geneid | 79908 |
---|---|
ensemblid | ENSG00000113303.12 |
hgncid | 26131 |
symbol | BTNL8 |
name | butyrophilin like 8 |
refseq_nuc | NM_001040462.3 |
refseq_prot | NP_001035552.1 |
ensembl_nuc | ENST00000340184.9 |
ensembl_prot | ENSP00000342197.4 |
mane_status | MANE Select |
chr | chr5 |
start | 180899159 |
end | 180950906 |
strand | + |
ver | v1.2 |
region | chr5:180899159-180950906 |
region5000 | chr5:180894159-180955906 |
regionname0 | BTNL8_chr5_180899159_180950906 |
regionname5000 | BTNL8_chr5_180894159_180955906 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 500 | 78 | 15 | 19 | 27 | 4 | 11 | 18 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002 | 0/0 | 500 | 43 | 25 | 4 | 9 | 1 | 4 | 5 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0003 | 0/0 | 500 | 28 | 5 | 1 | 14 | 0 | 8 | 9 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004 | 0/0 | 500 | 17 | 0 | 5 | 4 | 1 | 7 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005 | 0/0 | 500 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0006 | 0/0 | 500 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0007 | 0/0 | 500 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0008 | 0/0 | 500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0009 | 0/0 | 500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0010 | 0/0 | 500 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0011 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0012 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0013 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0014 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0015 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0016 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1503 | 78 | 15 | 19 | 27 | 4 | 11 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0002 | 0/0 | 1503 | 29 | 15 | 3 | 9 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0003 | 0/0 | 1503 | 21 | 2 | 1 | 14 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0004 | 0/0 | 1503 | 15 | 0 | 5 | 4 | 1 | 5 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0005 | 0/0 | 1503 | 9 | 5 | 1 | 0 | 1 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0006 | 0/0 | 1503 | 7 | 3 | 0 | 0 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0007 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0008 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0009 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0010 | 0/0 | 1503 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0011 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0012 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0013 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0014 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0015 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0016 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0017 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0018 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0019 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0020 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0021 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0022 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0023 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0024 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0025 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
c0026 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1503 | 78 | 15 | 19 | 27 | 4 | 11 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0002 | 0/0 | 1503 | 29 | 15 | 3 | 9 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0005 | 0/0 | 1503 | 9 | 5 | 1 | 0 | 1 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0007 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0024 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0003c0003 | 0/0 | 1503 | 21 | 2 | 1 | 14 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0003c0006 | 0/0 | 1503 | 7 | 3 | 0 | 0 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004c0004 | 0/0 | 1503 | 15 | 0 | 5 | 4 | 1 | 5 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004c0010 | 0/0 | 1503 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0009 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0012 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0021 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0006c0008 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0007c0013 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0007c0017 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0008c0019 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0008c0025 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0009c0018 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0009c0022 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0010c0011 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0011c0026 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0012c0023 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0013c0015 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0014c0014 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0015c0016 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0016c0020 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2017 | 77 | 15 | 19 | 27 | 4 | 10 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0001c0001t0002 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0002t0001 | 0/0 | 2017 | 29 | 15 | 3 | 9 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0005t0001 | 0/0 | 2017 | 9 | 5 | 1 | 0 | 1 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0007t0001 | 0/0 | 2017 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0002c0024t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0003c0003t0001 | 0/0 | 2017 | 21 | 2 | 1 | 14 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0003c0006t0001 | 0/0 | 2017 | 7 | 3 | 0 | 0 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004c0004t0001 | 0/0 | 2017 | 14 | 0 | 5 | 4 | 1 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004c0004t0002 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0004c0010t0001 | 0/0 | 2017 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0009t0001 | 0/0 | 2017 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0012t0001 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0005c0021t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0006c0008t0001 | 0/0 | 2017 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0007c0013t0001 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0007c0017t0001 | 0/0 | 2017 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0008c0019t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0008c0025t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0009c0018t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0009c0022t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0010c0011t0001 | 0/0 | 2017 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0011c0026t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0012c0023t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0013c0015t0001 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0014c0014t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0015c0016t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
a0016c0020t0001 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | copy fasta | chr5 | 180894159 | 180955906 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0002c0024t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0003c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0010t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0004c0010t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0009t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0012t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0012t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0005c0021t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0006c0008t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0006c0008t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0007c0013t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0007c0013t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0007c0017t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0008c0019t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0008c0025t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0009c0018t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0009c0022t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0010c0011t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0011c0026t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0012c0023t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0013c0015t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0014c0014t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0015c0016t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
a0016c0020t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0004 | c0004 | t0001 | g0154 | EUR | GBR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00280 | hp1 | a0002 | c0005 | t0001 | g0139 | EUR | FIN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01071 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01169 | hp1 | a0004 | c0004 | t0001 | g0153 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01192 | hp1 | a0002 | c0005 | t0001 | g0136 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01243 | hp2 | a0007 | c0017 | t0001 | g0052 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0068 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0074 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01884 | hp2 | a0005 | c0021 | t0001 | g0029 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0073 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0069 | EAS | CDX | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02257 | hp2 | a0002 | c0024 | t0001 | g0062 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02280 | hp1 | a0008 | c0019 | t0001 | g0046 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02451 | hp1 | a0002 | c0005 | t0001 | g0142 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0060 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02572 | hp2 | a0003 | c0006 | t0001 | g0146 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02615 | hp1 | a0005 | c0012 | t0001 | g0038 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02615 | hp2 | a0009 | c0018 | t0001 | g0047 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02622 | hp1 | a0003 | c0006 | t0001 | g0148 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02622 | hp2 | a0005 | c0009 | t0001 | g0035 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02630 | hp1 | a0005 | c0009 | t0001 | g0034 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02698 | hp1 | a0002 | c0005 | t0001 | g0138 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02698 | hp2 | a0003 | c0006 | t0001 | g0021 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02717 | hp2 | a0006 | c0008 | t0001 | g0143 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02723 | hp1 | a0006 | c0008 | t0001 | g0011 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02723 | hp2 | a0002 | c0007 | t0001 | g0042 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02735 | hp1 | a0002 | c0005 | t0001 | g0137 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02809 | hp1 | a0006 | c0008 | t0001 | g0011 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02809 | hp2 | a0008 | c0025 | t0001 | g0045 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02886 | hp2 | a0003 | c0006 | t0001 | g0145 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02922 | hp1 | a0007 | c0013 | t0001 | g0043 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02922 | hp2 | a0011 | c0026 | t0001 | g0077 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02970 | hp1 | a0005 | c0009 | t0001 | g0036 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02970 | hp2 | a0002 | c0005 | t0001 | g0058 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03017 | hp1 | a0013 | c0015 | t0001 | g0002 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03041 | hp1 | a0015 | c0016 | t0001 | g0064 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03130 | hp1 | a0002 | c0007 | t0001 | g0055 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03139 | hp1 | a0009 | c0022 | t0001 | g0053 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03139 | hp2 | a0005 | c0012 | t0001 | g0041 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03195 | hp1 | a0002 | c0007 | t0001 | g0044 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03209 | hp1 | a0002 | c0005 | t0001 | g0087 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03209 | hp2 | a0002 | c0007 | t0001 | g0039 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03239 | hp1 | a0003 | c0006 | t0001 | g0021 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03490 | hp1 | a0003 | c0006 | t0001 | g0157 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0149 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03492 | hp1 | a0003 | c0006 | t0001 | g0150 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03492 | hp2 | a0004 | c0004 | t0001 | g0156 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03540 | hp2 | a0002 | c0005 | t0001 | g0061 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03579 | hp1 | a0007 | c0013 | t0001 | g0040 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03669 | hp1 | a0004 | c0004 | t0002 | g0151 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03831 | hp1 | a0004 | c0004 | t0001 | g0158 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03927 | hp1 | a0004 | c0004 | t0001 | g0155 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG03927 | hp2 | a0016 | c0020 | t0001 | g0126 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04184 | hp1 | a0004 | c0010 | t0001 | g0122 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0070 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04199 | hp2 | a0004 | c0010 | t0001 | g0121 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | YRI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18522 | hp2 | a0012 | c0023 | t0001 | g0037 | AFR | YRI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18964 | hp2 | a0010 | c0011 | t0001 | g0014 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18980 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA18986 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19002 | hp1 | a0004 | c0004 | t0001 | g0152 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19043 | hp2 | a0014 | c0014 | t0001 | g0147 | AFR | LWK | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19054 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19063 | hp2 | a0010 | c0011 | t0001 | g0014 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19072 | hp1 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19082 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19086 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01123 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180908846
|
A | G | 1 | a0016 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.310A>G | p.Ile104Val | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 462/2017 | 310/1503 | 104/500 | chr5 | 180908846 | ||
chr5:180911368
|
A | G | 8 | a0002a0005a0006others(5): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
missense_variant | MODERATE | c.427A>G | p.Thr143Ala | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/8 | 579/2017 | 427/1503 | 143/500 | chr5 | 180911368 | ||
chr5:180911566
|
C | T | 1 | a0015 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.625C>T | p.Arg209Trp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/8 | 777/2017 | 625/1503 | 209/500 | chr5 | 180911566 | ||
chr5:180947523
|
G | A | 5 | a0002a0005a0007others(2): Show | 55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
missense_variant | MODERATE | c.685G>A | p.Glu229Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/8 | 837/2017 | 685/1503 | 229/500 | chr5 | 180947523 | ||
chr5:180949972
|
C | G | 6 | a0002a0004a0008others(3): Show | 66 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
missense_variant | MODERATE | c.931C>G | p.His311Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1083/2017 | 931/1503 | 311/500 | chr5 | 180949972 | ||
chr5:180949974
|
T | G | 6 | a0002a0004a0008others(3): Show | 66 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
missense_variant | MODERATE | c.933T>G | p.His311Gln | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1085/2017 | 933/1503 | 311/500 | chr5 | 180949974 | ||
chr5:180950018
|
C | A | 6 | a0003a0004a0005others(3): Show | 56 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(53): Show |
missense_variant | MODERATE | c.977C>A | p.Thr326Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1129/2017 | 977/1503 | 326/500 | chr5 | 180950018 | ||
chr5:180950407
|
C | T | 1 | a0013 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1366C>T | p.Pro456Ser | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1518/2017 | 1366/1503 | 456/500 | chr5 | 180950407 | ||
chr5:180950470
|
G | A | 5 | a0002a0007a0008others(2): Show | 50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
missense_variant | MODERATE | c.1429G>A | p.Ala477Thr | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1581/2017 | 1429/1503 | 477/500 | chr5 | 180950470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180908671
|
G | A | 4 | a0003c0006a0004c0004a0013c0015others(1): Show | 24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
synonymous_variant | LOW | c.135G>A | p.Lys45Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 287/2017 | 135/1503 | 45/500 | chr5 | 180908671 | ||
chr5:180908743
|
C | T | 11 | a0002c0002a0002c0007a0002c0024others(8): Show | 46 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(43): Show |
synonymous_variant | LOW | c.207C>T | p.Asp69Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 359/2017 | 207/1503 | 69/500 | chr5 | 180908743 | ||
chr5:180947534
|
G | A | 14 | a0002c0002a0002c0005a0002c0007others(11): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
synonymous_variant | LOW | c.696G>A | p.Ser232Ser | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/8 | 848/2017 | 696/1503 | 232/500 | chr5 | 180947534 | ||
chr5:180949249
|
C | T | 4 | a0002c0007a0005c0009a0005c0012others(1): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.846C>T | p.Asp282Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/8 | 998/2017 | 846/1503 | 282/500 | chr5 | 180949249 | ||
chr5:180949261
|
C | T | 1 | a0002c0024 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.858C>T | p.His286His | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/8 | 1010/2017 | 858/1503 | 286/500 | chr5 | 180949261 | ||
chr5:180950331
|
T | C | 12 | a0002c0002a0002c0005a0002c0007others(9): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
synonymous_variant | LOW | c.1290T>C | p.Tyr430Tyr | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1442/2017 | 1290/1503 | 430/500 | chr5 | 180950331 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180899274
|
G | A | 2 | a0001c0001t0002a0004c0004t0002 | 2 | HG03669.hp1 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/8 | 37 | chr5 | 180899274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180899502
|
C | T | 19 | a0003c0006t0001g0021a0003c0006t0001g0145a0003c0006t0001g0146others(16): Show | 24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+143C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899502 | ||||||
chr5:180899510
|
A | G | 1 | a0006c0008t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+151A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899510 | ||||||
chr5:180899568
|
C | T | 1 | a0002c0005t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49+209C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899568 | ||||||
chr5:180899569
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.49+210G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899569 | ||||||
chr5:180899571
|
T | A | 67 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(64): Show | 79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.49+212T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899571 | ||||||
chr5:180899590
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG01243.hp1 HG01952.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+231G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899590 | ||||||
chr5:180899617
|
C | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+258C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899617 | ||||||
chr5:180899961
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49+602T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899961 | ||||||
chr5:180900021
|
A | G | 3 | a0003c0003t0001g0006a0003c0003t0001g0140a0003c0003t0001g0141 | 5 | NA19054.hp1 NA19064.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+662A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900021 | ||||||
chr5:180900152
|
G | A | 25 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(22): Show | 31 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.49+793G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900152 | ||||||
chr5:180900158
|
G | A | 19 | a0003c0006t0001g0021a0003c0006t0001g0145a0003c0006t0001g0146others(16): Show | 24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+799G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900158 | ||||||
chr5:180900188
|
G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+829G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900188 | ||||||
chr5:180900428
|
G | A | 1 | a0004c0004t0001g0144 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.49+1069G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900428 | ||||||
chr5:180900543
|
G | A | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+1184G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900543 | ||||||
chr5:180900780
|
C | T | 12 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(9): Show | 12 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+1421C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900780 | ||||||
chr5:180900855
|
A | G | 2 | a0002c0002t0001g0010a0002c0002t0001g0033 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.49+1496A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900855 | ||||||
chr5:180900892
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+1533G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900892 | ||||||
chr5:180901001
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1642G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901001 | ||||||
chr5:180901003
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1644A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901003 | ||||||
chr5:180901071
|
G | A | 1 | a0006c0008t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+1712G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901071 | ||||||
chr5:180901103
|
A | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1744A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901103 | ||||||
chr5:180901133
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1774T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901133 | ||||||
chr5:180901331
|
A | G | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+1972A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901331 | ||||||
chr5:180901493
|
A | T | 19 | a0003c0006t0001g0021a0003c0006t0001g0145a0003c0006t0001g0146others(16): Show | 24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+2134A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901493 | ||||||
chr5:180901623
|
G | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2264G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901623 | ||||||
chr5:180901742
|
T | A | 1 | a0015c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.49+2383T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901742 | ||||||
chr5:180901743
|
T | A | 1 | a0015c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.49+2384T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901743 | ||||||
chr5:180901809
|
A | G | 12 | a0003c0006t0001g0157a0004c0004t0001g0002a0004c0004t0001g0022others(9): Show | 16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+2450A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901809 | ||||||
chr5:180902023
|
A | G | 1 | a0002c0005t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.49+2664A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902023 | ||||||
chr5:180902035
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.49+2676T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902035 | ||||||
chr5:180902041
|
T | TAAA | 2 | a0006c0008t0001g0011a0006c0008t0001g0143 | 3 | HG02717.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.49+2684_49+2686dup others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902041 | |||||
chr5:180902187
|
GT | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2838delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902187 | |||||
chr5:180902188
|
T | G | 38 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(35): Show | 50 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+2829T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902188 | ||||||
chr5:180902189
|
T | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2830T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902189 | ||||||
chr5:180902359
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3000T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902359 | ||||||
chr5:180902448
|
G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3089G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902448 | ||||||
chr5:180902452
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3093G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902452 | ||||||
chr5:180902458
|
C | G | 15 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+3099C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902458 | ||||||
chr5:180902517
|
GT | G | 68 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(65): Show | 87 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.49+3169delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902517 | |||||
chr5:180902536
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3177C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902536 | ||||||
chr5:180902673
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3314C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902673 | ||||||
chr5:180902678
|
C | T | 2 | a0002c0005t0001g0060a0002c0005t0001g0061 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.49+3319C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902678 | ||||||
chr5:180902682
|
T | C | 67 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(64): Show | 79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.49+3323T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902682 | ||||||
chr5:180902698
|
C | A | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.49+3339C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902698 | ||||||
chr5:180902770
|
C | T | 1 | a0002c0007t0001g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+3411C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902770 | ||||||
chr5:180902771
|
G | A | 12 | a0003c0006t0001g0157a0004c0004t0001g0002a0004c0004t0001g0022others(9): Show | 16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+3412G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902771 | ||||||
chr5:180902847
|
C | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3488C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902847 | ||||||
chr5:180902848
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3489A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902848 | ||||||
chr5:180902898
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3539T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902898 | ||||||
chr5:180902940
|
T | C | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+3581T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902940 | ||||||
chr5:180902969
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3610G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902969 | ||||||
chr5:180902973
|
C | T | 11 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+3614C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902973 | ||||||
chr5:180903081
|
T | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3722T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903081 | ||||||
chr5:180903168
|
A | AC | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3809_49+3810ins others(1): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903168 | ||||||
chr5:180903284
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3925A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903284 | ||||||
chr5:180903448
|
C | T | 1 | a0002c0005t0001g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.49+4089C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903448 | ||||||
chr5:180903571
|
T | C | 4 | a0002c0005t0001g0060a0002c0005t0001g0061a0002c0005t0001g0142others(1): Show | 4 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+4212T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903571 | ||||||
chr5:180903604
|
C | T | 5 | a0001c0001t0001g0020a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+4245C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903604 | ||||||
chr5:180903694
|
T | A | 1 | a0002c0007t0001g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+4335T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903694 | ||||||
chr5:180903707
|
T | C | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+4348T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903707 | ||||||
chr5:180903789
|
C | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4430C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903789 | ||||||
chr5:180903790
|
C | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4431C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903790 | ||||||
chr5:180903791
|
C | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4432C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903791 | ||||||
chr5:180903840
|
T | C | 2 | a0002c0005t0001g0142a0007c0017t0001g0052 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.49+4481T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903840 | ||||||
chr5:180903846
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.49+4487G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903846 | ||||||
chr5:180904006
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4580A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904006 | ||||||
chr5:180904042
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4544T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904042 | ||||||
chr5:180904116
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-4470G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904116 | ||||||
chr5:180904256
|
T | G | 15 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-4330T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904256 | ||||||
chr5:180904349
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4237C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904349 | ||||||
chr5:180904580
|
G | C | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.50-4006G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904580 | ||||||
chr5:180904584
|
G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-4002G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904584 | ||||||
chr5:180904670
|
G | C | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.50-3916G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904670 | ||||||
chr5:180904673
|
A | G | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-3913A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904673 | ||||||
chr5:180904694
|
C | T | 7 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0009others(4): Show | 11 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-3892C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904694 | ||||||
chr5:180904697
|
C | G | 5 | a0001c0001t0001g0020a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-3889C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904697 | ||||||
chr5:180904808
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-3778G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904808 | ||||||
chr5:180904850
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3736C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904850 | ||||||
chr5:180904953
|
T | C | 1 | a0002c0002t0001g0007 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.50-3633T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904953 | ||||||
chr5:180905011
|
G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-3575G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905011 | ||||||
chr5:180905033
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3553A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905033 | ||||||
chr5:180905102
|
T | C | 2 | a0002c0005t0001g0142a0007c0017t0001g0052 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.50-3484T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905102 | ||||||
chr5:180905135
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3451G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905135 | ||||||
chr5:180905170
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0081 | 4 | HG01167.hp2 HG01169.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-3416T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905170 | ||||||
chr5:180905218
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.50-3368G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905218 | ||||||
chr5:180905233
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.50-3353C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905233 | ||||||
chr5:180905259
|
G | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3327G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905259 | ||||||
chr5:180905362
|
C | T | 32 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(29): Show | 39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-3224C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905362 | ||||||
chr5:180905396
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3190A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905396 | ||||||
chr5:180905411
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3175C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905411 | ||||||
chr5:180905413
|
C | G | 1 | a0002c0002t0001g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-3173C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905413 | ||||||
chr5:180905441
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3145C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905441 | ||||||
chr5:180905520
|
A | C | 2 | a0003c0006t0001g0150a0004c0004t0001g0149 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.50-3066A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905520 | ||||||
chr5:180905938
|
T | TC | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2646dupC | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180905938 | |||||
chr5:180905959
|
T | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2627T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905959 | ||||||
chr5:180906007
|
C | T | 32 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(29): Show | 39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-2579C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906007 | ||||||
chr5:180906008
|
G | A | 14 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-2578G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906008 | ||||||
chr5:180906094
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2492G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906094 | ||||||
chr5:180906102
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2484A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906102 | ||||||
chr5:180906307
|
G | T | 12 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(9): Show | 18 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.50-2279G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906307 | ||||||
chr5:180906325
|
T | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-2261T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906325 | ||||||
chr5:180906332
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.50-2254C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906332 | ||||||
chr5:180906346
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2240C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906346 | ||||||
chr5:180906415
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2171C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906415 | ||||||
chr5:180906424
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2162G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906424 | ||||||
chr5:180906446
|
A | G | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-2140A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906446 | ||||||
chr5:180906528
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-2058C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906528 | ||||||
chr5:180906614
|
C | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1972C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906614 | ||||||
chr5:180906704
|
G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1882G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906704 | ||||||
chr5:180906707
|
A | G | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1879A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906707 | ||||||
chr5:180906712
|
G | C | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-1874G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906712 | ||||||
chr5:180906757
|
T | G | 49 | a0001c0001t0001g0083a0002c0002t0001g0003a0002c0002t0001g0007others(46): Show | 56 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.50-1829T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906757 | ||||||
chr5:180906805
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1781G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906805 | ||||||
chr5:180906882
|
C | T | 19 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(16): Show | 26 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-1704C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906882 | ||||||
chr5:180906929
|
G | A | 1 | a0010c0011t0001g0014 | 2 | NA18964.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.50-1657G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906929 | ||||||
chr5:180906992
|
T | C | 1 | a0002c0002t0001g0023 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.50-1594T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906992 | ||||||
chr5:180907036
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1550G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907036 | ||||||
chr5:180907061
|
C | T | 12 | a0003c0006t0001g0157a0004c0004t0001g0002a0004c0004t0001g0022others(9): Show | 16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-1525C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907061 | ||||||
chr5:180907066
|
T | G | 67 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(64): Show | 79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.50-1520T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907066 | ||||||
chr5:180907106
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.50-1480A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907106 | ||||||
chr5:180907238
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1348T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907238 | ||||||
chr5:180907253
|
C | T | 19 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(16): Show | 26 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-1333C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907253 | ||||||
chr5:180907315
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1271C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907315 | ||||||
chr5:180907351
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1235T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907351 | ||||||
chr5:180907404
|
T | C | 32 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(29): Show | 39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-1182T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907404 | ||||||
chr5:180907427
|
A | AT | 14 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-1151dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180907427 | |||||
chr5:180907661
|
C | T | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-925C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907661 | ||||||
chr5:180907700
|
T | C | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-886T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907700 | ||||||
chr5:180907722
|
T | TGTTA | 2 | a0003c0003t0001g0067a0003c0003t0001g0068 | 2 | HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.50-861_50-860insAG others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180907722 | |||||
chr5:180907740
|
G | C | 1 | a0003c0003t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-846G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907740 | ||||||
chr5:180907748
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.50-838T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907748 | ||||||
chr5:180907760
|
C | G | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-826C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907760 | ||||||
chr5:180907768
|
G | A | 1 | a0003c0003t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-818G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907768 | ||||||
chr5:180907777
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-809C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907777 | ||||||
chr5:180907787
|
G | A | 15 | a0001c0001t0001g0013a0002c0002t0001g0024a0002c0002t0001g0025others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-799G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907787 | ||||||
chr5:180907790
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-796A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907790 | ||||||
chr5:180907797
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-789C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907797 | ||||||
chr5:180907831
|
G | A | 2 | a0001c0001t0001g0015a0003c0006t0001g0148 | 3 | HG02109.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.50-755G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907831 | ||||||
chr5:180907847
|
G | T | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-739G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907847 | ||||||
chr5:180907851
|
T | A | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-735T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907851 | ||||||
chr5:180907851
|
T | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0131others(54): Show | 66 | HG00280.hp1 HG00544.hp2 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.50-735T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907851 | ||||||
chr5:180907859
|
G | A | 1 | a0001c0001t0001g0015 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.50-727G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907859 | ||||||
chr5:180907873
|
A | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG02040.hp2 HG04199.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.50-713A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907873 | ||||||
chr5:180907873
|
A | G | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-713A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907873 | ||||||
chr5:180908041
|
C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-545C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908041 | ||||||
chr5:180908063
|
T | G | 38 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0009others(35): Show | 43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-523T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908063 | ||||||
chr5:180908091
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.50-495C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908091 | ||||||
chr5:180908096
|
G | A | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.50-490G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908096 | ||||||
chr5:180908118
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.50-468T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908118 | ||||||
chr5:180908185
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-401T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908185 | ||||||
chr5:180908196
|
T | C | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-390T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908196 | ||||||
chr5:180908280
|
G | GC | 5 | a0001c0001t0001g0020a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-305dupC | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180908280 | |||||
chr5:180908285
|
C | T | 5 | a0001c0001t0001g0020a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-301C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908285 | ||||||
chr5:180908289
|
A | G | 5 | a0001c0001t0001g0020a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-297A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908289 | ||||||
chr5:180908376
|
C | T | 1 | a0002c0002t0001g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.50-210C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908376 | ||||||
chr5:180908382
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-204G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908382 | ||||||
chr5:180908384
|
G | A | 48 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(45): Show | 55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-202G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908384 | ||||||
chr5:180909022
|
T | TCTTTATT others(4): Show |
1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+89_397+90insCT others(9): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909022 | ||||||
chr5:180909024
|
G | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+91G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909024 | ||||||
chr5:180909025
|
G | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+92G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909025 | ||||||
chr5:180909027
|
C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+94C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909027 | ||||||
chr5:180909028
|
A | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+95A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909028 | ||||||
chr5:180909080
|
A | G | 1 | a0004c0004t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+147A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909080 | ||||||
chr5:180909276
|
C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397+343C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909276 | ||||||
chr5:180909434
|
C | A | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.397+501C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909434 | ||||||
chr5:180909581
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.397+648T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909581 | ||||||
chr5:180909678
|
G | C | 18 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0075others(15): Show | 25 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.397+745G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909678 | ||||||
chr5:180909716
|
T | TA | 27 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 35 | HG00438.hp2 HG00621.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.397+799dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | |||||
chr5:180909716
|
T | TAA | 6 | a0002c0002t0001g0033a0002c0002t0001g0057a0006c0008t0001g0011others(3): Show | 7 | HG01167.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+798_397+799dup others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | |||||
chr5:180909716
|
T | TAAA | 31 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 37 | HG00544.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.397+797_397+799dup others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | |||||
chr5:180909770
|
A | G | 1 | a0003c0003t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.397+837A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909770 | ||||||
chr5:180909781
|
C | T | 1 | a0002c0007t0001g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.397+848C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909781 | ||||||
chr5:180909782
|
G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397+849G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909782 | ||||||
chr5:180909849
|
C | T | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+916C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909849 | ||||||
chr5:180910369
|
C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-970C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910369 | ||||||
chr5:180910401
|
C | T | 1 | a0016c0020t0001g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.398-938C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910401 | ||||||
chr5:180910541
|
A | G | 54 | a0001c0001t0001g0081a0002c0002t0001g0003a0002c0002t0001g0007others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.398-798A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910541 | ||||||
chr5:180910543
|
A | G | 48 | a0001c0001t0001g0081a0002c0002t0001g0003a0002c0002t0001g0007others(45): Show | 55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.398-796A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910543 | ||||||
chr5:180910634
|
A | T | 1 | a0002c0002t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-705A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910634 | ||||||
chr5:180910753
|
C | G | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.398-586C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910753 | ||||||
chr5:180911212
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.398-127G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911212 | ||||||
chr5:180911300
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.398-39G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911300 | ||||||
chr5:180911318
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.398-21C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911318 | ||||||
chr5:180911743
|
A | C | 5 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+129A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911743 | ||||||
chr5:180911754
|
G | A | 41 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(38): Show | 48 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.673+140G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911754 | ||||||
chr5:180911952
|
A | C | 1 | a0002c0005t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.673+338A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911952 | ||||||
chr5:180911980
|
G | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+366G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911980 | ||||||
chr5:180912213
|
C | T | 36 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(33): Show | 43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+599C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912213 | ||||||
chr5:180912293
|
C | T | 1 | a0003c0003t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.673+679C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912293 | ||||||
chr5:180912415
|
A | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.673+801A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912415 | ||||||
chr5:180912427
|
G | GTA | 15 | a0001c0001t0001g0075a0003c0003t0001g0001a0003c0003t0001g0006others(12): Show | 22 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.673+829_673+830dup others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180912427 | |||||
chr5:180912427
|
GTATATA | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+825_673+830del others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180912427 | |||||
chr5:180912830
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1216G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912830 | ||||||
chr5:180912912
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1298C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912912 | ||||||
chr5:180912939
|
G | T | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+1325G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912939 | ||||||
chr5:180913020
|
C | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+1406C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913020 | ||||||
chr5:180913362
|
G | A | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+1748G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913362 | ||||||
chr5:180913378
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1764T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913378 | ||||||
chr5:180913503
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+1889A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913503 | ||||||
chr5:180913541
|
T | A | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+1927T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913541 | ||||||
chr5:180913569
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1955G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913569 | ||||||
chr5:180913652
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0088 | 4 | HG01109.hp2 HG01123.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.673+2038C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913652 | ||||||
chr5:180913705
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+2091G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913705 | ||||||
chr5:180913721
|
G | A | 5 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+2107G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913721 | ||||||
chr5:180914080
|
G | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+2466G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914080 | ||||||
chr5:180914119
|
C | T | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.673+2505C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914119 | ||||||
chr5:180914751
|
A | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+3137A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914751 | ||||||
chr5:180914845
|
G | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+3231G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914845 | ||||||
chr5:180914895
|
C | T | 21 | a0003c0006t0001g0021a0003c0006t0001g0145a0003c0006t0001g0146others(18): Show | 26 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.673+3281C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914895 | ||||||
chr5:180915059
|
A | T | 3 | a0003c0006t0001g0021a0003c0006t0001g0150a0004c0004t0001g0149 | 4 | HG02698.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3445A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915059 | ||||||
chr5:180915085
|
G | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+3471G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915085 | ||||||
chr5:180915243
|
T | G | 1 | a0003c0003t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.673+3629T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915243 | ||||||
chr5:180915278
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.673+3664G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915278 | ||||||
chr5:180915398
|
G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+3784G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915398 | ||||||
chr5:180915506
|
G | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+3892G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915506 | ||||||
chr5:180915568
|
G | C | 1 | a0002c0005t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.673+3954G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915568 | ||||||
chr5:180915600
|
A | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+3986A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915600 | ||||||
chr5:180915620
|
A | G | 91 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(88): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.673+4006A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915620 | ||||||
chr5:180915626
|
G | A | 5 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+4012G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915626 | ||||||
chr5:180915700
|
A | G | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+4086A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915700 | ||||||
chr5:180915707
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4093C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915707 | ||||||
chr5:180915806
|
G | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4192G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915806 | ||||||
chr5:180915859
|
C | T | 46 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(43): Show | 53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.673+4245C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915859 | ||||||
chr5:180915889
|
C | A | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.673+4275C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915889 | ||||||
chr5:180916025
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.673+4411C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916025 | ||||||
chr5:180916026
|
G | A | 2 | a0004c0004t0001g0152a0004c0004t0001g0158 | 2 | HG03831.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.673+4412G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916026 | ||||||
chr5:180916225
|
A | G | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+4611A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916225 | ||||||
chr5:180916376
|
AAAAG | A | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+4768_673+4771d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180916376 | |||||
chr5:180916530
|
A | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4916A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916530 | ||||||
chr5:180916749
|
C | T | 91 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(88): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.673+5135C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916749 | ||||||
chr5:180917048
|
T | TCAACAAA others(1097): Show |
1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5455_673+5456i others(1106): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917048 | |||||
chr5:180917048
|
T | TCAACAAA others(407): Show |
11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.673+5455_673+5456i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917048 | |||||
chr5:180917057
|
T | C | 1 | a0002c0005t0001g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.673+5443T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917057 | ||||||
chr5:180917070
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+5456G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917070 | ||||||
chr5:180917093
|
T | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+5479T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917093 | ||||||
chr5:180917095
|
T | C | 41 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(38): Show | 48 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.673+5481T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917095 | ||||||
chr5:180917109
|
G | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5495G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917109 | ||||||
chr5:180917113
|
T | C | 20 | a0002c0002t0001g0027a0002c0005t0001g0058a0002c0005t0001g0060others(17): Show | 21 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.673+5499T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917113 | ||||||
chr5:180917113
|
T | TAGGCCAA others(407): Show |
3 | a0002c0002t0001g0032a0002c0005t0001g0087a0011c0026t0001g0077 | 3 | HG02922.hp2 HG03209.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.673+5567_673+5568i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917113 | |||||
chr5:180917113
|
T | TAGGCCAA others(476): Show |
1 | a0002c0005t0001g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.673+5567_673+5568i others(485): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917113 | |||||
chr5:180917139
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.673+5525A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917139 | ||||||
chr5:180917164
|
CGGCACTA others(131): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0085 | 3 | NA18966.hp2 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.673+5688_673+5825d others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917164 | |||||
chr5:180917182
|
T | C | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5568T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917182 | ||||||
chr5:180917234
|
G | A | 2 | a0003c0006t0001g0145a0003c0006t0001g0146 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.673+5620G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917234 | ||||||
chr5:180917251
|
T | C | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5637T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917251 | ||||||
chr5:180917302
|
T | C | 57 | a0001c0001t0001g0123a0002c0002t0001g0003a0002c0002t0001g0007others(54): Show | 65 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.673+5688T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917302 | ||||||
chr5:180917305
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.673+5691C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917305 | ||||||
chr5:180917320
|
T | C | 37 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(34): Show | 44 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.673+5706T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917320 | ||||||
chr5:180917332
|
C | CTGGATAA others(407): Show |
30 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(27): Show | 37 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.673+5774_673+5775i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917332 | |||||
chr5:180917332
|
C | CTGGATAA others(269): Show |
1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+5774_673+5775i others(278): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917332 | |||||
chr5:180917332
|
C | T | 14 | a0002c0002t0001g0032a0002c0005t0001g0087a0002c0007t0001g0039others(11): Show | 14 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.673+5718C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917332 | ||||||
chr5:180917389
|
T | C | 7 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.673+5775T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917389 | ||||||
chr5:180917402
|
T | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5788T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917402 | ||||||
chr5:180917403
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5789G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917403 | ||||||
chr5:180917403
|
G | GGATAACC others(407): Show |
2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917403 | |||||
chr5:180917440
|
C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | |||||
chr5:180917440
|
C | CGGCACTA others(407): Show |
2 | a0002c0005t0001g0061a0007c0017t0001g0052 | 2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | |||||
chr5:180917440
|
C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | |||||
chr5:180917440
|
C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | |||||
chr5:180917440
|
C | T | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.673+5826C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917440 | ||||||
chr5:180917608
|
T | TA | 53 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(50): Show | 60 | HG00280.hp1 HG00544.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.673+5994_673+5995i others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917608 | ||||||
chr5:180917609
|
T | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+5995T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917609 | ||||||
chr5:180917609
|
T | TA | 37 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(34): Show | 49 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.673+6003dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917609 | |||||
chr5:180917750
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6136T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917750 | ||||||
chr5:180917763
|
G | A | 1 | a0002c0002t0001g0008 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.673+6149G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917763 | ||||||
chr5:180917810
|
C | T | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673+6196C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917810 | ||||||
chr5:180917817
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.673+6203A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917817 | ||||||
chr5:180917830
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673+6216C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917830 | ||||||
chr5:180917877
|
G | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6263G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917877 | ||||||
chr5:180917920
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6306T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917920 | ||||||
chr5:180917986
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+6372G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917986 | ||||||
chr5:180918028
|
C | CA | 50 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(47): Show | 57 | HG00280.hp1 HG00544.hp2 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.673+6429dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180918028 | |||||
chr5:180918028
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+6414C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918028 | ||||||
chr5:180918177
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6563T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918177 | ||||||
chr5:180918625
|
A | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7011A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918625 | ||||||
chr5:180918810
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+7196A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918810 | ||||||
chr5:180918814
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+7200G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918814 | ||||||
chr5:180919153
|
T | C | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.673+7539T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919153 | ||||||
chr5:180919231
|
T | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7617T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919231 | ||||||
chr5:180919363
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7749T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919363 | ||||||
chr5:180919616
|
T | G | 36 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(33): Show | 43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+8002T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919616 | ||||||
chr5:180919731
|
G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+8117G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919731 | ||||||
chr5:180919794
|
A | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8180A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919794 | ||||||
chr5:180919907
|
G | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8293G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919907 | ||||||
chr5:180920004
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8390C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920004 | ||||||
chr5:180920753
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+9139T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920753 | ||||||
chr5:180920980
|
C | T | 9 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.673+9366C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920980 | ||||||
chr5:180921220
|
T | C | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+9606T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921220 | ||||||
chr5:180921239
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02080.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.673+9625A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921239 | ||||||
chr5:180921459
|
T | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+9845T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921459 | ||||||
chr5:180921660
|
T | TAC | 20 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0123others(17): Show | 23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+10080_673+1008 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
T | TACAC | 3 | a0002c0005t0001g0060a0004c0004t0001g0153a0011c0026t0001g0077 | 3 | HG01169.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.673+10078_673+1008 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
T | TACACAC | 3 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050 | 3 | HG02965.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.673+10076_673+1008 others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
TAC | T | 20 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0065others(17): Show | 22 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.673+10080_673+1008 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
TACAC | T | 9 | a0001c0001t0001g0115a0002c0002t0001g0010a0002c0002t0001g0033others(6): Show | 10 | HG01167.hp1 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.673+10078_673+1008 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
TACACAC | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0075others(16): Show | 28 | HG00438.hp2 HG00621.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.673+10076_673+1008 others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180921660
|
TACACACA others(1): Show |
T | 3 | a0003c0006t0001g0145a0003c0006t0001g0146a0003c0006t0001g0148 | 3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.673+10074_673+1008 others(12): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | |||||
chr5:180922074
|
TA | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+10461delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922074 | ||||||
chr5:180922128
|
T | A | 11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.673+10514T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922128 | ||||||
chr5:180922352
|
C | T | 2 | a0002c0005t0001g0060a0002c0005t0001g0061 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+10738C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922352 | ||||||
chr5:180922514
|
G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0107others(3): Show | 7 | HG00438.hp1 HG02027.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+10900G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922514 | ||||||
chr5:180922533
|
C | T | 7 | a0002c0002t0001g0027a0002c0005t0001g0136a0002c0005t0001g0137others(4): Show | 7 | HG00280.hp1 HG01192.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.673+10919C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922533 | ||||||
chr5:180922554
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.673+10940A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922554 | ||||||
chr5:180922591
|
T | TAAGAAGT others(311): Show |
3 | a0002c0005t0001g0142a0002c0024t0001g0062a0009c0018t0001g0047 | 3 | HG02257.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922591
|
T | TAAGAAGT others(315): Show |
1 | a0008c0025t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.673+10990_673+1099 others(326): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922591
|
T | TAAGAAGT others(316): Show |
6 | a0002c0002t0001g0027a0002c0005t0001g0136a0002c0005t0001g0137others(3): Show | 6 | HG00280.hp1 HG01192.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(327): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922591
|
T | TAAGAAGT others(311): Show |
4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922591
|
T | TAAGAAGT others(310): Show |
2 | a0002c0002t0001g0030a0002c0002t0001g0057 | 2 | HG02897.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.673+10990_673+1099 others(321): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922591
|
T | TAAGAAGT others(311): Show |
38 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(35): Show | 45 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | |||||
chr5:180922618
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+11004G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922618 | ||||||
chr5:180922654
|
A | C | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.673+11040A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922654 | ||||||
chr5:180922778
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.673+11164C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922778 | ||||||
chr5:180922832
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.673+11218T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922832 | ||||||
chr5:180923052
|
A | T | 5 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+11438A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923052 | ||||||
chr5:180923084
|
C | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+11470C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923084 | ||||||
chr5:180923131
|
C | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+11517C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923131 | ||||||
chr5:180923167
|
A | G | 119 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(116): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.673+11553A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923167 | ||||||
chr5:180923423
|
A | G | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+11809A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923423 | ||||||
chr5:180923485
|
T | G | 1 | a0002c0002t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.673+11871T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923485 | ||||||
chr5:180923705
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.673+12091T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923705 | ||||||
chr5:180923779
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+12165C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923779 | ||||||
chr5:180923975
|
G | A | 1 | a0011c0026t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.673+12361G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923975 | ||||||
chr5:180924514
|
C | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+12900C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180924514 | ||||||
chr5:180924666
|
C | G | 1 | a0004c0004t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.673+13052C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180924666 | ||||||
chr5:180925753
|
T | C | 5 | a0002c0002t0001g0027a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 5 | HG00280.hp1 HG01192.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+14139T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180925753 | ||||||
chr5:180925879
|
T | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+14265T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180925879 | ||||||
chr5:180926005
|
CA | C | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+14398delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180926005 | |||||
chr5:180926206
|
C | G | 1 | a0003c0006t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.673+14592C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926206 | ||||||
chr5:180926220
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673+14606G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926220 | ||||||
chr5:180926318
|
C | T | 15 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(12): Show | 22 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.673+14704C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926318 | ||||||
chr5:180926553
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.673+14939A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926553 | ||||||
chr5:180926677
|
T | G | 40 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(37): Show | 47 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.673+15063T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926677 | ||||||
chr5:180926976
|
G | T | 6 | a0002c0007t0001g0039a0005c0012t0001g0038a0005c0012t0001g0041others(3): Show | 6 | HG02615.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+15362G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926976 | ||||||
chr5:180927003
|
C | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+15389C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927003 | ||||||
chr5:180927034
|
C | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+15420C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927034 | ||||||
chr5:180927303
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.673+15689C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927303 | ||||||
chr5:180927320
|
C | T | 1 | a0005c0012t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.673+15706C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927320 | ||||||
chr5:180927570
|
G | C | 2 | a0002c0005t0001g0060a0002c0005t0001g0061 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+15956G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927570 | ||||||
chr5:180927664
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+16050C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927664 | ||||||
chr5:180927720
|
G | T | 1 | a0002c0002t0001g0031 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.673+16106G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927720 | ||||||
chr5:180927858
|
T | C | 1 | a0002c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.673+16244T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927858 | ||||||
chr5:180927874
|
T | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+16260T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927874 | ||||||
chr5:180927910
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.673+16296C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927910 | ||||||
chr5:180928495
|
C | A | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.673+16881C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928495 | ||||||
chr5:180928527
|
A | G | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+16913A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928527 | ||||||
chr5:180928541
|
C | A | 5 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+16927C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928541 | ||||||
chr5:180928655
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.673+17041G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928655 | ||||||
chr5:180928741
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.673+17127A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928741 | ||||||
chr5:180928905
|
C | T | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+17291C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928905 | ||||||
chr5:180929028
|
A | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(43): Show | 53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.673+17414A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929028 | ||||||
chr5:180929227
|
G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+17613G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929227 | ||||||
chr5:180929293
|
C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.673+17679C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929293 | ||||||
chr5:180929314
|
C | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+17700C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929314 | ||||||
chr5:180929471
|
A | G | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+17857A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929471 | ||||||
chr5:180929550
|
AATAG | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+17942_673+1794 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180929550 | |||||
chr5:180929560
|
C | A | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+17946C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929560 | ||||||
chr5:180929603
|
T | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-17909T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929603 | ||||||
chr5:180929648
|
C | A | 1 | a0002c0005t0001g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.674-17864C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929648 | ||||||
chr5:180929684
|
C | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17828C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929684 | ||||||
chr5:180929736
|
C | T | 1 | a0005c0009t0001g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.674-17776C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929736 | ||||||
chr5:180929764
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0118a0001c0001t0001g0127 | 4 | HG01071.hp2 HG01255.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-17748G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929764 | ||||||
chr5:180929835
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.674-17677C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929835 | ||||||
chr5:180929947
|
CT | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17563delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180929947 | |||||
chr5:180930002
|
A | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17510A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930002 | ||||||
chr5:180930108
|
G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-17404G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930108 | ||||||
chr5:180930118
|
C | T | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.674-17394C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930118 | ||||||
chr5:180930164
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.674-17348C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930164 | ||||||
chr5:180930179
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17333G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930179 | ||||||
chr5:180930244
|
C | T | 46 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(43): Show | 53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.674-17268C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930244 | ||||||
chr5:180930325
|
T | C | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-17187T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930325 | ||||||
chr5:180930401
|
A | G | 2 | a0003c0006t0001g0145a0003c0006t0001g0146 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-17111A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930401 | ||||||
chr5:180930409
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG02027.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.674-17103A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930409 | ||||||
chr5:180930457
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.674-17055C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930457 | ||||||
chr5:180930607
|
C | G | 1 | a0004c0004t0001g0144 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.674-16905C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930607 | ||||||
chr5:180930710
|
A | G | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-16802A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930710 | ||||||
chr5:180930884
|
G | A | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-16628G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930884 | ||||||
chr5:180930923
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.674-16589G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930923 | ||||||
chr5:180931005
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.674-16507A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931005 | ||||||
chr5:180931260
|
T | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-16252T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931260 | ||||||
chr5:180931432
|
G | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-16080G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931432 | ||||||
chr5:180931438
|
C | T | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-16074C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931438 | ||||||
chr5:180931626
|
A | G | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.674-15886A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931626 | ||||||
chr5:180931635
|
G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-15877G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931635 | ||||||
chr5:180931990
|
T | C | 1 | a0011c0026t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.674-15522T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931990 | ||||||
chr5:180932083
|
T | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(154): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.674-15429T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932083 | ||||||
chr5:180932258
|
T | C | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 22 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.674-15254T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932258 | ||||||
chr5:180932440
|
G | A | 5 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-15072G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932440 | ||||||
chr5:180932448
|
G | A | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-15064G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932448 | ||||||
chr5:180932460
|
C | T | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-15052C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932460 | ||||||
chr5:180932480
|
G | A | 3 | a0002c0002t0001g0010a0002c0002t0001g0033a0002c0005t0001g0087 | 4 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-15032G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932480 | ||||||
chr5:180932515
|
T | G | 1 | a0004c0004t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.674-14997T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932515 | ||||||
chr5:180932571
|
G | C | 1 | a0015c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.674-14941G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932571 | ||||||
chr5:180932591
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.674-14921C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932591 | ||||||
chr5:180932733
|
A | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-14779A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932733 | ||||||
chr5:180933005
|
CA | C | 81 | a0001c0001t0001g0098a0002c0002t0001g0003a0002c0002t0001g0007others(78): Show | 99 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.674-14494delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933005 | |||||
chr5:180933005
|
CAA | C | 11 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0005t0001g0058others(8): Show | 12 | HG01243.hp2 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.674-14495_674-1449 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933005 | |||||
chr5:180933103
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-14409G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933103 | ||||||
chr5:180933106
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-14406G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933106 | ||||||
chr5:180933107
|
G | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-14405G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933107 | ||||||
chr5:180933127
|
A | G | 36 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(33): Show | 43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-14385A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933127 | ||||||
chr5:180933437
|
C | G | 1 | a0002c0002t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.674-14075C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933437 | ||||||
chr5:180933751
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.674-13761C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933751 | ||||||
chr5:180933880
|
G | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13632G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933880 | ||||||
chr5:180933979
|
G | GA | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13524dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933979 | |||||
chr5:180934037
|
C | G | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-13475C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934037 | ||||||
chr5:180934240
|
C | A | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13272C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934240 | ||||||
chr5:180934248
|
G | C | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-13264G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934248 | ||||||
chr5:180934266
|
A | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-13246A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934266 | ||||||
chr5:180934272
|
G | A | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-13240G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934272 | ||||||
chr5:180934516
|
C | T | 1 | a0003c0003t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.674-12996C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934516 | ||||||
chr5:180934665
|
C | G | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-12847C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934665 | ||||||
chr5:180934801
|
C | T | 2 | a0002c0005t0001g0060a0002c0005t0001g0061 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-12711C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934801 | ||||||
chr5:180934813
|
T | C | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-12699T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934813 | ||||||
chr5:180934838
|
G | A | 18 | a0003c0006t0001g0021a0003c0006t0001g0150a0003c0006t0001g0157others(15): Show | 23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-12674G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934838 | ||||||
chr5:180934887
|
A | G | 1 | a0002c0002t0001g0008 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.674-12625A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934887 | ||||||
chr5:180934946
|
G | GGTGA | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-12564_674-1256 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180934946 | |||||
chr5:180935131
|
T | C | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-12381T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935131 | ||||||
chr5:180935264
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0108 | 2 | NA18952.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.674-12248G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935264 | ||||||
chr5:180935269
|
G | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-12243G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935269 | ||||||
chr5:180935499
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-12013C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935499 | ||||||
chr5:180935614
|
C | T | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-11898C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935614 | ||||||
chr5:180935647
|
G | A | 5 | a0004c0004t0001g0002a0004c0004t0001g0153a0004c0004t0001g0154others(2): Show | 8 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-11865G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935647 | ||||||
chr5:180935775
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.674-11737C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935775 | ||||||
chr5:180935919
|
C | CT | 6 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0106others(3): Show | 6 | HG01192.hp2 HG01952.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.674-11580dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180935919 | |||||
chr5:180936042
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-11470G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936042 | ||||||
chr5:180936043
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-11469G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936043 | ||||||
chr5:180936093
|
G | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-11419G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936093 | ||||||
chr5:180936161
|
G | T | 11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-11351G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936161 | ||||||
chr5:180936220
|
A | C | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-11292A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936220 | ||||||
chr5:180936514
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.674-10998T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936514 | ||||||
chr5:180936573
|
G | T | 1 | a0011c0026t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.674-10939G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936573 | ||||||
chr5:180936610
|
T | C | 3 | a0005c0009t0001g0034a0005c0009t0001g0035a0005c0009t0001g0036 | 3 | HG02622.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.674-10902T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936610 | ||||||
chr5:180936668
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-10844G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936668 | ||||||
chr5:180937002
|
C | T | 11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-10510C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937002 | ||||||
chr5:180937072
|
C | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-10440C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937072 | ||||||
chr5:180937157
|
G | A | 5 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-10355G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937157 | ||||||
chr5:180937164
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.674-10348G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937164 | ||||||
chr5:180937888
|
G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-9624G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937888 | ||||||
chr5:180937942
|
T | TA | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(153): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.674-9559dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180937942 | |||||
chr5:180938103
|
A | G | 91 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(88): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.674-9409A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938103 | ||||||
chr5:180938159
|
T | C | 70 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(67): Show | 84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.674-9353T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938159 | ||||||
chr5:180938313
|
T | C | 53 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(50): Show | 60 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.674-9199T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938313 | ||||||
chr5:180938314
|
G | A | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-9198G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938314 | ||||||
chr5:180938488
|
A | G | 5 | a0002c0002t0001g0027a0002c0005t0001g0136a0002c0005t0001g0137others(2): Show | 5 | HG00280.hp1 HG01192.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-9024A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938488 | ||||||
chr5:180938515
|
T | TCTTCCTT others(1): Show |
3 | a0002c0005t0001g0060a0002c0005t0001g0061a0007c0017t0001g0052 | 3 | HG01243.hp2 HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-8981_674-8974d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938515 | |||||
chr5:180938535
|
CCTTT | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0073others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-8968_674-8965d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938535 | |||||
chr5:180938539
|
T | C | 8 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0009others(5): Show | 12 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.674-8973T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938539 | ||||||
chr5:180938541
|
TTTC | T | 12 | a0003c0003t0001g0001a0003c0003t0001g0006a0003c0003t0001g0012others(9): Show | 19 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.674-8968_674-8966d others(5): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938541 | |||||
chr5:180938543
|
T | C | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-8969T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938543 | ||||||
chr5:180938544
|
CT | C | 39 | a0002c0002t0001g0007a0002c0002t0001g0010a0002c0002t0001g0024others(36): Show | 42 | HG00280.hp1 HG01167.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.674-8954delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938544 | |||||
chr5:180938545
|
T | TTTC | 7 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0009others(4): Show | 11 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-8965_674-8964i others(5): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938545 | |||||
chr5:180938578
|
G | A | 47 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(44): Show | 54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-8934G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938578 | ||||||
chr5:180938591
|
C | G | 53 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(50): Show | 60 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.674-8921C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938591 | ||||||
chr5:180938727
|
G | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-8785G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938727 | ||||||
chr5:180938817
|
T | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-8695T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938817 | ||||||
chr5:180938890
|
G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-8622G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938890 | ||||||
chr5:180939298
|
G | C | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-8214G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939298 | ||||||
chr5:180939860
|
A | AT | 4 | a0001c0001t0001g0125a0001c0001t0001g0129a0003c0006t0001g0145others(1): Show | 4 | HG02572.hp2 HG02886.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-7644dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180939860 | |||||
chr5:180939869
|
A | T | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.674-7643A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939869 | ||||||
chr5:180939970
|
C | T | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7542C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939970 | ||||||
chr5:180940215
|
A | G | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-7297A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940215 | ||||||
chr5:180940231
|
C | T | 3 | a0002c0007t0001g0039a0008c0019t0001g0046a0008c0025t0001g0045 | 3 | HG02280.hp1 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.674-7281C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940231 | ||||||
chr5:180940308
|
C | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-7204C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940308 | ||||||
chr5:180940478
|
C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-7034C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940478 | ||||||
chr5:180940576
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.674-6936A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940576 | ||||||
chr5:180940787
|
G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-6725G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940787 | ||||||
chr5:180940895
|
C | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-6617C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940895 | ||||||
chr5:180940906
|
A | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-6606A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940906 | ||||||
chr5:180940933
|
A | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-6579A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940933 | ||||||
chr5:180940948
|
C | G | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.674-6564C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940948 | ||||||
chr5:180941086
|
AAGGG | A | 39 | a0002c0002t0001g0007a0002c0002t0001g0009a0002c0002t0001g0010others(36): Show | 43 | HG00280.hp1 HG01167.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-6414_674-6411d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941086 | |||||
chr5:180941098
|
G | A | 14 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0023others(11): Show | 17 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.674-6414G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941098 | ||||||
chr5:180941102
|
A | AAGGG | 3 | a0002c0005t0001g0060a0002c0005t0001g0061a0008c0025t0001g0045 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-6407_674-6406i others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941102 | |||||
chr5:180941106
|
A | G | 11 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0023others(8): Show | 14 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.674-6406A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941106 | ||||||
chr5:180941110
|
G | A | 15 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0023others(12): Show | 18 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.674-6402G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941110 | ||||||
chr5:180941110
|
G | GAGGA | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0088others(4): Show | 9 | HG00280.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.674-6361_674-6358d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941110
|
G | GAGGAAGG others(1): Show |
26 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0065others(23): Show | 36 | HG00621.hp1 HG00621.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.674-6365_674-6358d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941110
|
G | GAGGAAGG others(5): Show |
43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 49 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.674-6369_674-6358d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941110
|
G | GAGGAAGG others(9): Show |
7 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0106others(4): Show | 7 | HG01255.hp1 HG02155.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-6373_674-6358d others(18): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941110
|
GAGGA | G | 8 | a0002c0002t0001g0028a0002c0007t0001g0042a0002c0007t0001g0044others(5): Show | 9 | HG00140.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.674-6361_674-6358d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941110
|
GAGGAAGG others(1): Show |
G | 6 | a0001c0001t0001g0019a0001c0001t0001g0120a0002c0002t0001g0048others(3): Show | 7 | HG02027.hp1 HG02040.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-6365_674-6358d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | |||||
chr5:180941461
|
C | A | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.674-6051C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941461 | ||||||
chr5:180941784
|
A | G | 2 | a0002c0007t0001g0042a0002c0007t0001g0044 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.674-5728A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941784 | ||||||
chr5:180941895
|
T | TGCCCACT others(105): Show |
1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(114): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(111): Show |
1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(120): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(116): Show |
3 | a0002c0002t0001g0023a0002c0002t0001g0024a0009c0022t0001g0053 | 3 | HG03041.hp2 HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.674-5598_674-5597i others(125): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(117): Show |
1 | a0002c0005t0001g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.674-5598_674-5597i others(126): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(117): Show |
35 | a0002c0002t0001g0003a0002c0002t0001g0008a0002c0002t0001g0009others(32): Show | 41 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.674-5598_674-5597i others(126): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(118): Show |
12 | a0002c0002t0001g0007a0002c0002t0001g0048a0002c0002t0001g0050others(9): Show | 13 | HG02145.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.674-5598_674-5597i others(127): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180941895
|
T | TGCCCACT others(119): Show |
1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(128): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | |||||
chr5:180942129
|
T | C | 1 | a0002c0002t0001g0007 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.674-5383T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942129 | ||||||
chr5:180942282
|
G | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-5230G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942282 | ||||||
chr5:180942317
|
C | G | 11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-5195C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942317 | ||||||
chr5:180942360
|
C | T | 70 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(67): Show | 84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.674-5152C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942360 | ||||||
chr5:180942367
|
C | T | 11 | a0002c0007t0001g0039a0002c0007t0001g0042a0002c0007t0001g0044others(8): Show | 11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-5145C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942367 | ||||||
chr5:180942759
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0085 | 3 | NA18966.hp2 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.674-4753A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942759 | ||||||
chr5:180942779
|
A | T | 54 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(51): Show | 61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-4733A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942779 | ||||||
chr5:180943130
|
C | CT | 89 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(86): Show | 109 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.674-4360dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180943130 | |||||
chr5:180943181
|
C | G | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4331C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943181 | ||||||
chr5:180943230
|
G | T | 2 | a0003c0006t0001g0145a0003c0006t0001g0146 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-4282G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943230 | ||||||
chr5:180943323
|
C | T | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.674-4189C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943323 | ||||||
chr5:180943419
|
C | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 30 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.674-4093C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943419 | ||||||
chr5:180943499
|
G | A | 18 | a0003c0006t0001g0021a0003c0006t0001g0150a0003c0006t0001g0157others(15): Show | 23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-4013G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943499 | ||||||
chr5:180943503
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.674-4009A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943503 | ||||||
chr5:180943599
|
C | A | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-3913C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943599 | ||||||
chr5:180943812
|
A | G | 2 | a0002c0002t0001g0007a0005c0021t0001g0029 | 3 | HG01884.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.674-3700A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943812 | ||||||
chr5:180944194
|
GAA | G | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3316_674-3315d others(4): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180944194 | |||||
chr5:180944349
|
C | T | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3163C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944349 | ||||||
chr5:180944504
|
ACTAGAGG others(5): Show |
A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG01243.hp1 HG01952.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.674-3007_674-2996d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944504 | ||||||
chr5:180944569
|
T | C | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-2943T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944569 | ||||||
chr5:180944763
|
T | A | 2 | a0003c0006t0001g0145a0003c0006t0001g0146 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-2749T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944763 | ||||||
chr5:180944860
|
T | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.674-2652T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944860 | ||||||
chr5:180944958
|
A | G | 1 | a0002c0005t0001g0139 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674-2554A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944958 | ||||||
chr5:180945082
|
T | C | 5 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(2): Show | 5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-2430T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945082 | ||||||
chr5:180945237
|
T | C | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-2275T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945237 | ||||||
chr5:180945334
|
A | G | 67 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(64): Show | 80 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.674-2178A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945334 | ||||||
chr5:180945437
|
A | T | 1 | a0003c0003t0001g0012 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.674-2075A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945437 | ||||||
chr5:180945456
|
CA | C | 44 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(41): Show | 50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.674-2053delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945456 | |||||
chr5:180945473
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.674-2039A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945473 | ||||||
chr5:180945531
|
G | A | 1 | a0006c0008t0001g0011 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.674-1981G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945531 | ||||||
chr5:180945713
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.674-1799C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945713 | ||||||
chr5:180945838
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.674-1674T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945838 | ||||||
chr5:180945987
|
T | TAATA | 2 | a0003c0003t0001g0072a0003c0006t0001g0148 | 2 | HG02622.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.674-1497_674-1494d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | |||||
chr5:180945987
|
TAATA | T | 2 | a0001c0001t0001g0110a0003c0003t0001g0070 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.674-1497_674-1494d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | |||||
chr5:180945987
|
TAATAAAT others(1): Show |
T | 50 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(47): Show | 56 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.674-1501_674-1494d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | |||||
chr5:180945987
|
TAATAAAT others(5): Show |
T | 1 | a0002c0002t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.674-1505_674-1494d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | |||||
chr5:180946093
|
T | C | 1 | a0002c0007t0001g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674-1419T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946093 | ||||||
chr5:180946205
|
C | A | 9 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.674-1307C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946205 | ||||||
chr5:180946581
|
G | C | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-931G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946581 | ||||||
chr5:180946862
|
G | A | 49 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(46): Show | 55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.674-650G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946862 | ||||||
chr5:180947019
|
T | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-493T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947019 | ||||||
chr5:180947139
|
T | A | 4 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-373T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947139 | ||||||
chr5:180947379
|
A | C | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-133A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947379 | ||||||
chr5:180947387
|
G | A | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-125G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947387 | ||||||
chr5:180947898
|
A | G | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.787+273A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180947898 | ||||||
chr5:180947919
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.787+294A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180947919 | ||||||
chr5:180948095
|
T | C | 53 | a0001c0001t0001g0086a0001c0001t0001g0092a0002c0002t0001g0003others(50): Show | 59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.788-260T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948095 | ||||||
chr5:180948208
|
A | G | 44 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(41): Show | 50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.788-147A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948208 | ||||||
chr5:180948341
|
T | C | 1 | a0002c0005t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.788-14T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948341 | ||||||
chr5:180948469
|
G | A | 7 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+94G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948469 | ||||||
chr5:180948499
|
A | G | 7 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+124A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948499 | ||||||
chr5:180948512
|
G | A | 8 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(5): Show | 8 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.808+137G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948512 | ||||||
chr5:180948643
|
A | G | 52 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(49): Show | 58 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.808+268A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948643 | ||||||
chr5:180948672
|
C | G | 67 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0003others(64): Show | 80 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.809-248C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948672 | ||||||
chr5:180948682
|
G | GT | 16 | a0001c0001t0001g0075a0001c0001t0001g0076a0003c0003t0001g0001others(13): Show | 23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.809-237dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 180948682 | |||||
chr5:180948790
|
T | C | 49 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(46): Show | 55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.809-130T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948790 | ||||||
chr5:180948821
|
T | C | 5 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(2): Show | 5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-99T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948821 | ||||||
chr5:180948877
|
G | A | 4 | a0002c0002t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-43G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948877 | ||||||
chr5:180949083
|
G | T | 9 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+137G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949083 | ||||||
chr5:180949115
|
T | G | 1 | a0007c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.836-124T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949115 | ||||||
chr5:180949116
|
T | C | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-123T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949116 | ||||||
chr5:180949121
|
G | A | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-118G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949121 | ||||||
chr5:180949133
|
G | T | 5 | a0002c0005t0001g0058a0002c0005t0001g0060a0002c0005t0001g0061others(2): Show | 5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-106G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949133 | ||||||
chr5:180949208
|
T | G | 51 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(48): Show | 57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-31T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949208 | ||||||
chr5:180949223
|
G | C | 55 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(52): Show | 62 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.836-16G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949223 | ||||||
chr5:180949273
|
C | T | 2 | a0008c0019t0001g0046a0008c0025t0001g0045 | 2 | HG02280.hp1 HG02809.hp2 |
splice_region_variant&intron_variant | LOW | c.862+8C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949273 | ||||||
chr5:180949343
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.862+78C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949343 | ||||||
chr5:180949475
|
G | A | 1 | a0007c0013t0001g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.862+210G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949475 | ||||||
chr5:180949482
|
C | T | 1 | a0003c0006t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862+217C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949482 | ||||||
chr5:180949489
|
C | CG | 39 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(36): Show | 45 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.862+231dupG | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 180949489 | |||||
chr5:180949711
|
C | T | 34 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(31): Show | 40 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.863-193C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949711 | ||||||
chr5:180949719
|
T | C | 5 | a0002c0005t0001g0058a0002c0024t0001g0062a0008c0019t0001g0046others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-185T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949719 | ||||||
chr5:180949766
|
G | A | 3 | a0004c0004t0001g0149a0004c0004t0001g0155a0004c0004t0002g0151 | 3 | HG03490.hp2 HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.863-138G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949766 | ||||||
chr5:180949804
|
C | A | 34 | a0002c0002t0001g0003a0002c0002t0001g0007a0002c0002t0001g0008others(31): Show | 42 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.863-100C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949804 | ||||||
chr5:180949860
|
G | C | 47 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0135others(44): Show | 57 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.863-44G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949860 |