Item | Value |
---|---|
geneid | 6018 |
ensemblid | ENSG00000117000.9 |
hgncid | 10025 |
symbol | RLF |
name | RLF zinc finger |
refseq_nuc | NM_012421.4 |
refseq_prot | NP_036553.2 |
ensembl_nuc | ENST00000372771.5 |
ensembl_prot | ENSP00000361857.4 |
mane_status | MANE Select |
chr | chr1 |
start | 40161387 |
end | 40240921 |
strand | + |
ver | v1.2 |
region | chr1:40161387-40240921 |
region5000 | chr1:40156387-40245921 |
regionname0 | RLF_chr1_40161387_40240921 |
regionname5000 | RLF_chr1_40156387_40245921 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1914 | 212 | 44 | 30 | 101 | 7 | 28 | 73 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0002 | 0/0 | 1914 | 64 | 31 | 8 | 17 | 6 | 2 | 16 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0003 | 0/0 | 1914 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0004 | 0/0 | 1914 | 15 | 1 | 0 | 6 | 0 | 8 | 2 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0005 | 0/0 | 1914 | 13 | 0 | 1 | 12 | 0 | 0 | 9 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0006 | 0/0 | 1914 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0007 | 0/0 | 1914 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0008 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0009 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0010 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0011 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0012 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0013 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0014 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0015 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0016 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0017 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5745 | 196 | 42 | 28 | 89 | 7 | 28 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0002 | 0/0 | 5745 | 57 | 24 | 8 | 17 | 6 | 2 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0003 | 0/0 | 5745 | 16 | 15 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0004 | 0/0 | 5745 | 15 | 1 | 0 | 6 | 0 | 8 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0005 | 0/0 | 5745 | 13 | 0 | 1 | 12 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0006 | 0/0 | 5745 | 11 | 0 | 0 | 11 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0007 | 0/0 | 5745 | 4 | 4 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0008 | 0/0 | 5745 | 3 | 0 | 0 | 3 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0009 | 0/0 | 5745 | 3 | 1 | 2 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0010 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0011 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0012 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0013 | 0/0 | 5745 | 2 | 0 | 0 | 1 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0014 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0015 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0016 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0017 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0018 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0019 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0020 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0021 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0022 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0023 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
c0024 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 488 | 338 | 98 | 40 | 144 | 14 | 40 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5745 | 196 | 42 | 28 | 89 | 7 | 28 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0001c0006 | 0/0 | 5745 | 11 | 0 | 0 | 11 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0001c0009 | 0/0 | 5745 | 3 | 1 | 2 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0001c0016 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0001c0019 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0002c0002 | 0/0 | 5745 | 57 | 24 | 8 | 17 | 6 | 2 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0002c0007 | 0/0 | 5745 | 4 | 4 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0002c0011 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0002c0023 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0003c0003 | 0/0 | 5745 | 16 | 15 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0004c0004 | 0/0 | 5745 | 15 | 1 | 0 | 6 | 0 | 8 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0005c0005 | 0/0 | 5745 | 13 | 0 | 1 | 12 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0006c0008 | 0/0 | 5745 | 3 | 0 | 0 | 3 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0007c0013 | 0/0 | 5745 | 2 | 0 | 0 | 1 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0008c0010 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0009c0012 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0010c0014 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0011c0024 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0012c0020 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0013c0021 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0014c0018 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0015c0017 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0016c0022 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 | |
a0017c0015 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 6232 | 196 | 42 | 28 | 89 | 7 | 28 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0001c0006t0001 | 0/0 | 6232 | 11 | 0 | 0 | 11 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0001c0009t0001 | 0/0 | 6232 | 3 | 1 | 2 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0001c0016t0001 | 0/0 | 6232 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0001c0019t0001 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0002c0002t0001 | 0/0 | 6232 | 57 | 24 | 8 | 17 | 6 | 2 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0002c0007t0001 | 0/0 | 6232 | 4 | 4 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0002c0011t0001 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0002c0023t0001 | 0/0 | 6232 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0003c0003t0001 | 0/0 | 6232 | 16 | 15 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0004c0004t0001 | 0/0 | 6232 | 15 | 1 | 0 | 6 | 0 | 8 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0005c0005t0001 | 0/0 | 6232 | 13 | 0 | 1 | 12 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0006c0008t0001 | 0/0 | 6232 | 3 | 0 | 0 | 3 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0007c0013t0001 | 0/0 | 6232 | 2 | 0 | 0 | 1 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0008c0010t0001 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0009c0012t0001 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0010c0014t0001 | 0/0 | 6232 | 2 | 2 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0011c0024t0001 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0012c0020t0001 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0013c0021t0001 | 0/0 | 6232 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0014c0018t0001 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0015c0017t0001 | 0/0 | 6232 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0016c0022t0001 | 0/0 | 6232 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
a0017c0015t0001 | 0/0 | 6232 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | copy fasta | chr1 | 40156387 | 40245921 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0009t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0009t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0009t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0016t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0001c0019t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0007t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0007t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0007t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0011t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0002c0023t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0003c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0005c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0006c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0006c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0006c0008t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0007c0013t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0007c0013t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0008c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0008c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0009c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0009c0012t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0010c0014t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0010c0014t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0011c0024t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0012c0020t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0013c0021t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0014c0018t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0015c0017t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0016c0022t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
a0017c0015t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0261 | EUR | GBR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | GBR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00280 | hp1 | a0013 | c0021 | t0001 | g0051 | EUR | FIN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0249 | EUR | FIN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00423 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00423 | hp2 | a0005 | c0005 | t0001 | g0314 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00544 | hp2 | a0001 | c0006 | t0001 | g0065 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00558 | hp1 | a0005 | c0005 | t0001 | g0318 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0322 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01069 | hp1 | a0001 | c0009 | t0001 | g0241 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01071 | hp2 | a0001 | c0009 | t0001 | g0174 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01496 | hp1 | a0005 | c0005 | t0001 | g0307 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0272 | EUR | IBS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0271 | EUR | IBS | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0321 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01891 | hp2 | a0009 | c0012 | t0001 | g0237 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02015 | hp2 | a0014 | c0018 | t0001 | g0087 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02027 | hp1 | a0005 | c0005 | t0001 | g0306 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0323 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02074 | hp2 | a0004 | c0004 | t0001 | g0182 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02080 | hp1 | a0004 | c0004 | t0001 | g0180 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02083 | hp2 | a0004 | c0004 | t0001 | g0176 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02132 | hp1 | a0011 | c0024 | t0001 | g0201 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0326 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0335 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02258 | hp2 | a0002 | c0007 | t0001 | g0252 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02523 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02615 | hp2 | a0002 | c0023 | t0001 | g0268 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0288 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02630 | hp2 | a0016 | c0022 | t0001 | g0333 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02698 | hp2 | a0004 | c0004 | t0001 | g0304 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0334 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02735 | hp1 | a0004 | c0004 | t0001 | g0177 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02818 | hp2 | a0002 | c0011 | t0001 | g0230 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0320 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02895 | hp1 | a0010 | c0014 | t0001 | g0338 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0330 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02897 | hp1 | a0010 | c0014 | t0001 | g0337 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0329 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0332 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0327 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0324 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0173 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03209 | hp1 | a0002 | c0007 | t0001 | g0255 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03225 | hp1 | a0002 | c0007 | t0001 | g0253 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0331 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03453 | hp2 | a0002 | c0007 | t0001 | g0254 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03540 | hp2 | a0008 | c0010 | t0001 | g0228 | AFR | GWD | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03654 | hp1 | a0004 | c0004 | t0001 | g0086 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03688 | hp2 | a0004 | c0004 | t0001 | g0154 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03834 | hp2 | a0015 | c0017 | t0001 | g0137 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03927 | hp1 | a0004 | c0004 | t0001 | g0301 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04115 | hp1 | a0004 | c0004 | t0001 | g0302 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04199 | hp1 | a0007 | c0013 | t0001 | g0315 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04204 | hp2 | a0004 | c0004 | t0001 | g0178 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18522 | hp1 | a0008 | c0010 | t0001 | g0227 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18747 | hp2 | a0001 | c0006 | t0001 | g0159 | EAS | CHB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18906 | hp2 | a0001 | c0016 | t0001 | g0096 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18944 | hp2 | a0005 | c0005 | t0001 | g0316 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18949 | hp1 | a0005 | c0005 | t0001 | g0319 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18951 | hp2 | a0001 | c0019 | t0001 | g0204 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18952 | hp1 | a0005 | c0005 | t0001 | g0312 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18957 | hp2 | a0001 | c0006 | t0001 | g0049 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18960 | hp2 | a0012 | c0020 | t0001 | g0042 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18969 | hp1 | a0017 | c0015 | t0001 | g0282 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18971 | hp1 | a0006 | c0008 | t0001 | g0009 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18975 | hp2 | a0005 | c0005 | t0001 | g0317 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18977 | hp2 | a0001 | c0006 | t0001 | g0056 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18985 | hp2 | a0004 | c0004 | t0001 | g0184 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18986 | hp2 | a0005 | c0005 | t0001 | g0309 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18988 | hp1 | a0006 | c0008 | t0001 | g0010 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18992 | hp2 | a0006 | c0008 | t0001 | g0005 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18994 | hp1 | a0001 | c0006 | t0001 | g0046 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0029 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19002 | hp1 | a0005 | c0005 | t0001 | g0313 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19012 | hp1 | a0001 | c0006 | t0001 | g0047 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0280 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19054 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19057 | hp2 | a0007 | c0013 | t0001 | g0172 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19062 | hp2 | a0001 | c0006 | t0001 | g0024 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19064 | hp1 | a0005 | c0005 | t0001 | g0311 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19065 | hp1 | a0005 | c0005 | t0001 | g0308 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19066 | hp1 | a0005 | c0005 | t0001 | g0310 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19082 | hp1 | a0001 | c0006 | t0001 | g0058 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19240 | hp1 | a0004 | c0004 | t0001 | g0181 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA19240 | hp2 | a0009 | c0012 | t0001 | g0234 | AFR | YRI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ASW | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0325 | AFR | ASW | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0243 | EUR | TSI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20905 | hp2 | a0004 | c0004 | t0001 | g0303 | SAS | GIH | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | ACB | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0328 | AFR | USA | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA18955 | hp2 | a0004 | c0004 | t0001 | g0179 | EAS | JPT | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0336 | AFR | USA | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
NA21309 | hp2 | a0002 | c0011 | t0001 | g0278 | AFR | LWK | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | RLF_chr1_40156387_40245921 | RLF | chr1 | 40156387 | 40245921 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40161455 | C | T | 1 | a0011 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.56C>T | p.Pro19Leu | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/8 | 69/6232 | 56/5745 | 19/1914 | chr1 | 40161455 | ||
chr1:40202583 | C | G | 1 | a0005 | 13 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(10): Show |
missense_variant | MODERATE | c.779C>G | p.Ser260Cys | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/8 | 792/6232 | 779/5745 | 260/1914 | chr1 | 40202583 | ||
chr1:40235985 | T | C | 1 | a0017 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1283T>C | p.Met428Thr | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 1296/6232 | 1283/5745 | 428/1914 | chr1 | 40235985 | ||
chr1:40236581 | G | A | 1 | a0006 | 3 | NA18971.hp1 NA18988.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.1879G>A | p.Gly627Ser | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 1892/6232 | 1879/5745 | 627/1914 | chr1 | 40236581 | ||
chr1:40236633 | A | G | 1 | a0016 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1931A>G | p.Asn644Ser | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 1944/6232 | 1931/5745 | 644/1914 | chr1 | 40236633 | ||
chr1:40237302 | C | A | 2 | a0005a0007 | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
missense_variant | MODERATE | c.2600C>A | p.Pro867His | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2613/6232 | 2600/5745 | 867/1914 | chr1 | 40237302 | ||
chr1:40237497 | T | C | 1 | a0008 | 2 | HG03540.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.2795T>C | p.Val932Ala | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2808/6232 | 2795/5745 | 932/1914 | chr1 | 40237497 | ||
chr1:40237502 | G | C | 1 | a0015 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2800G>C | p.Gly934Arg | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2813/6232 | 2800/5745 | 934/1914 | chr1 | 40237502 | ||
chr1:40237532 | A | G | 1 | a0012 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.2830A>G | p.Ser944Gly | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2843/6232 | 2830/5745 | 944/1914 | chr1 | 40237532 | ||
chr1:40237572 | G | A | 1 | a0013 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.2870G>A | p.Gly957Asp | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2883/6232 | 2870/5745 | 957/1914 | chr1 | 40237572 | ||
chr1:40239265 | C | G | 2 | a0005a0007 | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
missense_variant | MODERATE | c.4563C>G | p.Ile1521Met | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4576/6232 | 4563/5745 | 1521/1914 | chr1 | 40239265 | ||
chr1:40239530 | A | G | 1 | a0010 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.4828A>G | p.Ile1610Val | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4841/6232 | 4828/5745 | 1610/1914 | chr1 | 40239530 | ||
chr1:40239566 | C | T | 3 | a0003a0010a0016 | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
missense_variant | MODERATE | c.4864C>T | p.Arg1622Cys | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4877/6232 | 4864/5745 | 1622/1914 | chr1 | 40239566 | ||
chr1:40239588 | C | T | 1 | a0009 | 2 | HG01891.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.4886C>T | p.Pro1629Leu | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4899/6232 | 4886/5745 | 1629/1914 | chr1 | 40239588 | ||
chr1:40239755 | C | G | 1 | a0004 | 15 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(12): Show |
missense_variant | MODERATE | c.5053C>G | p.Gln1685Glu | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5066/6232 | 5053/5745 | 1685/1914 | chr1 | 40239755 | ||
chr1:40240054 | A | T | 2 | a0002a0017 | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
missense_variant | MODERATE | c.5352A>T | p.Glu1784Asp | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5365/6232 | 5352/5745 | 1784/1914 | chr1 | 40240054 | ||
chr1:40240055 | G | A | 1 | a0014 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.5353G>A | p.Asp1785Asn | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5366/6232 | 5353/5745 | 1785/1914 | chr1 | 40240055 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40195691 | T | C | 1 | a0002c0007 | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.534T>C | p.Val178Val | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/8 | 547/6232 | 534/5745 | 178/1914 | chr1 | 40195691 | ||
chr1:40202572 | A | G | 1 | a0001c0009 | 3 | HG01069.hp1 HG01071.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.768A>G | p.Thr256Thr | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/8 | 781/6232 | 768/5745 | 256/1914 | chr1 | 40202572 | ||
chr1:40235998 | A | G | 1 | a0002c0023 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1296A>G | p.Leu432Leu | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 1309/6232 | 1296/5745 | 432/1914 | chr1 | 40235998 | ||
chr1:40236670 | A | G | 1 | a0013c0021 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.1968A>G | p.Thr656Thr | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 1981/6232 | 1968/5745 | 656/1914 | chr1 | 40236670 | ||
chr1:40236898 | C | T | 5 | a0003c0003a0005c0005a0007c0013others(2): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
synonymous_variant | LOW | c.2196C>T | p.His732His | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2209/6232 | 2196/5745 | 732/1914 | chr1 | 40236898 | ||
chr1:40237159 | G | A | 1 | a0001c0016 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2457G>A | p.Gln819Gln | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 2470/6232 | 2457/5745 | 819/1914 | chr1 | 40237159 | ||
chr1:40237768 | C | T | 1 | a0001c0006 | 11 | HG00423.hp1 HG00544.hp2 NA18747.hp2 others(8): Show |
synonymous_variant | LOW | c.3066C>T | p.Ser1022Ser | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 3079/6232 | 3066/5745 | 1022/1914 | chr1 | 40237768 | ||
chr1:40239121 | T | C | 5 | a0003c0003a0005c0005a0007c0013others(2): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
synonymous_variant | LOW | c.4419T>C | p.Tyr1473Tyr | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4432/6232 | 4419/5745 | 1473/1914 | chr1 | 40239121 | ||
chr1:40239589 | G | A | 1 | a0002c0011 | 2 | HG02818.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.4887G>A | p.Pro1629Pro | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 4900/6232 | 4887/5745 | 1629/1914 | chr1 | 40239589 | ||
chr1:40239727 | T | C | 5 | a0003c0003a0005c0005a0007c0013others(2): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
synonymous_variant | LOW | c.5025T>C | p.Asn1675Asn | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5038/6232 | 5025/5745 | 1675/1914 | chr1 | 40239727 | ||
chr1:40239850 | C | T | 2 | a0005c0005a0007c0013 | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
synonymous_variant | LOW | c.5148C>T | p.Phe1716Phe | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5161/6232 | 5148/5745 | 1716/1914 | chr1 | 40239850 | ||
chr1:40240357 | G | A | 1 | a0001c0019 | 1 | NA18951.hp2 | synonymous_variant | LOW | c.5655G>A | p.Val1885Val | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 8/8 | 5668/6232 | 5655/5745 | 1885/1914 | chr1 | 40240357 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40161717 | G | T | 33 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+81G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40161717 | ||||||
chr1:40161766 | G | C | 2 | a0001c0006t0001g0001a0001c0006t0001g0002 | 2 | HG00423.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.237+130G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40161766 | ||||||
chr1:40162165 | G | C | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.237+529G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162165 | ||||||
chr1:40162166 | T | C | 33 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+530T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162166 | ||||||
chr1:40162184 | C | CT | 6 | a0001c0001t0001g0300a0001c0001t0001g0305a0004c0004t0001g0301others(3): Show | 6 | HG02698.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+561dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40162184 | |||||
chr1:40162184 | CT | C | 14 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(11): Show | 14 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+561delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40162184 | |||||
chr1:40162399 | A | G | 58 | a0002c0002t0001g0003a0002c0002t0001g0243a0002c0002t0001g0244others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.237+763A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162399 | ||||||
chr1:40162447 | C | T | 167 | a0001c0001t0001g0175a0001c0001t0001g0185a0001c0001t0001g0186others(164): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.237+811C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162447 | ||||||
chr1:40162462 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.237+826A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162462 | ||||||
chr1:40162644 | C | T | 2 | a0001c0001t0001g0242a0001c0009t0001g0241 | 2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.237+1008C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162644 | ||||||
chr1:40162692 | T | C | 7 | a0002c0002t0001g0243a0002c0002t0001g0244a0002c0002t0001g0245others(4): Show | 7 | HG00280.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+1056T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162692 | ||||||
chr1:40162761 | G | A | 33 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+1125G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162761 | ||||||
chr1:40162842 | C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG00609.hp1 HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.237+1206C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162842 | ||||||
chr1:40162893 | G | A | 33 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+1257G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40162893 | ||||||
chr1:40163049 | G | A | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.237+1413G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163049 | ||||||
chr1:40163080 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+1444T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163080 | ||||||
chr1:40163116 | G | GT | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+1480_237+1481i others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163116 | ||||||
chr1:40163150 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+1514G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163150 | ||||||
chr1:40163416 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+1780A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163416 | ||||||
chr1:40163822 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237+2186C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163822 | ||||||
chr1:40163956 | A | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.237+2320A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40163956 | ||||||
chr1:40164022 | G | A | 19 | a0001c0001t0001g0175a0001c0001t0001g0240a0001c0001t0001g0242others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.237+2386G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164022 | ||||||
chr1:40164205 | G | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | NA18612.hp1 NA18747.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.237+2569G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164205 | ||||||
chr1:40164627 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+2991A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164627 | ||||||
chr1:40164649 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.237+3013A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164649 | ||||||
chr1:40164804 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.237+3168C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164804 | ||||||
chr1:40164850 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.237+3214G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164850 | ||||||
chr1:40164864 | G | C | 1 | a0006c0008t0001g0005 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.237+3228G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164864 | ||||||
chr1:40164906 | CA | C | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+3271delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40164906 | ||||||
chr1:40165103 | GAA | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+3470_237+3471d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40165103 | |||||
chr1:40165109 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.237+3473A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165109 | ||||||
chr1:40165110 | T | C | 5 | a0002c0002t0001g0256a0002c0002t0001g0257a0002c0002t0001g0258others(2): Show | 5 | HG02559.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+3474T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165110 | ||||||
chr1:40165172 | A | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+3536A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165172 | ||||||
chr1:40165184 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.237+3548A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165184 | ||||||
chr1:40165267 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.237+3631C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165267 | ||||||
chr1:40165464 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+3828C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165464 | ||||||
chr1:40165563 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.237+3927T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165563 | ||||||
chr1:40165581 | G | T | 114 | a0001c0001t0001g0233a0002c0002t0001g0003a0002c0002t0001g0166others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.237+3945G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165581 | ||||||
chr1:40165599 | C | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+3963C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165599 | ||||||
chr1:40165693 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.237+4057A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165693 | ||||||
chr1:40165759 | T | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0006c0008t0001g0005others(2): Show | 5 | NA18961.hp2 NA18971.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+4123T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165759 | ||||||
chr1:40165787 | C | G | 1 | a0001c0006t0001g0159 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.237+4151C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165787 | ||||||
chr1:40165788 | C | T | 56 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(53): Show | 56 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.237+4152C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165788 | ||||||
chr1:40165966 | C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | NA18948.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.237+4330C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40165966 | ||||||
chr1:40166003 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+4367T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166003 | ||||||
chr1:40166155 | G | A | 1 | a0002c0002t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.237+4519G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166155 | ||||||
chr1:40166187 | C | T | 1 | a0002c0002t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+4551C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166187 | ||||||
chr1:40166289 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.237+4653G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166289 | ||||||
chr1:40166578 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.237+4942A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166578 | ||||||
chr1:40166683 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+5047G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166683 | ||||||
chr1:40166775 | G | A | 1 | a0003c0003t0001g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.237+5139G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166775 | ||||||
chr1:40166777 | TCTCA | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+5146_237+5149d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40166777 | |||||
chr1:40166853 | G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+5217G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166853 | ||||||
chr1:40166909 | C | T | 49 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(46): Show | 49 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.237+5273C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166909 | ||||||
chr1:40166923 | C | T | 1 | a0004c0004t0001g0184 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.237+5287C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40166923 | ||||||
chr1:40167006 | T | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.237+5370T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167006 | ||||||
chr1:40167007 | A | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0239 | 2 | HG03516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.237+5371A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167007 | ||||||
chr1:40167090 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+5454A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167090 | ||||||
chr1:40167138 | T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01496.hp2 HG01943.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+5502T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167138 | ||||||
chr1:40167154 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+5518A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167154 | ||||||
chr1:40167158 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+5522G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167158 | ||||||
chr1:40167282 | T | A | 42 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(39): Show | 42 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.237+5646T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167282 | ||||||
chr1:40167327 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.237+5691G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167327 | ||||||
chr1:40167405 | A | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+5769A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167405 | ||||||
chr1:40167497 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237+5861G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167497 | ||||||
chr1:40167581 | A | G | 1 | a0004c0004t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.237+5945A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167581 | ||||||
chr1:40167851 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+6215T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40167851 | ||||||
chr1:40168041 | CA | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+6418delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40168041 | |||||
chr1:40168057 | A | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+6421A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168057 | ||||||
chr1:40168127 | A | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+6491A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168127 | ||||||
chr1:40168158 | T | G | 14 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+6522T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168158 | ||||||
chr1:40168302 | G | A | 4 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0261others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+6666G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168302 | ||||||
chr1:40168715 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.237+7079G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168715 | ||||||
chr1:40168953 | G | A | 335 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.237+7317G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168953 | ||||||
chr1:40168958 | A | C | 2 | a0002c0002t0001g0243a0002c0002t0001g0249 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.237+7322A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40168958 | ||||||
chr1:40169382 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.237+7746C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169382 | ||||||
chr1:40169473 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+7837G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169473 | ||||||
chr1:40169485 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+7849G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169485 | ||||||
chr1:40169559 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+7923T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169559 | ||||||
chr1:40169563 | C | CCGAGATT others(9): Show |
1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+7929_237+7944d others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40169563 | |||||
chr1:40169564 | C | T | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+7928C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169564 | ||||||
chr1:40169586 | G | A | 3 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.237+7950G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169586 | ||||||
chr1:40169601 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.237+7965C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169601 | ||||||
chr1:40169618 | G | A | 1 | a0001c0006t0001g0024 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.237+7982G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169618 | ||||||
chr1:40169622 | C | CA | 55 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(52): Show | 55 | HG00642.hp1 HG01071.hp2 HG01891.hp2 others(52): Show |
intron_variant | MODIFIER | c.237+8009dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40169622 | |||||
chr1:40169622 | C | CAA | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0239others(16): Show | 19 | HG00423.hp2 HG00642.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+8008_237+8009d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40169622 | |||||
chr1:40169632 | A | T | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+7996A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169632 | ||||||
chr1:40169638 | A | T | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+8002A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169638 | ||||||
chr1:40169684 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237+8048G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169684 | ||||||
chr1:40169695 | CTT | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+8072_237+8073d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40169695 | |||||
chr1:40169759 | C | T | 12 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(9): Show | 12 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+8123C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169759 | ||||||
chr1:40169761 | C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(45): Show | 48 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.237+8125C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169761 | ||||||
chr1:40169785 | C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0162 | 3 | HG01099.hp2 HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.237+8149C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169785 | ||||||
chr1:40169786 | G | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+8150G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169786 | ||||||
chr1:40169898 | T | C | 120 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(117): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.237+8262T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169898 | ||||||
chr1:40169959 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.237+8323G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169959 | ||||||
chr1:40169984 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+8348G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40169984 | ||||||
chr1:40170104 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.237+8468G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170104 | ||||||
chr1:40170222 | T | G | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8586T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170222 | ||||||
chr1:40170231 | A | T | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8595A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170231 | ||||||
chr1:40170252 | T | G | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8616T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170252 | ||||||
chr1:40170254 | G | T | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8618G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170254 | ||||||
chr1:40170255 | T | G | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8619T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170255 | ||||||
chr1:40170559 | T | C | 43 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(40): Show | 43 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.237+8923T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170559 | ||||||
chr1:40170575 | T | C | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+8939T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170575 | ||||||
chr1:40170603 | C | T | 1 | a0007c0013t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.237+8967C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170603 | ||||||
chr1:40170643 | C | T | 2 | a0004c0004t0001g0182a0004c0004t0001g0183 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.237+9007C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170643 | ||||||
chr1:40170650 | T | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+9014T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170650 | ||||||
chr1:40170664 | A | G | 6 | a0003c0003t0001g0323a0003c0003t0001g0327a0003c0003t0001g0328others(3): Show | 6 | HG02055.hp1 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.237+9028A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170664 | ||||||
chr1:40170707 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.237+9071A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170707 | ||||||
chr1:40170709 | G | A | 1 | a0002c0002t0001g0270 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.237+9073G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170709 | ||||||
chr1:40170715 | G | T | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.237+9079G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170715 | ||||||
chr1:40170803 | A | T | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+9167A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170803 | ||||||
chr1:40170909 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237+9273A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170909 | ||||||
chr1:40170950 | T | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0010c0014t0001g0337others(1): Show | 4 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+9314T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170950 | ||||||
chr1:40170953 | G | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+9317G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40170953 | ||||||
chr1:40171003 | A | G | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+9367A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171003 | ||||||
chr1:40171010 | TTTTG | T | 38 | a0001c0001t0001g0100a0001c0001t0001g0148a0001c0001t0001g0149others(35): Show | 38 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.237+9398_237+9401d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40171010 | |||||
chr1:40171010 | TTTTGTTT others(1): Show |
T | 55 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.237+9394_237+9401d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40171010 | |||||
chr1:40171027 | T | G | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.237+9391T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171027 | ||||||
chr1:40171030 | GTTTGTTT others(1): Show |
G | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+9395_237+9402d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171030 | ||||||
chr1:40171194 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237+9558T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171194 | ||||||
chr1:40171221 | G | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+9585G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171221 | ||||||
chr1:40171291 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.237+9655G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171291 | ||||||
chr1:40171519 | G | T | 31 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0026others(28): Show | 31 | HG00673.hp1 HG01070.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.237+9883G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171519 | ||||||
chr1:40171558 | G | A | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.237+9922G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171558 | ||||||
chr1:40171691 | C | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+10055C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171691 | ||||||
chr1:40171705 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+10069G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171705 | ||||||
chr1:40171763 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.237+10127C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171763 | ||||||
chr1:40171913 | A | G | 1 | a0015c0017t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.237+10277A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40171913 | ||||||
chr1:40172013 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.237+10377A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172013 | ||||||
chr1:40172082 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+10446T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172082 | ||||||
chr1:40172156 | TTTTTTAA others(16): Show |
T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+10523_237+1054 others(27): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40172156 | |||||
chr1:40172517 | G | T | 1 | a0002c0002t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.237+10881G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172517 | ||||||
chr1:40172555 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+10919C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172555 | ||||||
chr1:40172638 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.237+11002A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172638 | ||||||
chr1:40172723 | G | A | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.237+11087G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172723 | ||||||
chr1:40172761 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+11125A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172761 | ||||||
chr1:40172936 | C | T | 1 | a0004c0004t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.237+11300C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172936 | ||||||
chr1:40172969 | A | G | 2 | a0005c0005t0001g0316a0005c0005t0001g0317 | 2 | NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.237+11333A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40172969 | ||||||
chr1:40173039 | T | C | 1 | a0002c0002t0001g0273 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.237+11403T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173039 | ||||||
chr1:40173073 | G | GT | 36 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0081others(33): Show | 36 | HG00544.hp1 HG00673.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.237+11455dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173073 | |||||
chr1:40173073 | G | GTTTTTTT others(6): Show |
5 | a0003c0003t0001g0321a0003c0003t0001g0324a0003c0003t0001g0327others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+11443_237+1145 others(17): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173073 | |||||
chr1:40173073 | G | GTTTTTTT others(7): Show |
11 | a0003c0003t0001g0320a0003c0003t0001g0322a0003c0003t0001g0325others(8): Show | 11 | HG00642.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.237+11442_237+1145 others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173073 | |||||
chr1:40173073 | G | GTTTTTTT others(8): Show |
2 | a0003c0003t0001g0326a0003c0003t0001g0331 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.237+11441_237+1145 others(19): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173073 | |||||
chr1:40173073 | G | GTTTTTTT others(9): Show |
1 | a0003c0003t0001g0323 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237+11440_237+1145 others(20): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173073 | |||||
chr1:40173076 | T | TTG | 14 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(11): Show | 14 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+11441_237+1144 others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173076 | |||||
chr1:40173092 | G | T | 333 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.237+11456G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173092 | ||||||
chr1:40173187 | C | G | 1 | a0004c0004t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.237+11551C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173187 | ||||||
chr1:40173375 | C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.237+11739C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173375 | ||||||
chr1:40173514 | A | AT | 31 | a0001c0001t0001g0133a0001c0001t0001g0189a0001c0001t0001g0221others(28): Show | 31 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.237+11895dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173514 | |||||
chr1:40173514 | A | ATTT | 16 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(13): Show | 16 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.237+11893_237+1189 others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173514 | |||||
chr1:40173514 | AT | A | 72 | a0001c0001t0001g0099a0001c0001t0001g0157a0001c0001t0001g0175others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.237+11895delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40173514 | |||||
chr1:40173863 | G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0171 | 2 | NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.237+12227G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173863 | ||||||
chr1:40173998 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+12362A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40173998 | ||||||
chr1:40174370 | C | CA | 36 | a0001c0001t0001g0193a0002c0002t0001g0250a0002c0002t0001g0251others(33): Show | 36 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.237+12748dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40174370 | |||||
chr1:40174370 | CA | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0160a0001c0001t0001g0175others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+12748delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40174370 | |||||
chr1:40174487 | A | T | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237+12851A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40174487 | ||||||
chr1:40174699 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.237+13063A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40174699 | ||||||
chr1:40175198 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.237+13562G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175198 | ||||||
chr1:40175205 | T | TG | 39 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0193others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.237+13578dupG | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40175205 | |||||
chr1:40175338 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+13702C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175338 | ||||||
chr1:40175426 | G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0048 | 2 | HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.238-13629G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175426 | ||||||
chr1:40175446 | C | A | 7 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0261others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-13609C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175446 | ||||||
chr1:40175588 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238-13467G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175588 | ||||||
chr1:40175635 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-13420T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175635 | ||||||
chr1:40175636 | G | A | 14 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.238-13419G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175636 | ||||||
chr1:40175642 | C | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-13413C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175642 | ||||||
chr1:40175653 | A | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-13402A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175653 | ||||||
chr1:40175784 | C | CA | 61 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0016others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.238-13253dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40175784 | |||||
chr1:40175784 | CA | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0078a0001c0001t0001g0131others(7): Show | 10 | HG00099.hp2 HG01070.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-13253delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40175784 | |||||
chr1:40175801 | AAG | A | 17 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(14): Show | 17 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.238-13253_238-1325 others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175801 | ||||||
chr1:40175828 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.238-13227T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175828 | ||||||
chr1:40175870 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-13185C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175870 | ||||||
chr1:40175877 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.238-13178A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40175877 | ||||||
chr1:40176267 | G | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.238-12788G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176267 | ||||||
chr1:40176414 | G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.238-12641G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176414 | ||||||
chr1:40176438 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238-12617T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176438 | ||||||
chr1:40176513 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238-12542C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176513 | ||||||
chr1:40176533 | A | G | 2 | a0001c0001t0001g0175a0001c0009t0001g0174 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.238-12522A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176533 | ||||||
chr1:40176570 | G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-12485G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176570 | ||||||
chr1:40176759 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-12296A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176759 | ||||||
chr1:40176863 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.238-12192A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176863 | ||||||
chr1:40176876 | A | G | 335 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.238-12179A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176876 | ||||||
chr1:40176973 | A | C | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-12082A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40176973 | ||||||
chr1:40177232 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.238-11823C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177232 | ||||||
chr1:40177254 | G | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-11801G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177254 | ||||||
chr1:40177292 | C | CT | 6 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0226others(3): Show | 6 | HG02523.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-11750dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40177292 | |||||
chr1:40177292 | CT | C | 33 | a0003c0003t0001g0320a0003c0003t0001g0322a0003c0003t0001g0323others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.238-11750delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40177292 | |||||
chr1:40177529 | G | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-11526G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177529 | ||||||
chr1:40177634 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.238-11421T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177634 | ||||||
chr1:40177673 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.238-11382C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177673 | ||||||
chr1:40177785 | G | T | 1 | a0004c0004t0001g0184 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.238-11270G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177785 | ||||||
chr1:40177935 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-11120G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177935 | ||||||
chr1:40177961 | A | T | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-11094A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40177961 | ||||||
chr1:40178057 | C | CAT | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0022others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.238-10986_238-1098 others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178057 | |||||
chr1:40178057 | CAT | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-10986_238-1098 others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178057 | |||||
chr1:40178060 | A | G | 2 | a0004c0004t0001g0177a0004c0004t0001g0178 | 2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.238-10995A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178060 | ||||||
chr1:40178102 | ATGAG | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-10950_238-1094 others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178102 | |||||
chr1:40178105 | AGT | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-10947_238-1094 others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178105 | |||||
chr1:40178208 | C | T | 1 | a0007c0013t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.238-10847C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178208 | ||||||
chr1:40178265 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238-10790A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178265 | ||||||
chr1:40178522 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238-10533A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178522 | ||||||
chr1:40178545 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-10510G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178545 | ||||||
chr1:40178619 | G | GT | 7 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0083others(4): Show | 7 | HG02056.hp1 HG02056.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-10424dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178619 | |||||
chr1:40178627 | T | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-10428T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178627 | ||||||
chr1:40178628 | T | G | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.238-10427T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178628 | ||||||
chr1:40178628 | T | TG | 3 | a0001c0001t0001g0233a0008c0010t0001g0227a0008c0010t0001g0228 | 3 | HG02922.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-10427_238-1042 others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178628 | ||||||
chr1:40178631 | T | G | 1 | a0004c0004t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.238-10424T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178631 | ||||||
chr1:40178632 | G | GT | 36 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0136others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.238-10407dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178632 | |||||
chr1:40178632 | G | GTTTTGTT others(6): Show |
19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-10419_238-1041 others(17): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178632 | |||||
chr1:40178632 | G | T | 2 | a0002c0002t0001g0266a0004c0004t0001g0180 | 2 | HG02080.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.238-10423G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178632 | ||||||
chr1:40178633 | T | TTTTG | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-10419_238-1041 others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178633 | |||||
chr1:40178634 | T | TG | 3 | a0002c0002t0001g0267a0002c0002t0001g0275a0002c0002t0001g0297 | 3 | HG02056.hp1 NA18975.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.238-10421_238-1042 others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178634 | ||||||
chr1:40178640 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.238-10415T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178640 | ||||||
chr1:40178687 | G | GT | 17 | a0001c0001t0001g0099a0001c0001t0001g0130a0001c0001t0001g0215others(14): Show | 17 | HG02027.hp1 HG02080.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.238-10355dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40178687 | |||||
chr1:40178700 | T | C | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-10355T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178700 | ||||||
chr1:40178878 | A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0077 | 2 | HG01167.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.238-10177A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178878 | ||||||
chr1:40178921 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238-10134A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178921 | ||||||
chr1:40178979 | C | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-10076C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40178979 | ||||||
chr1:40179262 | G | T | 37 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(34): Show | 37 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.238-9793G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179262 | ||||||
chr1:40179488 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.238-9567C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179488 | ||||||
chr1:40179546 | C | CT | 21 | a0001c0001t0001g0128a0003c0003t0001g0320a0003c0003t0001g0321others(18): Show | 21 | HG00280.hp1 HG00642.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.238-9495dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40179546 | |||||
chr1:40179546 | CT | C | 84 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0175others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.238-9495delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40179546 | |||||
chr1:40179565 | C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0078 | 2 | HG00099.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.238-9490C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179565 | ||||||
chr1:40179587 | G | A | 3 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0011t0001g0230 | 3 | HG02257.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.238-9468G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179587 | ||||||
chr1:40179672 | C | CTCCA | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-9368_238-9365d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40179672 | |||||
chr1:40179672 | CTCCA | C | 3 | a0004c0004t0001g0176a0004c0004t0001g0182a0004c0004t0001g0183 | 3 | HG02074.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.238-9368_238-9365d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40179672 | |||||
chr1:40179716 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-9339G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179716 | ||||||
chr1:40179722 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-9333G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40179722 | ||||||
chr1:40180113 | T | C | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-8942T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180113 | ||||||
chr1:40180299 | C | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0132 | 3 | HG02083.hp1 NA18964.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.238-8756C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180299 | ||||||
chr1:40180524 | C | T | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-8531C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180524 | ||||||
chr1:40180587 | C | G | 3 | a0004c0004t0001g0176a0004c0004t0001g0182a0004c0004t0001g0183 | 3 | HG02074.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.238-8468C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180587 | ||||||
chr1:40180599 | G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0045 | 2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.238-8456G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180599 | ||||||
chr1:40180653 | A | T | 1 | a0007c0013t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.238-8402A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180653 | ||||||
chr1:40180701 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.238-8354A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180701 | ||||||
chr1:40180775 | A | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.238-8280A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180775 | ||||||
chr1:40180968 | A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.238-8087A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40180968 | ||||||
chr1:40181398 | C | G | 2 | a0002c0002t0001g0246a0002c0002t0001g0247 | 2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.238-7657C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40181398 | ||||||
chr1:40181735 | A | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.238-7320A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40181735 | ||||||
chr1:40181854 | G | A | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.238-7201G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40181854 | ||||||
chr1:40181909 | A | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-7146A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40181909 | ||||||
chr1:40181910 | G | A | 1 | a0005c0005t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.238-7145G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40181910 | ||||||
chr1:40182131 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-6924G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182131 | ||||||
chr1:40182136 | T | TA | 5 | a0002c0002t0001g0297a0002c0007t0001g0252a0002c0007t0001g0253others(2): Show | 5 | HG02056.hp1 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-6912dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182136 | |||||
chr1:40182184 | A | G | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-6871A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182184 | ||||||
chr1:40182347 | T | C | 1 | a0002c0002t0001g0273 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.238-6708T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182347 | ||||||
chr1:40182449 | A | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-6606A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182449 | ||||||
chr1:40182469 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-6586C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182469 | ||||||
chr1:40182528 | A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0213others(1): Show | 4 | HG02132.hp2 NA18939.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-6527A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182528 | ||||||
chr1:40182581 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.238-6474C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182581 | ||||||
chr1:40182617 | A | G | 3 | a0002c0002t0001g0279a0002c0002t0001g0280a0002c0002t0001g0299 | 3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.238-6438A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182617 | ||||||
chr1:40182634 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.238-6421A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182634 | ||||||
chr1:40182674 | C | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-6381C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182674 | ||||||
chr1:40182749 | A | ATAGGTAG others(1): Show |
7 | a0003c0003t0001g0321a0003c0003t0001g0325a0003c0003t0001g0332others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182749 | |||||
chr1:40182749 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-6306A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182749 | ||||||
chr1:40182753 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-6302G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182753 | ||||||
chr1:40182753 | G | GTAGA | 43 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0027others(40): Show | 43 | HG00140.hp1 HG00544.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.238-6265_238-6262d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGATAG others(1): Show |
13 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0109others(10): Show | 13 | HG01071.hp2 HG01074.hp1 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.238-6269_238-6262d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(1): Show |
18 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0190others(15): Show | 18 | HG00673.hp2 HG01123.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(5): Show |
21 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0189others(18): Show | 21 | HG00408.hp1 HG00558.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(9): Show |
2 | a0001c0001t0001g0192a0001c0001t0001g0212 | 2 | HG02135.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.238-6299_238-6298i others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(5): Show |
7 | a0003c0003t0001g0320a0003c0003t0001g0323a0003c0003t0001g0326others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(9): Show |
3 | a0005c0005t0001g0307a0005c0005t0001g0308a0005c0005t0001g0309 | 3 | HG01496.hp1 NA18986.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.238-6299_238-6298i others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(13): Show |
10 | a0005c0005t0001g0306a0005c0005t0001g0310a0005c0005t0001g0311others(7): Show | 10 | HG02027.hp1 HG04199.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(22): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(17): Show |
2 | a0005c0005t0001g0314a0005c0005t0001g0318 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.238-6299_238-6298i others(26): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | G | GTAGGTAG others(9): Show |
5 | a0003c0003t0001g0322a0003c0003t0001g0324a0003c0003t0001g0330others(2): Show | 5 | HG00642.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-6299_238-6298i others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | GTAGA | G | 135 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.238-6265_238-6262d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182753 | GTAGATAG others(5): Show |
G | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-6273_238-6262d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40182753 | |||||
chr1:40182761 | A | G | 1 | a0004c0004t0001g0154 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.238-6294A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182761 | ||||||
chr1:40182763 | A | T | 1 | a0001c0001t0001g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.238-6292A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182763 | ||||||
chr1:40182870 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-6185G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182870 | ||||||
chr1:40182994 | C | G | 120 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(117): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.238-6061C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182994 | ||||||
chr1:40182999 | C | G | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.238-6056C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40182999 | ||||||
chr1:40183026 | G | A | 120 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(117): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.238-6029G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183026 | ||||||
chr1:40183116 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238-5939C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183116 | ||||||
chr1:40183196 | C | T | 1 | a0013c0021t0001g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.238-5859C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183196 | ||||||
chr1:40183275 | C | T | 2 | a0010c0014t0001g0337a0010c0014t0001g0338 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238-5780C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183275 | ||||||
chr1:40183460 | C | A | 1 | a0001c0006t0001g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.238-5595C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183460 | ||||||
chr1:40183505 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-5550G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183505 | ||||||
chr1:40183619 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.238-5436C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183619 | ||||||
chr1:40183625 | G | A | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.238-5430G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183625 | ||||||
chr1:40183796 | A | G | 37 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(34): Show | 37 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.238-5259A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183796 | ||||||
chr1:40183804 | A | G | 1 | a0007c0013t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.238-5251A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183804 | ||||||
chr1:40183903 | T | C | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.238-5152T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183903 | ||||||
chr1:40183927 | T | C | 1 | a0005c0005t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.238-5128T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40183927 | ||||||
chr1:40184149 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.238-4906A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184149 | ||||||
chr1:40184212 | C | T | 2 | a0010c0014t0001g0337a0010c0014t0001g0338 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238-4843C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184212 | ||||||
chr1:40184232 | A | T | 2 | a0010c0014t0001g0337a0010c0014t0001g0338 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238-4823A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184232 | ||||||
chr1:40184249 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-4806A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184249 | ||||||
chr1:40184310 | A | G | 55 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0243others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.238-4745A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184310 | ||||||
chr1:40184361 | G | A | 6 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0279others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-4694G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184361 | ||||||
chr1:40184693 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.238-4362C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184693 | ||||||
chr1:40184935 | A | G | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.238-4120A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184935 | ||||||
chr1:40184949 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-4106G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184949 | ||||||
chr1:40184995 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-4060G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40184995 | ||||||
chr1:40185072 | C | G | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.238-3983C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185072 | ||||||
chr1:40185090 | T | A | 1 | a0003c0003t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.238-3965T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185090 | ||||||
chr1:40185206 | A | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-3849A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185206 | ||||||
chr1:40185226 | G | A | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.238-3829G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185226 | ||||||
chr1:40185292 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3763G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185292 | ||||||
chr1:40185348 | C | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0101a0003c0003t0001g0324 | 3 | HG02970.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.238-3707C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185348 | ||||||
chr1:40185517 | T | TA | 32 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0027others(29): Show | 32 | HG00544.hp1 HG01175.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.238-3512dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | T | TAA | 45 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0111others(42): Show | 45 | HG00408.hp1 HG00558.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.238-3513_238-3512d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | T | TAAA | 75 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.238-3514_238-3512d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | T | TAAAA | 44 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0014others(41): Show | 44 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.238-3515_238-3512d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | TAA | T | 6 | a0001c0001t0001g0165a0001c0001t0001g0240a0003c0003t0001g0320others(3): Show | 6 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-3513_238-3512d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | TAAA | T | 15 | a0001c0001t0001g0044a0003c0003t0001g0321a0003c0003t0001g0322others(12): Show | 15 | HG00642.hp2 HG01884.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-3514_238-3512d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | TAAAA | T | 13 | a0003c0003t0001g0335a0005c0005t0001g0307a0005c0005t0001g0308others(10): Show | 13 | HG00423.hp2 HG01496.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.238-3515_238-3512d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | TAAAAA | T | 8 | a0001c0001t0001g0043a0001c0001t0001g0140a0001c0001t0001g0141others(5): Show | 8 | HG00558.hp1 HG02723.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-3516_238-3512d others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185517 | TAAAAAA | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0144others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-3517_238-3512d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185517 | |||||
chr1:40185550 | C | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0212a0001c0001t0001g0214 | 3 | NA18954.hp2 NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.238-3505C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185550 | ||||||
chr1:40185578 | C | T | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-3477C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185578 | ||||||
chr1:40185656 | C | CA | 43 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.238-3377dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185656 | |||||
chr1:40185656 | C | CAA | 19 | a0001c0001t0001g0067a0001c0001t0001g0072a0003c0003t0001g0334others(16): Show | 19 | HG00408.hp2 HG00558.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-3378_238-3377d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185656 | |||||
chr1:40185656 | C | CAAAA | 11 | a0003c0003t0001g0321a0003c0003t0001g0322a0003c0003t0001g0323others(8): Show | 11 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.238-3380_238-3377d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185656 | |||||
chr1:40185656 | CA | C | 19 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0059others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-3377delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185656 | |||||
chr1:40185684 | C | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-3371C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185684 | ||||||
chr1:40185777 | A | G | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3278A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185777 | ||||||
chr1:40185826 | C | CA | 71 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0095others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.238-3214dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185826 | |||||
chr1:40185826 | CA | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-3214delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185826 | |||||
chr1:40185826 | CAA | C | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.238-3215_238-3214d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185826 | |||||
chr1:40185826 | CAAAAAAA others(16): Show |
C | 1 | a0004c0004t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.238-3213_238-3191d others(25): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185826 | |||||
chr1:40185842 | G | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0145a0002c0007t0001g0253others(9): Show | 12 | HG00639.hp2 HG02074.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-3213G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185842 | ||||||
chr1:40185843 | C | CA | 48 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0027others(45): Show | 48 | HG01109.hp2 HG01123.hp2 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.238-3190dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185843 | |||||
chr1:40185843 | C | G | 12 | a0001c0001t0001g0101a0001c0001t0001g0145a0002c0007t0001g0253others(9): Show | 12 | HG00639.hp2 HG02074.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-3212C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185843 | ||||||
chr1:40185843 | CA | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.238-3190delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185843 | |||||
chr1:40185843 | CAA | C | 79 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0018others(76): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.238-3191_238-3190d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185843 | |||||
chr1:40185843 | CAAA | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0036a0003c0003t0001g0321others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.238-3192_238-3190d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40185843 | |||||
chr1:40185844 | A | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0145a0002c0007t0001g0253others(9): Show | 12 | HG00639.hp2 HG02074.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.238-3211A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185844 | ||||||
chr1:40185859 | A | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-3196A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185859 | ||||||
chr1:40185920 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.238-3135G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185920 | ||||||
chr1:40185931 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.238-3124C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185931 | ||||||
chr1:40185983 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.238-3072C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40185983 | ||||||
chr1:40186026 | G | A | 1 | a0005c0005t0001g0307 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.238-3029G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186026 | ||||||
chr1:40186108 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-2947A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186108 | ||||||
chr1:40186121 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-2934G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186121 | ||||||
chr1:40186130 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.238-2925C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186130 | ||||||
chr1:40186149 | CTT | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-2905_238-2904d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186149 | ||||||
chr1:40186283 | T | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-2772T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186283 | ||||||
chr1:40186284 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.238-2771A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186284 | ||||||
chr1:40186292 | AG | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-2762delG | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186292 | ||||||
chr1:40186368 | C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0015 | 2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.238-2687C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186368 | ||||||
chr1:40186418 | T | C | 1 | a0003c0003t0001g0324 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.238-2637T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186418 | ||||||
chr1:40186487 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-2568G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186487 | ||||||
chr1:40186522 | C | T | 1 | a0002c0002t0001g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.238-2533C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186522 | ||||||
chr1:40186598 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.238-2457G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186598 | ||||||
chr1:40186618 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-2437T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186618 | ||||||
chr1:40186713 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.238-2342C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186713 | ||||||
chr1:40186955 | A | G | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-2100A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40186955 | ||||||
chr1:40187041 | G | GT | 16 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0076others(13): Show | 16 | HG00544.hp1 HG01978.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.238-2003dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40187041 | |||||
chr1:40187082 | AG | A | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.238-1972delG | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187082 | ||||||
chr1:40187151 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238-1904C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187151 | ||||||
chr1:40187193 | ATC | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-1858_238-1857d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40187193 | |||||
chr1:40187257 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.238-1798C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187257 | ||||||
chr1:40187323 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.238-1732C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187323 | ||||||
chr1:40187362 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-1693G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187362 | ||||||
chr1:40187375 | A | G | 1 | a0002c0002t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.238-1680A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187375 | ||||||
chr1:40187402 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-1653G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187402 | ||||||
chr1:40187514 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.238-1541G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187514 | ||||||
chr1:40187573 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.238-1482G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187573 | ||||||
chr1:40187579 | C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.238-1476C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187579 | ||||||
chr1:40187598 | CTG | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.238-1455_238-1454d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40187598 | |||||
chr1:40187719 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.238-1336T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187719 | ||||||
chr1:40187776 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-1279A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187776 | ||||||
chr1:40187814 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.238-1241C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187814 | ||||||
chr1:40187827 | C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(45): Show | 48 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.238-1228C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40187827 | ||||||
chr1:40188029 | C | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0084 | 2 | HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.238-1026C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40188029 | ||||||
chr1:40188062 | T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG00609.hp1 HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.238-993T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40188062 | ||||||
chr1:40188175 | C | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-880C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40188175 | ||||||
chr1:40188618 | G | GA | 95 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.238-425dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 40188618 | |||||
chr1:40188685 | G | A | 1 | a0004c0004t0001g0184 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.238-370G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40188685 | ||||||
chr1:40188854 | T | C | 2 | a0002c0007t0001g0254a0002c0007t0001g0255 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.238-201T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 1/7 | chr1 | 40188854 | ||||||
chr1:40189349 | C | T | 3 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.392+140C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40189349 | ||||||
chr1:40189353 | C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0085 | 2 | HG00673.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.392+144C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40189353 | ||||||
chr1:40189607 | G | C | 2 | a0002c0007t0001g0254a0002c0007t0001g0255 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.392+398G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40189607 | ||||||
chr1:40189806 | C | A | 76 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.392+597C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40189806 | ||||||
chr1:40189809 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.392+600A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40189809 | ||||||
chr1:40190244 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.393-528G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190244 | ||||||
chr1:40190296 | T | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.393-476T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190296 | ||||||
chr1:40190334 | A | G | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.393-438A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190334 | ||||||
chr1:40190370 | T | C | 2 | a0002c0007t0001g0254a0002c0007t0001g0255 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393-402T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190370 | ||||||
chr1:40190388 | A | AT | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.393-381dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 40190388 | |||||
chr1:40190402 | A | G | 1 | a0002c0002t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393-370A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190402 | ||||||
chr1:40190463 | G | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.393-309G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190463 | ||||||
chr1:40190624 | T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.393-148T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 2/7 | chr1 | 40190624 | ||||||
chr1:40190933 | C | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0131others(3): Show | 6 | NA18961.hp2 NA18971.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.474+80C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40190933 | ||||||
chr1:40191181 | C | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.474+328C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191181 | ||||||
chr1:40191358 | C | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+505C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191358 | ||||||
chr1:40191448 | T | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.474+595T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191448 | ||||||
chr1:40191490 | A | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.474+637A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191490 | ||||||
chr1:40191539 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.474+686G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191539 | ||||||
chr1:40191777 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+924G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191777 | ||||||
chr1:40191800 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.474+947C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40191800 | ||||||
chr1:40192085 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.474+1232T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40192085 | ||||||
chr1:40192168 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.474+1315A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40192168 | ||||||
chr1:40192874 | T | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.474+2021T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40192874 | ||||||
chr1:40192975 | C | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.474+2122C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40192975 | ||||||
chr1:40192979 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.474+2126C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40192979 | ||||||
chr1:40193127 | C | CA | 57 | a0001c0001t0001g0060a0001c0001t0001g0144a0001c0001t0001g0165others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.474+2293dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40193127 | |||||
chr1:40193127 | CA | C | 16 | a0001c0001t0001g0210a0005c0005t0001g0306a0005c0005t0001g0307others(13): Show | 16 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.474+2293delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40193127 | |||||
chr1:40193127 | CAA | C | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.474+2292_474+2293d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40193127 | |||||
chr1:40193139 | A | G | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+2286A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193139 | ||||||
chr1:40193287 | TTA | T | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-2343_475-2342d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40193287 | |||||
chr1:40193559 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.475-2073T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193559 | ||||||
chr1:40193764 | TGTGGGTG others(1): Show |
T | 9 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0052others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-1864_475-1857d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40193764 | |||||
chr1:40193768 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.475-1864G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193768 | ||||||
chr1:40193809 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.475-1823G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193809 | ||||||
chr1:40193816 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.475-1816G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193816 | ||||||
chr1:40193938 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.475-1694G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193938 | ||||||
chr1:40193958 | G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.475-1674G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40193958 | ||||||
chr1:40194163 | A | ATAACT | 278 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.475-1467_475-1466i others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194163 | |||||
chr1:40194313 | A | G | 1 | a0004c0004t0001g0303 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.475-1319A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194313 | ||||||
chr1:40194372 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.475-1260C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194372 | ||||||
chr1:40194404 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.475-1228T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194404 | ||||||
chr1:40194530 | C | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-1102C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194530 | ||||||
chr1:40194531 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.475-1101T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194531 | ||||||
chr1:40194586 | C | CA | 7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0240others(4): Show | 7 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-1034dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194586 | |||||
chr1:40194750 | G | A | 19 | a0001c0001t0001g0175a0001c0001t0001g0240a0001c0001t0001g0242others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.475-882G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194750 | ||||||
chr1:40194769 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.475-863G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194769 | ||||||
chr1:40194807 | G | GTTAT | 4 | a0001c0001t0001g0064a0001c0001t0001g0170a0001c0006t0001g0046others(1): Show | 4 | HG02129.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-784_475-781dup others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194807 | |||||
chr1:40194807 | GTTAT | G | 101 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0016others(98): Show | 101 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.475-784_475-781del others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194807 | |||||
chr1:40194807 | GTTATTTA others(1): Show |
G | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.475-788_475-781del others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194807 | |||||
chr1:40194807 | GTTATTTA others(5): Show |
G | 4 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0233others(1): Show | 4 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-792_475-781del others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194807 | |||||
chr1:40194807 | GTTATTTA others(9): Show |
G | 33 | a0001c0001t0001g0240a0003c0003t0001g0320a0003c0003t0001g0321others(30): Show | 33 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.475-796_475-781del others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194807 | |||||
chr1:40194828 | T | G | 1 | a0002c0002t0001g0287 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.475-804T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194828 | ||||||
chr1:40194851 | T | A | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.475-781T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40194851 | ||||||
chr1:40194998 | TA | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.475-632delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40194998 | |||||
chr1:40195001 | T | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.475-631T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195001 | ||||||
chr1:40195098 | G | T | 3 | a0002c0002t0001g0279a0002c0002t0001g0280a0002c0002t0001g0299 | 3 | HG02622.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.475-534G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195098 | ||||||
chr1:40195150 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.475-482T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195150 | ||||||
chr1:40195290 | A | C | 1 | a0005c0005t0001g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.475-342A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195290 | ||||||
chr1:40195310 | G | A | 1 | a0004c0004t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.475-322G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195310 | ||||||
chr1:40195355 | A | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0060others(1): Show | 4 | HG03710.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-277A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195355 | ||||||
chr1:40195368 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.475-264G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195368 | ||||||
chr1:40195436 | A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0225 | 2 | HG02132.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.475-196A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195436 | ||||||
chr1:40195449 | TA | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0103a0001c0001t0001g0107others(3): Show | 6 | HG01070.hp1 HG01515.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-169delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40195449 | |||||
chr1:40195449 | TAAAA | T | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.475-172_475-169del others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 40195449 | |||||
chr1:40195495 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.475-137A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195495 | ||||||
chr1:40195539 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.475-93C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 3/7 | chr1 | 40195539 | ||||||
chr1:40195808 | C | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.607+44C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40195808 | ||||||
chr1:40195825 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.607+61G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40195825 | ||||||
chr1:40196020 | A | G | 1 | a0002c0002t0001g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.607+256A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196020 | ||||||
chr1:40196056 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.607+292G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196056 | ||||||
chr1:40196078 | C | CT | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.607+326dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40196078 | |||||
chr1:40196263 | G | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.607+499G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196263 | ||||||
chr1:40196263 | G | C | 14 | a0001c0001t0001g0240a0004c0004t0001g0176a0004c0004t0001g0177others(11): Show | 14 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.607+499G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196263 | ||||||
chr1:40196356 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.607+592G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196356 | ||||||
chr1:40196418 | A | C | 51 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.607+654A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196418 | ||||||
chr1:40196420 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.607+656G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196420 | ||||||
chr1:40196461 | GT | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02647.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.607+701delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40196461 | |||||
chr1:40196498 | TTTTTGTT others(3): Show |
T | 4 | a0002c0002t0001g0244a0002c0002t0001g0246a0002c0002t0001g0247others(1): Show | 4 | HG01109.hp2 HG01433.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.607+744_607+753del others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40196498 | |||||
chr1:40196610 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.607+846C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196610 | ||||||
chr1:40196635 | G | T | 1 | a0001c0006t0001g0029 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.607+871G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196635 | ||||||
chr1:40196734 | CAA | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.607+971_607+972del others(2): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196734 | ||||||
chr1:40196832 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.607+1068G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40196832 | ||||||
chr1:40197301 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.607+1537T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197301 | ||||||
chr1:40197393 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.607+1629A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197393 | ||||||
chr1:40197452 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.607+1688A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197452 | ||||||
chr1:40197710 | A | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.607+1946A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197710 | ||||||
chr1:40197726 | T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0123 | 2 | HG01981.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.607+1962T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197726 | ||||||
chr1:40197753 | T | A | 1 | a0002c0002t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.607+1989T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197753 | ||||||
chr1:40197973 | T | C | 1 | a0002c0002t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.607+2209T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197973 | ||||||
chr1:40197977 | T | C | 2 | a0001c0001t0001g0213a0001c0001t0001g0225 | 2 | HG02132.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.607+2213T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40197977 | ||||||
chr1:40198046 | C | G | 1 | a0007c0013t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.607+2282C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198046 | ||||||
chr1:40198060 | A | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.607+2296A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198060 | ||||||
chr1:40198254 | C | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.607+2490C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198254 | ||||||
chr1:40198301 | CT | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(199): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.607+2556delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40198301 | |||||
chr1:40198301 | CTT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0157others(8): Show | 11 | HG00099.hp1 HG01167.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.607+2555_607+2556d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40198301 | |||||
chr1:40198361 | A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG00609.hp1 HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.607+2597A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198361 | ||||||
chr1:40198365 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.607+2601C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198365 | ||||||
chr1:40198870 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.607+3106C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198870 | ||||||
chr1:40198915 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.607+3151C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40198915 | ||||||
chr1:40199144 | G | C | 2 | a0002c0002t0001g0250a0002c0002t0001g0251 | 2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.608-3268G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199144 | ||||||
chr1:40199210 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.608-3202T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199210 | ||||||
chr1:40199274 | G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0111others(5): Show | 8 | NA18961.hp2 NA18971.hp1 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-3138G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199274 | ||||||
chr1:40199447 | G | T | 3 | a0002c0002t0001g0267a0002c0002t0001g0275a0002c0002t0001g0297 | 3 | HG02056.hp1 NA18975.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.608-2965G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199447 | ||||||
chr1:40199477 | A | G | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-2935A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199477 | ||||||
chr1:40199616 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.608-2796C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199616 | ||||||
chr1:40199830 | T | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.608-2582T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199830 | ||||||
chr1:40199946 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.608-2466G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199946 | ||||||
chr1:40199966 | T | C | 1 | a0003c0003t0001g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.608-2446T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40199966 | ||||||
chr1:40200327 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.608-2085C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200327 | ||||||
chr1:40200397 | A | G | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-2015A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200397 | ||||||
chr1:40200491 | G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0052others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.608-1921G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200491 | ||||||
chr1:40200618 | T | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0124others(4): Show | 7 | HG00544.hp1 NA18944.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-1794T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200618 | ||||||
chr1:40200667 | T | C | 33 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.608-1745T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200667 | ||||||
chr1:40200667 | T | G | 1 | a0003c0003t0001g0330 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.608-1745T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200667 | ||||||
chr1:40200750 | T | TTA | 35 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(32): Show | 35 | HG00639.hp2 HG00642.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.608-1648_608-1647d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200750 | |||||
chr1:40200811 | C | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.608-1601C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200811 | ||||||
chr1:40200851 | T | C | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-1561T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200851 | ||||||
chr1:40200867 | T | TAC | 33 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0036others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.608-1474_608-1473d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACAC | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0039others(15): Show | 18 | HG00408.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.608-1476_608-1473d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACAC | 9 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0001g0120others(6): Show | 9 | HG00558.hp2 HG01167.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-1478_608-1473d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0100others(1): Show | 4 | NA18957.hp1 NA18982.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-1480_608-1473d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0119a0001c0001t0001g0226a0002c0002t0001g0243others(1): Show | 4 | HG02523.hp2 NA18942.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-1482_608-1473d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0170others(3): Show | 6 | HG02056.hp1 HG02080.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-1484_608-1473d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0127a0001c0001t0001g0220a0002c0002t0001g0290others(1): Show | 4 | HG02083.hp1 NA18974.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-1486_608-1473d others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0200 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.608-1488_608-1473d others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TAC | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0037others(33): Show | 36 | HG00280.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.608-1474_608-1473d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACAC | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0017others(43): Show | 46 | HG00544.hp1 HG00639.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.608-1476_608-1473d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACAC | T | 31 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0034others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.608-1478_608-1473d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(1): Show |
T | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.608-1480_608-1473d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0022a0001c0001t0001g0076a0001c0001t0001g0088others(3): Show | 6 | HG00741.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-1482_608-1473d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(5): Show |
T | 12 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0001g0117others(9): Show | 12 | HG00673.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.608-1484_608-1473d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(7): Show |
T | 5 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0114others(2): Show | 5 | HG02280.hp2 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-1486_608-1473d others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0004a0001c0001t0001g0191a0001c0001t0001g0215others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.608-1488_608-1473d others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(11): Show |
T | 5 | a0001c0001t0001g0132a0001c0001t0001g0145a0002c0002t0001g0264others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1490_608-1473d others(20): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(13): Show |
T | 2 | a0001c0001t0001g0027a0001c0001t0001g0136 | 2 | HG04184.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.608-1492_608-1473d others(22): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(15): Show |
T | 2 | a0001c0001t0001g0123a0002c0011t0001g0278 | 2 | HG03492.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.608-1494_608-1473d others(24): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(17): Show |
T | 1 | a0006c0008t0001g0010 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.608-1496_608-1473d others(26): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(19): Show |
T | 2 | a0001c0001t0001g0153a0001c0001t0001g0213 | 2 | HG01243.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.608-1498_608-1473d others(28): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.608-1500_608-1473d others(30): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(23): Show |
T | 3 | a0001c0001t0001g0023a0002c0002t0001g0277a0002c0002t0001g0295 | 3 | HG01070.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.608-1502_608-1473d others(32): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200867 | TACACACA others(27): Show |
T | 1 | a0002c0002t0001g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.608-1506_608-1473d others(36): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200867 | |||||
chr1:40200893 | C | T | 1 | a0008c0010t0001g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.608-1519C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200893 | ||||||
chr1:40200895 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.608-1517C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200895 | ||||||
chr1:40200897 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.608-1515C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200897 | ||||||
chr1:40200897 | C | T | 1 | a0008c0010t0001g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.608-1515C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200897 | ||||||
chr1:40200904 | ACACACAC others(29): Show |
A | 1 | a0002c0002t0001g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.608-1507_608-1472d others(38): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200904 | ||||||
chr1:40200913 | C | CAGTGGTT others(23): Show |
1 | a0003c0003t0001g0322 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.608-1498_608-1497i others(32): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200913 | |||||
chr1:40200914 | A | AGTGGTTT others(26): Show |
3 | a0005c0005t0001g0306a0007c0013t0001g0172a0007c0013t0001g0315 | 3 | HG02027.hp1 HG04199.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.608-1498_608-1497i others(35): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200914 | ||||||
chr1:40200915 | C | CACACAGT others(32): Show |
10 | a0005c0005t0001g0307a0005c0005t0001g0308a0005c0005t0001g0309others(7): Show | 10 | HG01496.hp1 NA18944.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-1492_608-1491i others(41): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200915 | |||||
chr1:40200915 | C | CACAGTGG others(30): Show |
2 | a0005c0005t0001g0314a0005c0005t0001g0318 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.608-1494_608-1493i others(39): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200915 | |||||
chr1:40200915 | C | T | 3 | a0005c0005t0001g0306a0007c0013t0001g0172a0007c0013t0001g0315 | 3 | HG02027.hp1 HG04199.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.608-1497C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200915 | ||||||
chr1:40200916 | A | T | 1 | a0003c0003t0001g0322 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.608-1496A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200916 | ||||||
chr1:40200917 | C | CACACACA others(34): Show |
1 | a0003c0003t0001g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.608-1488_608-1487i others(43): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200917 | |||||
chr1:40200919 | C | CACACACA others(50): Show |
1 | a0003c0003t0001g0321 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.608-1473_608-1472i others(59): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACACA others(44): Show |
1 | a0003c0003t0001g0330 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.608-1476_608-1475i others(53): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACACA others(42): Show |
1 | a0003c0003t0001g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.608-1478_608-1477i others(51): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACACA others(38): Show |
3 | a0003c0003t0001g0323a0003c0003t0001g0328a0003c0003t0001g0332 | 3 | HG02055.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.608-1482_608-1481i others(47): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACACA others(36): Show |
1 | a0003c0003t0001g0327 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.608-1484_608-1483i others(45): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACACA others(34): Show |
3 | a0003c0003t0001g0324a0003c0003t0001g0325a0016c0022t0001g0333 | 3 | HG02630.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.608-1486_608-1485i others(43): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACACAGT others(32): Show |
2 | a0003c0003t0001g0320a0003c0003t0001g0326 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.608-1488_608-1487i others(41): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200919 | C | CACAGTGG others(30): Show |
5 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1490_608-1489i others(39): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40200919 | |||||
chr1:40200922 | A | G | 1 | a0004c0004t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.608-1490A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200922 | ||||||
chr1:40200926 | A | G | 1 | a0004c0004t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.608-1486A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200926 | ||||||
chr1:40200932 | A | G | 1 | a0004c0004t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.608-1480A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200932 | ||||||
chr1:40200935 | CACACTGG others(47): Show |
C | 1 | a0001c0006t0001g0047 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.608-1476_608-1423d others(56): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200935 | ||||||
chr1:40200981 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.608-1431A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200981 | ||||||
chr1:40200983 | A | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0052others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-1429A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40200983 | ||||||
chr1:40201041 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.608-1371A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201041 | ||||||
chr1:40201043 | C | A | 47 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(44): Show | 47 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.608-1369C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201043 | ||||||
chr1:40201045 | CCCCCACA others(17): Show |
C | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.608-1362_608-1339d others(26): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201045 | |||||
chr1:40201046 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.608-1366C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201046 | ||||||
chr1:40201048 | C | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.608-1364C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201048 | ||||||
chr1:40201052 | A | C | 5 | a0003c0003t0001g0323a0003c0003t0001g0328a0003c0003t0001g0329others(2): Show | 5 | HG02055.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1360A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201052 | ||||||
chr1:40201055 | TCA | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0112others(17): Show | 20 | HG01069.hp2 HG01243.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.608-1343_608-1342d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201055 | |||||
chr1:40201055 | TCACA | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0133others(7): Show | 10 | HG00140.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-1345_608-1342d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201055 | |||||
chr1:40201055 | TCACACA | T | 5 | a0002c0002t0001g0262a0003c0003t0001g0328a0003c0003t0001g0329others(2): Show | 5 | HG01943.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1347_608-1342d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201055 | |||||
chr1:40201055 | TCACACAC others(1): Show |
T | 7 | a0003c0003t0001g0327a0005c0005t0001g0307a0005c0005t0001g0309others(4): Show | 7 | HG00423.hp2 HG01496.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-1349_608-1342d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201055 | |||||
chr1:40201055 | TCACACAC others(3): Show |
T | 3 | a0003c0003t0001g0320a0010c0014t0001g0337a0010c0014t0001g0338 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.608-1351_608-1342d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201055 | |||||
chr1:40201059 | ACACACAC others(4): Show |
A | 4 | a0003c0003t0001g0326a0003c0003t0001g0334a0003c0003t0001g0335others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-1351_608-1341d others(13): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201059 | |||||
chr1:40201060 | CACACACA others(2): Show |
C | 3 | a0003c0003t0001g0324a0003c0003t0001g0325a0003c0003t0001g0332 | 3 | HG02970.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.608-1351_608-1343d others(11): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201060 | ||||||
chr1:40201061 | ACACACAC others(3): Show |
A | 2 | a0005c0005t0001g0308a0005c0005t0001g0313 | 2 | NA19002.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.608-1349_608-1340d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201061 | |||||
chr1:40201063 | A | AC | 4 | a0001c0001t0001g0118a0002c0002t0001g0229a0002c0002t0001g0231others(1): Show | 4 | HG01981.hp1 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-1348dupC | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201063 | |||||
chr1:40201063 | A | ACC | 4 | a0001c0001t0001g0060a0001c0001t0001g0150a0006c0008t0001g0009others(1): Show | 4 | HG03710.hp2 HG03834.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-1348_608-1347i others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201063 | |||||
chr1:40201063 | A | ACCC | 4 | a0001c0001t0001g0037a0001c0001t0001g0104a0001c0001t0001g0123others(1): Show | 4 | HG01175.hp2 HG03492.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-1348_608-1347i others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201063 | |||||
chr1:40201064 | CA | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0136others(2): Show | 5 | NA18949.hp2 NA18985.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1347delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201064 | ||||||
chr1:40201064 | CACA | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0106a0001c0001t0001g0108others(3): Show | 6 | HG03239.hp1 HG04228.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-1347_608-1345d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201064 | ||||||
chr1:40201064 | CACACA | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0120others(3): Show | 6 | HG00099.hp1 HG01070.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-1347_608-1343d others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201064 | ||||||
chr1:40201065 | A | AC | 6 | a0001c0001t0001g0030a0001c0001t0001g0064a0001c0001t0001g0101others(3): Show | 6 | HG02970.hp1 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-1346dupC | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201065 | |||||
chr1:40201065 | A | C | 21 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0060others(18): Show | 21 | HG01175.hp2 HG01981.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.608-1347A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201065 | ||||||
chr1:40201065 | ACACACC | A | 25 | a0001c0001t0001g0239a0002c0002t0001g0167a0002c0002t0001g0251others(22): Show | 25 | HG01167.hp2 HG01517.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.608-1345_608-1340d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201065 | |||||
chr1:40201065 | ACACACCC | A | 20 | a0002c0002t0001g0243a0002c0002t0001g0245a0002c0002t0001g0258others(17): Show | 20 | HG02273.hp2 HG02559.hp2 HG02698.hp2 others(17): Show |
intron_variant | MODIFIER | c.608-1345_608-1339d others(9): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201065 | |||||
chr1:40201066 | CACA | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0134a0001c0001t0001g0235others(4): Show | 7 | HG00544.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-1345_608-1343d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201066 | ||||||
chr1:40201067 | A | AC | 15 | a0001c0001t0001g0025a0001c0001t0001g0061a0001c0001t0001g0073others(12): Show | 15 | HG01123.hp1 HG02015.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.608-1344dupC | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201067 | |||||
chr1:40201067 | A | ACC | 17 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0069others(14): Show | 17 | HG01167.hp1 HG01175.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.608-1344_608-1343i others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201067 | |||||
chr1:40201067 | A | ACCC | 10 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0062others(7): Show | 10 | HG02129.hp2 HG02451.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.608-1344_608-1343i others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201067 | |||||
chr1:40201067 | A | ACCCC | 6 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0084others(3): Show | 6 | HG00673.hp1 HG01070.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-1344_608-1343i others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201067 | |||||
chr1:40201067 | A | ACCCCC | 7 | a0001c0001t0001g0031a0001c0001t0001g0079a0001c0001t0001g0163others(4): Show | 7 | HG00609.hp1 HG02109.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-1344_608-1343i others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201067 | |||||
chr1:40201067 | A | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0030others(46): Show | 49 | HG00544.hp2 HG01175.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.608-1345A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201067 | ||||||
chr1:40201068 | CA | C | 18 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0045others(15): Show | 18 | HG00280.hp1 HG00408.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.608-1343delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201068 | ||||||
chr1:40201069 | A | C | 156 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 156 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.608-1343A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201069 | ||||||
chr1:40201070 | C | CA | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0144others(2): Show | 5 | HG00639.hp2 HG01884.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-1342_608-1341i others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201070 | ||||||
chr1:40201079 | C | A | 3 | a0002c0002t0001g0231a0002c0002t0001g0232a0002c0011t0001g0230 | 3 | HG02717.hp1 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.608-1333C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201079 | ||||||
chr1:40201082 | C | T | 1 | a0002c0002t0001g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.608-1330C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201082 | ||||||
chr1:40201180 | C | G | 1 | a0002c0002t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.608-1232C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201180 | ||||||
chr1:40201193 | G | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG01070.hp2 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-1219G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201193 | ||||||
chr1:40201296 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.608-1116T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201296 | ||||||
chr1:40201348 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.608-1064G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201348 | ||||||
chr1:40201495 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-917G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201495 | ||||||
chr1:40201550 | C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.608-862C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201550 | ||||||
chr1:40201558 | G | A | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-854G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201558 | ||||||
chr1:40201625 | C | CA | 31 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0261others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.608-765dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201625 | |||||
chr1:40201625 | CA | C | 218 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.608-765delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201625 | |||||
chr1:40201625 | CAA | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0057others(7): Show | 10 | HG01496.hp2 HG02055.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-766_608-765del others(2): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201625 | |||||
chr1:40201625 | CAAA | C | 32 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.608-767_608-765del others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40201625 | |||||
chr1:40201626 | A | G | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.608-786A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | chr1 | 40201626 | ||||||
chr1:40202387 | CTG | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.608-23_608-22delGT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 40202387 | |||||
chr1:40202776 | A | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG00609.hp1 HG01496.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+162A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40202776 | ||||||
chr1:40202917 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+303A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40202917 | ||||||
chr1:40202976 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810+362G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40202976 | ||||||
chr1:40203055 | C | T | 42 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(39): Show | 42 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.810+441C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203055 | ||||||
chr1:40203100 | G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(45): Show | 48 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.810+486G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203100 | ||||||
chr1:40203108 | T | G | 2 | a0002c0002t0001g0243a0002c0002t0001g0249 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.810+494T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203108 | ||||||
chr1:40203109 | C | CT | 11 | a0001c0001t0001g0032a0001c0001t0001g0097a0001c0001t0001g0116others(8): Show | 11 | HG01978.hp2 HG02135.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.810+518dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40203109 | |||||
chr1:40203109 | C | CTT | 7 | a0003c0003t0001g0323a0003c0003t0001g0334a0003c0003t0001g0336others(4): Show | 7 | HG02055.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.810+517_810+518dup others(2): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40203109 | |||||
chr1:40203109 | C | CTTT | 23 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.810+516_810+518dup others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40203109 | |||||
chr1:40203109 | CT | C | 27 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0001t0001g0212others(24): Show | 27 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.810+518delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40203109 | |||||
chr1:40203133 | G | A | 14 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(11): Show | 14 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.810+519G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203133 | ||||||
chr1:40203136 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+522A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203136 | ||||||
chr1:40203263 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.810+649C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203263 | ||||||
chr1:40203318 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+704G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203318 | ||||||
chr1:40203551 | C | CAAAA | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+939_810+940ins others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40203551 | |||||
chr1:40203566 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+952G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203566 | ||||||
chr1:40203590 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+976A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203590 | ||||||
chr1:40203951 | T | A | 1 | a0004c0004t0001g0184 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.810+1337T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40203951 | ||||||
chr1:40204005 | T | C | 1 | a0002c0002t0001g0266 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.810+1391T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204005 | ||||||
chr1:40204034 | C | CT | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0112others(4): Show | 7 | HG00423.hp1 HG02165.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1438dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40204034 | |||||
chr1:40204034 | CT | C | 46 | a0001c0001t0001g0091a0001c0001t0001g0140a0001c0001t0001g0150others(43): Show | 46 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.810+1438delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40204034 | |||||
chr1:40204036 | T | C | 8 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.810+1422T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204036 | ||||||
chr1:40204093 | C | T | 3 | a0001c0001t0001g0239a0009c0012t0001g0234a0009c0012t0001g0237 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.810+1479C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204093 | ||||||
chr1:40204101 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+1487T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204101 | ||||||
chr1:40204102 | T | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+1488T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204102 | ||||||
chr1:40204310 | C | T | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.810+1696C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204310 | ||||||
chr1:40204337 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.810+1723C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204337 | ||||||
chr1:40204398 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810+1784G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204398 | ||||||
chr1:40204515 | T | G | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810+1901T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204515 | ||||||
chr1:40204556 | G | A | 7 | a0002c0002t0001g0243a0002c0002t0001g0244a0002c0002t0001g0245others(4): Show | 7 | HG00280.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1942G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204556 | ||||||
chr1:40204569 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+1955A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204569 | ||||||
chr1:40204581 | T | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.810+1967T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204581 | ||||||
chr1:40204699 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.810+2085G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204699 | ||||||
chr1:40204744 | T | G | 1 | a0002c0002t0001g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.810+2130T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40204744 | ||||||
chr1:40205140 | T | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+2526T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205140 | ||||||
chr1:40205219 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.810+2605C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205219 | ||||||
chr1:40205331 | G | C | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.810+2717G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205331 | ||||||
chr1:40205485 | C | CCT | 17 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(14): Show | 17 | HG00642.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.810+2871_810+2872i others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205485 | ||||||
chr1:40205485 | C | CT | 69 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00140.hp1 HG00423.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.810+2893dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40205485 | |||||
chr1:40205485 | C | CTT | 6 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0110others(3): Show | 6 | HG00544.hp1 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.810+2892_810+2893d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40205485 | |||||
chr1:40205485 | CT | C | 51 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(48): Show | 51 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.810+2893delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40205485 | |||||
chr1:40205485 | CTT | C | 24 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(21): Show | 24 | HG01069.hp2 HG01243.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.810+2892_810+2893d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40205485 | |||||
chr1:40205556 | C | T | 5 | a0002c0002t0001g0256a0002c0002t0001g0257a0002c0002t0001g0258others(2): Show | 5 | HG02559.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+2942C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205556 | ||||||
chr1:40205575 | C | T | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+2961C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205575 | ||||||
chr1:40205650 | C | T | 2 | a0002c0002t0001g0277a0002c0002t0001g0295 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.810+3036C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205650 | ||||||
chr1:40205651 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.810+3037G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205651 | ||||||
chr1:40205733 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.810+3119C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205733 | ||||||
chr1:40205734 | G | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0219 | 2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.810+3120G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205734 | ||||||
chr1:40205769 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+3155G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205769 | ||||||
chr1:40205834 | G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02647.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.810+3220G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205834 | ||||||
chr1:40205838 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.810+3224G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205838 | ||||||
chr1:40205838 | G | C | 7 | a0002c0002t0001g0243a0002c0002t0001g0244a0002c0002t0001g0245others(4): Show | 7 | HG00280.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+3224G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205838 | ||||||
chr1:40205925 | G | A | 120 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(117): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.810+3311G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40205925 | ||||||
chr1:40206093 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+3479A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206093 | ||||||
chr1:40206113 | A | T | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.810+3499A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206113 | ||||||
chr1:40206133 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.810+3519C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206133 | ||||||
chr1:40206134 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+3520G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206134 | ||||||
chr1:40206355 | T | C | 1 | a0007c0013t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.810+3741T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206355 | ||||||
chr1:40206598 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810+3984G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206598 | ||||||
chr1:40206658 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.810+4044A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206658 | ||||||
chr1:40206736 | G | A | 228 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(225): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.810+4122G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40206736 | ||||||
chr1:40207017 | A | G | 1 | a0004c0004t0001g0303 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.810+4403A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207017 | ||||||
chr1:40207108 | C | T | 2 | a0002c0007t0001g0254a0002c0007t0001g0255 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.810+4494C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207108 | ||||||
chr1:40207140 | C | T | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+4526C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207140 | ||||||
chr1:40207173 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.810+4559A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207173 | ||||||
chr1:40207245 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.810+4631G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207245 | ||||||
chr1:40207245 | G | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.810+4631G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207245 | ||||||
chr1:40207389 | C | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+4775C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207389 | ||||||
chr1:40207545 | T | C | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+4931T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207545 | ||||||
chr1:40207546 | G | T | 60 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.810+4932G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207546 | ||||||
chr1:40207623 | G | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+5009G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207623 | ||||||
chr1:40207674 | G | T | 2 | a0002c0002t0001g0231a0002c0011t0001g0230 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.810+5060G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207674 | ||||||
chr1:40207685 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.810+5071A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207685 | ||||||
chr1:40207812 | C | G | 1 | a0001c0001t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.810+5198C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207812 | ||||||
chr1:40207817 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.810+5203C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40207817 | ||||||
chr1:40208106 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.810+5492G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40208106 | ||||||
chr1:40208106 | G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0082 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.810+5492G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40208106 | ||||||
chr1:40208693 | C | CT | 169 | a0001c0001t0001g0175a0001c0001t0001g0185a0001c0001t0001g0186others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.810+6079_810+6080i others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40208693 | ||||||
chr1:40208910 | G | A | 1 | a0004c0004t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.810+6296G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40208910 | ||||||
chr1:40209009 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.810+6395C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209009 | ||||||
chr1:40209129 | T | G | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+6515T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209129 | ||||||
chr1:40209187 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.810+6573G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209187 | ||||||
chr1:40209195 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.810+6581A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209195 | ||||||
chr1:40209283 | G | A | 1 | a0002c0002t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.810+6669G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209283 | ||||||
chr1:40209319 | A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.810+6705A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209319 | ||||||
chr1:40209391 | AAC | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+6781_810+6782d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40209391 | |||||
chr1:40209482 | C | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+6868C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209482 | ||||||
chr1:40209648 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.810+7034C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209648 | ||||||
chr1:40209717 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.810+7103G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209717 | ||||||
chr1:40209825 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.810+7211C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209825 | ||||||
chr1:40209839 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.810+7225T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40209839 | ||||||
chr1:40209877 | T | TA | 20 | a0001c0001t0001g0198a0003c0003t0001g0320a0003c0003t0001g0322others(17): Show | 20 | HG00642.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.810+7279dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40209877 | |||||
chr1:40209877 | TAA | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG00408.hp2 HG00609.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+7278_810+7279d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40209877 | |||||
chr1:40210220 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.810+7606G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40210220 | ||||||
chr1:40210595 | C | T | 2 | a0002c0002t0001g0258a0002c0002t0001g0259 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.810+7981C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40210595 | ||||||
chr1:40210734 | T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(56): Show | 59 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.810+8120T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40210734 | ||||||
chr1:40210997 | G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+8383G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40210997 | ||||||
chr1:40211229 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.810+8615T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211229 | ||||||
chr1:40211322 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+8708A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211322 | ||||||
chr1:40211378 | A | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.810+8764A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211378 | ||||||
chr1:40211593 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.810+8979G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211593 | ||||||
chr1:40211601 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.810+8987A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211601 | ||||||
chr1:40211788 | A | AT | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.810+9179dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40211788 | |||||
chr1:40211889 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.810+9275A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40211889 | ||||||
chr1:40212041 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.810+9427A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212041 | ||||||
chr1:40212116 | CAGG | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01496.hp2 HG01943.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+9505_810+9507d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40212116 | |||||
chr1:40212473 | G | C | 1 | a0004c0004t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.810+9859G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212473 | ||||||
chr1:40212636 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-9938G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212636 | ||||||
chr1:40212685 | G | C | 2 | a0010c0014t0001g0337a0010c0014t0001g0338 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.811-9889G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212685 | ||||||
chr1:40212730 | A | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG00609.hp1 HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.811-9844A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212730 | ||||||
chr1:40212779 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.811-9795A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212779 | ||||||
chr1:40212895 | T | TCCAGATG others(346): Show |
1 | a0002c0002t0001g0251 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.811-9666_811-9665i others(355): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40212895 | |||||
chr1:40212926 | A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0153 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.811-9648A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40212926 | ||||||
chr1:40213064 | A | T | 1 | a0002c0002t0001g0295 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.811-9510A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213064 | ||||||
chr1:40213200 | C | A | 1 | a0002c0002t0001g0274 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.811-9374C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213200 | ||||||
chr1:40213238 | T | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-9336T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213238 | ||||||
chr1:40213367 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-9207G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213367 | ||||||
chr1:40213659 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-8915A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213659 | ||||||
chr1:40213669 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.811-8905A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213669 | ||||||
chr1:40213825 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-8749A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213825 | ||||||
chr1:40213830 | A | G | 3 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0011t0001g0230 | 3 | HG02257.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.811-8744A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213830 | ||||||
chr1:40213855 | C | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.811-8719C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40213855 | ||||||
chr1:40214022 | G | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(56): Show | 59 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.811-8552G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214022 | ||||||
chr1:40214037 | G | A | 240 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(237): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.811-8537G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214037 | ||||||
chr1:40214075 | A | G | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.811-8499A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214075 | ||||||
chr1:40214168 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.811-8406A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214168 | ||||||
chr1:40214432 | G | C | 1 | a0002c0002t0001g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.811-8142G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214432 | ||||||
chr1:40214456 | A | G | 56 | a0002c0002t0001g0071a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.811-8118A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214456 | ||||||
chr1:40214918 | C | CA | 89 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0037others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.811-7629dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAA | 41 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0197others(38): Show | 41 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.811-7630_811-7629d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAA | 18 | a0001c0001t0001g0175a0001c0009t0001g0174a0001c0009t0001g0241others(15): Show | 18 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.811-7631_811-7629d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAA | 15 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0054others(12): Show | 15 | HG01074.hp1 HG01243.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.811-7632_811-7629d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAAA | 18 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 18 | HG00140.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.811-7633_811-7629d others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0105a0001c0001t0001g0107others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.811-7636_811-7629d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0013a0001c0001t0001g0110a0001c0001t0001g0116others(6): Show | 9 | HG01981.hp1 HG02015.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.811-7637_811-7629d others(11): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0134others(2): Show | 5 | HG00544.hp1 HG03834.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-7638_811-7629d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.811-7642_811-7629d others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | CA | C | 6 | a0001c0001t0001g0034a0001c0006t0001g0046a0003c0003t0001g0321others(3): Show | 6 | HG01884.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-7629delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | CAA | C | 29 | a0003c0003t0001g0320a0003c0003t0001g0322a0003c0003t0001g0324others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.811-7630_811-7629d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0189a0001c0001t0001g0240 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.811-7639_811-7629d others(13): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214918 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.811-7640_811-7629d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40214918 | |||||
chr1:40214943 | A | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.811-7631A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40214943 | ||||||
chr1:40215004 | A | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-7570A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40215004 | ||||||
chr1:40215186 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-7388C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40215186 | ||||||
chr1:40215439 | C | G | 1 | a0002c0002t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.811-7135C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40215439 | ||||||
chr1:40215771 | T | C | 1 | a0003c0003t0001g0332 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.811-6803T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40215771 | ||||||
chr1:40215787 | A | G | 1 | a0002c0002t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.811-6787A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40215787 | ||||||
chr1:40216206 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-6368G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216206 | ||||||
chr1:40216209 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.811-6365C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216209 | ||||||
chr1:40216430 | G | T | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-6144G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216430 | ||||||
chr1:40216436 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-6138T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216436 | ||||||
chr1:40216454 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.811-6120C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216454 | ||||||
chr1:40216487 | TA | T | 13 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0164others(10): Show | 13 | HG02015.hp1 HG02080.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.811-6073delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40216487 | |||||
chr1:40216488 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.811-6086A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216488 | ||||||
chr1:40216500 | A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0090a0001c0001t0001g0094 | 3 | NA18960.hp1 NA18964.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.811-6074A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216500 | ||||||
chr1:40216500 | AAGAG | A | 36 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(33): Show | 36 | HG00408.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.811-6066_811-6063d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40216500 | |||||
chr1:40216600 | A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0132 | 3 | HG02083.hp1 NA18964.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.811-5974A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216600 | ||||||
chr1:40216631 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.811-5943C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216631 | ||||||
chr1:40216694 | C | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-5880C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216694 | ||||||
chr1:40216782 | C | T | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.811-5792C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216782 | ||||||
chr1:40216815 | G | A | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.811-5759G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216815 | ||||||
chr1:40216952 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-5622T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216952 | ||||||
chr1:40216991 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.811-5583A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40216991 | ||||||
chr1:40217004 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-5570G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217004 | ||||||
chr1:40217048 | C | G | 6 | a0003c0003t0001g0323a0003c0003t0001g0327a0003c0003t0001g0328others(3): Show | 6 | HG02055.hp1 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-5526C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217048 | ||||||
chr1:40217119 | A | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02647.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.811-5455A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217119 | ||||||
chr1:40217190 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.811-5384G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217190 | ||||||
chr1:40217268 | C | A | 1 | a0002c0002t0001g0003 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.811-5306C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217268 | ||||||
chr1:40217343 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.811-5231T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217343 | ||||||
chr1:40217542 | C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0202 | 2 | HG01175.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.811-5032C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217542 | ||||||
chr1:40217570 | G | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.811-5004G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217570 | ||||||
chr1:40217624 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-4950T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217624 | ||||||
chr1:40217830 | A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0218 | 3 | HG00408.hp1 HG00558.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.811-4744A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217830 | ||||||
chr1:40217864 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.811-4710C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40217864 | ||||||
chr1:40218284 | C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0130 | 2 | NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.811-4290C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218284 | ||||||
chr1:40218297 | C | G | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-4277C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218297 | ||||||
chr1:40218362 | T | TA | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.811-4211dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40218362 | |||||
chr1:40218391 | T | C | 1 | a0003c0003t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.811-4183T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218391 | ||||||
chr1:40218490 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.811-4084G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218490 | ||||||
chr1:40218548 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.811-4026C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218548 | ||||||
chr1:40218561 | C | T | 1 | a0002c0002t0001g0273 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.811-4013C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218561 | ||||||
chr1:40218637 | A | G | 1 | a0001c0019t0001g0204 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.811-3937A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218637 | ||||||
chr1:40218751 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.811-3823A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218751 | ||||||
chr1:40218888 | A | G | 14 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.811-3686A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218888 | ||||||
chr1:40218903 | C | T | 19 | a0001c0001t0001g0175a0001c0001t0001g0240a0001c0001t0001g0242others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.811-3671C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40218903 | ||||||
chr1:40218990 | TTAAGTA | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-3579_811-3574d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40218990 | |||||
chr1:40219132 | T | C | 55 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0243others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.811-3442T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219132 | ||||||
chr1:40219168 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.811-3406G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219168 | ||||||
chr1:40219383 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-3191T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219383 | ||||||
chr1:40219394 | G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.811-3180G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219394 | ||||||
chr1:40219450 | A | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.811-3124A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219450 | ||||||
chr1:40219494 | A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0153 | 2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.811-3080A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219494 | ||||||
chr1:40219596 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-2978A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219596 | ||||||
chr1:40219742 | G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0238 | 3 | HG02647.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.811-2832G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219742 | ||||||
chr1:40219860 | A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.811-2714A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219860 | ||||||
chr1:40219975 | G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0015 | 2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.811-2599G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219975 | ||||||
chr1:40219998 | G | T | 2 | a0002c0002t0001g0243a0002c0002t0001g0249 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.811-2576G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40219998 | ||||||
chr1:40220246 | A | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.811-2328A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40220246 | ||||||
chr1:40220320 | T | G | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.811-2254T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40220320 | ||||||
chr1:40220335 | C | A | 1 | a0002c0002t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.811-2239C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40220335 | ||||||
chr1:40220970 | T | TA | 31 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0053others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.811-1585dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40220970 | |||||
chr1:40220970 | TA | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0023others(8): Show | 11 | HG01070.hp2 HG02922.hp2 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.811-1585delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40220970 | |||||
chr1:40220971 | A | T | 2 | a0002c0007t0001g0252a0002c0007t0001g0253 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.811-1603A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40220971 | ||||||
chr1:40221082 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-1492G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221082 | ||||||
chr1:40221119 | G | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.811-1455G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221119 | ||||||
chr1:40221167 | G | A | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.811-1407G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221167 | ||||||
chr1:40221188 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-1386G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221188 | ||||||
chr1:40221209 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.811-1365C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221209 | ||||||
chr1:40221321 | GA | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-1243delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221321 | |||||
chr1:40221491 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811-1083A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221491 | ||||||
chr1:40221606 | C | CA | 15 | a0001c0001t0001g0045a0001c0001t0001g0082a0004c0004t0001g0176others(12): Show | 15 | HG01109.hp1 HG02055.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.811-956dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221606 | |||||
chr1:40221627 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-947A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221627 | ||||||
chr1:40221639 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.811-935G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221639 | ||||||
chr1:40221689 | T | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0221others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.811-885T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221689 | ||||||
chr1:40221689 | T | C | 35 | a0002c0002t0001g0264a0003c0003t0001g0320a0003c0003t0001g0321others(32): Show | 35 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.811-885T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221689 | ||||||
chr1:40221696 | T | A | 3 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0274 | 3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.811-878T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221696 | ||||||
chr1:40221696 | T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0048others(45): Show | 48 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.811-878T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221696 | ||||||
chr1:40221712 | A | T | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.811-862A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221712 | ||||||
chr1:40221722 | A | G | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-852A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221722 | ||||||
chr1:40221808 | G | A | 1 | a0001c0001t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.811-766G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221808 | ||||||
chr1:40221817 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.811-757T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221817 | ||||||
chr1:40221870 | G | A | 1 | a0004c0004t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.811-704G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221870 | ||||||
chr1:40221871 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.811-703G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221871 | ||||||
chr1:40221878 | C | T | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-696C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221878 | ||||||
chr1:40221899 | C | CA | 6 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0101others(3): Show | 6 | HG00741.hp1 HG02273.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.811-656dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(1): Show |
32 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.811-663_811-656dup others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(3): Show |
47 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.811-665_811-656dup others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(4): Show |
7 | a0002c0002t0001g0251a0002c0002t0001g0276a0002c0002t0001g0277others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.811-666_811-656dup others(11): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(5): Show |
1 | a0002c0002t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.811-667_811-656dup others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.811-670_811-656dup others(15): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(10): Show |
4 | a0004c0004t0001g0179a0004c0004t0001g0301a0004c0004t0001g0303others(1): Show | 4 | HG02698.hp2 HG03927.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-672_811-656dup others(17): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(11): Show |
4 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0184others(1): Show | 4 | HG02083.hp2 HG02735.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-673_811-656dup others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(12): Show |
2 | a0004c0004t0001g0180a0004c0004t0001g0181 | 2 | HG02080.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.811-674_811-656dup others(19): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(13): Show |
1 | a0004c0004t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.811-656_811-655ins others(20): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(14): Show |
1 | a0004c0004t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.811-656_811-655ins others(21): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221899 | C | CAAAAAAA others(15): Show |
1 | a0004c0004t0001g0182 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.811-656_811-655ins others(22): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221899 | |||||
chr1:40221915 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.811-659A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221915 | ||||||
chr1:40221917 | A | AAAAAAAA others(17): Show |
1 | a0008c0010t0001g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.811-656_811-655ins others(24): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 40221917 | |||||
chr1:40221917 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.811-657A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221917 | ||||||
chr1:40221952 | G | T | 1 | a0001c0001t0001g0033 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.811-622G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221952 | ||||||
chr1:40221996 | A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0242 | 2 | HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.811-578A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40221996 | ||||||
chr1:40222049 | C | T | 3 | a0002c0002t0001g0290a0002c0002t0001g0291a0002c0002t0001g0292 | 3 | NA18939.hp2 NA18948.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.811-525C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222049 | ||||||
chr1:40222143 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-431C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222143 | ||||||
chr1:40222213 | T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.811-361T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222213 | ||||||
chr1:40222327 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.811-247G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222327 | ||||||
chr1:40222460 | C | T | 49 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(46): Show | 49 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.811-114C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222460 | ||||||
chr1:40222507 | C | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.811-67C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 5/7 | chr1 | 40222507 | ||||||
chr1:40222888 | G | A | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.947+178G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40222888 | ||||||
chr1:40222989 | TGTTA | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+285_947+288del others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40222989 | |||||
chr1:40222991 | T | C | 1 | a0001c0006t0001g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.947+281T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40222991 | ||||||
chr1:40223019 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.947+309T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40223019 | ||||||
chr1:40223434 | C | T | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.947+724C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40223434 | ||||||
chr1:40223489 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.947+779T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40223489 | ||||||
chr1:40224027 | C | G | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.947+1317C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224027 | ||||||
chr1:40224041 | C | T | 1 | a0002c0002t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.947+1331C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224041 | ||||||
chr1:40224047 | ATAAAT | A | 3 | a0004c0004t0001g0176a0004c0004t0001g0182a0004c0004t0001g0183 | 3 | HG02074.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.947+1343_947+1347d others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224047 | |||||
chr1:40224161 | T | C | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.947+1451T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224161 | ||||||
chr1:40224271 | G | GA | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+1562dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224271 | |||||
chr1:40224306 | C | CT | 17 | a0001c0001t0001g0025a0001c0001t0001g0045a0001c0001t0001g0088others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+1616dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224306 | |||||
chr1:40224306 | CT | C | 11 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG02922.hp2 HG02965.hp1 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.947+1616delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224306 | |||||
chr1:40224306 | CTT | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.947+1615_947+1616d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224306 | |||||
chr1:40224306 | CTTT | C | 18 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(15): Show | 18 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.947+1614_947+1616d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224306 | |||||
chr1:40224533 | CA | C | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.947+1826delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224533 | |||||
chr1:40224578 | CT | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.947+1890delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224578 | |||||
chr1:40224578 | CTT | C | 10 | a0001c0001t0001g0168a0001c0001t0001g0175a0001c0001t0001g0233others(7): Show | 10 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.947+1889_947+1890d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224578 | |||||
chr1:40224578 | CTTTT | C | 17 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(14): Show | 17 | HG00642.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.947+1887_947+1890d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224578 | |||||
chr1:40224578 | CTTTTT | C | 16 | a0003c0003t0001g0334a0003c0003t0001g0336a0005c0005t0001g0306others(13): Show | 16 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.947+1886_947+1890d others(7): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224578 | |||||
chr1:40224600 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.947+1890T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224600 | ||||||
chr1:40224600 | T | TC | 4 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0145others(1): Show | 4 | HG00639.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+1894dupC | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224600 | |||||
chr1:40224623 | C | CT | 31 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(28): Show | 31 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.947+1944dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTT | 15 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0016others(12): Show | 15 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.947+1943_947+1944d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTT | 6 | a0001c0001t0001g0168a0001c0006t0001g0049a0001c0006t0001g0058others(3): Show | 6 | HG00609.hp1 HG02723.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+1942_947+1944d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.947+1931_947+1944d others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0199a0001c0001t0001g0212a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+1930_947+1944d others(17): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0218 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.947+1929_947+1944d others(18): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0214 | 2 | HG00408.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.947+1928_947+1944d others(19): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.947+1927_947+1944d others(20): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0200 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.947+1926_947+1944d others(21): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.947+1925_947+1944d others(22): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.947+1924_947+1944d others(23): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0198a0001c0001t0001g0215a0001c0001t0001g0226 | 3 | HG02523.hp2 HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.947+1921_947+1944d others(26): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.947+1920_947+1944d others(27): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0001g0221a0001c0001t0001g0225 | 2 | NA18522.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.947+1919_947+1944d others(28): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0188 | 2 | HG01175.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.947+1918_947+1944d others(29): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0217 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.947+1915_947+1944d others(32): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0224 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.947+1944_947+1945i others(34): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTT | C | 6 | a0001c0001t0001g0305a0002c0007t0001g0252a0002c0007t0001g0253others(3): Show | 6 | HG00423.hp2 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.947+1943_947+1944d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTT | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0203a0001c0001t0001g0233others(3): Show | 6 | HG01099.hp1 HG02027.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+1942_947+1944d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTT | C | 14 | a0001c0001t0001g0208a0001c0001t0001g0216a0002c0002t0001g0003others(11): Show | 14 | HG00558.hp1 HG01433.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+1941_947+1944d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTT | C | 12 | a0001c0001t0001g0210a0001c0001t0001g0235a0001c0001t0001g0236others(9): Show | 12 | HG00558.hp2 HG01981.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.947+1939_947+1944d others(8): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT | C | 47 | a0001c0001t0001g0082a0002c0002t0001g0166a0002c0002t0001g0167others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.947+1938_947+1944d others(9): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0110others(4): Show | 7 | HG01175.hp2 HG03942.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.947+1937_947+1944d others(10): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT others(2): Show |
C | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(54): Show | 57 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.947+1936_947+1944d others(11): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0117a0001c0019t0001g0204 | 2 | NA18951.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.947+1935_947+1944d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT others(5): Show |
C | 14 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.947+1933_947+1944d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224623 | CTTTTTTT others(7): Show |
C | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.947+1931_947+1944d others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40224623 | |||||
chr1:40224665 | T | C | 5 | a0002c0002t0001g0256a0002c0002t0001g0257a0002c0002t0001g0258others(2): Show | 5 | HG02559.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+1955T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224665 | ||||||
chr1:40224709 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.947+1999G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224709 | ||||||
chr1:40224717 | T | G | 1 | a0002c0002t0001g0299 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.947+2007T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224717 | ||||||
chr1:40224718 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+2008G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224718 | ||||||
chr1:40224830 | T | C | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.947+2120T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224830 | ||||||
chr1:40224913 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.947+2203G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40224913 | ||||||
chr1:40225213 | C | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.947+2503C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225213 | ||||||
chr1:40225522 | C | T | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+2812C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225522 | ||||||
chr1:40225578 | C | CA | 8 | a0001c0001t0001g0015a0001c0001t0001g0059a0001c0001t0001g0067others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.947+2885dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | C | CAAAAAAA others(2): Show |
8 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0309others(5): Show | 8 | HG01496.hp1 HG02027.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.947+2877_947+2885d others(11): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | C | CAAAAAAA others(3): Show |
7 | a0005c0005t0001g0308a0005c0005t0001g0311a0005c0005t0001g0313others(4): Show | 7 | HG00423.hp2 HG00558.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.947+2876_947+2885d others(12): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | C | CAAAAAAA others(5): Show |
7 | a0003c0003t0001g0320a0003c0003t0001g0322a0003c0003t0001g0324others(4): Show | 7 | HG00642.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.947+2874_947+2885d others(14): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | C | CAAAAAAA others(6): Show |
9 | a0003c0003t0001g0321a0003c0003t0001g0323a0003c0003t0001g0325others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.947+2873_947+2885d others(15): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | C | CAAAAAAA others(8): Show |
3 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.947+2871_947+2885d others(17): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225578 | CA | C | 76 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.947+2885delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225578 | |||||
chr1:40225599 | G | A | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(56): Show | 59 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.947+2889G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225599 | ||||||
chr1:40225615 | G | T | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.947+2905G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225615 | ||||||
chr1:40225634 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.947+2924T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225634 | ||||||
chr1:40225642 | C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0115a0001c0001t0001g0135others(1): Show | 4 | HG02027.hp2 NA18952.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+2932C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225642 | ||||||
chr1:40225721 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.947+3011G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225721 | ||||||
chr1:40225765 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.947+3055T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225765 | ||||||
chr1:40225770 | G | A | 1 | a0004c0004t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.947+3060G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225770 | ||||||
chr1:40225810 | G | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.947+3100G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225810 | ||||||
chr1:40225835 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.947+3125C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225835 | ||||||
chr1:40225878 | C | CA | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.947+3194dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225878 | |||||
chr1:40225878 | C | CAA | 23 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0165others(20): Show | 23 | HG01175.hp1 HG01433.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.947+3193_947+3194d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225878 | |||||
chr1:40225878 | C | CAAA | 12 | a0001c0001t0001g0191a0001c0001t0001g0212a0001c0001t0001g0233others(9): Show | 12 | HG00642.hp2 HG01884.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.947+3192_947+3194d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225878 | |||||
chr1:40225878 | C | CAAAA | 7 | a0003c0003t0001g0320a0003c0003t0001g0323a0003c0003t0001g0326others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.947+3191_947+3194d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225878 | |||||
chr1:40225878 | C | CAAAAAAA | 10 | a0005c0005t0001g0306a0005c0005t0001g0308a0005c0005t0001g0310others(7): Show | 10 | HG00423.hp2 HG00558.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.947+3188_947+3194d others(9): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40225878 | |||||
chr1:40225879 | A | C | 3 | a0002c0002t0001g0264a0002c0002t0001g0265a0002c0002t0001g0269 | 3 | HG02451.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.947+3169A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225879 | ||||||
chr1:40225910 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.947+3200A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40225910 | ||||||
chr1:40226003 | A | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+3293A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226003 | ||||||
chr1:40226367 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.947+3657C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226367 | ||||||
chr1:40226571 | G | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+3861G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226571 | ||||||
chr1:40226648 | A | AT | 5 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+3939dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40226648 | |||||
chr1:40226677 | T | C | 2 | a0002c0002t0001g0279a0002c0002t0001g0280 | 2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.947+3967T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226677 | ||||||
chr1:40226683 | T | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.947+3973T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226683 | ||||||
chr1:40226744 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.947+4034T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226744 | ||||||
chr1:40226785 | A | G | 60 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.947+4075A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226785 | ||||||
chr1:40226921 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.947+4211A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40226921 | ||||||
chr1:40227021 | G | A | 2 | a0008c0010t0001g0227a0008c0010t0001g0228 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.947+4311G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227021 | ||||||
chr1:40227085 | G | C | 13 | a0004c0004t0001g0176a0004c0004t0001g0177a0004c0004t0001g0178others(10): Show | 13 | HG02074.hp2 HG02080.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.947+4375G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227085 | ||||||
chr1:40227244 | G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA18968.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.948-4273G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227244 | ||||||
chr1:40227419 | G | C | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-4098G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227419 | ||||||
chr1:40227498 | G | A | 3 | a0004c0004t0001g0176a0004c0004t0001g0182a0004c0004t0001g0183 | 3 | HG02074.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.948-4019G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227498 | ||||||
chr1:40227742 | C | T | 1 | a0007c0013t0001g0172 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.948-3775C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227742 | ||||||
chr1:40227752 | C | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-3765C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227752 | ||||||
chr1:40227776 | A | G | 121 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(118): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.948-3741A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227776 | ||||||
chr1:40227831 | C | T | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-3686C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227831 | ||||||
chr1:40227864 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-3653A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227864 | ||||||
chr1:40227909 | A | G | 1 | a0003c0003t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.948-3608A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227909 | ||||||
chr1:40227957 | C | T | 14 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.948-3560C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227957 | ||||||
chr1:40227981 | G | C | 121 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(118): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.948-3536G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40227981 | ||||||
chr1:40228218 | AGAGGTTG others(290): Show |
A | 3 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0165 | 3 | NA18949.hp2 NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.948-3282_948-2986d others(2): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40228218 | |||||
chr1:40228233 | C | T | 2 | a0002c0007t0001g0252a0002c0007t0001g0253 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.948-3284C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228233 | ||||||
chr1:40228259 | C | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.948-3258C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228259 | ||||||
chr1:40228285 | C | CA | 16 | a0002c0002t0001g0267a0005c0005t0001g0306a0005c0005t0001g0307others(13): Show | 16 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.948-3220dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40228285 | |||||
chr1:40228287 | A | G | 1 | a0001c0001t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.948-3230A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228287 | ||||||
chr1:40228391 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.948-3126C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228391 | ||||||
chr1:40228483 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.948-3034T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228483 | ||||||
chr1:40228581 | C | CA | 57 | a0001c0001t0001g0233a0002c0002t0001g0003a0002c0002t0001g0071others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.948-2921dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40228581 | |||||
chr1:40228591 | A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA18939.hp1 NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.948-2926A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228591 | ||||||
chr1:40228661 | T | C | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-2856T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228661 | ||||||
chr1:40228726 | A | AT | 121 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(118): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.948-2790dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40228726 | |||||
chr1:40228907 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.948-2610G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228907 | ||||||
chr1:40228935 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-2582A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228935 | ||||||
chr1:40228972 | T | C | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-2545T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40228972 | ||||||
chr1:40229006 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.948-2511G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229006 | ||||||
chr1:40229118 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.948-2399C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229118 | ||||||
chr1:40229132 | T | C | 24 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(21): Show | 24 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.948-2385T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229132 | ||||||
chr1:40229209 | A | C | 1 | a0002c0002t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.948-2308A>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229209 | ||||||
chr1:40229349 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.948-2168T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229349 | ||||||
chr1:40229448 | C | CT | 24 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0052others(21): Show | 24 | HG00408.hp2 HG01175.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.948-2045dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40229448 | |||||
chr1:40229448 | C | CTT | 6 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0083others(3): Show | 6 | HG01891.hp1 HG01981.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.948-2046_948-2045d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40229448 | |||||
chr1:40229448 | CT | C | 85 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0163others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.948-2045delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40229448 | |||||
chr1:40229448 | CTT | C | 8 | a0002c0002t0001g0269a0002c0007t0001g0252a0002c0007t0001g0253others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.948-2046_948-2045d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40229448 | |||||
chr1:40229559 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.948-1958A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229559 | ||||||
chr1:40229642 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.948-1875A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229642 | ||||||
chr1:40229675 | G | A | 2 | a0002c0002t0001g0166a0002c0002t0001g0167 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.948-1842G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229675 | ||||||
chr1:40229706 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.948-1811G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229706 | ||||||
chr1:40229748 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.948-1769C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229748 | ||||||
chr1:40229822 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-1695A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229822 | ||||||
chr1:40229842 | C | T | 1 | a0003c0003t0001g0324 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.948-1675C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229842 | ||||||
chr1:40229843 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.948-1674G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40229843 | ||||||
chr1:40230025 | C | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-1492C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230025 | ||||||
chr1:40230068 | G | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-1449G>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230068 | ||||||
chr1:40230085 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.948-1432G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230085 | ||||||
chr1:40230114 | C | CA | 15 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(12): Show | 15 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.948-1389dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40230114 | |||||
chr1:40230126 | A | G | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(54): Show | 57 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.948-1391A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230126 | ||||||
chr1:40230582 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.948-935A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230582 | ||||||
chr1:40230587 | C | T | 1 | a0003c0003t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.948-930C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230587 | ||||||
chr1:40230648 | G | T | 1 | a0002c0002t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.948-869G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230648 | ||||||
chr1:40230656 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-861C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230656 | ||||||
chr1:40230666 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-851C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230666 | ||||||
chr1:40230669 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-848G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230669 | ||||||
chr1:40230671 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-846G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230671 | ||||||
chr1:40230681 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-836C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230681 | ||||||
chr1:40230682 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-835C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230682 | ||||||
chr1:40230684 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-833T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230684 | ||||||
chr1:40230685 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-832C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230685 | ||||||
chr1:40230687 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-830C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230687 | ||||||
chr1:40230688 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-829C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230688 | ||||||
chr1:40230690 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-827C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230690 | ||||||
chr1:40230691 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-826C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230691 | ||||||
chr1:40230692 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-825C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230692 | ||||||
chr1:40230697 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-820T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230697 | ||||||
chr1:40230698 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-819G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230698 | ||||||
chr1:40230699 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-818C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230699 | ||||||
chr1:40230702 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-815G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230702 | ||||||
chr1:40230703 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-814G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230703 | ||||||
chr1:40230707 | A | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-810A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230707 | ||||||
chr1:40230708 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-809C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230708 | ||||||
chr1:40230710 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-807G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230710 | ||||||
chr1:40230711 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-806G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230711 | ||||||
chr1:40230712 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-805C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230712 | ||||||
chr1:40230715 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-802G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230715 | ||||||
chr1:40230717 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-800G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230717 | ||||||
chr1:40230718 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-799C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230718 | ||||||
chr1:40230719 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-798C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230719 | ||||||
chr1:40230720 | ACCCGCCA others(9): Show |
A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-796_948-781del others(16): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230720 | ||||||
chr1:40230737 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-780T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230737 | ||||||
chr1:40230738 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-779C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230738 | ||||||
chr1:40230745 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-772G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230745 | ||||||
chr1:40230753 | A | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-764A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230753 | ||||||
chr1:40230757 | G | A | 2 | a0002c0023t0001g0268a0011c0024t0001g0201 | 2 | HG02132.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.948-760G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230757 | ||||||
chr1:40230760 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-757G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230760 | ||||||
chr1:40230762 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-755G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230762 | ||||||
chr1:40230765 | A | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-752A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230765 | ||||||
chr1:40230767 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-750C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230767 | ||||||
chr1:40230771 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-746C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230771 | ||||||
chr1:40230778 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-739G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230778 | ||||||
chr1:40230782 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-735C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230782 | ||||||
chr1:40230784 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-733C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230784 | ||||||
chr1:40230790 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-727G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230790 | ||||||
chr1:40230791 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-726C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230791 | ||||||
chr1:40230792 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-725T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230792 | ||||||
chr1:40230795 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-722C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230795 | ||||||
chr1:40230796 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-721C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230796 | ||||||
chr1:40230799 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-718G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230799 | ||||||
chr1:40230800 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-717C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230800 | ||||||
chr1:40230806 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-711C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230806 | ||||||
chr1:40230813 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-704C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230813 | ||||||
chr1:40230814 | A | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-703A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230814 | ||||||
chr1:40230816 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-701T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230816 | ||||||
chr1:40230817 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-700C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230817 | ||||||
chr1:40230819 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-698C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230819 | ||||||
chr1:40230820 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-697T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230820 | ||||||
chr1:40230821 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-696C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230821 | ||||||
chr1:40230827 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-690C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230827 | ||||||
chr1:40230832 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-685C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230832 | ||||||
chr1:40230836 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-681C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230836 | ||||||
chr1:40230837 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-680C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230837 | ||||||
chr1:40230838 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-679T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230838 | ||||||
chr1:40230840 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-677G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230840 | ||||||
chr1:40230841 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-676G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230841 | ||||||
chr1:40230842 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-675C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230842 | ||||||
chr1:40230845 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-672T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230845 | ||||||
chr1:40230846 | G | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-671G>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230846 | ||||||
chr1:40230848 | T | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-669T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230848 | ||||||
chr1:40230849 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-668G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230849 | ||||||
chr1:40230851 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-666G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230851 | ||||||
chr1:40230855 | C | T | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-662C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230855 | ||||||
chr1:40230860 | G | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-657G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230860 | ||||||
chr1:40230861 | C | A | 1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-656C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230861 | ||||||
chr1:40230865 | T | TAATAAAA others(8): Show |
1 | a0002c0023t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948-652_948-651ins others(15): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40230865 | ||||||
chr1:40231082 | A | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.948-435A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40231082 | ||||||
chr1:40231110 | C | CTA | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.948-406_948-405ins others(2): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 40231110 | |||||
chr1:40231223 | T | C | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-294T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40231223 | ||||||
chr1:40231326 | G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0130 | 2 | NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.948-191G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40231326 | ||||||
chr1:40231335 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.948-182C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40231335 | ||||||
chr1:40231336 | G | A | 3 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0274 | 3 | HG00140.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.948-181G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 6/7 | chr1 | 40231336 | ||||||
chr1:40231967 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1089+309G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40231967 | ||||||
chr1:40232148 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089+490T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232148 | ||||||
chr1:40232215 | T | TA | 13 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(10): Show | 13 | HG00423.hp2 HG00558.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1089+557_1089+558i others(3): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232215 | ||||||
chr1:40232216 | T | A | 37 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0162others(34): Show | 37 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1089+558T>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232216 | ||||||
chr1:40232216 | T | TA | 7 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(4): Show | 7 | HG02074.hp2 HG02083.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1089+572dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40232216 | |||||
chr1:40232216 | TA | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0098a0001c0001t0001g0185others(5): Show | 8 | HG01069.hp1 HG01517.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+572delA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40232216 | |||||
chr1:40232217 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1089+559A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232217 | ||||||
chr1:40232367 | A | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0090a0001c0001t0001g0094 | 3 | NA18960.hp1 NA18964.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1089+709A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232367 | ||||||
chr1:40232371 | A | G | 3 | a0004c0004t0001g0176a0004c0004t0001g0182a0004c0004t0001g0183 | 3 | HG02074.hp2 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1089+713A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232371 | ||||||
chr1:40232433 | G | A | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+775G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232433 | ||||||
chr1:40232487 | C | T | 7 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(4): Show | 7 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1089+829C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232487 | ||||||
chr1:40232522 | T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0111others(4): Show | 7 | NA18961.hp2 NA18971.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089+864T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232522 | ||||||
chr1:40232682 | C | G | 1 | a0004c0004t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1089+1024C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232682 | ||||||
chr1:40232768 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1089+1110G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232768 | ||||||
chr1:40232787 | T | C | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089+1129T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232787 | ||||||
chr1:40232793 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1089+1135C>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232793 | ||||||
chr1:40232923 | A | G | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089+1265A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40232923 | ||||||
chr1:40233004 | C | A | 34 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(31): Show | 34 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089+1346C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40233004 | ||||||
chr1:40233094 | C | CA | 50 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(47): Show | 50 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1089+1452dupA | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40233094 | |||||
chr1:40233523 | C | A | 122 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(119): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1089+1865C>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40233523 | ||||||
chr1:40233749 | G | A | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1090-2043G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40233749 | ||||||
chr1:40233824 | C | CCTTCTCA others(8): Show |
1 | a0002c0002t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1090-1964_1090-195 others(19): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40233824 | |||||
chr1:40233971 | C | T | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-1821C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40233971 | ||||||
chr1:40234008 | G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1090-1784G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234008 | ||||||
chr1:40234130 | A | G | 4 | a0002c0007t0001g0252a0002c0007t0001g0253a0002c0007t0001g0254others(1): Show | 4 | HG02258.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-1662A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234130 | ||||||
chr1:40234172 | A | G | 19 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(16): Show | 19 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1090-1620A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234172 | ||||||
chr1:40234181 | C | T | 1 | a0004c0004t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1090-1611C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234181 | ||||||
chr1:40234283 | T | C | 1 | a0005c0005t0001g0319 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1090-1509T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234283 | ||||||
chr1:40234353 | C | T | 122 | a0001c0001t0001g0175a0001c0001t0001g0233a0001c0001t0001g0240others(119): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1090-1439C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234353 | ||||||
chr1:40234366 | T | C | 5 | a0004c0004t0001g0086a0004c0004t0001g0154a0004c0004t0001g0176others(2): Show | 5 | HG02074.hp2 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-1426T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234366 | ||||||
chr1:40234391 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1090-1401T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234391 | ||||||
chr1:40234398 | G | A | 3 | a0001c0009t0001g0173a0001c0009t0001g0174a0001c0009t0001g0241 | 3 | HG01069.hp1 HG01071.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1090-1394G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234398 | ||||||
chr1:40234445 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1090-1347G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234445 | ||||||
chr1:40234699 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1090-1093A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234699 | ||||||
chr1:40234733 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1090-1059C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234733 | ||||||
chr1:40234755 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1090-1037T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234755 | ||||||
chr1:40234886 | C | T | 1 | a0002c0002t0001g0298 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1090-906C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40234886 | ||||||
chr1:40235055 | A | AT | 111 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0030others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1090-714dupT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235055 | A | ATT | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1090-715_1090-714d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235055 | A | ATTT | 12 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(9): Show | 12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1090-716_1090-714d others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235055 | AT | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0115a0001c0001t0001g0146others(3): Show | 6 | HG00423.hp2 HG03041.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-714delT | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235055 | ATT | A | 14 | a0005c0005t0001g0306a0005c0005t0001g0307a0005c0005t0001g0308others(11): Show | 14 | HG00558.hp1 HG01496.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.1090-715_1090-714d others(4): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235055 | ATTTT | A | 15 | a0003c0003t0001g0320a0003c0003t0001g0321a0003c0003t0001g0322others(12): Show | 15 | HG00642.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1090-717_1090-714d others(6): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235055 | |||||
chr1:40235084 | G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0211 | 2 | NA19056.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1090-708G>A | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235084 | ||||||
chr1:40235126 | A | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0072 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1090-666A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235126 | ||||||
chr1:40235198 | A | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0106 | 2 | HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1090-594A>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235198 | ||||||
chr1:40235383 | T | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090-409T>C | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235383 | ||||||
chr1:40235420 | A | G | 1 | a0002c0002t0001g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1090-372A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235420 | ||||||
chr1:40235467 | C | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0242a0001c0009t0001g0173others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-325C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235467 | ||||||
chr1:40235527 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1090-265C>T | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235527 | ||||||
chr1:40235592 | A | G | 4 | a0002c0002t0001g0229a0002c0002t0001g0231a0002c0002t0001g0232others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090-200A>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235592 | ||||||
chr1:40235706 | T | G | 56 | a0002c0002t0001g0003a0002c0002t0001g0166a0002c0002t0001g0167others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1090-86T>G | RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | chr1 | 40235706 | ||||||
chr1:40235709 | CAAGCT | C | 3 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336 | 3 | HG02145.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1090-80_1090-76del others(5): Show |
RLF | ENSG00000117000.9 | transcript | ENST00000372771.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 40235709 |