ||||||
chr19:41239934
|
A | G | 1 | a0001c0001t0006g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1312+214A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239934 | ||||||
chr19:41239981
|
G | C | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312+261G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239981 | ||||||
chr19:41239999
|
C | G | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+279C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239999 | ||||||
chr19:41240025
|
C | T | 41 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(38): Show | 42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1312+305C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240025 | ||||||
chr19:41240073
|
A | C | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312+353A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240073 | ||||||
chr19:41240086
|
G | C | 1 | a0001c0001t0015g0286 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1312+366G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240086 | ||||||
chr19:41240095
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1312+375A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240095 | ||||||
chr19:41240376
|
G | GTGGA | 145 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(142): Show | 157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1312+679_1312+682d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41240376 | |||||
chr19:41240630
|
C | T | 64 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(61): Show | 70 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1312+910C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240630 | ||||||
chr19:41240655
|
A | G | 3 | a0001c0001t0002g0220a0001c0001t0025g0173a0001c0001t0054g0159 | 3 | HG01123.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1312+935A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240655 | ||||||
chr19:41240952
|
A | G | 1 | a0001c0001t0002g0243 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1312+1232A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240952 | ||||||
chr19:41241414
|
C | T | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-1469C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241414 | ||||||
chr19:41241433
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-1450G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241433 | ||||||
chr19:41241543
|
C | CA | 76 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0132others(73): Show | 85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1313-1324dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41241543 | |||||
chr19:41241543
|
CA | C | 6 | a0001c0001t0005g0275a0001c0001t0047g0277a0001c0003t0009g0006others(3): Show | 7 | HG01884.hp1 HG02145.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-1324delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41241543 | |||||
chr19:41241576
|
A | G | 1 | a0001c0001t0007g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1313-1307A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241576 | ||||||
chr19:41241922
|
C | T | 41 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(38): Show | 42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1313-961C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241922 | ||||||
chr19:41241990
|
AT | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-892delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241990 | ||||||
chr19:41242103
|
C | A | 1 | a0001c0001t0004g0236 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1313-780C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242103 | ||||||
chr19:41242186
|
T | C | 42 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(39): Show | 46 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.1313-697T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242186 | ||||||
chr19:41242248
|
A | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(111): Show | 125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1313-635A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242248 | ||||||
chr19:41242282
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1313-601G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242282 | ||||||
chr19:41242315
|
C | CT | 10 | a0001c0001t0001g0056a0001c0001t0001g0083a0001c0001t0001g0105others(7): Show | 10 | HG01071.hp2 HG01934.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-542dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242315
|
CT | C | 48 | a0001c0001t0001g0079a0001c0001t0002g0220a0001c0001t0004g0134others(45): Show | 48 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1313-542delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242315
|
CTT | C | 24 | a0001c0001t0001g0099a0001c0001t0004g0139a0001c0001t0004g0162others(21): Show | 28 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1313-543_1313-542d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242315
|
CTTT | C | 8 | a0001c0001t0003g0025a0001c0001t0004g0265a0001c0001t0006g0160others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-544_1313-542d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242315
|
CTTTT | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(76): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1313-545_1313-542d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242315
|
CTTTTT | C | 8 | a0001c0001t0002g0149a0001c0001t0002g0228a0001c0001t0003g0072others(5): Show | 9 | HG01169.hp2 HG02145.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1313-546_1313-542d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | |||||
chr19:41242392
|
C | T | 1 | a0001c0001t0011g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1313-491C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242392 | ||||||
chr19:41242479
|
C | A | 1 | a0001c0001t0011g0221 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1313-404C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242479 | ||||||
chr19:41242498
|
A | G | 1 | a0001c0001t0004g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1313-385A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242498 | ||||||
chr19:41242848
|
T | C | 149 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(146): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1313-35T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242848 | ||||||
chr19:41243140
|
C | T | 4 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019others(1): Show | 5 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1445+125C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243140 | ||||||
chr19:41243143
|
G | T | 44 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(41): Show | 48 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1445+128G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243143 | ||||||
chr19:41243422
|
A | G | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1446-194A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243422 | ||||||
chr19:41243607
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1446-9C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243607 | ||||||
chr19:41243941
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0019g0108 | 2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+234C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41243941 | ||||||
chr19:41244398
|
C | T | 1 | a0001c0001t0012g0198 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1537+691C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244398 | ||||||
chr19:41244451
|
A | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1537+744A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244451 | ||||||
chr19:41244492
|
T | G | 5 | a0001c0001t0034g0034a0001c0001t0036g0215a0001c0001t0036g0216others(2): Show | 5 | HG00642.hp2 HG00738.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1537+785T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244492 | ||||||
chr19:41244582
|
T | C | 5 | a0001c0001t0006g0128a0001c0003t0009g0006a0001c0003t0009g0018others(2): Show | 6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537+875T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244582 | ||||||
chr19:41244596
|
C | T | 1 | a0001c0001t0010g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1537+889C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244596 | ||||||
chr19:41244645
|
A | G | 12 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0100others(9): Show | 12 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537+938A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244645 | ||||||
chr19:41244790
|
C | T | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1537+1083C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244790 | ||||||
chr19:41244852
|
A | G | 1 | a0001c0001t0027g0205 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1537+1145A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244852 | ||||||
chr19:41244934
|
AT | A | 125 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(122): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1537+1243delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41244934 | |||||
chr19:41245007
|
T | C | 20 | a0001c0001t0004g0014a0001c0001t0004g0169a0001c0001t0004g0235others(17): Show | 21 | HG00423.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1537+1300T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245007 | ||||||
chr19:41245275
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+1568G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245275 | ||||||
chr19:41245339
|
C | A | 1 | a0001c0003t0009g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1537+1632C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245339 | ||||||
chr19:41245450
|
G | A | 1 | a0001c0001t0031g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1537+1743G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245450 | ||||||
chr19:41245504
|
C | T | 10 | a0001c0001t0011g0210a0001c0001t0011g0217a0001c0001t0018g0115others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537+1797C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245504 | ||||||
chr19:41245534
|
C | G | 1 | a0001c0001t0023g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1537+1827C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245534 | ||||||
chr19:41245615
|
G | A | 12 | a0001c0001t0014g0064a0001c0001t0014g0065a0001c0001t0014g0100others(9): Show | 12 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537+1908G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245615 | ||||||
chr19:41245639
|
G | A | 5 | a0001c0001t0006g0128a0001c0003t0009g0006a0001c0003t0009g0018others(2): Show | 6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537+1932G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245639 | ||||||
chr19:41245674
|
A | C | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1537+1967A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245674 | ||||||
chr19:41245713
|
C | CA | 6 | a0001c0001t0005g0208a0001c0001t0015g0166a0001c0001t0022g0096others(3): Show | 6 | HG01192.hp2 HG04199.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537+2026dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41245713 | |||||
chr19:41245713
|
CA | C | 30 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0131others(27): Show | 31 | HG00735.hp1 HG01070.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1537+2026delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41245713 | |||||
chr19:41245793
|
T | C | 4 | a0001c0001t0011g0256a0001c0001t0011g0259a0001c0001t0028g0238others(1): Show | 4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+2086T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245793 | ||||||
chr19:41245810
|
G | C | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1537+2103G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245810 | ||||||
chr19:41245866
|
T | C | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1537+2159T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245866 | ||||||
chr19:41245876
|
G | C | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+2169G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245876 | ||||||
chr19:41246222
|
C | A | 58 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(55): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1538-2292C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246222 | ||||||
chr19:41246315
|
T | G | 1 | a0001c0001t0011g0256 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1538-2199T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246315 | ||||||
chr19:41246429
|
A | G | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1538-2085A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246429 | ||||||
chr19:41246444
|
C | CA | 34 | a0001c0001t0003g0280a0001c0001t0009g0030a0001c0001t0009g0225others(31): Show | 34 | HG00642.hp1 HG00735.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1538-2056dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41246444 | |||||
chr19:41246483
|
T | G | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1538-2031T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246483 | ||||||
chr19:41246489
|
G | GC | 124 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(121): Show | 135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1538-2023dupC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41246489 | |||||
chr19:41246540
|
T | A | 1 | a0001c0001t0056g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1538-1974T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246540 | ||||||
chr19:41246569
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1538-1945G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246569 | ||||||
chr19:41246589
|
C | T | 1 | a0001c0001t0013g0051 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1538-1925C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246589 | ||||||
chr19:41246598
|
C | T | 1 | a0001c0001t0047g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1538-1916C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246598 | ||||||
chr19:41246611
|
A | G | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1538-1903A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246611 | ||||||
chr19:41246615
|
T | C | 1 | a0001c0001t0020g0196 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1538-1899T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246615 | ||||||
chr19:41246730
|
A | C | 125 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(122): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1538-1784A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246730 | ||||||
chr19:41246826
|
T | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1688T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246826 | ||||||
chr19:41246827
|
G | T | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1687G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246827 | ||||||
chr19:41246828
|
A | T | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1686A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246828 | ||||||
chr19:41246831
|
C | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1683C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246831 | ||||||
chr19:41246833
|
C | G | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1681C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246833 | ||||||
chr19:41246834
|
T | C | 147 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0132others(144): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1680T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246834 | ||||||
chr19:41247010
|
T | TCAA | 125 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(122): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1538-1499_1538-149 others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247010 | |||||
chr19:41247036
|
T | G | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1538-1478T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247036 | ||||||
chr19:41247325
|
C | A | 4 | a0001c0001t0017g0101a0001c0001t0017g0103a0001c0001t0023g0102others(1): Show | 4 | HG02896.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-1189C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247325 | ||||||
chr19:41247358
|
A | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0222 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1538-1156A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247358 | ||||||
chr19:41247375
|
T | A | 1 | a0001c0001t0052g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1538-1139T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247375 | ||||||
chr19:41247460
|
G | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-1054G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247460 | ||||||
chr19:41247474
|
G | T | 3 | a0001c0001t0024g0005a0001c0001t0031g0005a0001c0001t0053g0005 | 3 | HG01109.hp2 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1538-1040G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247474 | ||||||
chr19:41247503
|
CA | C | 6 | a0001c0001t0001g0061a0001c0001t0003g0072a0001c0001t0004g0237others(3): Show | 6 | HG02896.hp2 NA18962.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1538-1000delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247503 | |||||
chr19:41247729
|
G | A | 59 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(56): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1538-785G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247729 | ||||||
chr19:41247773
|
C | T | 1 | a0001c0001t0046g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1538-741C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247773 | ||||||
chr19:41247794
|
A | G | 4 | a0001c0002t0009g0282a0001c0002t0023g0283a0001c0002t0023g0284others(1): Show | 4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1538-720A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247794 | ||||||
chr19:41247842
|
C | T | 1 | a0001c0001t0027g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1538-672C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247842 | ||||||
chr19:41247877
|
A | G | 123 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0002g0003others(120): Show | 134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1538-637A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247877 | ||||||
chr19:41247879
|
C | T | 1 | a0001c0001t0010g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1538-635C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247879 | ||||||
chr19:41247895
|
T | TTTTTA | 7 | a0001c0001t0017g0037a0001c0001t0017g0101a0001c0001t0018g0038others(4): Show | 7 | HG01109.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-579_1538-575d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | |||||
chr19:41247895
|
TTTTTA | T | 84 | a0001c0001t0001g0099a0001c0001t0002g0194a0001c0001t0003g0045others(81): Show | 89 | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1538-579_1538-575d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | |||||
chr19:41247895
|
TTTTTATT others(3): Show |
T | 64 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0129others(61): Show | 71 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1538-584_1538-575d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | |||||
chr19:41247945
|
C | T | 5 | a0001c0001t0006g0128a0001c0003t0009g0006a0001c0003t0009g0018others(2): Show | 6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1538-569C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247945 | ||||||
chr19:41248204
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0150a0001c0001t0005g0254 | 3 | HG02056.hp1 NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1538-310G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248204 | ||||||
chr19:41248285
|
C | T | 1 | a0001c0001t0005g0224 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1538-229C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248285 | ||||||
chr19:41248312
|
G | T | 119 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(116): Show | 130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1538-202G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248312 | ||||||
chr19:41248321
|
T | C | 2 | a0001c0001t0018g0115a0001c0001t0019g0114 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1538-193T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248321 | ||||||
chr19:41248632
|
C | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0222 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1633+23C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 13/19 | chr19 | 41248632 | ||||||
chr19:41248882
|
G | A | 1 | a0001c0001t0014g0049 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1711+62G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41248882 | ||||||
chr19:41249272
|
C | G | 1 | a0001c0001t0006g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1711+452C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249272 | ||||||
chr19:41249333
|
T | G | 57 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(54): Show | 63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1711+513T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249333 | ||||||
chr19:41249353
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1711+533A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249353 | ||||||
chr19:41249383
|
C | T | 4 | a0001c0002t0009g0282a0001c0002t0023g0283a0001c0002t0023g0284others(1): Show | 4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1711+563C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249383 | ||||||
chr19:41249452
|
C | T | 40 | a0001c0001t0001g0016a0001c0001t0002g0136a0001c0001t0002g0144others(37): Show | 44 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1711+632C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249452 | ||||||
chr19:41249481
|
C | T | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711+661C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249481 | ||||||
chr19:41249482
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1711+662G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249482 | ||||||
chr19:41249485
|
G | A | 15 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(12): Show | 15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1711+665G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249485 | ||||||
chr19:41249520
|
C | A | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711+700C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249520 | ||||||
chr19:41249523
|
A | G | 1 | a0001c0001t0037g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1711+703A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249523 | ||||||
chr19:41249587
|
C | G | 5 | a0001c0001t0006g0128a0001c0003t0009g0006a0001c0003t0009g0018others(2): Show | 6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1711+767C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249587 | ||||||
chr19:41249705
|
G | A | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1711+885G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249705 | ||||||
chr19:41249710
|
C | T | 1 | a0008c0014t0001g0138 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1711+890C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249710 | ||||||
chr19:41249892
|
G | A | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1711+1072G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249892 | ||||||
chr19:41249933
|
G | A | 3 | a0001c0001t0032g0163a0001c0001t0032g0164a0001c0001t0032g0288 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1711+1113G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249933 | ||||||
chr19:41250044
|
C | T | 8 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0005g0204others(5): Show | 8 | HG00280.hp1 HG01099.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711+1224C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250044 | ||||||
chr19:41250099
|
A | G | 1 | a0001c0001t0006g0165 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1711+1279A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250099 | ||||||
chr19:41250133
|
T | G | 117 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(114): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1711+1313T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250133 | ||||||
chr19:41250180
|
T | C | 15 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(12): Show | 15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1711+1360T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250180 | ||||||
chr19:41250183
|
A | G | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1711+1363A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250183 | ||||||
chr19:41250382
|
A | ACCCACTC others(32): Show |
1 | a0001c0001t0010g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1711+1563_1711+160 others(43): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41250382 | |||||
chr19:41250598
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(53): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-1753A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250598 | ||||||
chr19:41250658
|
G | T | 15 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(12): Show | 15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-1693G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250658 | ||||||
chr19:41250836
|
T | C | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-1515T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250836 | ||||||
chr19:41250886
|
G | T | 1 | a0001c0001t0052g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1712-1465G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250886 | ||||||
chr19:41251001
|
G | T | 15 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(12): Show | 15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-1350G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251001 | ||||||
chr19:41251151
|
A | T | 1 | a0001c0001t0020g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1712-1200A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251151 | ||||||
chr19:41251354
|
G | C | 1 | a0001c0001t0015g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1712-997G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251354 | ||||||
chr19:41251418
|
T | G | 2 | a0001c0001t0001g0067a0001c0001t0005g0180 | 2 | NA18990.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1712-933T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251418 | ||||||
chr19:41251470
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02040.hp2 HG02129.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.1712-881G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251470 | ||||||
chr19:41251519
|
G | A | 15 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146others(12): Show | 15 | HG00597.hp1 HG00621.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-832G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251519 | ||||||
chr19:41251539
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(53): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-812G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251539 | ||||||
chr19:41251562
|
C | CA | 7 | a0001c0001t0006g0183a0001c0001t0026g0245a0001c0001t0026g0248others(4): Show | 7 | HG02155.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1712-773dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41251562 | |||||
chr19:41251698
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(53): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-653C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251698 | ||||||
chr19:41251746
|
A | G | 1 | a0001c0001t0008g0040 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1712-605A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251746 | ||||||
chr19:41251802
|
A | G | 11 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(8): Show | 11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1712-549A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251802 | ||||||
chr19:41251938
|
C | A | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-413C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251938 | ||||||
chr19:41252045
|
G | A | 1 | a0007c0009t0033g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1712-306G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252045 | ||||||
chr19:41252111
|
TA | T | 50 | a0001c0001t0001g0086a0001c0001t0004g0014a0001c0001t0004g0134others(47): Show | 54 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1712-223delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252111 | |||||
chr19:41252111
|
TAA | T | 6 | a0001c0001t0004g0213a0001c0001t0008g0040a0001c0002t0009g0282others(3): Show | 6 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1712-224_1712-223d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252111 | |||||
chr19:41252128
|
A | T | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1712-223A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252128 | ||||||
chr19:41252139
|
ATT | A | 19 | a0001c0001t0006g0160a0001c0001t0014g0048a0001c0001t0014g0049others(16): Show | 19 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1712-209_1712-208d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252139 | |||||
chr19:41252142
|
T | A | 56 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(53): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-209T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252142 | ||||||
chr19:41252144
|
A | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-207A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252144 | ||||||
chr19:41252256
|
GTGA | G | 4 | a0001c0001t0006g0160a0001c0001t0037g0031a0001c0001t0047g0277others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1712-71_1712-69del others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252256 | |||||
chr19:41252975
|
G | C | 6 | a0001c0001t0009g0141a0001c0001t0009g0142a0001c0001t0009g0143others(3): Show | 6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1926+8G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41252975 | ||||||
chr19:41253186
|
G | T | 4 | a0001c0001t0011g0256a0001c0001t0011g0259a0001c0001t0028g0238others(1): Show | 4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1926+219G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253186 | ||||||
chr19:41253234
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0078 | 2 | NA18944.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1926+267G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253234 | ||||||
chr19:41253348
|
G | A | 1 | a0001c0001t0004g0265 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1927-251G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253348 | ||||||
chr19:41253505
|
C | T | 1 | a0001c0001t0006g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1927-94C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253505 | ||||||
chr19:41253569
|
C | T | 11 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(8): Show | 11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1927-30C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253569 | ||||||
chr19:41253726
|
A | AC | 96 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0035others(93): Show | 99 | HG00639.hp1 HG01099.hp1 HG01099.hp2 others(96): Show |
intron_variant | MODIFIER | c.2036+30dupC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | |||||
chr19:41253726
|
AC | A | 14 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0105others(11): Show | 14 | HG00323.hp1 HG01074.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.2036+30delC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | |||||
chr19:41253726
|
ACCC | A | 74 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(71): Show | 80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2036+28_2036+30del others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | |||||
chr19:41253732
|
C | T | 74 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(71): Show | 80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2036+24C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253732 | ||||||
chr19:41253736
|
C | A | 1 | a0001c0001t0038g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2036+28C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253736 | ||||||
chr19:41253972
|
G | T | 2 | a0001c0001t0017g0026a0001c0001t0029g0193 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2036+264G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253972 | ||||||
chr19:41254128
|
T | C | 78 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(75): Show | 85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2036+420T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254128 | ||||||
chr19:41254376
|
CA | C | 18 | a0001c0001t0006g0128a0001c0001t0012g0231a0001c0001t0014g0048others(15): Show | 19 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2036+685delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41254376 | |||||
chr19:41254390
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0037g0031others(1): Show | 4 | HG02896.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2036+682A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254390 | ||||||
chr19:41254391
|
AAAG | A | 53 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(50): Show | 59 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2036+686_2036+688d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41254391 | |||||
chr19:41254551
|
A | T | 1 | a0001c0001t0015g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2036+843A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254551 | ||||||
chr19:41254710
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2036+1002G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254710 | ||||||
chr19:41254913
|
A | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0172 | 2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2036+1205A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254913 | ||||||
chr19:41254992
|
C | A | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2036+1284C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254992 | ||||||
chr19:41255008
|
A | G | 11 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0014g0064others(8): Show | 11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2036+1300A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255008 | ||||||
chr19:41255348
|
CTTCT | C | 74 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(71): Show | 80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2037-1097_2037-109 others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41255348 | |||||
chr19:41255355
|
C | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1097C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255355 | ||||||
chr19:41255356
|
T | C | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1096T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255356 | ||||||
chr19:41255362
|
T | C | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1090T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255362 | ||||||
chr19:41255364
|
C | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1088C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255364 | ||||||
chr19:41255368
|
T | C | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1084T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255368 | ||||||
chr19:41255368
|
T | TTC | 74 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(71): Show | 80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2037-1076_2037-107 others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41255368 | |||||
chr19:41255591
|
C | T | 1 | a0001c0001t0015g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2037-861C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255591 | ||||||
chr19:41255625
|
G | C | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2037-827G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255625 | ||||||
chr19:41255745
|
T | G | 2 | a0001c0001t0037g0031a0001c0001t0047g0277 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2037-707T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255745 | ||||||
chr19:41255804
|
G | A | 4 | a0001c0001t0011g0256a0001c0001t0011g0259a0001c0001t0028g0238others(1): Show | 4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2037-648G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255804 | ||||||
chr19:41255849
|
A | T | 1 | a0001c0001t0034g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2037-603A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255849 | ||||||
chr19:41255964
|
C | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-488C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255964 | ||||||
chr19:41256080
|
G | GGTGT | 55 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(52): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2037-354_2037-351d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | |||||
chr19:41256080
|
G | GGTGTGT | 4 | a0001c0001t0014g0048a0001c0001t0014g0049a0001c0001t0037g0031others(1): Show | 4 | HG00642.hp1 HG01123.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2037-356_2037-351d others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | |||||
chr19:41256080
|
G | GGTGTGTG others(1): Show |
5 | a0001c0001t0006g0128a0001c0001t0047g0277a0001c0003t0009g0006others(2): Show | 6 | HG02145.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037-358_2037-351d others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | |||||
chr19:41256080
|
G | GGTGTGTG others(3): Show |
12 | a0001c0001t0014g0064a0001c0001t0014g0100a0001c0001t0020g0195others(9): Show | 12 | HG00735.hp1 HG01346.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2037-360_2037-351d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | |||||
chr19:41256080
|
G | GGTGTGTG others(5): Show |
2 | a0001c0001t0014g0065a0001c0011t0011g0260 | 2 | HG01515.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2037-362_2037-351d others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | |||||
chr19:41256095
|
G | T | 11 | a0001c0001t0010g0012a0001c0001t0010g0122a0001c0001t0010g0123others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2037-357G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256095 | ||||||
chr19:41256137
|
C | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-315C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256137 | ||||||
chr19:41256245
|
G | A | 3 | a0001c0001t0037g0031a0001c0001t0047g0277a0001c0001t0048g0112 | 3 | HG02896.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2037-207G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256245 | ||||||
chr19:41256404
|
T | C | 1 | a0001c0001t0004g0265 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2037-48T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256404 | ||||||
chr19:41256620
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(53): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2196+9A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256620 | ||||||
chr19:41256765
|
T | C | 63 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(60): Show | 69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2196+154T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256765 | ||||||
chr19:41256794
|
TA | T | 63 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(60): Show | 69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2196+184delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256794 | ||||||
chr19:41256961
|
A | T | 36 | a0001c0001t0004g0014a0001c0001t0004g0134a0001c0001t0004g0139others(33): Show | 40 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.2196+350A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256961 | ||||||
chr19:41257023
|
T | C | 1 | a0001c0001t0006g0165 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2196+412T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257023 | ||||||
chr19:41257075
|
G | A | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2197-418G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257075 | ||||||
chr19:41257334
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2197-159G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257334 | ||||||
chr19:41257726
|
A | G | 3 | a0001c0003t0009g0006a0001c0003t0009g0018a0001c0003t0009g0019 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2333+97A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257726 | ||||||
chr19:41257886
|
A | C | 1 | a0001c0003t0009g0019 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2333+257A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257886 | ||||||
chr19:41257889
|
C | G | 1 | a0001c0001t0048g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2333+260C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257889 | ||||||
chr19:41257993
|
C | T | 3 | a0001c0001t0012g0191a0001c0001t0012g0192a0001c0001t0012g0231 | 3 | HG03017.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2333+364C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257993 | ||||||
chr19:41258068
|
C | A | 5 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0019g0114others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2333+439C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258068 | ||||||
chr19:41258099
|
G | T | 3 | a0001c0001t0014g0048a0001c0001t0014g0049a0006c0008t0014g0047 | 3 | HG00642.hp1 HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2333+470G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258099 | ||||||
chr19:41258221
|
C | T | 1 | a0001c0001t0022g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2333+592C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258221 | ||||||
chr19:41258353
|
T | C | 2 | a0001c0001t0017g0103a0001c0001t0023g0102 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2333+724T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258353 | ||||||
chr19:41258378
|
AT | A | 55 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(52): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2333+751delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 41258378 | |||||
chr19:41258519
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A | G | 4 | a0001c0001t0002g0220a0001c0001t0012g0157a0001c0001t0042g0015others(1): Show | 4 | HG01123.hp1 HG01496.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2333+890A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258519 | ||||||
chr19:41258540
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A | G | 1 | a0001c0001t0002g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2333+911A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258540 | ||||||
chr19:41258663
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G | T | 12 | a0001c0001t0006g0128a0001c0001t0014g0048a0001c0001t0014g0049others(9): Show | 12 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2334-890G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258663 | ||||||
chr19:41258823
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C | A | 2 | a0001c0001t0006g0181a0001c0001t0006g0182 | 2 | NA18997.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2334-730C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258823 | ||||||
chr19:41258840
|
G | T | 2 | a0001c0001t0032g0163a0001c0001t0032g0164 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2334-713G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258840 | ||||||
chr19:41258853
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A | G | 40 | a0001c0001t0001g0016a0001c0001t0002g0136a0001c0001t0002g0144others(37): Show | 44 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2334-700A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258853 | ||||||
chr19:41258869
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A | G | 4 | a0001c0002t0009g0282a0001c0002t0023g0283a0001c0002t0023g0284others(1): Show | 4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2334-684A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258869 | ||||||
chr19:41259241
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G | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2334-312G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259241 | ||||||
chr19:41259324
|
T | C | 68 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(65): Show | 74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2334-229T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259324 | ||||||
chr19:41259339
|
C | T | 1 | a0001c0011t0011g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2334-214C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259339 | ||||||
chr19:41259356
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C | T | 4 | a0001c0001t0010g0012a0001c0001t0014g0049a0001c0001t0022g0096others(1): Show | 5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2334-197C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259356 | ||||||
chr19:41259409
|
T | C | 1 | a0002c0004t0005g0226 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2334-144T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259409 | ||||||
chr19:41259502
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A | C | 57 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0136others(54): Show | 63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2334-51A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259502 |