geneid | 200558 |
---|---|
ensemblid | ENSG00000169621.11 |
hgncid | 28724 |
symbol | APLF |
name | aprataxin and PNKP like factor |
refseq_nuc | NM_173545.3 |
refseq_prot | NP_775816.1 |
ensembl_nuc | ENST00000303795.9 |
ensembl_prot | ENSP00000307004.4 |
mane_status | MANE Select |
chr | chr2 |
start | 68467585 |
end | 68580162 |
strand | + |
ver | v1.2 |
region | chr2:68467585-68580162 |
region5000 | chr2:68462585-68585162 |
regionname0 | APLF_chr2_68467585_68580162 |
regionname5000 | APLF_chr2_68462585_68585162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 511 | 84 | 25 | 18 | 21 | 3 | 15 | 18 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002 | 0/0 | 511 | 39 | 33 | 6 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0003 | 0/0 | 511 | 21 | 14 | 5 | 0 | 1 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0004 | 0/0 | 511 | 13 | 0 | 2 | 7 | 2 | 2 | 6 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0005 | 0/0 | 510 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006 | 0/0 | 511 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0007 | 0/0 | 511 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0008 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0009 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0010 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0011 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0012 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1536 | 83 | 25 | 18 | 20 | 3 | 15 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0002 | 0/0 | 1536 | 38 | 32 | 6 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0003 | 0/0 | 1536 | 21 | 14 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0004 | 0/0 | 1536 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0005 | 0/0 | 1533 | 5 | 0 | 3 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0006 | 0/0 | 1536 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0007 | 0/0 | 1536 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0008 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0009 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0010 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0011 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0012 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0013 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0014 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
c0015 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2288 | 90 | 29 | 20 | 19 | 3 | 17 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0002 | 0/0 | 2288 | 21 | 19 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0003 | 0/0 | 2288 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0004 | 0/0 | 2288 | 12 | 5 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0005 | 0/0 | 2288 | 9 | 9 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0006 | 0/0 | 2281 | 8 | 8 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0007 | 0/0 | 2288 | 6 | 3 | 3 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0008 | 0/0 | 2288 | 3 | 2 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0009 | 0/0 | 2288 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0010 | 0/0 | 2288 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0011 | 0/0 | 2288 | 2 | 0 | 0 | 2 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0012 | 0/0 | 2281 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0013 | 0/0 | 2288 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0014 | 0/0 | 2288 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0015 | 0/0 | 2288 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0016 | 0/0 | 2281 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
t0017 | 0/0 | 2281 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1536 | 83 | 25 | 18 | 20 | 3 | 15 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0001c0009 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002 | 0/0 | 1536 | 38 | 32 | 6 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0011 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0003c0003 | 0/0 | 1536 | 21 | 14 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0004c0004 | 0/0 | 1536 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0005c0005 | 0/0 | 1533 | 5 | 0 | 3 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006c0007 | 0/0 | 1536 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006c0013 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0007c0006 | 0/0 | 1536 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0008c0008 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0009c0010 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0010c0014 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0011c0015 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0012c0012 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3823 | 80 | 24 | 18 | 18 | 3 | 15 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0001c0001t0011 | 0/0 | 3823 | 2 | 0 | 0 | 2 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0001c0001t0015 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0001c0009t0001 | 0/0 | 3823 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0002 | 0/0 | 3823 | 20 | 18 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0006 | 0/0 | 3816 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0007 | 0/0 | 3823 | 5 | 2 | 3 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0008 | 0/0 | 3823 | 3 | 2 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0009 | 0/0 | 3823 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0010 | 0/0 | 3823 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0002t0012 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0002c0011t0002 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0003c0003t0004 | 0/0 | 3823 | 12 | 5 | 5 | 0 | 1 | 1 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0003c0003t0005 | 0/0 | 3823 | 9 | 9 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0004c0004t0003 | 0/0 | 3823 | 13 | 0 | 2 | 7 | 2 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0005c0005t0001 | 0/0 | 3820 | 4 | 0 | 2 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0005c0005t0014 | 0/0 | 3820 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006c0007t0006 | 0/0 | 3816 | 3 | 3 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006c0007t0017 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0006c0013t0016 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0007c0006t0001 | 0/0 | 3823 | 4 | 4 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0008c0008t0006 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0009c0010t0001 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0010c0014t0009 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0011c0015t0013 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
a0012c0012t0007 | 0/0 | 3823 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | copy fasta | chr2 | 68462585 | 68585162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0001t0015g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0001c0009t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0008g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0002t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0002c0011t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0003c0003t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0004c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0005c0005t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0005c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0005c0005t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0005c0005t0014g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0006c0007t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0006c0007t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0006c0007t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0006c0013t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0007c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0007c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0007c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0007c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0008c0008t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0009c0010t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0010c0014t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0011c0015t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
a0012c0012t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00639 | hp1 | a0003 | c0003 | t0004 | g0119 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00639 | hp2 | a0005 | c0005 | t0001 | g0154 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00673 | hp2 | a0001 | c0009 | t0001 | g0155 | EAS | CHS | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00738 | hp1 | a0003 | c0003 | t0004 | g0126 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01109 | hp1 | a0002 | c0002 | t0007 | g0030 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01109 | hp2 | a0005 | c0005 | t0014 | g0142 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01167 | hp1 | a0002 | c0002 | t0007 | g0001 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01167 | hp2 | a0002 | c0002 | t0008 | g0024 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01169 | hp1 | a0002 | c0002 | t0007 | g0001 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01192 | hp1 | a0003 | c0003 | t0004 | g0124 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01192 | hp2 | a0005 | c0005 | t0001 | g0149 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01261 | hp2 | a0003 | c0003 | t0004 | g0114 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01884 | hp1 | a0007 | c0006 | t0001 | g0141 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01943 | hp1 | a0003 | c0003 | t0004 | g0115 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02055 | hp1 | a0002 | c0002 | t0008 | g0023 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02055 | hp2 | a0007 | c0006 | t0001 | g0136 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02129 | hp1 | a0004 | c0004 | t0003 | g0010 | EAS | KHV | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02257 | hp1 | a0003 | c0003 | t0005 | g0130 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02280 | hp1 | a0002 | c0002 | t0006 | g0162 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02293 | hp1 | a0004 | c0004 | t0003 | g0009 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02300 | hp2 | a0004 | c0004 | t0003 | g0014 | AMR | PEL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02451 | hp2 | a0002 | c0002 | t0010 | g0169 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02572 | hp2 | a0003 | c0003 | t0005 | g0128 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02615 | hp1 | a0007 | c0006 | t0001 | g0140 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02615 | hp2 | a0003 | c0003 | t0004 | g0123 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02622 | hp1 | a0002 | c0002 | t0006 | g0161 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02622 | hp2 | a0010 | c0014 | t0009 | g0028 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02717 | hp2 | a0003 | c0003 | t0005 | g0132 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02738 | hp1 | a0004 | c0004 | t0003 | g0015 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02738 | hp2 | a0005 | c0005 | t0001 | g0153 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0003 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02897 | hp2 | a0002 | c0002 | t0009 | g0003 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02965 | hp1 | a0003 | c0003 | t0005 | g0134 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02970 | hp1 | a0003 | c0003 | t0004 | g0122 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03041 | hp2 | a0002 | c0002 | t0010 | g0167 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03098 | hp1 | a0006 | c0007 | t0006 | g0002 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0090 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03130 | hp1 | a0003 | c0003 | t0005 | g0105 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03139 | hp2 | a0003 | c0003 | t0005 | g0129 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03195 | hp1 | a0006 | c0007 | t0017 | g0022 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03209 | hp1 | a0002 | c0002 | t0007 | g0031 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03225 | hp1 | a0003 | c0003 | t0005 | g0131 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03225 | hp2 | a0002 | c0002 | t0012 | g0021 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03453 | hp2 | a0003 | c0003 | t0004 | g0151 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03486 | hp1 | a0006 | c0013 | t0016 | g0166 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03486 | hp2 | a0006 | c0007 | t0006 | g0002 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03516 | hp2 | a0002 | c0002 | t0010 | g0168 | AFR | ESN | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03540 | hp1 | a0012 | c0012 | t0007 | g0027 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03540 | hp2 | a0003 | c0003 | t0004 | g0121 | AFR | GWD | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03579 | hp1 | a0007 | c0006 | t0001 | g0139 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03834 | hp2 | a0003 | c0003 | t0004 | g0125 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03942 | hp2 | a0004 | c0004 | t0003 | g0012 | SAS | BEB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG04228 | hp2 | a0005 | c0005 | t0001 | g0144 | SAS | STU | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18522 | hp2 | a0011 | c0015 | t0013 | g0165 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18906 | hp1 | a0003 | c0003 | t0005 | g0133 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18943 | hp2 | a0004 | c0004 | t0003 | g0020 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18966 | hp1 | a0004 | c0004 | t0003 | g0016 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18971 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18978 | hp1 | a0004 | c0004 | t0003 | g0018 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA18984 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19005 | hp1 | a0004 | c0004 | t0003 | g0017 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19058 | hp1 | a0004 | c0004 | t0003 | g0013 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19079 | hp1 | a0004 | c0004 | t0003 | g0011 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19240 | hp1 | a0006 | c0007 | t0006 | g0032 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | YRI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ASW | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20129 | hp2 | a0002 | c0002 | t0008 | g0025 | AFR | ASW | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20752 | hp1 | a0004 | c0004 | t0003 | g0008 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20805 | hp1 | a0003 | c0003 | t0004 | g0104 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20805 | hp2 | a0004 | c0004 | t0003 | g0019 | EUR | TSI | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02109 | hp1 | a0002 | c0002 | t0006 | g0163 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02109 | hp2 | a0009 | c0010 | t0001 | g0111 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02486 | hp1 | a0008 | c0008 | t0006 | g0026 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03471 | hp1 | a0003 | c0003 | t0005 | g0127 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG06807 | hp1 | a0002 | c0002 | t0007 | g0029 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
HG06807 | hp2 | a0002 | c0011 | t0002 | g0040 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20300 | hp1 | a0002 | c0002 | t0006 | g0164 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
NA21309 | hp2 | a0003 | c0003 | t0004 | g0120 | AFR | LWK | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0072 | REF | REF | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | APLF_chr2_68462585_68585162 | APLF | chr2 | 68462585 | 68585162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68502860
|
A | G | 6 | a0002a0004a0006others(3): Show | 60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
missense_variant | MODERATE | c.298A>G | p.Ile100Val | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/10 | 445/3823 | 298/1536 | 100/511 | chr2 | 68502860 | ||
chr2:68513576
|
A | G | 1 | a0009 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.518A>G | p.Asn173Ser | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/10 | 665/3823 | 518/1536 | 173/511 | chr2 | 68513576 | ||
chr2:68526108
|
T | A | 7 | a0002a0003a0004others(4): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
missense_variant | MODERATE | c.670T>A | p.Ser224Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/10 | 817/3823 | 670/1536 | 224/511 | chr2 | 68526108 | ||
chr2:68538002
|
AAAG | A | 1 | a0005 | 5 | HG00639.hp2 HG01109.hp2 HG01192.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.938_940delGAA | p.Arg313del | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1085/3823 | 938/1536 | 313/511 | INFO_REALIGN_3_PRIME | chr2 | 68538002 | |
chr2:68538073
|
C | T | 2 | a0003a0006 | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
missense_variant | MODERATE | c.1006C>T | p.Leu336Phe | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1153/3823 | 1006/1536 | 336/511 | chr2 | 68538073 | ||
chr2:68545278
|
C | T | 1 | a0012 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1252C>T | p.Arg418Trp | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1399/3823 | 1252/1536 | 418/511 | chr2 | 68545278 | ||
chr2:68545302
|
T | C | 1 | a0007 | 4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.1276T>C | p.Ser426Pro | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1423/3823 | 1276/1536 | 426/511 | chr2 | 68545302 | ||
chr2:68545305
|
T | C | 1 | a0011 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1279T>C | p.Cys427Arg | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/10 | 1426/3823 | 1279/1536 | 427/511 | chr2 | 68545305 | ||
chr2:68567351
|
C | A | 1 | a0004 | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
missense_variant | MODERATE | c.1297C>A | p.Gln433Lys | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/10 | 1444/3823 | 1297/1536 | 433/511 | chr2 | 68567351 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68502799
|
A | G | 2 | a0004c0004a0011c0015 | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
synonymous_variant | LOW | c.237A>G | p.Leu79Leu | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/10 | 384/3823 | 237/1536 | 79/511 | chr2 | 68502799 | ||
chr2:68538153
|
T | C | 1 | a0006c0013 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1086T>C | p.Thr362Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/10 | 1233/3823 | 1086/1536 | 362/511 | chr2 | 68538153 | ||
chr2:68567350
|
C | T | 1 | a0002c0011 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1296C>T | p.Pro432Pro | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/10 | 1443/3823 | 1296/1536 | 432/511 | chr2 | 68567350 | ||
chr2:68577923
|
A | C | 1 | a0001c0009 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1437A>C | p.Thr479Thr | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1584/3823 | 1437/1536 | 479/511 | chr2 | 68577923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68467605
|
G | C | 1 | a0002c0002t0012 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/10 | 127 | chr2 | 68467605 | |||||
chr2:68467715
|
C | T | 1 | a0001c0001t0011 | 2 | NA18971.hp1 NA18984.hp2 |
5_prime_UTR_variant | MODIFIER | c.-17C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/10 | 17 | chr2 | 68467715 | |||||
chr2:68578612
|
G | A | 1 | a0011c0015t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 590 | chr2 | 68578612 | |||||
chr2:68578785
|
C | T | 10 | a0002c0002t0006a0002c0002t0010a0002c0002t0012others(7): Show | 36 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*763C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 763 | chr2 | 68578785 | |||||
chr2:68578970
|
A | G | 2 | a0002c0002t0002a0002c0011t0002 | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 948 | chr2 | 68578970 | |||||
chr2:68578987
|
G | A | 2 | a0002c0002t0002a0002c0011t0002 | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 965 | chr2 | 68578987 | |||||
chr2:68579085
|
C | T | 1 | a0006c0007t0017 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1063 | chr2 | 68579085 | |||||
chr2:68579304
|
T | A | 1 | a0005c0005t0014 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1282 | chr2 | 68579304 | |||||
chr2:68579411
|
A | G | 1 | a0011c0015t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1389 | chr2 | 68579411 | |||||
chr2:68579453
|
G | A | 11 | a0002c0002t0006a0002c0002t0008a0002c0002t0010others(8): Show | 39 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1431G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1431 | chr2 | 68579453 | |||||
chr2:68579540
|
A | AT | 18 | a0002c0002t0002a0002c0002t0006a0002c0002t0007others(15): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1518_*1519insT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1519 | chr2 | 68579540 | |||||
chr2:68579543
|
C | G | 2 | a0002c0002t0007a0012c0012t0007 | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1521C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1521 | chr2 | 68579543 | |||||
chr2:68579551
|
TATCAACT others(1): Show |
T | 6 | a0002c0002t0006a0002c0002t0012a0006c0007t0006others(3): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1530_*1537delATCA others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1530 | chr2 | 68579551 | |||||
chr2:68579558
|
TG | T | 12 | a0002c0002t0002a0002c0002t0007a0002c0002t0008others(9): Show | 71 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1539delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1539 | INFO_REALIGN_3_PRIME | chr2 | 68579558 | ||||
chr2:68579561
|
G | A | 1 | a0001c0001t0015 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1539 | chr2 | 68579561 | |||||
chr2:68579734
|
C | T | 1 | a0002c0002t0010 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1712C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1712 | chr2 | 68579734 | |||||
chr2:68579813
|
G | A | 1 | a0004c0004t0003 | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1791G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1791 | chr2 | 68579813 | |||||
chr2:68579951
|
T | C | 5 | a0002c0002t0006a0002c0002t0012a0006c0007t0006others(2): Show | 10 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1929T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 1929 | chr2 | 68579951 | |||||
chr2:68580092
|
C | T | 1 | a0003c0003t0004 | 12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2070C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 10/10 | 2070 | chr2 | 68580092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:68467851
|
G | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.96+24G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467851 | ||||||
chr2:68467897
|
C | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+70C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467897 | ||||||
chr2:68467908
|
C | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+81C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467908 | ||||||
chr2:68467927
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+100G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467927 | ||||||
chr2:68467954
|
T | A | 2 | a0002c0002t0012g0021a0011c0015t0013g0165 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.96+127T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467954 | ||||||
chr2:68467976
|
A | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+149A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68467976 | ||||||
chr2:68468070
|
G | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+243G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468070 | ||||||
chr2:68468159
|
T | C | 58 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(55): Show | 61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+332T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468159 | ||||||
chr2:68468321
|
C | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+494C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468321 | ||||||
chr2:68468387
|
A | G | 33 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(30): Show | 36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.96+560A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468387 | ||||||
chr2:68468438
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+611A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468438 | ||||||
chr2:68468480
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.96+653G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468480 | ||||||
chr2:68468485
|
C | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+658C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468485 | ||||||
chr2:68468512
|
T | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+685T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468512 | ||||||
chr2:68468825
|
C | T | 24 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(21): Show | 26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.96+998C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468825 | ||||||
chr2:68468969
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+1142A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468969 | ||||||
chr2:68468989
|
G | GGT | 11 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(8): Show | 12 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1193_96+1194dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
G | GGTGT | 41 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0065others(38): Show | 42 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.96+1191_96+1194dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
G | GGTGTGT | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 7 | HG01943.hp2 HG02109.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+1189_96+1194dup others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
G | GGTGTGTG others(1): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0061a0002c0002t0006g0161others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1187_96+1194dup others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
G | GTGT | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG03579.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.96+1162_96+1163ins others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468989 | ||||||
chr2:68468989
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.96+1162G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468989 | ||||||
chr2:68468989
|
GGT | G | 7 | a0001c0001t0001g0157a0002c0002t0009g0003a0002c0002t0010g0167others(4): Show | 8 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1193_96+1194del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
GGTGT | G | 7 | a0002c0002t0012g0021a0004c0004t0003g0008a0004c0004t0003g0009others(4): Show | 7 | HG02129.hp1 HG02293.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+1191_96+1194del others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468989
|
GGTGTGT | G | 9 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(6): Show | 9 | HG02300.hp2 HG02738.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1189_96+1194del others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68468989 | |||||
chr2:68468991
|
T | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02280.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1164T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68468991 | ||||||
chr2:68469014
|
G | GTGTGTGT | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1207_96+1213dup others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | |||||
chr2:68469014
|
G | GTGTGTGT others(4): Show |
1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+1194_96+1195ins others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | |||||
chr2:68469014
|
GTGTGTGT | G | 8 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(5): Show | 8 | HG01243.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1207_96+1213del others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469014 | |||||
chr2:68469016
|
GTGTGT | G | 10 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(7): Show | 10 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1195_96+1199del others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68469016 | |||||
chr2:68469091
|
G | A | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1264G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469091 | ||||||
chr2:68469145
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+1318A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469145 | ||||||
chr2:68469287
|
A | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1460A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469287 | ||||||
chr2:68469291
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.96+1464G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469291 | ||||||
chr2:68469316
|
T | A | 2 | a0002c0002t0002g0043a0002c0002t0002g0044 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.96+1489T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469316 | ||||||
chr2:68469325
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1498T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469325 | ||||||
chr2:68469516
|
T | G | 2 | a0003c0003t0004g0114a0003c0003t0004g0115 | 2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.96+1689T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469516 | ||||||
chr2:68469599
|
G | A | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1772G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469599 | ||||||
chr2:68469613
|
A | T | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+1786A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469613 | ||||||
chr2:68469816
|
A | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+1989A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469816 | ||||||
chr2:68469999
|
G | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+2172G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68469999 | ||||||
chr2:68470463
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+2636A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470463 | ||||||
chr2:68470521
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+2694G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470521 | ||||||
chr2:68470559
|
G | A | 37 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(34): Show | 40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.96+2732G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470559 | ||||||
chr2:68470571
|
C | T | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2744C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470571 | ||||||
chr2:68470623
|
A | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+2796A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470623 | ||||||
chr2:68470667
|
A | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+2840A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470667 | ||||||
chr2:68470846
|
C | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0117others(1): Show | 6 | HG01071.hp1 HG01106.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+3019C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68470846 | ||||||
chr2:68471124
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3297G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471124 | ||||||
chr2:68471144
|
C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+3317C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471144 | ||||||
chr2:68471278
|
T | TAAG | 58 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(55): Show | 61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+3451_96+3452ins others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471278 | ||||||
chr2:68471339
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+3512G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471339 | ||||||
chr2:68471396
|
G | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3569G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471396 | ||||||
chr2:68471408
|
G | A | 1 | a0004c0004t0003g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.96+3581G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471408 | ||||||
chr2:68471445
|
T | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3618T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471445 | ||||||
chr2:68471460
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3633A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471460 | ||||||
chr2:68471520
|
C | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+3693C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471520 | ||||||
chr2:68471853
|
G | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4026G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471853 | ||||||
chr2:68471886
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4059C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471886 | ||||||
chr2:68471947
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+4120A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68471947 | ||||||
chr2:68472163
|
G | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4336G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472163 | ||||||
chr2:68472291
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+4464G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472291 | ||||||
chr2:68472328
|
G | A | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.96+4501G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472328 | ||||||
chr2:68472392
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+4565C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472392 | ||||||
chr2:68472408
|
A | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+4581A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472408 | ||||||
chr2:68472518
|
A | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4691A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472518 | ||||||
chr2:68472520
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4693A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472520 | ||||||
chr2:68472809
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+4982G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68472809 | ||||||
chr2:68473073
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+5246C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473073 | ||||||
chr2:68473134
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5307G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473134 | ||||||
chr2:68473159
|
T | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5332T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473159 | ||||||
chr2:68473194
|
G | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+5367G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473194 | ||||||
chr2:68473271
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+5444T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473271 | ||||||
chr2:68473284
|
C | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+5457C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473284 | ||||||
chr2:68473298
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5471C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473298 | ||||||
chr2:68473418
|
G | C | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.96+5591G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473418 | ||||||
chr2:68473441
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5614A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473441 | ||||||
chr2:68473462
|
A | G | 2 | a0002c0002t0010g0168a0002c0002t0010g0169 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.96+5635A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473462 | ||||||
chr2:68473488
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+5661G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473488 | ||||||
chr2:68473518
|
A | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+5691A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473518 | ||||||
chr2:68473591
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.96+5764A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473591 | ||||||
chr2:68473719
|
G | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+5892G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473719 | ||||||
chr2:68473868
|
A | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+6041A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68473868 | ||||||
chr2:68474019
|
G | A | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+6192G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474019 | ||||||
chr2:68474032
|
C | T | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+6205C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474032 | ||||||
chr2:68474059
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96+6232G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474059 | ||||||
chr2:68474094
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.96+6267T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474094 | ||||||
chr2:68474203
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+6376C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474203 | ||||||
chr2:68474210
|
G | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+6383G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474210 | ||||||
chr2:68474212
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6385A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474212 | ||||||
chr2:68474213
|
G | GGGCGGGG others(74): Show |
1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6386_96+6387ins others(81): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474213 | ||||||
chr2:68474215
|
T | G | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6388T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474215 | ||||||
chr2:68474216
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6389T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474216 | ||||||
chr2:68474217
|
T | G | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6390T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474217 | ||||||
chr2:68474228
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6401T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474228 | ||||||
chr2:68474233
|
TTTGGGTT others(70): Show |
T | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.96+6407_96+6483del others(77): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474233 | ||||||
chr2:68474396
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.96+6569C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474396 | ||||||
chr2:68474707
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.96+6880T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474707 | ||||||
chr2:68474740
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+6913C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474740 | ||||||
chr2:68474754
|
T | C | 44 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(41): Show | 47 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.96+6927T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474754 | ||||||
chr2:68474829
|
C | T | 5 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+7002C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474829 | ||||||
chr2:68474834
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7007G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474834 | ||||||
chr2:68474858
|
C | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7031C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474858 | ||||||
chr2:68474928
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+7101A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474928 | ||||||
chr2:68474968
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7141A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68474968 | ||||||
chr2:68475014
|
C | T | 1 | a0002c0002t0010g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96+7187C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475014 | ||||||
chr2:68475146
|
G | C | 1 | a0002c0002t0002g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.96+7319G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475146 | ||||||
chr2:68475276
|
G | A | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+7449G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475276 | ||||||
chr2:68475306
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.96+7479G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475306 | ||||||
chr2:68475588
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7761G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475588 | ||||||
chr2:68475634
|
T | C | 24 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(21): Show | 26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.96+7807T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475634 | ||||||
chr2:68475673
|
C | T | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+7846C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475673 | ||||||
chr2:68475821
|
G | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7994G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475821 | ||||||
chr2:68475823
|
C | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+7996C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475823 | ||||||
chr2:68475881
|
T | TTATATA | 18 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(15): Show | 19 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+8066_96+8071dup others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | |||||
chr2:68475881
|
T | TTATATAT others(1): Show |
3 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0046 | 3 | HG02886.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.96+8064_96+8071dup others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | |||||
chr2:68475881
|
T | TTATATAT others(3): Show |
1 | a0002c0002t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.96+8062_96+8071dup others(10): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | |||||
chr2:68475881
|
T | TTATATAT others(7): Show |
1 | a0006c0007t0006g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.96+8058_96+8071dup others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | |||||
chr2:68475881
|
T | TTATATAT others(13): Show |
1 | a0006c0007t0006g0002 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.96+8071_96+8072ins others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68475881 | |||||
chr2:68475891
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+8064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68475891 | ||||||
chr2:68476122
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+8295G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476122 | ||||||
chr2:68476158
|
G | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8331G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476158 | ||||||
chr2:68476234
|
C | T | 1 | a0002c0002t0008g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.96+8407C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476234 | ||||||
chr2:68476240
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8413C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476240 | ||||||
chr2:68476255
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8428A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476255 | ||||||
chr2:68476271
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8444A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476271 | ||||||
chr2:68476305
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+8478G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476305 | ||||||
chr2:68476366
|
T | C | 57 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(54): Show | 60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.96+8539T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476366 | ||||||
chr2:68476371
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+8544T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476371 | ||||||
chr2:68476476
|
C | CA | 18 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(15): Show | 18 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+8669dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68476476 | |||||
chr2:68476476
|
CA | C | 41 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0064others(38): Show | 44 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.96+8669delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68476476 | |||||
chr2:68476554
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+8727A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476554 | ||||||
chr2:68476565
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.96+8738A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476565 | ||||||
chr2:68476585
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8758A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476585 | ||||||
chr2:68476652
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+8825G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476652 | ||||||
chr2:68476698
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+8871A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476698 | ||||||
chr2:68476832
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+9005T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476832 | ||||||
chr2:68476880
|
C | T | 1 | a0002c0002t0008g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.96+9053C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476880 | ||||||
chr2:68476992
|
T | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+9165T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68476992 | ||||||
chr2:68477093
|
A | C | 1 | a0002c0002t0008g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.96+9266A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477093 | ||||||
chr2:68477104
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+9277C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477104 | ||||||
chr2:68477111
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+9284A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477111 | ||||||
chr2:68477152
|
GAT | G | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.96+9328_96+9329del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68477152 | |||||
chr2:68477709
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.96+9882T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477709 | ||||||
chr2:68477766
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+9939A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477766 | ||||||
chr2:68477773
|
G | A | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+9946G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477773 | ||||||
chr2:68477948
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+10121A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477948 | ||||||
chr2:68477998
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+10171A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68477998 | ||||||
chr2:68478017
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.96+10190G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478017 | ||||||
chr2:68478149
|
G | A | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+10322G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478149 | ||||||
chr2:68478224
|
GAT | G | 2 | a0002c0002t0012g0021a0011c0015t0013g0165 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.96+10398_96+10399d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478224 | ||||||
chr2:68478268
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.96+10441A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478268 | ||||||
chr2:68478291
|
A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.96+10464A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478291 | ||||||
chr2:68478315
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.96+10488A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478315 | ||||||
chr2:68478520
|
C | G | 58 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(55): Show | 61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.96+10693C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478520 | ||||||
chr2:68478529
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.96+10702A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478529 | ||||||
chr2:68478711
|
C | T | 1 | a0001c0009t0001g0155 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.96+10884C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478711 | ||||||
chr2:68478804
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+10977T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478804 | ||||||
chr2:68478887
|
G | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+11060G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478887 | ||||||
chr2:68478888
|
A | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+11061A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478888 | ||||||
chr2:68478889
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.96+11062A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68478889 | ||||||
chr2:68479244
|
C | T | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-10946C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479244 | ||||||
chr2:68479270
|
A | G | 1 | a0003c0003t0004g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.97-10920A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479270 | ||||||
chr2:68479348
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-10842T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479348 | ||||||
chr2:68479374
|
C | G | 1 | a0005c0005t0001g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-10816C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479374 | ||||||
chr2:68479378
|
G | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-10812G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479378 | ||||||
chr2:68479441
|
C | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-10749C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479441 | ||||||
chr2:68479449
|
A | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10741A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479449 | ||||||
chr2:68479523
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10667G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479523 | ||||||
chr2:68479591
|
G | C | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.97-10599G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479591 | ||||||
chr2:68479857
|
T | C | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.97-10333T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479857 | ||||||
chr2:68479915
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-10275A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479915 | ||||||
chr2:68479964
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-10226C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479964 | ||||||
chr2:68479969
|
G | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-10221G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68479969 | ||||||
chr2:68480147
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG01071.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-10043A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480147 | ||||||
chr2:68480160
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-10030C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480160 | ||||||
chr2:68480300
|
T | G | 2 | a0002c0002t0002g0047a0002c0002t0002g0048 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.97-9890T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480300 | ||||||
chr2:68480301
|
CCTTTTTT others(7): Show |
C | 2 | a0002c0002t0012g0021a0011c0015t0013g0165 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-9888_97-9875del others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480301 | ||||||
chr2:68480307
|
T | C | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9883T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480307 | ||||||
chr2:68480449
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-9741G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480449 | ||||||
chr2:68480597
|
C | T | 1 | a0003c0003t0004g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97-9593C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480597 | ||||||
chr2:68480619
|
T | G | 4 | a0007c0006t0001g0136a0007c0006t0001g0139a0007c0006t0001g0140others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9571T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480619 | ||||||
chr2:68480691
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-9499C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480691 | ||||||
chr2:68480857
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0078 | 2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.97-9333T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480857 | ||||||
chr2:68480981
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-9209A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68480981 | ||||||
chr2:68481017
|
A | AT | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-9166dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481017 | |||||
chr2:68481112
|
G | A | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9078G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481112 | ||||||
chr2:68481185
|
A | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.97-9005A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481185 | ||||||
chr2:68481289
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97-8901C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481289 | ||||||
chr2:68481293
|
T | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8897T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481293 | ||||||
chr2:68481361
|
A | AGTTTT | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 167 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(164): Show |
intron_variant | MODIFIER | c.97-8808_97-8804dup others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481361 | |||||
chr2:68481361
|
AGTTTT | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-8808_97-8804del others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481361 | |||||
chr2:68481504
|
TTGA | T | 3 | a0003c0003t0004g0114a0003c0003t0004g0115a0003c0003t0004g0124 | 3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.97-8681_97-8679del others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68481504 | |||||
chr2:68481543
|
G | A | 1 | a0002c0002t0007g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97-8647G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481543 | ||||||
chr2:68481568
|
A | G | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-8622A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481568 | ||||||
chr2:68481662
|
G | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-8528G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481662 | ||||||
chr2:68481675
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-8515A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481675 | ||||||
chr2:68481752
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8438C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68481752 | ||||||
chr2:68482027
|
A | G | 1 | a0004c0004t0003g0020 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.97-8163A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482027 | ||||||
chr2:68482046
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-8144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482046 | ||||||
chr2:68482094
|
CT | C | 53 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(50): Show | 56 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.97-8085delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68482094 | |||||
chr2:68482104
|
T | G | 1 | a0001c0001t0011g0069 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97-8086T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482104 | ||||||
chr2:68482146
|
T | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-8044T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482146 | ||||||
chr2:68482458
|
G | A | 1 | a0004c0004t0003g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-7732G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482458 | ||||||
chr2:68482484
|
C | T | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-7706C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482484 | ||||||
chr2:68482499
|
C | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97-7691C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482499 | ||||||
chr2:68482847
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.97-7343G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482847 | ||||||
chr2:68482876
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97-7314G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68482876 | ||||||
chr2:68483369
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-6821C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483369 | ||||||
chr2:68483371
|
A | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-6819A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483371 | ||||||
chr2:68483547
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6643A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483547 | ||||||
chr2:68483752
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6438A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483752 | ||||||
chr2:68483756
|
T | TA | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-6428dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68483756 | |||||
chr2:68483798
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-6392A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483798 | ||||||
chr2:68483815
|
G | A | 1 | a0002c0002t0002g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97-6375G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483815 | ||||||
chr2:68483870
|
C | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-6320C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483870 | ||||||
chr2:68483932
|
A | G | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-6258A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483932 | ||||||
chr2:68483961
|
G | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-6229G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68483961 | ||||||
chr2:68484143
|
A | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-6047A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484143 | ||||||
chr2:68484168
|
T | TAACA | 57 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(54): Show | 60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.97-6021_97-6018dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484168 | |||||
chr2:68484301
|
A | G | 20 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-5889A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484301 | ||||||
chr2:68484316
|
A | G | 2 | a0004c0004t0003g0014a0004c0004t0003g0019 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.97-5874A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484316 | ||||||
chr2:68484340
|
A | G | 2 | a0002c0002t0012g0021a0011c0015t0013g0165 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-5850A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484340 | ||||||
chr2:68484553
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-5637A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484553 | ||||||
chr2:68484572
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-5618A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484572 | ||||||
chr2:68484584
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-5606C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484584 | ||||||
chr2:68484678
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-5512C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484678 | ||||||
chr2:68484691
|
G | GA | 52 | a0001c0001t0001g0099a0002c0002t0002g0033a0002c0002t0002g0034others(49): Show | 55 | HG00738.hp2 HG01109.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.97-5482dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484691 | |||||
chr2:68484749
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-5441C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484749 | ||||||
chr2:68484802
|
G | T | 1 | a0004c0004t0003g0011 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.97-5388G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68484802 | ||||||
chr2:68484964
|
C | CTG | 31 | a0001c0001t0001g0101a0002c0002t0002g0033a0002c0002t0002g0034others(28): Show | 33 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-5209_97-5208dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484964 | |||||
chr2:68484964
|
C | CTGTG | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-5211_97-5208dup others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484964 | |||||
chr2:68484981
|
T | TGC | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-5206_97-5205dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68484981 | |||||
chr2:68485157
|
C | T | 1 | a0002c0002t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.97-5033C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485157 | ||||||
chr2:68485171
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-5019G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485171 | ||||||
chr2:68485202
|
A | T | 1 | a0003c0003t0004g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-4988A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485202 | ||||||
chr2:68485325
|
A | C | 2 | a0002c0002t0012g0021a0011c0015t0013g0165 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.97-4865A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485325 | ||||||
chr2:68485563
|
A | G | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-4627A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485563 | ||||||
chr2:68485586
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-4604T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485586 | ||||||
chr2:68485616
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-4574C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485616 | ||||||
chr2:68485666
|
G | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-4524G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485666 | ||||||
chr2:68485780
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.97-4410T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485780 | ||||||
chr2:68485809
|
C | CT | 6 | a0001c0001t0001g0113a0001c0009t0001g0155a0003c0003t0004g0104others(3): Show | 6 | HG00673.hp2 HG01243.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-4363dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | |||||
chr2:68485809
|
CT | C | 50 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(47): Show | 53 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.97-4363delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | |||||
chr2:68485809
|
CTT | C | 5 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(2): Show | 5 | HG01433.hp2 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-4364_97-4363del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68485809 | |||||
chr2:68485811
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.97-4379T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485811 | ||||||
chr2:68485873
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0078a0002c0002t0008g0023others(2): Show | 5 | HG01167.hp2 HG02055.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-4317G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68485873 | ||||||
chr2:68486094
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-4096T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486094 | ||||||
chr2:68486108
|
C | G | 1 | a0004c0004t0003g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.97-4082C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486108 | ||||||
chr2:68486121
|
G | T | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-4069G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486121 | ||||||
chr2:68486225
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-3965G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486225 | ||||||
chr2:68486289
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-3901A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486289 | ||||||
chr2:68486389
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-3801C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486389 | ||||||
chr2:68486527
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-3663C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486527 | ||||||
chr2:68486763
|
AATT | A | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3423_97-3421del others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68486763 | |||||
chr2:68486807
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-3383G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68486807 | ||||||
chr2:68487151
|
C | T | 1 | a0004c0004t0003g0012 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.97-3039C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487151 | ||||||
chr2:68487212
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-2978T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487212 | ||||||
chr2:68487249
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.97-2941A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487249 | ||||||
chr2:68487416
|
T | C | 24 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(21): Show | 26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.97-2774T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487416 | ||||||
chr2:68487435
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG01169.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.97-2755G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487435 | ||||||
chr2:68487528
|
A | C | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-2662A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68487528 | ||||||
chr2:68488018
|
GCTTA | G | 37 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(34): Show | 40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-2168_97-2165del others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488018 | |||||
chr2:68488098
|
G | T | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.97-2092G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488098 | ||||||
chr2:68488329
|
CT | C | 47 | a0001c0001t0001g0107a0002c0002t0002g0033a0002c0002t0002g0034others(44): Show | 49 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.97-1842delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488329 | |||||
chr2:68488329
|
CTT | C | 6 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(3): Show | 7 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-1843_97-1842del others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68488329 | |||||
chr2:68488334
|
T | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-1856T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488334 | ||||||
chr2:68488573
|
G | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-1617G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488573 | ||||||
chr2:68488729
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1461T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488729 | ||||||
chr2:68488976
|
A | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-1214A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68488976 | ||||||
chr2:68489076
|
T | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.97-1114T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489076 | ||||||
chr2:68489108
|
A | G | 1 | a0003c0003t0004g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-1082A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489108 | ||||||
chr2:68489173
|
G | A | 1 | a0003c0003t0005g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-1017G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489173 | ||||||
chr2:68489402
|
A | G | 1 | a0004c0004t0003g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-788A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489402 | ||||||
chr2:68489567
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-623A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489567 | ||||||
chr2:68489569
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0080others(1): Show | 4 | HG00741.hp1 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-621G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489569 | ||||||
chr2:68489742
|
C | T | 1 | a0003c0003t0004g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97-448C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489742 | ||||||
chr2:68489869
|
G | C | 75 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(72): Show | 78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-321G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489869 | ||||||
chr2:68489930
|
C | T | 1 | a0003c0003t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.97-260C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489930 | ||||||
chr2:68489950
|
G | A | 2 | a0002c0002t0002g0038a0002c0002t0002g0039 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.97-240G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68489950 | ||||||
chr2:68490010
|
T | A | 22 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-180T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490010 | ||||||
chr2:68490014
|
C | CTCTGAGT others(1): Show |
2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-174_97-173insTG others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 68490014 | |||||
chr2:68490052
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-138C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490052 | ||||||
chr2:68490059
|
T | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.97-131T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490059 | ||||||
chr2:68490107
|
G | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-83G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 1/9 | chr2 | 68490107 | ||||||
chr2:68490367
|
A | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+106A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490367 | ||||||
chr2:68490551
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.168+290A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490551 | ||||||
chr2:68490710
|
T | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+449T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490710 | ||||||
chr2:68490846
|
G | A | 1 | a0002c0002t0006g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+585G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68490846 | ||||||
chr2:68491059
|
G | C | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.168+798G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491059 | ||||||
chr2:68491072
|
G | A | 2 | a0003c0003t0004g0114a0003c0003t0004g0115 | 2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.168+811G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491072 | ||||||
chr2:68491101
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.168+840T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491101 | ||||||
chr2:68491725
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1464C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491725 | ||||||
chr2:68491727
|
G | A | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.168+1466G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491727 | ||||||
chr2:68491890
|
T | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0063others(29): Show | 34 | HG00323.hp1 HG00323.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.168+1629T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68491890 | ||||||
chr2:68492154
|
A | C | 1 | a0002c0002t0002g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+1893A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492154 | ||||||
chr2:68492244
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+1983C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492244 | ||||||
chr2:68492244
|
CG | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1987delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68492244 | |||||
chr2:68492249
|
T | C | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.168+1988T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492249 | ||||||
chr2:68492281
|
A | G | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+2020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492281 | ||||||
chr2:68492282
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+2021T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492282 | ||||||
chr2:68492313
|
C | T | 19 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+2052C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492313 | ||||||
chr2:68492338
|
C | T | 2 | a0003c0003t0004g0114a0003c0003t0004g0115 | 2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.168+2077C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492338 | ||||||
chr2:68492388
|
G | T | 20 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+2127G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492388 | ||||||
chr2:68492403
|
G | A | 20 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+2142G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492403 | ||||||
chr2:68492457
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+2196G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492457 | ||||||
chr2:68492560
|
C | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(31): Show | 35 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.168+2299C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492560 | ||||||
chr2:68492666
|
C | T | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+2405C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492666 | ||||||
chr2:68492702
|
C | A | 2 | a0002c0002t0012g0021a0003c0003t0005g0128 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.168+2441C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492702 | ||||||
chr2:68492826
|
T | A | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2565T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492826 | ||||||
chr2:68492959
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.168+2698A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492959 | ||||||
chr2:68492987
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68492987 | ||||||
chr2:68493016
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.168+2755A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493016 | ||||||
chr2:68493061
|
T | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+2800T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493061 | ||||||
chr2:68493101
|
A | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+2840A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493101 | ||||||
chr2:68493327
|
G | GA | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3075dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68493327 | |||||
chr2:68493334
|
A | C | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3073A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493334 | ||||||
chr2:68493609
|
C | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3348C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493609 | ||||||
chr2:68493613
|
A | G | 3 | a0002c0002t0012g0021a0003c0003t0005g0128a0011c0015t0013g0165 | 3 | HG02572.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.168+3352A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493613 | ||||||
chr2:68493825
|
G | A | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3564G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493825 | ||||||
chr2:68493846
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168+3585C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493846 | ||||||
chr2:68493890
|
C | T | 24 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(21): Show | 26 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.168+3629C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493890 | ||||||
chr2:68493935
|
C | T | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+3674C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493935 | ||||||
chr2:68493967
|
G | A | 11 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+3706G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68493967 | ||||||
chr2:68494113
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+3852A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494113 | ||||||
chr2:68494207
|
G | T | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+3946G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494207 | ||||||
chr2:68494277
|
C | CA | 26 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0065others(23): Show | 26 | HG00323.hp1 HG00673.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.168+4041dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | |||||
chr2:68494277
|
C | CAA | 5 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0080others(2): Show | 5 | HG00741.hp1 HG01433.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+4040_168+4041d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | |||||
chr2:68494277
|
CA | C | 39 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(36): Show | 41 | HG01167.hp2 HG01243.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.168+4041delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | |||||
chr2:68494277
|
CAAAAAAA others(4): Show |
C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4031_168+4041d others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | |||||
chr2:68494277
|
CAAAAAAA others(6): Show |
C | 1 | a0007c0006t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.168+4029_168+4041d others(15): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68494277 | |||||
chr2:68494280
|
A | C | 1 | a0002c0002t0008g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.168+4019A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494280 | ||||||
chr2:68494281
|
A | C | 2 | a0002c0002t0008g0024a0002c0002t0008g0025 | 2 | HG01167.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.168+4020A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494281 | ||||||
chr2:68494309
|
A | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4048A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494309 | ||||||
chr2:68494337
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+4076G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494337 | ||||||
chr2:68494362
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+4101A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494362 | ||||||
chr2:68494530
|
G | C | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.168+4269G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494530 | ||||||
chr2:68494649
|
C | T | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+4388C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494649 | ||||||
chr2:68494691
|
T | A | 9 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+4430T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494691 | ||||||
chr2:68494820
|
A | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+4559A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494820 | ||||||
chr2:68494844
|
C | T | 58 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(55): Show | 61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.168+4583C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494844 | ||||||
chr2:68494876
|
A | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+4615A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494876 | ||||||
chr2:68494895
|
G | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168+4634G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494895 | ||||||
chr2:68494900
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+4639T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494900 | ||||||
chr2:68494975
|
C | T | 1 | a0004c0004t0003g0012 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+4714C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68494975 | ||||||
chr2:68495063
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+4802A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495063 | ||||||
chr2:68495389
|
C | T | 20 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+5128C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495389 | ||||||
chr2:68495394
|
G | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5133G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495394 | ||||||
chr2:68495465
|
C | A | 75 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(72): Show | 78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.168+5204C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495465 | ||||||
chr2:68495478
|
C | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5217C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495478 | ||||||
chr2:68495577
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5316A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495577 | ||||||
chr2:68495650
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5389T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495650 | ||||||
chr2:68495803
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5542T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495803 | ||||||
chr2:68495822
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+5561G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495822 | ||||||
chr2:68495868
|
G | C | 1 | a0004c0004t0003g0020 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.168+5607G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495868 | ||||||
chr2:68495885
|
G | A | 11 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+5624G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68495885 | ||||||
chr2:68496076
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+5815G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496076 | ||||||
chr2:68496136
|
G | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+5875G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496136 | ||||||
chr2:68496138
|
G | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+5877G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496138 | ||||||
chr2:68496262
|
C | T | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+6001C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496262 | ||||||
chr2:68496263
|
G | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.168+6002G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496263 | ||||||
chr2:68496395
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+6134G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496395 | ||||||
chr2:68496461
|
G | A | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.168+6200G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496461 | ||||||
chr2:68496504
|
G | A | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-6227G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496504 | ||||||
chr2:68496524
|
T | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-6207T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496524 | ||||||
chr2:68496607
|
G | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-6124G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496607 | ||||||
chr2:68496675
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169-6056A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496675 | ||||||
chr2:68496780
|
G | A | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-5951G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496780 | ||||||
chr2:68496781
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-5950A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496781 | ||||||
chr2:68496997
|
C | G | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-5734C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68496997 | ||||||
chr2:68497103
|
T | C | 10 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071others(7): Show | 10 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-5628T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497103 | ||||||
chr2:68497149
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5582T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497149 | ||||||
chr2:68497181
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5550A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497181 | ||||||
chr2:68497193
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-5538A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497193 | ||||||
chr2:68497219
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5512T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497219 | ||||||
chr2:68497488
|
CT | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5241delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68497488 | |||||
chr2:68497594
|
T | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-5137T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497594 | ||||||
chr2:68497628
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-5103T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497628 | ||||||
chr2:68497643
|
G | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-5088G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497643 | ||||||
chr2:68497702
|
C | T | 7 | a0001c0001t0001g0150a0002c0002t0002g0033a0002c0002t0002g0034others(4): Show | 7 | HG00639.hp2 HG01175.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-5029C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497702 | ||||||
chr2:68497813
|
C | A | 22 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.169-4918C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68497813 | ||||||
chr2:68498000
|
GTAT | G | 37 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(34): Show | 40 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.169-4729_169-4727d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68498000 | |||||
chr2:68498044
|
C | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4687C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498044 | ||||||
chr2:68498299
|
A | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-4432A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498299 | ||||||
chr2:68498300
|
A | G | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-4431A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498300 | ||||||
chr2:68498308
|
G | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4423G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498308 | ||||||
chr2:68498378
|
G | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-4353G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498378 | ||||||
chr2:68498560
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-4171T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68498560 | ||||||
chr2:68499014
|
T | TAA | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-3708_169-3707d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499014 | |||||
chr2:68499014
|
TA | T | 15 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(12): Show | 16 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.169-3707delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499014 | |||||
chr2:68499036
|
TAAAC | T | 2 | a0004c0004t0003g0009a0004c0004t0003g0011 | 2 | HG02293.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.169-3683_169-3680d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68499036 | |||||
chr2:68499170
|
A | G | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-3561A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499170 | ||||||
chr2:68499329
|
C | T | 55 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(52): Show | 58 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.169-3402C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499329 | ||||||
chr2:68499366
|
G | A | 2 | a0006c0007t0017g0022a0006c0013t0016g0166 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169-3365G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499366 | ||||||
chr2:68499387
|
G | A | 56 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(53): Show | 59 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-3344G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499387 | ||||||
chr2:68499440
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-3291T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499440 | ||||||
chr2:68499606
|
G | A | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(133): Show | 141 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.169-3125G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499606 | ||||||
chr2:68499711
|
C | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-3020C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499711 | ||||||
chr2:68499724
|
A | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.169-3007A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499724 | ||||||
chr2:68499927
|
G | A | 33 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(30): Show | 36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.169-2804G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68499927 | ||||||
chr2:68500014
|
G | A | 57 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(54): Show | 60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.169-2717G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500014 | ||||||
chr2:68500016
|
G | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2715G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500016 | ||||||
chr2:68500076
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.169-2655T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68500076 | ||||||
chr2:68500386
|
T | TTAAA | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-2342_169-2339d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68500386 | |||||
chr2:68501085
|
T | C | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1646T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501085 | ||||||
chr2:68501165
|
C | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1566C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501165 | ||||||
chr2:68501165
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-1566C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501165 | ||||||
chr2:68501180
|
G | T | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-1551G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501180 | ||||||
chr2:68501220
|
T | C | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1511T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501220 | ||||||
chr2:68501351
|
G | A | 56 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(53): Show | 59 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-1380G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501351 | ||||||
chr2:68501371
|
T | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.169-1360T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501371 | ||||||
chr2:68501436
|
AAACACC | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-1292_169-1287d others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 68501436 | |||||
chr2:68501569
|
A | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-1162A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501569 | ||||||
chr2:68501590
|
A | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-1141A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501590 | ||||||
chr2:68501641
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.169-1090G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501641 | ||||||
chr2:68501815
|
G | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-916G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68501815 | ||||||
chr2:68502166
|
C | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.169-565C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502166 | ||||||
chr2:68502166
|
C | T | 41 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(38): Show | 43 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.169-565C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502166 | ||||||
chr2:68502174
|
T | C | 2 | a0002c0002t0012g0021a0003c0003t0005g0128 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.169-557T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502174 | ||||||
chr2:68502185
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-546C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 2/9 | chr2 | 68502185 | ||||||
chr2:68502938
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.341+35T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68502938 | ||||||
chr2:68503179
|
G | C | 57 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(54): Show | 60 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.341+276G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503179 | ||||||
chr2:68503294
|
T | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.341+391T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503294 | ||||||
chr2:68503358
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+455G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503358 | ||||||
chr2:68503451
|
T | G | 1 | a0003c0003t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.341+548T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503451 | ||||||
chr2:68503491
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 6 | HG01243.hp2 HG01891.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+588G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503491 | ||||||
chr2:68503507
|
A | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+604A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503507 | ||||||
chr2:68503581
|
C | T | 55 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(52): Show | 58 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.341+678C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503581 | ||||||
chr2:68503783
|
T | G | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.341+880T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503783 | ||||||
chr2:68503967
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341+1064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68503967 | ||||||
chr2:68504011
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.341+1108A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504011 | ||||||
chr2:68504022
|
T | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341+1119T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504022 | ||||||
chr2:68504055
|
C | T | 22 | a0002c0002t0012g0021a0003c0003t0004g0104a0003c0003t0004g0114others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.341+1152C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504055 | ||||||
chr2:68504094
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+1191A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504094 | ||||||
chr2:68504221
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+1318A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504221 | ||||||
chr2:68504241
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+1338A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504241 | ||||||
chr2:68504259
|
T | C | 1 | a0002c0002t0002g0037 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.341+1356T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504259 | ||||||
chr2:68504332
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.341+1429A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504332 | ||||||
chr2:68504451
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+1548C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504451 | ||||||
chr2:68504576
|
T | C | 8 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(5): Show | 8 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+1673T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504576 | ||||||
chr2:68504628
|
CA | C | 30 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(27): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.341+1731delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68504628 | |||||
chr2:68504799
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+1896A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68504799 | ||||||
chr2:68505004
|
C | T | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341+2101C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505004 | ||||||
chr2:68505186
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(31): Show | 35 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+2283G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505186 | ||||||
chr2:68505195
|
G | A | 2 | a0001c0001t0001g0065a0010c0014t0009g0028 | 2 | HG02622.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.341+2292G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505195 | ||||||
chr2:68505298
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+2395A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68505298 | ||||||
chr2:68506239
|
T | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+3336T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506239 | ||||||
chr2:68506257
|
T | C | 78 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(75): Show | 81 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(78): Show |
intron_variant | MODIFIER | c.341+3354T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506257 | ||||||
chr2:68506277
|
T | TGGGGGCA others(316): Show |
1 | a0002c0002t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.341+3387_341+3388i others(325): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(317): Show |
3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(326): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(318): Show |
5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(327): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(319): Show |
1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.341+3387_341+3388i others(328): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(320): Show |
5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(329): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(328): Show |
2 | a0002c0002t0002g0049a0002c0002t0002g0052 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(337): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(328): Show |
2 | a0002c0002t0002g0047a0002c0002t0002g0048 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(337): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(329): Show |
9 | a0002c0002t0002g0037a0002c0002t0002g0038a0002c0002t0002g0039others(6): Show | 10 | HG01884.hp2 HG02886.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(338): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(329): Show |
1 | a0002c0002t0002g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.341+3387_341+3388i others(338): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(330): Show |
6 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0041others(3): Show | 7 | HG01243.hp1 HG01433.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+3387_341+3388i others(339): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506277
|
T | TGGGGGCA others(331): Show |
3 | a0002c0002t0002g0035a0002c0002t0002g0051a0002c0002t0002g0053 | 3 | HG02145.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.341+3387_341+3388i others(340): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68506277 | |||||
chr2:68506385
|
T | G | 8 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(5): Show | 8 | HG01433.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+3482T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506385 | ||||||
chr2:68506674
|
C | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+3771C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506674 | ||||||
chr2:68506744
|
G | A | 2 | a0001c0001t0001g0145a0001c0009t0001g0155 | 2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.341+3841G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506744 | ||||||
chr2:68506875
|
T | G | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.341+3972T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68506875 | ||||||
chr2:68507057
|
G | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.341+4154G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507057 | ||||||
chr2:68507123
|
G | A | 1 | a0004c0004t0003g0010 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.341+4220G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507123 | ||||||
chr2:68507174
|
A | G | 8 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(5): Show | 8 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.341+4271A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507174 | ||||||
chr2:68507246
|
C | G | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+4343C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507246 | ||||||
chr2:68507843
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+4940T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507843 | ||||||
chr2:68507861
|
T | G | 1 | a0002c0002t0010g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.341+4958T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68507861 | ||||||
chr2:68508012
|
T | C | 1 | a0002c0002t0002g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.342-5068T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508012 | ||||||
chr2:68508106
|
A | ATATT | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-4972_342-4971i others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68508106 | |||||
chr2:68508204
|
G | T | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.342-4876G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508204 | ||||||
chr2:68508249
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-4831G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508249 | ||||||
chr2:68508426
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-4654T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508426 | ||||||
chr2:68508492
|
T | C | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-4588T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508492 | ||||||
chr2:68508513
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-4567A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508513 | ||||||
chr2:68508586
|
G | A | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.342-4494G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508586 | ||||||
chr2:68508764
|
ACAATCCT others(4): Show |
A | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.342-4312_342-4302d others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 68508764 | |||||
chr2:68508776
|
C | A | 39 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-4304C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508776 | ||||||
chr2:68508802
|
T | G | 39 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-4278T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508802 | ||||||
chr2:68508966
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.342-4114G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68508966 | ||||||
chr2:68509112
|
A | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3968A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509112 | ||||||
chr2:68509120
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3960A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509120 | ||||||
chr2:68509179
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-3901A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509179 | ||||||
chr2:68509184
|
C | T | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.342-3896C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509184 | ||||||
chr2:68509401
|
G | A | 18 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(15): Show | 18 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.342-3679G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509401 | ||||||
chr2:68509470
|
C | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-3610C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509470 | ||||||
chr2:68509501
|
G | A | 39 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-3579G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509501 | ||||||
chr2:68509544
|
T | C | 1 | a0003c0003t0004g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342-3536T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509544 | ||||||
chr2:68509545
|
G | A | 1 | a0003c0003t0004g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342-3535G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509545 | ||||||
chr2:68509602
|
A | G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.342-3478A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509602 | ||||||
chr2:68509617
|
G | C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-3463G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509617 | ||||||
chr2:68509627
|
A | T | 1 | a0005c0005t0014g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342-3453A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509627 | ||||||
chr2:68509768
|
C | T | 20 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.342-3312C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509768 | ||||||
chr2:68509831
|
A | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3249A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509831 | ||||||
chr2:68509860
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0063others(108): Show | 116 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.342-3220T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509860 | ||||||
chr2:68509861
|
G | A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.342-3219G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68509861 | ||||||
chr2:68510081
|
G | C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2999G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510081 | ||||||
chr2:68510123
|
C | T | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342-2957C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510123 | ||||||
chr2:68510188
|
G | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.342-2892G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510188 | ||||||
chr2:68510307
|
C | T | 5 | a0004c0004t0003g0013a0004c0004t0003g0016a0004c0004t0003g0017others(2): Show | 5 | NA18943.hp2 NA18966.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-2773C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510307 | ||||||
chr2:68510324
|
C | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.342-2756C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510324 | ||||||
chr2:68510638
|
G | A | 31 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(28): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.342-2442G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510638 | ||||||
chr2:68510745
|
C | T | 1 | a0003c0003t0004g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.342-2335C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510745 | ||||||
chr2:68510776
|
T | G | 1 | a0002c0002t0008g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.342-2304T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510776 | ||||||
chr2:68510835
|
T | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.342-2245T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510835 | ||||||
chr2:68510851
|
A | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2229A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510851 | ||||||
chr2:68510995
|
A | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2085A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68510995 | ||||||
chr2:68511030
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-2050A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511030 | ||||||
chr2:68511199
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.342-1881T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511199 | ||||||
chr2:68511279
|
G | A | 39 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-1801G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511279 | ||||||
chr2:68511448
|
T | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.342-1632T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511448 | ||||||
chr2:68511458
|
C | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-1622C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511458 | ||||||
chr2:68511488
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.342-1592T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511488 | ||||||
chr2:68511840
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-1240A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511840 | ||||||
chr2:68511869
|
C | T | 40 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(37): Show | 42 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.342-1211C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511869 | ||||||
chr2:68511960
|
C | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-1120C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68511960 | ||||||
chr2:68512129
|
T | C | 1 | a0002c0002t0008g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.342-951T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512129 | ||||||
chr2:68512154
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.342-926T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512154 | ||||||
chr2:68512158
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0116 | 2 | NA18962.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.342-922A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512158 | ||||||
chr2:68512196
|
G | C | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-884G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512196 | ||||||
chr2:68512206
|
C | G | 1 | a0002c0002t0007g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342-874C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512206 | ||||||
chr2:68512259
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-821A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512259 | ||||||
chr2:68512391
|
T | C | 2 | a0004c0004t0003g0014a0004c0004t0003g0019 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.342-689T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512391 | ||||||
chr2:68512505
|
A | G | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-575A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512505 | ||||||
chr2:68512661
|
A | G | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-419A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512661 | ||||||
chr2:68512831
|
T | C | 1 | a0004c0004t0003g0010 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.342-249T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512831 | ||||||
chr2:68512869
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342-211G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512869 | ||||||
chr2:68512926
|
G | T | 2 | a0003c0003t0004g0121a0003c0003t0004g0123 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.342-154G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68512926 | ||||||
chr2:68513003
|
T | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.342-77T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 3/9 | chr2 | 68513003 | ||||||
chr2:68513387
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(30): Show | 34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.489+160C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513387 | ||||||
chr2:68513466
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-82G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513466 | ||||||
chr2:68513469
|
A | G | 2 | a0002c0002t0002g0043a0002c0002t0002g0044 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.490-79A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513469 | ||||||
chr2:68513470
|
G | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-78G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513470 | ||||||
chr2:68513473
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-75T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513473 | ||||||
chr2:68513501
|
A | G | 1 | a0002c0002t0010g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-47A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 4/9 | chr2 | 68513501 | ||||||
chr2:68513770
|
TATAGAG | T | 54 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(51): Show | 56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+97_622+102delA others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513770 | |||||
chr2:68513814
|
G | GT | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.622+141dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513814 | |||||
chr2:68513886
|
AT | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+214delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68513886 | |||||
chr2:68513958
|
G | T | 2 | a0004c0004t0003g0014a0004c0004t0003g0019 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.622+278G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68513958 | ||||||
chr2:68514034
|
T | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+354T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514034 | ||||||
chr2:68514154
|
G | T | 54 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(51): Show | 56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+474G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514154 | ||||||
chr2:68514264
|
C | T | 54 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(51): Show | 56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+584C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514264 | ||||||
chr2:68514420
|
C | T | 1 | a0004c0004t0003g0017 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.622+740C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514420 | ||||||
chr2:68514508
|
G | A | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+828G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514508 | ||||||
chr2:68514549
|
C | T | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+869C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514549 | ||||||
chr2:68514802
|
A | G | 58 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(55): Show | 61 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.622+1122A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514802 | ||||||
chr2:68514828
|
C | T | 36 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(33): Show | 38 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.622+1148C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68514828 | ||||||
chr2:68515292
|
A | AAT | 33 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(30): Show | 34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.622+1630_622+1631d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | |||||
chr2:68515292
|
AAT | A | 54 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(51): Show | 56 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.622+1630_622+1631d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | |||||
chr2:68515292
|
AATAT | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+1628_622+1631d others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68515292 | |||||
chr2:68515361
|
G | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+1681G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515361 | ||||||
chr2:68515532
|
A | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+1852A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515532 | ||||||
chr2:68515721
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.622+2041G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515721 | ||||||
chr2:68515742
|
C | G | 1 | a0003c0003t0004g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.622+2062C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515742 | ||||||
chr2:68515892
|
C | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+2212C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68515892 | ||||||
chr2:68516311
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0138 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.622+2631G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516311 | ||||||
chr2:68516352
|
T | G | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.622+2672T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516352 | ||||||
chr2:68516416
|
T | A | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+2736T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516416 | ||||||
chr2:68516431
|
C | T | 22 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.622+2751C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516431 | ||||||
chr2:68516494
|
G | T | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+2814G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516494 | ||||||
chr2:68516518
|
T | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+2838T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516518 | ||||||
chr2:68516700
|
T | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.622+3020T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516700 | ||||||
chr2:68516813
|
T | C | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3133T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516813 | ||||||
chr2:68516844
|
G | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3164G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516844 | ||||||
chr2:68516896
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+3216A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516896 | ||||||
chr2:68516912
|
T | C | 31 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(28): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.622+3232T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516912 | ||||||
chr2:68516929
|
AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0070a0001c0001t0001g0109a0006c0007t0006g0002others(3): Show | 7 | HG00741.hp1 HG03098.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.622+3269_622+3282d others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516929 | |||||
chr2:68516931
|
TATATA | T | 2 | a0002c0002t0002g0034a0002c0002t0002g0035 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+3262_622+3266d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516931 | |||||
chr2:68516959
|
TATA | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0093 | 2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.622+3286_622+3288d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516959 | |||||
chr2:68516985
|
T | A | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+3305T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516985 | ||||||
chr2:68516986
|
A | T | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+3306A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68516986 | ||||||
chr2:68516987
|
TATA | T | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+3314_622+3316d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68516987 | |||||
chr2:68517017
|
AATAATAT others(8): Show |
A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+3347_622+3361d others(17): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517017 | |||||
chr2:68517018
|
A | T | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+3338A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517018 | ||||||
chr2:68517025
|
AT | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3347delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517025 | |||||
chr2:68517050
|
GTTA | G | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3374_622+3376d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517050 | |||||
chr2:68517078
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.622+3398A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517078 | ||||||
chr2:68517083
|
GTTA | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3407_622+3409d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517083 | |||||
chr2:68517138
|
T | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3458T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517138 | ||||||
chr2:68517167
|
C | T | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3487C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517167 | ||||||
chr2:68517172
|
TATA | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+3498_622+3500d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517172 | |||||
chr2:68517202
|
AAT | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.622+3527_622+3528d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517202 | |||||
chr2:68517224
|
A | AAATATAT others(21): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0099 | 2 | HG00738.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.622+3644_622+3671d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | |||||
chr2:68517224
|
AAATATAT others(21): Show |
A | 66 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(63): Show | 68 | HG00323.hp1 HG00741.hp1 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.622+3644_622+3671d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | |||||
chr2:68517224
|
AAATATAT others(49): Show |
A | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622+3616_622+3671d others(58): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517224 | |||||
chr2:68517248
|
TATATAAT others(26): Show |
T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+3574_622+3606d others(35): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517248 | |||||
chr2:68517261
|
AATATATG others(23): Show |
A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.622+3586_622+3615d others(32): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517261 | |||||
chr2:68517315
|
T | G | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+3635T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517315 | ||||||
chr2:68517326
|
C | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3646C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517326 | ||||||
chr2:68517327
|
A | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+3647A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517327 | ||||||
chr2:68517359
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0159 | 2 | NA19005.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.622+3679A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517359 | ||||||
chr2:68517397
|
A | G | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.622+3717A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517397 | ||||||
chr2:68517409
|
C | CTA | 75 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(72): Show | 78 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.622+3735_622+3736d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517409 | |||||
chr2:68517425
|
A | G | 1 | a0001c0001t0015g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.622+3745A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517425 | ||||||
chr2:68517435
|
CTA | C | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+3761_622+3762d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517435 | |||||
chr2:68517470
|
GTTA | G | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+3794_622+3796d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517470 | |||||
chr2:68517538
|
CAT | C | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+3861_622+3862d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517538 | |||||
chr2:68517612
|
CTAA | C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+3934_622+3936d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517612 | |||||
chr2:68517632
|
C | CAAT | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+3954_622+3956d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517632 | |||||
chr2:68517661
|
TAAC | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+3984_622+3986d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517661 | |||||
chr2:68517722
|
T | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4042T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517722 | ||||||
chr2:68517762
|
A | C | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+4082A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517762 | ||||||
chr2:68517802
|
A | ACAGTAAT others(27): Show |
3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4196_622+4229d others(36): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517802 | |||||
chr2:68517802
|
A | ACAGTAAT others(61): Show |
1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4162_622+4229d others(70): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517802 | |||||
chr2:68517838
|
AGTAATAT others(95): Show |
A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+4190_622+4291d others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517838 | |||||
chr2:68517951
|
A | C | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.622+4271A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517951 | ||||||
chr2:68517975
|
G | A | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+4295G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68517975 | ||||||
chr2:68517988
|
AAT | A | 31 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(28): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.622+4311_622+4312d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68517988 | |||||
chr2:68518111
|
CAT | C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4435_622+4436d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518111 | |||||
chr2:68518129
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.622+4449A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518129 | ||||||
chr2:68518166
|
GTAATA | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4494_622+4498d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518166 | |||||
chr2:68518174
|
A | C | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.622+4494A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518174 | ||||||
chr2:68518214
|
C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+4534C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518214 | ||||||
chr2:68518215
|
G | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4535G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518215 | ||||||
chr2:68518279
|
TATA | T | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4603_622+4605d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518279 | |||||
chr2:68518310
|
T | C | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+4630T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518310 | ||||||
chr2:68518363
|
T | C | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+4683T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518363 | ||||||
chr2:68518376
|
CTG | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0101 | 2 | NA18962.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.622+4698_622+4699d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518376 | |||||
chr2:68518378
|
G | A | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.622+4698G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518378 | ||||||
chr2:68518404
|
A | ATAT | 66 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(63): Show | 68 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.622+4728_622+4730d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518404 | |||||
chr2:68518404
|
A | ATATTATT others(18): Show |
9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+4730_622+4731i others(27): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518404 | |||||
chr2:68518408
|
T | TATTATAT others(30): Show |
3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+4730_622+4731i others(39): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518408 | |||||
chr2:68518408
|
T | TATTATAT others(64): Show |
1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4730_622+4731i others(73): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518408 | |||||
chr2:68518425
|
T | A | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+4745T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518425 | ||||||
chr2:68518444
|
T | C | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.622+4764T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518444 | ||||||
chr2:68518466
|
CATATTA | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.622+4790_622+4795d others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518466 | |||||
chr2:68518467
|
ATAT | A | 4 | a0002c0002t0007g0029a0002c0002t0007g0030a0002c0002t0007g0031others(1): Show | 4 | HG01109.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+4790_622+4792d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518467 | |||||
chr2:68518478
|
A | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+4798A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518478 | ||||||
chr2:68518479
|
C | T | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+4799C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518479 | ||||||
chr2:68518487
|
C | T | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.622+4807C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518487 | ||||||
chr2:68518513
|
A | G | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+4833A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518513 | ||||||
chr2:68518543
|
A | ATATCAAT others(14): Show |
14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4863_622+4864i others(23): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518543 | ||||||
chr2:68518557
|
G | A | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4877G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518557 | ||||||
chr2:68518581
|
A | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4901A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518581 | ||||||
chr2:68518598
|
T | TATA | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4922_622+4924d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518598 | |||||
chr2:68518598
|
TATAATAT others(25): Show |
T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.622+4955_622+4986d others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518598 | |||||
chr2:68518603
|
T | TA | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4924dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518603 | |||||
chr2:68518607
|
TC | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4928delC | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518607 | ||||||
chr2:68518611
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+4931T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518611 | ||||||
chr2:68518611
|
T | TAATATAT others(22): Show |
20 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(17): Show | 22 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.622+4933_622+4961d others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | |||||
chr2:68518611
|
T | TAATATAT others(54): Show |
21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+4986_622+4987i others(63): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | |||||
chr2:68518611
|
T | TAATATAT others(22): Show |
21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.622+4957_622+4958i others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | |||||
chr2:68518611
|
T | TAATATAT others(19): Show |
1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+4953_622+4954i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518611 | |||||
chr2:68518627
|
TATA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0063others(10): Show | 15 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.622+4954_622+4956d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518627 | |||||
chr2:68518637
|
T | TATCAATA others(19): Show |
1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+4961_622+4962i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518637 | |||||
chr2:68518711
|
CAAT | C | 2 | a0001c0001t0001g0089a0001c0001t0015g0090 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.622+5036_622+5038d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518711 | |||||
chr2:68518742
|
AT | A | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5063delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518742 | ||||||
chr2:68518746
|
T | A | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5066T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518746 | ||||||
chr2:68518749
|
A | ATATATAA others(19): Show |
1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5083_622+5084i others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518749 | |||||
chr2:68518754
|
T | TC | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5074_622+5075i others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518754 | ||||||
chr2:68518756
|
A | T | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5076A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518756 | ||||||
chr2:68518760
|
A | T | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5080A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518760 | ||||||
chr2:68518764
|
TTAA | T | 3 | a0002c0002t0002g0038a0002c0002t0002g0039a0002c0002t0012g0021 | 3 | HG01884.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622+5090_622+5092d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518764 | |||||
chr2:68518765
|
T | C | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5085T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518765 | ||||||
chr2:68518767
|
A | T | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5087A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518767 | ||||||
chr2:68518768
|
T | G | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5088T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518768 | ||||||
chr2:68518774
|
A | ATCATTAT others(80): Show |
6 | a0003c0003t0005g0105a0003c0003t0005g0128a0003c0003t0005g0130others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.622+5120_622+5121i others(89): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518774 | |||||
chr2:68518778
|
T | TTAA | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5100_622+5101i others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518778 | |||||
chr2:68518801
|
C | A | 97 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(94): Show | 100 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(97): Show |
intron_variant | MODIFIER | c.622+5121C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518801 | ||||||
chr2:68518802
|
T | TGTCATTA others(25): Show |
3 | a0003c0003t0004g0114a0003c0003t0004g0115a0003c0003t0004g0124 | 3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.622+5122_622+5123i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518802 | ||||||
chr2:68518805
|
C | CATT | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 149 | HG00323.hp1 HG00323.hp2 HG00673.hp1 others(146): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | |||||
chr2:68518805
|
C | CATTATAT others(25): Show |
4 | a0002c0002t0002g0052a0006c0007t0006g0002a0006c0007t0006g0032others(1): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | |||||
chr2:68518805
|
C | CATTATAT others(83): Show |
3 | a0003c0003t0005g0127a0003c0003t0005g0129a0003c0003t0005g0134 | 3 | HG02965.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.622+5127_622+5128i others(92): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | |||||
chr2:68518805
|
C | CATTATAT others(54): Show |
9 | a0003c0003t0004g0104a0003c0003t0004g0119a0003c0003t0004g0120others(6): Show | 9 | HG00639.hp1 HG00738.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.622+5127_622+5128i others(63): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518805 | |||||
chr2:68518805
|
C | T | 3 | a0003c0003t0004g0114a0003c0003t0004g0115a0003c0003t0004g0124 | 3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.622+5125C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518805 | ||||||
chr2:68518814
|
A | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622+5134A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518814 | ||||||
chr2:68518822
|
G | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+5142G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518822 | ||||||
chr2:68518837
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.622+5157T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518837 | ||||||
chr2:68518861
|
G | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.622+5181G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518861 | ||||||
chr2:68518886
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.622+5206A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518886 | ||||||
chr2:68518891
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.622+5211A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518891 | ||||||
chr2:68518928
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5248A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518928 | ||||||
chr2:68518932
|
T | G | 1 | a0004c0004t0003g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.622+5252T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518932 | ||||||
chr2:68518958
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0063others(11): Show | 16 | HG00323.hp2 HG00673.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.622+5278A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518958 | ||||||
chr2:68518962
|
CATA | C | 2 | a0002c0002t0008g0023a0002c0002t0008g0025 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+5289_622+5291d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518962 | |||||
chr2:68518985
|
C | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.622+5305C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68518985 | ||||||
chr2:68518993
|
G | GATAATAT others(21): Show |
13 | a0003c0003t0004g0120a0003c0003t0004g0121a0003c0003t0004g0122others(10): Show | 13 | HG00738.hp1 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.622+5323_622+5350d others(30): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518993 | |||||
chr2:68518993
|
G | GATAATAT others(49): Show |
6 | a0003c0003t0004g0114a0003c0003t0004g0115a0003c0003t0005g0105others(3): Show | 6 | HG01261.hp2 HG01943.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.622+5350_622+5351i others(58): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518993 | |||||
chr2:68518997
|
ATATAT | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+5321_622+5325d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68518997 | |||||
chr2:68519003
|
T | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5323T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519003 | ||||||
chr2:68519031
|
G | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.622+5351G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519031 | ||||||
chr2:68519039
|
T | TATAATAA others(22): Show |
20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.622+5395_622+5423d others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | |||||
chr2:68519039
|
T | TATAATAA others(51): Show |
1 | a0002c0002t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.622+5366_622+5423d others(60): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | |||||
chr2:68519039
|
T | TATAATAA others(22): Show |
1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+5374_622+5375i others(31): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519039 | |||||
chr2:68519045
|
A | AAT | 2 | a0003c0003t0004g0104a0003c0003t0004g0119 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.622+5369_622+5370d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519045 | |||||
chr2:68519057
|
A | T | 2 | a0003c0003t0004g0104a0003c0003t0004g0119 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.622+5377A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519057 | ||||||
chr2:68519068
|
A | AATAATAT others(18): Show |
1 | a0003c0003t0004g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.622+5394_622+5395i others(27): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519068 | |||||
chr2:68519085
|
T | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5405T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519085 | ||||||
chr2:68519087
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.622+5407A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519087 | ||||||
chr2:68519094
|
T | TATA | 24 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(21): Show | 25 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.622+5421_622+5423d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | |||||
chr2:68519094
|
T | TATAATAA others(25): Show |
1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5423_622+5424i others(34): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | |||||
chr2:68519094
|
TATA | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+5421_622+5423d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519094 | |||||
chr2:68519117
|
A | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.622+5437A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519117 | ||||||
chr2:68519139
|
TTA | T | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+5470_622+5471d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519139 | |||||
chr2:68519180
|
G | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.622+5500G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519180 | ||||||
chr2:68519237
|
ATATAT | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.622+5563_622+5567d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519237 | |||||
chr2:68519267
|
ATATAT | A | 22 | a0002c0002t0009g0003a0003c0003t0004g0104a0003c0003t0004g0114others(19): Show | 23 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.622+5593_622+5597d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68519267 | |||||
chr2:68519464
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+5784A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519464 | ||||||
chr2:68519709
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.622+6029C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519709 | ||||||
chr2:68519857
|
G | A | 1 | a0002c0002t0008g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.622+6177G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68519857 | ||||||
chr2:68520014
|
C | G | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.623-6047C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520014 | ||||||
chr2:68520143
|
T | C | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-5918T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520143 | ||||||
chr2:68520244
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(30): Show | 34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.623-5817A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520244 | ||||||
chr2:68520310
|
T | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-5751T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520310 | ||||||
chr2:68520496
|
G | A | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.623-5565G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520496 | ||||||
chr2:68520708
|
C | T | 24 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(21): Show | 25 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.623-5353C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520708 | ||||||
chr2:68520735
|
G | A | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.623-5326G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520735 | ||||||
chr2:68520791
|
T | A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623-5270T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520791 | ||||||
chr2:68520968
|
T | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-5093T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68520968 | ||||||
chr2:68521189
|
G | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.623-4872G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521189 | ||||||
chr2:68521263
|
A | G | 2 | a0001c0001t0001g0145a0001c0009t0001g0155 | 2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.623-4798A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521263 | ||||||
chr2:68521422
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623-4639A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521422 | ||||||
chr2:68521457
|
A | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-4604A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521457 | ||||||
chr2:68521521
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-4540A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68521521 | ||||||
chr2:68522139
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623-3922T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522139 | ||||||
chr2:68522190
|
A | G | 47 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(44): Show | 49 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.623-3871A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522190 | ||||||
chr2:68522200
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.623-3861C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522200 | ||||||
chr2:68522202
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.623-3859G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522202 | ||||||
chr2:68522365
|
C | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-3696C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522365 | ||||||
chr2:68522394
|
T | C | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.623-3667T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522394 | ||||||
chr2:68522411
|
T | TA | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-3649dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68522411 | |||||
chr2:68522594
|
A | G | 1 | a0002c0002t0010g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.623-3467A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522594 | ||||||
chr2:68522714
|
C | T | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.623-3347C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522714 | ||||||
chr2:68522716
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-3345T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522716 | ||||||
chr2:68522915
|
A | C | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.623-3146A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68522915 | ||||||
chr2:68523005
|
G | T | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.623-3056G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523005 | ||||||
chr2:68523094
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-2967C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523094 | ||||||
chr2:68523204
|
G | A | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.623-2857G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523204 | ||||||
chr2:68523315
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623-2746G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523315 | ||||||
chr2:68523360
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-2701T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523360 | ||||||
chr2:68523402
|
TATACA | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-2653_623-2649d others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523402 | |||||
chr2:68523493
|
A | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2568A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523493 | ||||||
chr2:68523559
|
A | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-2502A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523559 | ||||||
chr2:68523580
|
T | A | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-2481T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523580 | ||||||
chr2:68523917
|
T | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(29): Show | 33 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.623-2144T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523917 | ||||||
chr2:68523971
|
CT | C | 80 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(77): Show | 83 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.623-2088delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523971 | |||||
chr2:68523984
|
A | AAT | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2068_623-2067d others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68523984 | |||||
chr2:68523994
|
T | TA | 2 | a0004c0004t0003g0009a0004c0004t0003g0011 | 2 | HG02293.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.623-2067_623-2066i others(3): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523994 | ||||||
chr2:68523995
|
T | A | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.623-2066T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68523995 | ||||||
chr2:68524016
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.623-2045G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524016 | ||||||
chr2:68524293
|
A | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-1768A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524293 | ||||||
chr2:68524446
|
G | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1615G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524446 | ||||||
chr2:68524452
|
G | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1609G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524452 | ||||||
chr2:68524568
|
G | T | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.623-1493G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524568 | ||||||
chr2:68524587
|
T | G | 1 | a0002c0002t0008g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623-1474T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524587 | ||||||
chr2:68524790
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-1271A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524790 | ||||||
chr2:68524927
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623-1134A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524927 | ||||||
chr2:68524934
|
G | T | 1 | a0002c0002t0002g0037 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.623-1127G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524934 | ||||||
chr2:68524966
|
G | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.623-1095G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68524966 | ||||||
chr2:68525069
|
G | A | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-992G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525069 | ||||||
chr2:68525109
|
C | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.623-952C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525109 | ||||||
chr2:68525120
|
T | C | 27 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.623-941T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525120 | ||||||
chr2:68525250
|
T | C | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.623-811T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525250 | ||||||
chr2:68525251
|
G | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.623-810G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525251 | ||||||
chr2:68525509
|
T | A | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.623-552T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525509 | ||||||
chr2:68525512
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.623-549A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525512 | ||||||
chr2:68525555
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-506C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525555 | ||||||
chr2:68525738
|
CTTTCTTT others(13): Show |
C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-319_623-300del others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525738 | |||||
chr2:68525742
|
C | CT | 14 | a0001c0001t0001g0067a0001c0001t0001g0113a0003c0003t0005g0105others(11): Show | 14 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.623-294dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTT | 14 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.623-295_623-294dup others(2): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(4): Show |
1 | a0002c0002t0002g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.623-304_623-294dup others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(5): Show |
12 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-305_623-294dup others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(6): Show |
5 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0039others(2): Show | 5 | HG03453.hp1 HG03516.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-306_623-294dup others(13): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(7): Show |
2 | a0002c0002t0002g0033a0002c0002t0002g0051 | 2 | HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.623-307_623-294dup others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(9): Show |
1 | a0002c0002t0002g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.623-309_623-294dup others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(16): Show |
1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.623-316_623-294dup others(23): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | CTTTTTTT others(21): Show |
1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.623-294_623-293ins others(28): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
C | T | 6 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(3): Show | 6 | HG01167.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-319C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68525742 | ||||||
chr2:68525742
|
CT | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0061others(30): Show | 34 | HG00323.hp1 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.623-294delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68525742
|
CTTTTTTT others(1): Show |
C | 12 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(9): Show | 12 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.623-301_623-294del others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 68525742 | |||||
chr2:68526003
|
A | C | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.623-58A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | chr2 | 68526003 | ||||||
chr2:68526711
|
C | T | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+469C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526711 | ||||||
chr2:68526733
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.804+491G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526733 | ||||||
chr2:68526750
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+508C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526750 | ||||||
chr2:68526876
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.804+634C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526876 | ||||||
chr2:68526901
|
C | T | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.804+659C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526901 | ||||||
chr2:68526969
|
C | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+727C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526969 | ||||||
chr2:68526973
|
A | T | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+731A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68526973 | ||||||
chr2:68527074
|
G | A | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.804+832G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527074 | ||||||
chr2:68527092
|
G | A | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.804+850G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527092 | ||||||
chr2:68527101
|
G | T | 28 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(25): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+859G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527101 | ||||||
chr2:68527142
|
C | T | 4 | a0007c0006t0001g0136a0007c0006t0001g0139a0007c0006t0001g0140others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+900C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527142 | ||||||
chr2:68527172
|
G | C | 1 | a0002c0002t0010g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804+930G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527172 | ||||||
chr2:68527316
|
C | T | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+1074C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527316 | ||||||
chr2:68527557
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01106.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.804+1315C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527557 | ||||||
chr2:68527576
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.804+1334T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527576 | ||||||
chr2:68527609
|
C | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1367C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527609 | ||||||
chr2:68527610
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0092others(1): Show | 4 | HG02717.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+1368G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527610 | ||||||
chr2:68527627
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.804+1385C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527627 | ||||||
chr2:68527660
|
C | T | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+1418C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527660 | ||||||
chr2:68527704
|
G | A | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804+1462G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527704 | ||||||
chr2:68527747
|
C | T | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1505C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527747 | ||||||
chr2:68527785
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+1543G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527785 | ||||||
chr2:68527787
|
C | T | 4 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025others(1): Show | 4 | HG01167.hp2 HG02055.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1545C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527787 | ||||||
chr2:68527893
|
G | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1651G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527893 | ||||||
chr2:68527940
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.804+1698C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68527940 | ||||||
chr2:68528011
|
C | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.804+1769C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528011 | ||||||
chr2:68528140
|
C | T | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+1898C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528140 | ||||||
chr2:68528158
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1916A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528158 | ||||||
chr2:68528345
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+2103G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528345 | ||||||
chr2:68528613
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0011g0069 | 2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.804+2371G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528613 | ||||||
chr2:68528638
|
G | A | 1 | a0004c0004t0003g0011 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.804+2396G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528638 | ||||||
chr2:68528754
|
A | T | 17 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(14): Show | 17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+2512A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68528754 | ||||||
chr2:68529019
|
A | G | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.804+2777A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529019 | ||||||
chr2:68529164
|
A | AG | 28 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(25): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+2929dupG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68529164 | |||||
chr2:68529165
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804+2923G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529165 | ||||||
chr2:68529170
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.804+2928G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529170 | ||||||
chr2:68529340
|
G | A | 3 | a0002c0002t0002g0047a0002c0002t0002g0048a0002c0002t0002g0050 | 3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.804+3098G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529340 | ||||||
chr2:68529348
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.804+3106C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529348 | ||||||
chr2:68529383
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.804+3141G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529383 | ||||||
chr2:68529458
|
T | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+3216T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529458 | ||||||
chr2:68529506
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+3264G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529506 | ||||||
chr2:68529522
|
A | T | 1 | a0003c0003t0004g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804+3280A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529522 | ||||||
chr2:68529722
|
G | A | 1 | a0003c0003t0004g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+3480G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529722 | ||||||
chr2:68529746
|
G | T | 1 | a0002c0011t0002g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.804+3504G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529746 | ||||||
chr2:68529753
|
C | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+3511C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529753 | ||||||
chr2:68529840
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+3598T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529840 | ||||||
chr2:68529850
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.804+3608G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529850 | ||||||
chr2:68529871
|
G | GGGCCAGA others(23): Show |
1 | a0002c0002t0010g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804+3630_804+3659d others(32): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68529871 | |||||
chr2:68529903
|
G | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804+3661G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529903 | ||||||
chr2:68529931
|
C | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+3689C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68529931 | ||||||
chr2:68530007
|
T | C | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.804+3765T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530007 | ||||||
chr2:68530008
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+3766C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530008 | ||||||
chr2:68530009
|
G | A | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.804+3767G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530009 | ||||||
chr2:68530028
|
A | G | 1 | a0003c0003t0005g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.804+3786A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530028 | ||||||
chr2:68530060
|
A | G | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.804+3818A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530060 | ||||||
chr2:68530087
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.804+3845G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530087 | ||||||
chr2:68530175
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 7 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3933T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530175 | ||||||
chr2:68530327
|
C | A | 23 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 24 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+4085C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530327 | ||||||
chr2:68530460
|
C | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+4218C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530460 | ||||||
chr2:68530592
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.804+4350T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530592 | ||||||
chr2:68530797
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.804+4555A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530797 | ||||||
chr2:68530877
|
TA | T | 17 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(14): Show | 17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+4644delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68530877 | |||||
chr2:68530893
|
G | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.804+4651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530893 | ||||||
chr2:68530986
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.804+4744C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68530986 | ||||||
chr2:68531048
|
A | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.804+4806A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531048 | ||||||
chr2:68531154
|
G | A | 10 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.804+4912G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531154 | ||||||
chr2:68531257
|
C | T | 34 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(31): Show | 36 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.804+5015C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531257 | ||||||
chr2:68531301
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804+5059A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531301 | ||||||
chr2:68531459
|
C | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.804+5217C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531459 | ||||||
chr2:68531731
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.804+5489T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531731 | ||||||
chr2:68531783
|
C | T | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+5541C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531783 | ||||||
chr2:68531872
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.804+5630A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68531872 | ||||||
chr2:68532030
|
G | A | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.804+5788G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532030 | ||||||
chr2:68532106
|
C | T | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.805-5766C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532106 | ||||||
chr2:68532339
|
T | G | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-5533T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532339 | ||||||
chr2:68532448
|
C | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-5424C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532448 | ||||||
chr2:68532482
|
T | C | 52 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(49): Show | 54 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.805-5390T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532482 | ||||||
chr2:68532599
|
G | A | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.805-5273G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532599 | ||||||
chr2:68532623
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.805-5249G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532623 | ||||||
chr2:68532852
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-5020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532852 | ||||||
chr2:68532986
|
G | A | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4886G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68532986 | ||||||
chr2:68533071
|
T | C | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4801T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533071 | ||||||
chr2:68533181
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-4691G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533181 | ||||||
chr2:68533274
|
T | C | 47 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(44): Show | 49 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.805-4598T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533274 | ||||||
chr2:68533285
|
A | G | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-4587A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533285 | ||||||
chr2:68533405
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.805-4467G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533405 | ||||||
chr2:68533515
|
C | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-4357C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533515 | ||||||
chr2:68533605
|
T | C | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-4267T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68533605 | ||||||
chr2:68534209
|
T | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-3663T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534209 | ||||||
chr2:68534283
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-3589A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534283 | ||||||
chr2:68534298
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-3574A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534298 | ||||||
chr2:68534468
|
T | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.805-3404T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534468 | ||||||
chr2:68534622
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-3250C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534622 | ||||||
chr2:68534771
|
T | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-3101T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534771 | ||||||
chr2:68534861
|
G | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.805-3011G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534861 | ||||||
chr2:68534869
|
A | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-3003A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68534869 | ||||||
chr2:68535055
|
A | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2817A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535055 | ||||||
chr2:68535079
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.805-2793A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535079 | ||||||
chr2:68535127
|
G | GT | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2743dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68535127 | |||||
chr2:68535274
|
A | G | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.805-2598A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535274 | ||||||
chr2:68535369
|
G | A | 26 | a0001c0001t0001g0083a0003c0003t0004g0104a0003c0003t0004g0114others(23): Show | 27 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.805-2503G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535369 | ||||||
chr2:68535466
|
T | G | 2 | a0002c0002t0002g0041a0002c0002t0002g0042 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.805-2406T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535466 | ||||||
chr2:68535603
|
CT | C | 17 | a0002c0002t0008g0024a0004c0004t0003g0008a0004c0004t0003g0009others(14): Show | 18 | HG01167.hp2 HG02129.hp1 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.805-2254delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68535603 | |||||
chr2:68535834
|
G | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2038G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535834 | ||||||
chr2:68535857
|
G | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2015G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535857 | ||||||
chr2:68535943
|
A | G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-1929A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68535943 | ||||||
chr2:68536105
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-1767G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536105 | ||||||
chr2:68536170
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-1702T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536170 | ||||||
chr2:68536432
|
C | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1440C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536432 | ||||||
chr2:68536470
|
C | T | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805-1402C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536470 | ||||||
chr2:68536514
|
T | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-1358T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536514 | ||||||
chr2:68536562
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.805-1310A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536562 | ||||||
chr2:68536568
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.805-1304A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536568 | ||||||
chr2:68536639
|
A | T | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.805-1233A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536639 | ||||||
chr2:68536721
|
C | A | 1 | a0002c0002t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.805-1151C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536721 | ||||||
chr2:68536834
|
A | G | 17 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(14): Show | 17 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.805-1038A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536834 | ||||||
chr2:68536913
|
T | TATTA | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.805-959_805-958ins others(4): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536913 | ||||||
chr2:68536925
|
G | C | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-947G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536925 | ||||||
chr2:68536964
|
C | T | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.805-908C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68536964 | ||||||
chr2:68537004
|
A | G | 1 | a0003c0003t0004g0124 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.805-868A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537004 | ||||||
chr2:68537057
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.805-815C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537057 | ||||||
chr2:68537133
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0074others(2): Show | 5 | HG00741.hp1 HG02886.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-739C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537133 | ||||||
chr2:68537164
|
C | CA | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.805-694dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537164 | |||||
chr2:68537164
|
CA | C | 7 | a0001c0001t0001g0056a0002c0002t0010g0167a0002c0002t0010g0168others(4): Show | 8 | HG02280.hp2 HG02451.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-694delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537164 | |||||
chr2:68537221
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.805-651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537221 | ||||||
chr2:68537293
|
AT | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-575delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 68537293 | |||||
chr2:68537350
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.805-522G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537350 | ||||||
chr2:68537394
|
T | C | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-478T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537394 | ||||||
chr2:68537414
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.805-458C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537414 | ||||||
chr2:68537584
|
G | T | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-288G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537584 | ||||||
chr2:68537637
|
T | C | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.805-235T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537637 | ||||||
chr2:68537655
|
C | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-217C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537655 | ||||||
chr2:68537741
|
G | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-131G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537741 | ||||||
chr2:68537810
|
A | T | 1 | a0002c0002t0002g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.805-62A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 6/9 | chr2 | 68537810 | ||||||
chr2:68538361
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1160+134T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538361 | ||||||
chr2:68538495
|
G | A | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1160+268G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538495 | ||||||
chr2:68538605
|
T | TTTAGGTG others(52): Show |
12 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(9): Show | 12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+379_1160+437d others(61): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68538605 | |||||
chr2:68538642
|
TTGA | T | 28 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(25): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1160+416_1160+418d others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538642 | ||||||
chr2:68538741
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160+514C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538741 | ||||||
chr2:68538816
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1160+589G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538816 | ||||||
chr2:68538935
|
A | G | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160+708A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538935 | ||||||
chr2:68538973
|
A | C | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1160+746A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68538973 | ||||||
chr2:68539118
|
A | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1160+891A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539118 | ||||||
chr2:68539249
|
T | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1160+1022T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539249 | ||||||
chr2:68539260
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1160+1033G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539260 | ||||||
chr2:68539373
|
T | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+1146T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539373 | ||||||
chr2:68539379
|
G | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1160+1152G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539379 | ||||||
chr2:68539552
|
C | A | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1160+1325C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539552 | ||||||
chr2:68539768
|
C | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+1541C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539768 | ||||||
chr2:68539781
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1160+1554C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539781 | ||||||
chr2:68539954
|
T | A | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160+1727T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68539954 | ||||||
chr2:68540108
|
A | G | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160+1881A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540108 | ||||||
chr2:68540169
|
C | T | 1 | a0002c0002t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1160+1942C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540169 | ||||||
chr2:68540199
|
C | T | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1160+1972C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540199 | ||||||
chr2:68540234
|
C | G | 3 | a0003c0003t0004g0114a0003c0003t0004g0115a0003c0003t0004g0124 | 3 | HG01192.hp1 HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1160+2007C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540234 | ||||||
chr2:68540538
|
A | G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+2311A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540538 | ||||||
chr2:68540576
|
G | A | 1 | a0002c0002t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1160+2349G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540576 | ||||||
chr2:68540599
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1160+2372A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540599 | ||||||
chr2:68540771
|
C | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+2544C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540771 | ||||||
chr2:68540778
|
GTGTGTGT others(3): Show |
G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+2569_1160+257 others(14): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68540778 | |||||
chr2:68540862
|
A | G | 28 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(25): Show | 30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.1160+2635A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540862 | ||||||
chr2:68540886
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160+2659C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68540886 | ||||||
chr2:68541195
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1160+2968A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541195 | ||||||
chr2:68541214
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1160+2987T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541214 | ||||||
chr2:68541339
|
TAGA | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+3115_1160+311 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68541339 | |||||
chr2:68541354
|
G | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1160+3127G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541354 | ||||||
chr2:68541386
|
C | T | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(161): Show | 169 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.1160+3159C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541386 | ||||||
chr2:68541676
|
C | T | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+3449C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541676 | ||||||
chr2:68541735
|
A | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161-3452A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541735 | ||||||
chr2:68541745
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1161-3442T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68541745 | ||||||
chr2:68542014
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-3173A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542014 | ||||||
chr2:68542135
|
ATATAACT | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-3049_1161-304 others(11): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68542135 | |||||
chr2:68542233
|
A | T | 1 | a0006c0007t0006g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1161-2954A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542233 | ||||||
chr2:68542253
|
C | T | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-2934C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542253 | ||||||
chr2:68542358
|
G | GAAATGAC others(90): Show |
5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-2750_1161-274 others(101): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68542358 | |||||
chr2:68542403
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1161-2784A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542403 | ||||||
chr2:68542415
|
T | C | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1161-2772T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542415 | ||||||
chr2:68542436
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2751G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542436 | ||||||
chr2:68542597
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2590G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542597 | ||||||
chr2:68542767
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161-2420A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542767 | ||||||
chr2:68542789
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1161-2398A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542789 | ||||||
chr2:68542942
|
A | G | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2245A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68542942 | ||||||
chr2:68543072
|
T | G | 2 | a0002c0002t0008g0023a0002c0002t0008g0025 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-2115T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543072 | ||||||
chr2:68543099
|
T | G | 22 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(19): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-2088T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543099 | ||||||
chr2:68543144
|
A | G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1161-2043A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543144 | ||||||
chr2:68543348
|
C | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1161-1839C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543348 | ||||||
chr2:68543398
|
G | A | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1161-1789G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543398 | ||||||
chr2:68543436
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1161-1751A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543436 | ||||||
chr2:68543547
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1161-1640T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543547 | ||||||
chr2:68543554
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161-1633C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543554 | ||||||
chr2:68543636
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1161-1551G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68543636 | ||||||
chr2:68543981
|
CT | C | 61 | a0001c0001t0001g0073a0002c0002t0002g0033a0002c0002t0002g0034others(58): Show | 63 | HG00323.hp1 HG01109.hp1 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.1161-1188delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68543981 | |||||
chr2:68543981
|
CTT | C | 17 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(14): Show | 18 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161-1189_1161-118 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68543981 | |||||
chr2:68544003
|
A | T | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-1184A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544003 | ||||||
chr2:68544197
|
C | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1161-990C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544197 | ||||||
chr2:68544342
|
C | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-845C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544342 | ||||||
chr2:68544403
|
T | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1161-784T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544403 | ||||||
chr2:68544420
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1161-767A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544420 | ||||||
chr2:68544535
|
A | C | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161-652A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544535 | ||||||
chr2:68544583
|
T | C | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-604T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544583 | ||||||
chr2:68544811
|
G | T | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1161-376G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544811 | ||||||
chr2:68544859
|
A | G | 1 | a0002c0002t0008g0024 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1161-328A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544859 | ||||||
chr2:68544863
|
A | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1161-324A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68544863 | ||||||
chr2:68545026
|
A | G | 1 | a0003c0003t0005g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1161-161A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545026 | ||||||
chr2:68545043
|
A | G | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1161-144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545043 | ||||||
chr2:68545149
|
AT | A | 20 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1161-28delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 68545149 | |||||
chr2:68545169
|
T | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1161-18T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 7/9 | chr2 | 68545169 | ||||||
chr2:68545619
|
T | C | 22 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(19): Show | 23 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1286+307T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68545619 | ||||||
chr2:68545676
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1286+364A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68545676 | ||||||
chr2:68546069
|
G | T | 14 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(11): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1286+757G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546069 | ||||||
chr2:68546275
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1286+963T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546275 | ||||||
chr2:68546416
|
T | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+1104T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546416 | ||||||
chr2:68546491
|
T | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+1179T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546491 | ||||||
chr2:68546676
|
A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1286+1364A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546676 | ||||||
chr2:68546888
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1286+1576G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546888 | ||||||
chr2:68546941
|
G | A | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286+1629G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546941 | ||||||
chr2:68546968
|
A | G | 32 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(29): Show | 33 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1286+1656A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68546968 | ||||||
chr2:68547078
|
G | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+1766G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547078 | ||||||
chr2:68547180
|
A | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+1868A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547180 | ||||||
chr2:68547227
|
A | G | 2 | a0002c0002t0006g0161a0002c0002t0006g0162 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1286+1915A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547227 | ||||||
chr2:68547303
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+1991C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547303 | ||||||
chr2:68547410
|
A | G | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1286+2098A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547410 | ||||||
chr2:68547552
|
T | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+2240T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547552 | ||||||
chr2:68547588
|
G | C | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+2276G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547588 | ||||||
chr2:68547675
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1286+2363C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547675 | ||||||
chr2:68547794
|
G | A | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+2482G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547794 | ||||||
chr2:68547813
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+2501A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547813 | ||||||
chr2:68547856
|
A | G | 1 | a0002c0002t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1286+2544A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547856 | ||||||
chr2:68547866
|
A | G | 1 | a0004c0004t0003g0010 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1286+2554A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68547866 | ||||||
chr2:68548005
|
C | G | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+2693C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548005 | ||||||
chr2:68548205
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+2893A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548205 | ||||||
chr2:68548545
|
A | C | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1286+3233A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548545 | ||||||
chr2:68548604
|
A | G | 8 | a0004c0004t0003g0013a0004c0004t0003g0014a0004c0004t0003g0015others(5): Show | 8 | HG02300.hp2 HG02738.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1286+3292A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548604 | ||||||
chr2:68548691
|
C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1286+3379C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548691 | ||||||
chr2:68548833
|
AG | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+3522delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68548833 | ||||||
chr2:68548868
|
TTCA | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+3560_1286+356 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68548868 | |||||
chr2:68549028
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1286+3716T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549028 | ||||||
chr2:68549448
|
T | G | 2 | a0002c0002t0010g0168a0002c0002t0010g0169 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+4136T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549448 | ||||||
chr2:68549480
|
A | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+4168A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549480 | ||||||
chr2:68549499
|
A | G | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+4187A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549499 | ||||||
chr2:68549580
|
T | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+4268T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549580 | ||||||
chr2:68549671
|
G | A | 1 | a0005c0005t0001g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1286+4359G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549671 | ||||||
chr2:68549851
|
A | G | 1 | a0002c0002t0010g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1286+4539A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549851 | ||||||
chr2:68549881
|
T | C | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+4569T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68549881 | ||||||
chr2:68550161
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+4849A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550161 | ||||||
chr2:68550235
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+4923A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550235 | ||||||
chr2:68550292
|
C | T | 1 | a0002c0002t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1286+4980C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550292 | ||||||
chr2:68550389
|
G | A | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1286+5077G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550389 | ||||||
chr2:68550525
|
C | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+5213C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550525 | ||||||
chr2:68550948
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+5636C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550948 | ||||||
chr2:68550971
|
A | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+5659A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68550971 | ||||||
chr2:68551032
|
T | G | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1286+5720T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551032 | ||||||
chr2:68551084
|
C | G | 1 | a0004c0004t0003g0010 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1286+5772C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551084 | ||||||
chr2:68551163
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1286+5851C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551163 | ||||||
chr2:68551241
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+5929C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551241 | ||||||
chr2:68551298
|
C | G | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+5986C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551298 | ||||||
chr2:68551345
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+6033A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551345 | ||||||
chr2:68551383
|
T | C | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1286+6071T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551383 | ||||||
chr2:68551591
|
A | ATTC | 23 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 23 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1286+6291_1286+629 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551591 | |||||
chr2:68551601
|
T | TCCTTC | 2 | a0002c0002t0008g0023a0002c0002t0008g0025 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+6289_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551601 | ||||||
chr2:68551603
|
C | CTT | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+6307_1286+630 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | |||||
chr2:68551603
|
C | CTTCT | 13 | a0002c0002t0002g0051a0002c0002t0009g0003a0002c0002t0012g0021others(10): Show | 14 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | |||||
chr2:68551603
|
C | CTTCTT | 8 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | |||||
chr2:68551603
|
C | CTTT | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+6306_1286+630 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551603 | |||||
chr2:68551603
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+6291C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551603 | ||||||
chr2:68551604
|
T | TTCTTC | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+6293_1286+629 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551604 | |||||
chr2:68551679
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1286+6367C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551679 | ||||||
chr2:68551684
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+6372T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551684 | ||||||
chr2:68551697
|
A | G | 1 | a0003c0003t0004g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1286+6385A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551697 | ||||||
chr2:68551715
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+6403A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551715 | ||||||
chr2:68551754
|
C | CTT | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+6453_1286+645 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68551754 | |||||
chr2:68551763
|
T | C | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+6451T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551763 | ||||||
chr2:68551811
|
C | T | 3 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035 | 3 | HG01433.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1286+6499C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551811 | ||||||
chr2:68551851
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+6539A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551851 | ||||||
chr2:68551944
|
T | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+6632T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68551944 | ||||||
chr2:68552224
|
A | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+6912A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552224 | ||||||
chr2:68552335
|
T | C | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1286+7023T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552335 | ||||||
chr2:68552382
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+7070C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552382 | ||||||
chr2:68552402
|
TAACC | T | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+7093_1286+709 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68552402 | |||||
chr2:68552831
|
G | A | 1 | a0006c0007t0006g0002 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1286+7519G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552831 | ||||||
chr2:68552927
|
C | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1286+7615C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68552927 | ||||||
chr2:68553088
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1286+7776C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553088 | ||||||
chr2:68553175
|
TC | T | 4 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286+7864delC | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553175 | ||||||
chr2:68553236
|
A | G | 1 | a0002c0002t0002g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1286+7924A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553236 | ||||||
chr2:68553247
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1286+7935A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553247 | ||||||
chr2:68553291
|
T | A | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286+7979T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553291 | ||||||
chr2:68553342
|
A | T | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8030A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553342 | ||||||
chr2:68553392
|
C | T | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(132): Show | 140 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.1286+8080C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553392 | ||||||
chr2:68553446
|
GTATAT | G | 17 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(14): Show | 17 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1286+8138_1286+814 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68553446 | |||||
chr2:68553531
|
A | G | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8219A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553531 | ||||||
chr2:68553603
|
C | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1286+8291C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68553603 | ||||||
chr2:68553791
|
ACTTG | A | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+8483_1286+848 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68553791 | |||||
chr2:68554086
|
A | C | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+8774A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554086 | ||||||
chr2:68554161
|
T | A | 1 | a0005c0005t0014g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1286+8849T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554161 | ||||||
chr2:68554249
|
T | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1286+8937T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554249 | ||||||
chr2:68554277
|
G | C | 1 | a0005c0005t0014g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1286+8965G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554277 | ||||||
chr2:68554372
|
A | C | 1 | a0002c0002t0007g0001 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1286+9060A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554372 | ||||||
chr2:68554638
|
G | GT | 10 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(7): Show | 11 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1286+9340dupT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68554638 | |||||
chr2:68554735
|
G | A | 1 | a0002c0002t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+9423G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554735 | ||||||
chr2:68554739
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+9427A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68554739 | ||||||
chr2:68555037
|
T | C | 28 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(25): Show | 29 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1286+9725T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555037 | ||||||
chr2:68555042
|
G | A | 25 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(22): Show | 26 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1286+9730G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555042 | ||||||
chr2:68555234
|
C | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+9922C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555234 | ||||||
chr2:68555250
|
A | G | 96 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(93): Show | 99 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.1286+9938A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555250 | ||||||
chr2:68555430
|
C | T | 1 | a0001c0001t0011g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1286+10118C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555430 | ||||||
chr2:68555474
|
G | A | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+10162G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555474 | ||||||
chr2:68555536
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286+10224A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555536 | ||||||
chr2:68555605
|
A | G | 1 | a0008c0008t0006g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1286+10293A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555605 | ||||||
chr2:68555631
|
A | C | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1286+10319A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555631 | ||||||
chr2:68555705
|
A | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1286+10393A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68555705 | ||||||
chr2:68556032
|
A | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+10720A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556032 | ||||||
chr2:68556225
|
A | T | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286+10913A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556225 | ||||||
chr2:68556356
|
A | T | 1 | a0004c0004t0003g0020 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1287-10985A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556356 | ||||||
chr2:68556608
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-10733A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556608 | ||||||
chr2:68556722
|
A | G | 1 | a0002c0002t0010g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1287-10619A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556722 | ||||||
chr2:68556813
|
G | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-10528G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556813 | ||||||
chr2:68556832
|
G | C | 10 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-10509G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68556832 | ||||||
chr2:68557200
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1287-10141C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557200 | ||||||
chr2:68557225
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1287-10116T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557225 | ||||||
chr2:68557258
|
G | A | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-10083G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557258 | ||||||
chr2:68557277
|
A | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-10064A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557277 | ||||||
chr2:68557344
|
A | G | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-9997A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557344 | ||||||
chr2:68557538
|
A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-9803A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557538 | ||||||
chr2:68557652
|
C | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-9689C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557652 | ||||||
chr2:68557677
|
T | G | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-9664T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557677 | ||||||
chr2:68557890
|
G | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-9451G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557890 | ||||||
chr2:68557910
|
G | GA | 5 | a0001c0001t0001g0066a0001c0001t0001g0089a0005c0005t0001g0149others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-9417dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68557910 | |||||
chr2:68557910
|
GA | G | 23 | a0002c0002t0007g0030a0003c0003t0005g0105a0003c0003t0005g0127others(20): Show | 23 | HG01109.hp1 HG02129.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1287-9417delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68557910 | |||||
chr2:68557925
|
T | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-9416T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557925 | ||||||
chr2:68557938
|
T | C | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-9403T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68557938 | ||||||
chr2:68558126
|
T | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG00323.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1287-9215T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558126 | ||||||
chr2:68558139
|
A | T | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-9202A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558139 | ||||||
chr2:68558211
|
G | A | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1287-9130G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558211 | ||||||
chr2:68558274
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-9067A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558274 | ||||||
chr2:68558304
|
A | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-9037A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558304 | ||||||
chr2:68558447
|
G | A | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-8894G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558447 | ||||||
chr2:68558486
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-8855T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558486 | ||||||
chr2:68558734
|
G | A | 10 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-8607G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558734 | ||||||
chr2:68558797
|
G | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-8544G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558797 | ||||||
chr2:68558800
|
C | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-8541C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558800 | ||||||
chr2:68558802
|
G | C | 32 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(29): Show | 33 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1287-8539G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558802 | ||||||
chr2:68558858
|
A | G | 32 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(29): Show | 33 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1287-8483A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68558858 | ||||||
chr2:68559238
|
T | C | 10 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-8103T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559238 | ||||||
chr2:68559345
|
G | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-7996G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559345 | ||||||
chr2:68559381
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7960A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559381 | ||||||
chr2:68559431
|
G | A | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1287-7910G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559431 | ||||||
chr2:68559477
|
G | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7864G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559477 | ||||||
chr2:68559645
|
C | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-7696C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559645 | ||||||
chr2:68559747
|
T | C | 2 | a0002c0002t0002g0047a0002c0002t0002g0048 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1287-7594T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559747 | ||||||
chr2:68559910
|
C | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-7431C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559910 | ||||||
chr2:68559993
|
A | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0078others(2): Show | 5 | NA18962.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-7348A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68559993 | ||||||
chr2:68560002
|
C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-7339C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560002 | ||||||
chr2:68560043
|
G | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-7298G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560043 | ||||||
chr2:68560059
|
T | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-7282T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560059 | ||||||
chr2:68560177
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-7164A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560177 | ||||||
chr2:68560362
|
G | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-6979G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560362 | ||||||
chr2:68560413
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1287-6928C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560413 | ||||||
chr2:68560426
|
T | TAGAA | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-6913_1287-691 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68560426 | |||||
chr2:68560458
|
T | G | 6 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(3): Show | 7 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-6883T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560458 | ||||||
chr2:68560612
|
C | T | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-6729C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560612 | ||||||
chr2:68560615
|
C | T | 1 | a0003c0003t0005g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1287-6726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560615 | ||||||
chr2:68560668
|
C | T | 1 | a0003c0003t0004g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1287-6673C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560668 | ||||||
chr2:68560795
|
C | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-6546C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560795 | ||||||
chr2:68560915
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-6426T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560915 | ||||||
chr2:68560923
|
G | A | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-6418G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560923 | ||||||
chr2:68560955
|
C | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-6386C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68560955 | ||||||
chr2:68560989
|
ATAT | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-6348_1287-634 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68560989 | |||||
chr2:68561162
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-6179A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561162 | ||||||
chr2:68561170
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-6171A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561170 | ||||||
chr2:68561269
|
A | G | 1 | a0002c0002t0002g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1287-6072A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561269 | ||||||
chr2:68561382
|
A | C | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-5959A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561382 | ||||||
chr2:68561421
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-5920A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561421 | ||||||
chr2:68561623
|
G | A | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-5718G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561623 | ||||||
chr2:68561733
|
C | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-5608C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68561733 | ||||||
chr2:68562037
|
C | T | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-5304C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562037 | ||||||
chr2:68562137
|
G | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-5204G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562137 | ||||||
chr2:68562150
|
G | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-5191G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562150 | ||||||
chr2:68562289
|
A | T | 1 | a0001c0001t0011g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1287-5052A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562289 | ||||||
chr2:68562324
|
A | G | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-5017A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562324 | ||||||
chr2:68562598
|
T | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-4743T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562598 | ||||||
chr2:68562749
|
A | G | 2 | a0001c0001t0001g0145a0001c0009t0001g0155 | 2 | HG00673.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1287-4592A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562749 | ||||||
chr2:68562784
|
A | C | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-4557A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562784 | ||||||
chr2:68562916
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-4425A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68562916 | ||||||
chr2:68563029
|
C | T | 76 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(73): Show | 79 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1287-4312C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563029 | ||||||
chr2:68563135
|
T | C | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-4206T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563135 | ||||||
chr2:68563217
|
A | T | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-4124A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563217 | ||||||
chr2:68563424
|
C | T | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-3917C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563424 | ||||||
chr2:68563440
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1287-3901G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563440 | ||||||
chr2:68563635
|
A | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-3706A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563635 | ||||||
chr2:68563670
|
G | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-3671G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563670 | ||||||
chr2:68563764
|
A | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-3577A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563764 | ||||||
chr2:68563853
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-3488C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563853 | ||||||
chr2:68563918
|
A | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287-3423A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68563918 | ||||||
chr2:68564162
|
G | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-3179G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564162 | ||||||
chr2:68564197
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1287-3144A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564197 | ||||||
chr2:68564308
|
T | C | 2 | a0002c0002t0002g0038a0002c0002t0002g0039 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1287-3033T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564308 | ||||||
chr2:68564335
|
A | G | 1 | a0002c0002t0002g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1287-3006A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564335 | ||||||
chr2:68564392
|
A | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1287-2949A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564392 | ||||||
chr2:68564496
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-2845A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564496 | ||||||
chr2:68564509
|
A | G | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1287-2832A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564509 | ||||||
chr2:68564665
|
T | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2676T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564665 | ||||||
chr2:68564674
|
A | G | 1 | a0002c0002t0002g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1287-2667A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564674 | ||||||
chr2:68564762
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2579A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564762 | ||||||
chr2:68564830
|
G | T | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287-2511G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68564830 | ||||||
chr2:68565028
|
T | C | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-2313T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565028 | ||||||
chr2:68565207
|
AG | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1287-2133delG | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565207 | ||||||
chr2:68565321
|
A | G | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1287-2020A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565321 | ||||||
chr2:68565322
|
A | G | 12 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(9): Show | 12 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-2019A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565322 | ||||||
chr2:68565504
|
T | C | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1837T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565504 | ||||||
chr2:68565508
|
C | CAGAT | 8 | a0002c0002t0002g0047a0002c0002t0002g0050a0002c0002t0002g0051others(5): Show | 9 | HG01167.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287-1827_1287-182 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | |||||
chr2:68565508
|
C | CAGATAGA others(1): Show |
22 | a0002c0002t0002g0052a0002c0002t0006g0161a0002c0002t0006g0164others(19): Show | 23 | HG00639.hp1 HG01192.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1287-1831_1287-182 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | |||||
chr2:68565508
|
C | CAGATAGA others(5): Show |
2 | a0002c0002t0006g0163a0008c0008t0006g0026 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | |||||
chr2:68565508
|
C | CAGATAGA others(9): Show |
1 | a0002c0002t0006g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1287-1824_1287-182 others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565508 | |||||
chr2:68565514
|
G | C | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1287-1827G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565514 | ||||||
chr2:68565514
|
G | GATAC | 26 | a0001c0001t0001g0066a0001c0001t0001g0085a0001c0001t0001g0086others(23): Show | 26 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1287-1787_1287-178 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
G | GATACATA others(1): Show |
5 | a0001c0001t0001g0137a0004c0004t0003g0012a0004c0004t0003g0013others(2): Show | 5 | HG02630.hp2 HG03942.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-1791_1287-178 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
G | GATACATA others(5): Show |
2 | a0002c0002t0006g0161a0002c0002t0006g0164 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1287-1795_1287-178 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
G | GATAGATA others(1): Show |
13 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(10): Show | 13 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(12): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
G | GATAGATA others(5): Show |
7 | a0002c0002t0002g0044a0002c0002t0002g0045a0003c0003t0004g0120others(4): Show | 7 | HG00738.hp1 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(16): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
G | GATAGATA others(9): Show |
2 | a0002c0002t0002g0043a0002c0002t0002g0046 | 2 | HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1287-1824_1287-182 others(20): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565514
|
GATAC | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1287-1787_1287-178 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 68565514 | |||||
chr2:68565518
|
C | G | 6 | a0002c0002t0002g0051a0002c0002t0002g0053a0002c0002t0009g0003others(3): Show | 7 | HG02145.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287-1823C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565518 | ||||||
chr2:68565522
|
C | G | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1287-1819C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565522 | ||||||
chr2:68565558
|
G | C | 41 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(38): Show | 43 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1287-1783G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565558 | ||||||
chr2:68565572
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1287-1769A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565572 | ||||||
chr2:68565595
|
C | A | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1287-1746C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565595 | ||||||
chr2:68565669
|
T | C | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-1672T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565669 | ||||||
chr2:68565690
|
G | A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1287-1651G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565690 | ||||||
chr2:68565703
|
A | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1638A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565703 | ||||||
chr2:68565720
|
T | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-1621T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565720 | ||||||
chr2:68565789
|
G | T | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1287-1552G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565789 | ||||||
chr2:68565844
|
G | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0054others(159): Show | 167 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.1287-1497G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565844 | ||||||
chr2:68565942
|
G | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1287-1399G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68565942 | ||||||
chr2:68566289
|
C | T | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1287-1052C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566289 | ||||||
chr2:68566449
|
C | T | 1 | a0004c0004t0003g0009 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1287-892C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566449 | ||||||
chr2:68566457
|
G | A | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-884G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566457 | ||||||
chr2:68566615
|
C | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1287-726C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566615 | ||||||
chr2:68566995
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1287-346C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68566995 | ||||||
chr2:68567072
|
T | C | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1287-269T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 8/9 | chr2 | 68567072 | ||||||
chr2:68567396
|
G | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+9G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567396 | ||||||
chr2:68567534
|
T | TA | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1333+156dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68567534 | |||||
chr2:68567665
|
A | G | 5 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(2): Show | 5 | HG02129.hp1 HG02293.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333+278A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567665 | ||||||
chr2:68567693
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1333+306C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567693 | ||||||
chr2:68567836
|
C | T | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+449C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567836 | ||||||
chr2:68567949
|
T | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+562T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68567949 | ||||||
chr2:68568008
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+621C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568008 | ||||||
chr2:68568019
|
C | T | 1 | a0002c0002t0010g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1333+632C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568019 | ||||||
chr2:68568533
|
G | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+1146G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568533 | ||||||
chr2:68568535
|
A | T | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+1148A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568535 | ||||||
chr2:68568580
|
T | C | 1 | a0006c0007t0017g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1333+1193T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568580 | ||||||
chr2:68568632
|
C | G | 1 | a0002c0002t0002g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1333+1245C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568632 | ||||||
chr2:68568638
|
C | T | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1333+1251C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568638 | ||||||
chr2:68568711
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1333+1324C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568711 | ||||||
chr2:68568814
|
A | C | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+1427A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568814 | ||||||
chr2:68568876
|
A | G | 18 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(15): Show | 18 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333+1489A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568876 | ||||||
chr2:68568929
|
A | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+1542A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568929 | ||||||
chr2:68568956
|
C | T | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+1569C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68568956 | ||||||
chr2:68569100
|
A | T | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1333+1713A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569100 | ||||||
chr2:68569192
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0011g0069 | 2 | NA18984.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1333+1805A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569192 | ||||||
chr2:68569201
|
G | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+1814G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569201 | ||||||
chr2:68569486
|
A | G | 73 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(70): Show | 76 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.1333+2099A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569486 | ||||||
chr2:68569574
|
C | T | 1 | a0012c0012t0007g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1333+2187C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569574 | ||||||
chr2:68569641
|
A | AT | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+2254_1333+225 others(5): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569641 | ||||||
chr2:68569643
|
T | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+2256T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569643 | ||||||
chr2:68569748
|
G | A | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+2361G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569748 | ||||||
chr2:68569839
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333+2452G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68569839 | ||||||
chr2:68570042
|
T | C | 41 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(38): Show | 43 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.1333+2655T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570042 | ||||||
chr2:68570233
|
T | C | 1 | a0002c0002t0002g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1333+2846T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570233 | ||||||
chr2:68570285
|
TTAA | T | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+2901_1333+290 others(7): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68570285 | |||||
chr2:68570287
|
A | T | 35 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(32): Show | 36 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1333+2900A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570287 | ||||||
chr2:68570287
|
AAT | A | 31 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(28): Show | 33 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333+2913_1333+291 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68570287 | |||||
chr2:68570288
|
A | T | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+2901A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570288 | ||||||
chr2:68570288
|
AT | A | 30 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1333+2902delT | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570288 | ||||||
chr2:68570289
|
T | A | 18 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(15): Show | 18 | HG02109.hp1 HG02129.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333+2902T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570289 | ||||||
chr2:68570314
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1333+2927T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570314 | ||||||
chr2:68570340
|
T | C | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+2953T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570340 | ||||||
chr2:68570437
|
C | T | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+3050C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570437 | ||||||
chr2:68570629
|
T | C | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1333+3242T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570629 | ||||||
chr2:68570654
|
C | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1333+3267C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570654 | ||||||
chr2:68570719
|
G | A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1333+3332G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570719 | ||||||
chr2:68570743
|
G | T | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+3356G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570743 | ||||||
chr2:68570799
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1333+3412G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570799 | ||||||
chr2:68570865
|
T | G | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333+3478T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570865 | ||||||
chr2:68570868
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1333+3481C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570868 | ||||||
chr2:68570931
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1333+3544G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68570931 | ||||||
chr2:68571094
|
C | G | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+3707C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571094 | ||||||
chr2:68571254
|
C | A | 3 | a0002c0002t0008g0023a0002c0002t0008g0024a0002c0002t0008g0025 | 3 | HG01167.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1333+3867C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571254 | ||||||
chr2:68571300
|
T | G | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1333+3913T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571300 | ||||||
chr2:68571332
|
C | A | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1333+3945C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571332 | ||||||
chr2:68571462
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333+4075A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571462 | ||||||
chr2:68571462
|
A | T | 1 | a0003c0003t0004g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1333+4075A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571462 | ||||||
chr2:68571576
|
C | G | 1 | a0002c0002t0012g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333+4189C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571576 | ||||||
chr2:68571641
|
C | T | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1333+4254C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571641 | ||||||
chr2:68571646
|
A | G | 1 | a0002c0002t0002g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1333+4259A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571646 | ||||||
chr2:68571684
|
A | T | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+4297A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571684 | ||||||
chr2:68571786
|
G | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+4399G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571786 | ||||||
chr2:68571940
|
T | C | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333+4553T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571940 | ||||||
chr2:68571941
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1333+4554G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571941 | ||||||
chr2:68571951
|
A | G | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333+4564A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68571951 | ||||||
chr2:68572063
|
A | C | 1 | a0002c0002t0009g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1333+4676A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572063 | ||||||
chr2:68572087
|
A | AGGCTTAG others(10): Show |
11 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4700_1333+470 others(21): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572087 | ||||||
chr2:68572089
|
A | T | 11 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4702A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572089 | ||||||
chr2:68572094
|
A | T | 11 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4707A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572094 | ||||||
chr2:68572095
|
C | T | 11 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333+4708C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572095 | ||||||
chr2:68572170
|
T | C | 1 | a0005c0005t0001g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1333+4783T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572170 | ||||||
chr2:68572272
|
T | G | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1333+4885T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572272 | ||||||
chr2:68572273
|
A | T | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333+4886A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572273 | ||||||
chr2:68572322
|
G | A | 79 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(76): Show | 82 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.1333+4935G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572322 | ||||||
chr2:68572518
|
G | C | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1333+5131G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572518 | ||||||
chr2:68572646
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0015g0090 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1334-5174G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572646 | ||||||
chr2:68572679
|
T | TA | 20 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1334-5133dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68572679 | |||||
chr2:68572819
|
A | G | 13 | a0004c0004t0003g0008a0004c0004t0003g0009a0004c0004t0003g0010others(10): Show | 13 | HG02129.hp1 HG02293.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1334-5001A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68572819 | ||||||
chr2:68572838
|
CAACAA | C | 30 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(27): Show | 31 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334-4962_1334-495 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68572838 | |||||
chr2:68573090
|
A | T | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-4730A>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573090 | ||||||
chr2:68573091
|
T | C | 2 | a0006c0007t0006g0002a0006c0007t0006g0032 | 3 | HG03098.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-4729T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573091 | ||||||
chr2:68573113
|
T | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0159 | 2 | NA19005.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1334-4707T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573113 | ||||||
chr2:68573336
|
A | G | 4 | a0001c0001t0001g0066a0005c0005t0001g0149a0005c0005t0001g0153others(1): Show | 4 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-4484A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573336 | ||||||
chr2:68573370
|
G | A | 2 | a0002c0002t0002g0043a0002c0002t0002g0044 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1334-4450G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573370 | ||||||
chr2:68573459
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1334-4361G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573459 | ||||||
chr2:68573569
|
A | G | 10 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(7): Show | 11 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1334-4251A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573569 | ||||||
chr2:68573598
|
G | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-4222G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573598 | ||||||
chr2:68573672
|
C | CA | 34 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(31): Show | 36 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1334-4129dupA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573672 | |||||
chr2:68573672
|
C | CAA | 32 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(29): Show | 32 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1334-4130_1334-412 others(6): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573672 | |||||
chr2:68573787
|
C | T | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1334-4033C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573787 | ||||||
chr2:68573795
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1334-4025G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573795 | ||||||
chr2:68573803
|
T | C | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-4017T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573803 | ||||||
chr2:68573880
|
GTTTCC | G | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-3935_1334-393 others(9): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68573880 | |||||
chr2:68573917
|
C | T | 4 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(1): Show | 5 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-3903C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68573917 | ||||||
chr2:68574004
|
T | C | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-3816T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574004 | ||||||
chr2:68574080
|
TA | T | 5 | a0001c0001t0001g0117a0002c0002t0010g0167a0002c0002t0010g0168others(2): Show | 5 | HG01169.hp2 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334-3725delA | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68574080 | |||||
chr2:68574142
|
A | G | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-3678A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574142 | ||||||
chr2:68574221
|
A | G | 1 | a0002c0002t0002g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1334-3599A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574221 | ||||||
chr2:68574280
|
T | A | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-3540T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574280 | ||||||
chr2:68574534
|
A | G | 18 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(15): Show | 18 | HG00323.hp1 HG00741.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1334-3286A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574534 | ||||||
chr2:68574572
|
G | A | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334-3248G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574572 | ||||||
chr2:68574706
|
C | T | 9 | a0003c0003t0005g0105a0003c0003t0005g0127a0003c0003t0005g0128others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1334-3114C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574706 | ||||||
chr2:68574760
|
A | G | 1 | a0002c0002t0002g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1334-3060A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574760 | ||||||
chr2:68574807
|
T | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-3013T>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574807 | ||||||
chr2:68574956
|
G | A | 5 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0041others(2): Show | 5 | HG01891.hp2 HG02809.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-2864G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574956 | ||||||
chr2:68574958
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-2862G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574958 | ||||||
chr2:68574962
|
C | A | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-2858C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574962 | ||||||
chr2:68574975
|
G | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2845G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68574975 | ||||||
chr2:68575135
|
T | C | 3 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022 | 4 | HG03098.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-2685T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575135 | ||||||
chr2:68575155
|
C | CAGAT | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-2663_1334-266 others(8): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 68575155 | |||||
chr2:68575340
|
G | A | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-2480G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575340 | ||||||
chr2:68575683
|
A | G | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-2137A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575683 | ||||||
chr2:68575793
|
T | C | 1 | a0006c0013t0016g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1334-2027T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575793 | ||||||
chr2:68575972
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-1848C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68575972 | ||||||
chr2:68576074
|
C | T | 1 | a0001c0001t0001g0007 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1334-1746C>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576074 | ||||||
chr2:68576079
|
T | C | 21 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0035others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1334-1741T>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576079 | ||||||
chr2:68576217
|
A | C | 5 | a0002c0002t0007g0001a0002c0002t0007g0029a0002c0002t0007g0030others(2): Show | 6 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334-1603A>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576217 | ||||||
chr2:68576300
|
T | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0116 | 2 | NA18962.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1334-1520T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576300 | ||||||
chr2:68576327
|
A | G | 21 | a0003c0003t0004g0104a0003c0003t0004g0114a0003c0003t0004g0115others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1334-1493A>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576327 | ||||||
chr2:68576380
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1334-1440C>G | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576380 | ||||||
chr2:68576991
|
G | T | 3 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169 | 3 | HG02451.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1334-829G>T | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576991 | ||||||
chr2:68576993
|
T | A | 31 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(28): Show | 32 | HG00639.hp1 HG00738.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-827T>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576993 | ||||||
chr2:68576995
|
G | A | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-825G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68576995 | ||||||
chr2:68577123
|
G | C | 1 | a0011c0015t0013g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334-697G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577123 | ||||||
chr2:68577167
|
G | A | 4 | a0002c0002t0010g0167a0002c0002t0010g0168a0002c0002t0010g0169others(1): Show | 4 | HG02451.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334-653G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577167 | ||||||
chr2:68577200
|
G | A | 4 | a0006c0007t0006g0002a0006c0007t0006g0032a0006c0007t0017g0022others(1): Show | 5 | HG03098.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-620G>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577200 | ||||||
chr2:68577320
|
G | C | 1 | a0010c0014t0009g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334-500G>C | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577320 | ||||||
chr2:68577436
|
C | A | 5 | a0002c0002t0006g0161a0002c0002t0006g0162a0002c0002t0006g0163others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-384C>A | APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 9/9 | chr2 | 68577436 |