geneid | 84910 |
---|---|
ensemblid | ENSG00000153214.11 |
hgncid | 25913 |
symbol | TMEM87B |
name | transmembrane protein 87B |
refseq_nuc | NM_032824.3 |
refseq_prot | NP_116213.1 |
ensembl_nuc | ENST00000283206.9 |
ensembl_prot | ENSP00000283206.4 |
mane_status | MANE Select |
chr | chr2 |
start | 112055269 |
end | 112119314 |
strand | + |
ver | v1.2 |
region | chr2:112055269-112119314 |
region5000 | chr2:112050269-112124314 |
regionname0 | TMEM87B_chr2_112055269_112119314 |
regionname5000 | TMEM87B_chr2_112050269_112124314 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 555 | 233 | 59 | 51 | 86 | 7 | 28 | 63 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002 | 0/0 | 554 | 77 | 23 | 17 | 22 | 7 | 8 | 21 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0003 | 0/0 | 555 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1668 | 228 | 55 | 50 | 86 | 7 | 28 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
c0002 | 0/0 | 1665 | 77 | 23 | 17 | 22 | 7 | 8 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
c0003 | 0/0 | 1668 | 6 | 0 | 2 | 0 | 2 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
c0004 | 0/0 | 1668 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
c0005 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3495 | 88 | 17 | 14 | 50 | 1 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0002 | 1/1 | 3495 | 80 | 3 | 30 | 24 | 4 | 17 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0003 | 0/0 | 3495 | 41 | 5 | 4 | 21 | 5 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0004 | 0/0 | 3495 | 19 | 13 | 5 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0005 | 0/0 | 3496 | 15 | 13 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0006 | 0/0 | 3495 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0007 | 0/0 | 3496 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0008 | 0/0 | 3494 | 5 | 0 | 2 | 0 | 1 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0009 | 0/0 | 3496 | 4 | 0 | 2 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0010 | 0/0 | 3495 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0011 | 0/0 | 3495 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0012 | 0/0 | 3495 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0013 | 0/0 | 3496 | 3 | 0 | 0 | 0 | 2 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0014 | 0/0 | 3494 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0015 | 0/0 | 3495 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0016 | 0/0 | 3495 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0017 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0018 | 0/0 | 3495 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0019 | 0/0 | 3495 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0020 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0021 | 0/0 | 3495 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0022 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0023 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0024 | 0/0 | 3496 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0025 | 0/0 | 3495 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0026 | 0/0 | 3496 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0027 | 0/0 | 3496 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0028 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0029 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0030 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0031 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0032 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0033 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0034 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0035 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0036 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0037 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0038 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0039 | 0/0 | 3494 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0040 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0041 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0042 | 0/0 | 3496 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
t0043 | 0/0 | 3495 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1668 | 228 | 55 | 50 | 86 | 7 | 28 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0004 | 0/0 | 1668 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0005 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002 | 0/0 | 1665 | 77 | 23 | 17 | 22 | 7 | 8 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0003c0003 | 0/0 | 1668 | 6 | 0 | 2 | 0 | 2 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5162 | 84 | 15 | 14 | 48 | 1 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0002 | 1/1 | 5162 | 80 | 3 | 30 | 24 | 4 | 17 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0003 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0004 | 0/0 | 5162 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0005 | 0/0 | 5163 | 15 | 13 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0006 | 0/0 | 5162 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0007 | 0/0 | 5163 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0011 | 0/0 | 5162 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0013 | 0/0 | 5163 | 3 | 0 | 0 | 0 | 2 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0015 | 0/0 | 5162 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0017 | 0/0 | 5162 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0019 | 0/0 | 5162 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0021 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0022 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0023 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0024 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0025 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0026 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0027 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0028 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0029 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0030 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0031 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0032 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0033 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0034 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0035 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0036 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0037 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0038 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0039 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0040 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0001t0042 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0004t0010 | 0/0 | 5162 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0001c0005t0020 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0001 | 0/0 | 5159 | 4 | 2 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0003 | 0/0 | 5159 | 40 | 5 | 4 | 20 | 5 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0004 | 0/0 | 5159 | 17 | 11 | 5 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0008 | 0/0 | 5158 | 5 | 0 | 2 | 0 | 1 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0012 | 0/0 | 5159 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0014 | 0/0 | 5158 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0018 | 0/0 | 5159 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0041 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0002c0002t0043 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0003c0003t0009 | 0/0 | 5163 | 4 | 0 | 2 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
a0003c0003t0016 | 0/0 | 5162 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | copy fasta | chr2 | 112050269 | 112124314 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0013g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0013g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0019g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0019g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0021g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0022g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0023g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0025g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0026g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0027g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0028g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0029g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0030g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0031g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0032g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0033g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0034g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0035g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0036g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0037g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0038g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0039g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0040g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0001t0042g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0004t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0004t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0004t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0004t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0001c0005t0020g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0012g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0014g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0014g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0014g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0018g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0018g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0041g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0002c0002t0043g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0009g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0009g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0009g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0016g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
a0003c0003t0016g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00099 | hp2 | a0002 | c0002 | t0003 | g0157 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0132 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00323 | hp1 | a0002 | c0002 | t0004 | g0118 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00323 | hp2 | a0001 | c0001 | t0013 | g0285 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00408 | hp2 | a0001 | c0001 | t0023 | g0048 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00438 | hp1 | a0001 | c0001 | t0038 | g0192 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00621 | hp2 | a0001 | c0001 | t0032 | g0210 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0112 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00642 | hp2 | a0001 | c0001 | t0030 | g0045 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00738 | hp2 | a0002 | c0002 | t0004 | g0116 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00741 | hp1 | a0002 | c0002 | t0003 | g0166 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0131 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01070 | hp2 | a0003 | c0003 | t0009 | g0304 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0130 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01074 | hp2 | a0002 | c0002 | t0014 | g0149 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01081 | hp1 | a0002 | c0002 | t0014 | g0150 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01099 | hp1 | a0002 | c0002 | t0014 | g0177 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01109 | hp1 | a0002 | c0002 | t0008 | g0152 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01109 | hp2 | a0001 | c0005 | t0020 | g0292 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01169 | hp1 | a0002 | c0002 | t0043 | g0154 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01175 | hp1 | a0002 | c0002 | t0004 | g0023 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0259 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0086 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01255 | hp1 | a0002 | c0002 | t0008 | g0142 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01255 | hp2 | a0001 | c0001 | t0022 | g0059 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01256 | hp2 | a0002 | c0002 | t0004 | g0113 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01257 | hp1 | a0002 | c0002 | t0018 | g0294 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01258 | hp1 | a0002 | c0002 | t0004 | g0114 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01258 | hp2 | a0002 | c0002 | t0018 | g0293 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01261 | hp1 | a0002 | c0002 | t0003 | g0147 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01346 | hp2 | a0003 | c0003 | t0009 | g0303 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01515 | hp1 | a0002 | c0002 | t0008 | g0159 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0004 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01516 | hp2 | a0003 | c0003 | t0016 | g0301 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01517 | hp1 | a0003 | c0003 | t0016 | g0302 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01517 | hp2 | a0002 | c0002 | t0003 | g0004 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG01993 | hp2 | a0001 | c0001 | t0031 | g0073 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02015 | hp2 | a0001 | c0001 | t0034 | g0213 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0239 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02056 | hp2 | a0002 | c0002 | t0003 | g0137 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0115 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02145 | hp2 | a0001 | c0001 | t0027 | g0298 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02451 | hp1 | a0002 | c0002 | t0041 | g0279 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0231 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0111 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0224 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0170 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02698 | hp2 | a0002 | c0002 | t0008 | g0162 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02723 | hp1 | a0001 | c0001 | t0035 | g0001 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02723 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02735 | hp1 | a0001 | c0001 | t0021 | g0028 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0156 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0117 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0169 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02895 | hp1 | a0002 | c0002 | t0012 | g0280 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02895 | hp2 | a0001 | c0004 | t0010 | g0290 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02896 | hp2 | a0001 | c0001 | t0042 | g0299 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02897 | hp2 | a0001 | c0004 | t0010 | g0291 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0206 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02922 | hp2 | a0001 | c0004 | t0010 | g0289 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02970 | hp1 | a0002 | c0002 | t0012 | g0282 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0200 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03098 | hp1 | a0001 | c0004 | t0010 | g0288 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03195 | hp1 | a0002 | c0002 | t0004 | g0128 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03195 | hp2 | a0001 | c0001 | t0033 | g0087 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03209 | hp1 | a0002 | c0002 | t0004 | g0296 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03209 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0179 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03239 | hp2 | a0001 | c0001 | t0025 | g0106 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03453 | hp1 | a0001 | c0001 | t0026 | g0015 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03490 | hp2 | a0003 | c0003 | t0009 | g0300 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0164 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03516 | hp2 | a0002 | c0002 | t0003 | g0175 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03654 | hp1 | a0003 | c0003 | t0009 | g0305 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0161 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03669 | hp2 | a0001 | c0001 | t0013 | g0286 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03704 | hp1 | a0002 | c0002 | t0008 | g0146 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03710 | hp2 | a0001 | c0001 | t0019 | g0168 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03942 | hp2 | a0001 | c0001 | t0019 | g0129 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04115 | hp1 | a0002 | c0002 | t0003 | g0141 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0144 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18522 | hp1 | a0001 | c0001 | t0036 | g0001 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18522 | hp2 | a0002 | c0002 | t0012 | g0283 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18906 | hp1 | a0002 | c0002 | t0012 | g0281 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18939 | hp1 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18941 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18947 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0148 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18954 | hp2 | a0001 | c0001 | t0037 | g0243 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18957 | hp2 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18962 | hp2 | a0001 | c0001 | t0029 | g0097 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18984 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18987 | hp1 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18988 | hp2 | a0002 | c0002 | t0003 | g0160 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18992 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18992 | hp2 | a0001 | c0001 | t0039 | g0201 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18993 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18994 | hp2 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18995 | hp2 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0134 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19004 | hp1 | a0002 | c0002 | t0003 | g0143 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19030 | hp1 | a0001 | c0001 | t0028 | g0016 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19043 | hp1 | a0001 | c0001 | t0040 | g0295 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19043 | hp2 | a0002 | c0002 | t0004 | g0024 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19057 | hp2 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0176 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19081 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA20805 | hp1 | a0002 | c0002 | t0003 | g0178 | EUR | TSI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA20805 | hp2 | a0001 | c0001 | t0013 | g0284 | EUR | TSI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0180 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
HG03471 | hp2 | a0001 | c0001 | t0015 | g0173 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA20300 | hp1 | a0002 | c0002 | t0004 | g0126 | AFR | USA | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | USA | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA21309 | hp1 | a0002 | c0002 | t0004 | g0109 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0076 | REF | REF | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0060 | REF | REF | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112055613
|
G | C | 1 | a0003 | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
missense_variant | MODERATE | c.22G>C | p.Val8Leu | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 345/5162 | 22/1668 | 8/555 | chr2 | 112055613 | ||
chr2:112074958
|
CAAT | C | 1 | a0002 | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(74): Show |
disruptive_inframe_deletion&splice_region_variant | MODERATE | c.498_500delAAT | p.Met167del | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/19 | 821/5162 | 498/1668 | 166/555 | chr2 | 112074958 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112055717
|
G | C | 1 | a0001c0004 | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.126G>C | p.Ala42Ala | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 449/5162 | 126/1668 | 42/555 | chr2 | 112055717 | ||
chr2:112060006
|
T | C | 1 | a0001c0005 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.195T>C | p.Thr65Thr | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/19 | 518/5162 | 195/1668 | 65/555 | chr2 | 112060006 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112055279
|
C | G | 8 | a0001c0001t0003a0001c0001t0015a0001c0001t0019others(5): Show | 56 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-313C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 313 | chr2 | 112055279 | |||||
chr2:112055305
|
C | T | 3 | a0001c0001t0013a0002c0002t0012a0002c0002t0041 | 8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-287C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 287 | chr2 | 112055305 | |||||
chr2:112055307
|
C | T | 2 | a0001c0001t0040a0002c0002t0018 | 3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | chr2 | 112055307 | ||||||
chr2:112055428
|
G | A | 2 | a0003c0003t0009a0003c0003t0016 | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-164G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 164 | chr2 | 112055428 | |||||
chr2:112055489
|
G | C | 12 | a0001c0001t0003a0001c0001t0013a0001c0001t0015others(9): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-103G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 103 | chr2 | 112055489 | |||||
chr2:112055586
|
G | A | 13 | a0001c0001t0003a0001c0001t0013a0001c0001t0015others(10): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 6 | chr2 | 112055586 | |||||
chr2:112116153
|
G | A | 1 | a0001c0001t0021 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 10 | chr2 | 112116153 | |||||
chr2:112116289
|
G | C | 1 | a0001c0001t0022 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 146 | chr2 | 112116289 | |||||
chr2:112116307
|
T | A | 1 | a0001c0001t0023 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 164 | chr2 | 112116307 | |||||
chr2:112116308
|
A | T | 1 | a0001c0001t0023 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 165 | chr2 | 112116308 | |||||
chr2:112116311
|
G | C | 2 | a0001c0001t0017a0001c0004t0010 | 6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 168 | chr2 | 112116311 | |||||
chr2:112116313
|
T | C | 2 | a0001c0001t0013a0001c0001t0024 | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 170 | chr2 | 112116313 | |||||
chr2:112116514
|
T | C | 1 | a0001c0001t0025 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 371 | chr2 | 112116514 | |||||
chr2:112116565
|
C | T | 1 | a0001c0001t0011 | 4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 422 | chr2 | 112116565 | |||||
chr2:112116594
|
G | T | 2 | a0001c0001t0005a0003c0003t0009 | 19 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*451G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 451 | chr2 | 112116594 | |||||
chr2:112116676
|
A | G | 1 | a0001c0001t0006 | 6 | HG02027.hp2 NA18978.hp2 NA18992.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 533 | chr2 | 112116676 | |||||
chr2:112116879
|
G | A | 2 | a0001c0001t0017a0001c0004t0010 | 6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*736G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 736 | chr2 | 112116879 | |||||
chr2:112116910
|
G | A | 3 | a0001c0001t0007a0001c0001t0013a0001c0001t0024 | 9 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*767G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 767 | chr2 | 112116910 | |||||
chr2:112117007
|
T | C | 3 | a0001c0001t0026a0001c0001t0027a0001c0001t0042 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*864T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 864 | chr2 | 112117007 | |||||
chr2:112117366
|
AT | A | 1 | a0002c0002t0014 | 3 | HG01074.hp2 HG01081.hp1 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1225delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1225 | INFO_REALIGN_3_PRIME | chr2 | 112117366 | ||||
chr2:112117462
|
A | G | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(21): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1319A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1319 | chr2 | 112117462 | |||||
chr2:112117514
|
A | T | 1 | a0002c0002t0043 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1371 | chr2 | 112117514 | |||||
chr2:112117662
|
GA | G | 2 | a0001c0001t0039a0002c0002t0008 | 6 | HG01109.hp1 HG01255.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1530delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1530 | INFO_REALIGN_3_PRIME | chr2 | 112117662 | ||||
chr2:112117697
|
A | G | 1 | a0001c0001t0027 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1554A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1554 | chr2 | 112117697 | |||||
chr2:112117722
|
G | A | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1579 | chr2 | 112117722 | |||||
chr2:112117967
|
T | C | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1824 | chr2 | 112117967 | |||||
chr2:112118021
|
G | A | 1 | a0002c0002t0018 | 2 | HG01257.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1878 | chr2 | 112118021 | |||||
chr2:112118037
|
C | CT | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0013others(5): Show | 31 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1894_*1895insT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1895 | chr2 | 112118037 | |||||
chr2:112118141
|
G | T | 1 | a0001c0001t0038 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1998 | chr2 | 112118141 | |||||
chr2:112118149
|
T | C | 1 | a0001c0001t0029 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2006T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2006 | chr2 | 112118149 | |||||
chr2:112118231
|
C | T | 1 | a0001c0001t0031 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2088 | chr2 | 112118231 | |||||
chr2:112118233
|
T | C | 1 | a0001c0001t0032 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2090T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2090 | chr2 | 112118233 | |||||
chr2:112118379
|
C | G | 2 | a0001c0001t0017a0001c0004t0010 | 6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2236 | chr2 | 112118379 | |||||
chr2:112118462
|
T | C | 4 | a0001c0001t0004a0001c0001t0015a0001c0001t0033others(1): Show | 23 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2319 | chr2 | 112118462 | |||||
chr2:112118677
|
G | T | 1 | a0001c0001t0025 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2534G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2534 | chr2 | 112118677 | |||||
chr2:112118734
|
T | G | 1 | a0001c0001t0034 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2591 | chr2 | 112118734 | |||||
chr2:112118798
|
T | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2655T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2655 | chr2 | 112118798 | |||||
chr2:112118893
|
C | A | 1 | a0001c0001t0036 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2750C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2750 | chr2 | 112118893 | |||||
chr2:112119001
|
T | G | 1 | a0001c0001t0033 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2858T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2858 | chr2 | 112119001 | |||||
chr2:112119037
|
T | C | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2894 | chr2 | 112119037 | |||||
chr2:112119045
|
C | G | 1 | a0001c0001t0030 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2902C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2902 | chr2 | 112119045 | |||||
chr2:112119204
|
G | A | 1 | a0001c0001t0037 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3061G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 3061 | chr2 | 112119204 | |||||
chr2:112119212
|
G | T | 1 | a0001c0001t0027 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 3069 | chr2 | 112119212 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112055814
|
C | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.165+58C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112055814 | ||||||
chr2:112055938
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.165+182C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112055938 | ||||||
chr2:112056107
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.165+351G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056107 | ||||||
chr2:112056195
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.165+439A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056195 | ||||||
chr2:112056202
|
TAGAA | T | 6 | a0003c0003t0009g0300a0003c0003t0009g0303a0003c0003t0009g0304others(3): Show | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+449_165+452del others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112056202 | |||||
chr2:112056206
|
A | C | 1 | a0001c0001t0005g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+450A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056206 | ||||||
chr2:112056223
|
C | A | 6 | a0003c0003t0009g0300a0003c0003t0009g0303a0003c0003t0009g0304others(3): Show | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+467C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056223 | ||||||
chr2:112056315
|
T | C | 55 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(52): Show | 55 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.165+559T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056315 | ||||||
chr2:112056351
|
A | T | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+595A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056351 | ||||||
chr2:112056356
|
G | A | 1 | a0001c0001t0019g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165+600G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056356 | ||||||
chr2:112056468
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.165+712T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056468 | ||||||
chr2:112056749
|
G | A | 54 | a0001c0001t0003g0151a0001c0001t0015g0170a0001c0001t0015g0173others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.165+993G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056749 | ||||||
chr2:112056895
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 5 | HG02572.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1139T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056895 | ||||||
chr2:112057044
|
T | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.165+1288T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057044 | ||||||
chr2:112057074
|
G | A | 8 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(5): Show | 8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+1318G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057074 | ||||||
chr2:112057144
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.165+1388G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057144 | ||||||
chr2:112057314
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+1558C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057314 | ||||||
chr2:112057315
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+1559C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057315 | ||||||
chr2:112057344
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.165+1588T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057344 | ||||||
chr2:112057425
|
G | A | 56 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(53): Show | 56 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.165+1669G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057425 | ||||||
chr2:112057496
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.165+1740T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057496 | ||||||
chr2:112057713
|
C | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.165+1957C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057713 | ||||||
chr2:112057827
|
C | CT | 45 | a0001c0001t0001g0123a0001c0001t0001g0278a0001c0001t0002g0080others(42): Show | 45 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.165+2088dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112057827 | |||||
chr2:112057827
|
CT | C | 71 | a0001c0001t0002g0182a0001c0001t0003g0151a0001c0001t0013g0284others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+2088delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112057827 | |||||
chr2:112057857
|
C | T | 3 | a0001c0001t0040g0295a0002c0002t0018g0293a0002c0002t0018g0294 | 3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.165+2101C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057857 | ||||||
chr2:112057893
|
T | G | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.166-2084T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057893 | ||||||
chr2:112057908
|
A | G | 8 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(5): Show | 8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-2069A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057908 | ||||||
chr2:112057920
|
C | T | 1 | a0001c0001t0013g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-2057C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057920 | ||||||
chr2:112057928
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.166-2049G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057928 | ||||||
chr2:112057985
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-1992G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057985 | ||||||
chr2:112058103
|
G | A | 3 | a0001c0001t0040g0295a0002c0002t0018g0293a0002c0002t0018g0294 | 3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.166-1874G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058103 | ||||||
chr2:112058106
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.166-1871C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058106 | ||||||
chr2:112058122
|
C | T | 2 | a0002c0002t0004g0023a0002c0002t0004g0024 | 2 | HG01175.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-1855C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058122 | ||||||
chr2:112058131
|
T | G | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1846T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058131 | ||||||
chr2:112058299
|
G | C | 12 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0005g0081others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1678G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058299 | ||||||
chr2:112058389
|
T | A | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1588T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058389 | ||||||
chr2:112058445
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0024g0012 | 3 | HG02723.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.166-1532T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058445 | ||||||
chr2:112058470
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.166-1507T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058470 | ||||||
chr2:112058548
|
T | TAA | 123 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(120): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.166-1427_166-1426d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112058548 | |||||
chr2:112058557
|
A | T | 6 | a0003c0003t0009g0300a0003c0003t0009g0303a0003c0003t0009g0304others(3): Show | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1420A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058557 | ||||||
chr2:112058659
|
G | T | 67 | a0001c0001t0003g0151a0001c0001t0013g0284a0001c0001t0013g0285others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-1318G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058659 | ||||||
chr2:112058671
|
A | G | 1 | a0001c0001t0013g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-1306A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058671 | ||||||
chr2:112058692
|
T | A | 12 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0005g0081others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1285T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058692 | ||||||
chr2:112058720
|
C | G | 12 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0005g0081others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1257C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058720 | ||||||
chr2:112058771
|
A | G | 54 | a0001c0001t0003g0151a0001c0001t0015g0170a0001c0001t0015g0173others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.166-1206A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058771 | ||||||
chr2:112058788
|
G | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0030others(4): Show | 7 | HG01361.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1189G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058788 | ||||||
chr2:112059157
|
G | T | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-820G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059157 | ||||||
chr2:112059311
|
A | G | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-666A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059311 | ||||||
chr2:112059328
|
G | T | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.166-649G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059328 | ||||||
chr2:112059487
|
G | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(12): Show | 16 | HG01175.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-490G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059487 | ||||||
chr2:112059562
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.166-415C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059562 | ||||||
chr2:112059643
|
A | G | 1 | a0001c0001t0002g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.166-334A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059643 | ||||||
chr2:112059649
|
C | T | 12 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(9): Show | 12 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-328C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059649 | ||||||
chr2:112059881
|
A | T | 55 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(52): Show | 55 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.166-96A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059881 | ||||||
chr2:112059928
|
CA | C | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-41delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112059928 | |||||
chr2:112060152
|
C | A | 22 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(19): Show | 22 | HG01257.hp2 HG01516.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+115C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060152 | ||||||
chr2:112060251
|
A | G | 12 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(9): Show | 12 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+214A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060251 | ||||||
chr2:112060262
|
T | C | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.226+225T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060262 | ||||||
chr2:112060285
|
C | G | 126 | a0001c0001t0001g0123a0001c0001t0001g0274a0001c0001t0001g0275others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.226+248C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060285 | ||||||
chr2:112060339
|
ACT | A | 71 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.226+305_226+306del others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | 112060339 | |||||
chr2:112060381
|
A | C | 42 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(39): Show | 42 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.226+344A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060381 | ||||||
chr2:112060408
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 6 | HG02572.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+371C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060408 | ||||||
chr2:112060434
|
A | G | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.226+397A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060434 | ||||||
chr2:112060816
|
C | T | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226+779C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060816 | ||||||
chr2:112060931
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+894A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060931 | ||||||
chr2:112060996
|
A | C | 1 | a0001c0001t0002g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.226+959A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060996 | ||||||
chr2:112061027
|
C | T | 42 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(39): Show | 42 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.226+990C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061027 | ||||||
chr2:112061054
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226+1017G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061054 | ||||||
chr2:112061159
|
G | C | 2 | a0002c0002t0003g0130a0002c0002t0003g0131 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.226+1122G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061159 | ||||||
chr2:112061439
|
G | A | 54 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(51): Show | 54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.226+1402G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061439 | ||||||
chr2:112061778
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.226+1741G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061778 | ||||||
chr2:112061896
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.226+1859A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061896 | ||||||
chr2:112061925
|
G | C | 1 | a0002c0002t0003g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226+1888G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061925 | ||||||
chr2:112062024
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.226+1987A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062024 | ||||||
chr2:112062049
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.226+2012C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062049 | ||||||
chr2:112062284
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.227-1878C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062284 | ||||||
chr2:112062426
|
A | G | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-1736A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062426 | ||||||
chr2:112062532
|
G | A | 57 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.227-1630G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062532 | ||||||
chr2:112062854
|
C | G | 1 | a0002c0002t0003g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.227-1308C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062854 | ||||||
chr2:112062885
|
T | C | 126 | a0001c0001t0001g0123a0001c0001t0001g0274a0001c0001t0001g0275others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.227-1277T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062885 | ||||||
chr2:112062961
|
C | G | 3 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0025g0106 | 3 | HG01993.hp1 HG02129.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.227-1201C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062961 | ||||||
chr2:112063057
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-1105G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063057 | ||||||
chr2:112063063
|
A | G | 3 | a0001c0001t0005g0127a0002c0002t0004g0126a0002c0002t0004g0128 | 3 | HG02055.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.227-1099A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063063 | ||||||
chr2:112063287
|
G | T | 19 | a0001c0001t0001g0123a0001c0001t0002g0119a0001c0001t0004g0082others(16): Show | 19 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-875G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063287 | ||||||
chr2:112063288
|
C | T | 19 | a0001c0001t0001g0123a0001c0001t0002g0119a0001c0001t0004g0082others(16): Show | 19 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-874C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063288 | ||||||
chr2:112063411
|
T | A | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.227-751T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063411 | ||||||
chr2:112063535
|
C | T | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0007g0084others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-627C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063535 | ||||||
chr2:112063649
|
A | G | 72 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.227-513A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063649 | ||||||
chr2:112063710
|
A | G | 1 | a0002c0002t0004g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.227-452A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063710 | ||||||
chr2:112063769
|
C | G | 9 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(6): Show | 9 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.227-393C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063769 | ||||||
chr2:112064020
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.227-142G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112064020 | ||||||
chr2:112064044
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.227-118A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112064044 | ||||||
chr2:112064303
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.318+50A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064303 | ||||||
chr2:112064343
|
A | G | 1 | a0002c0002t0003g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.318+90A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064343 | ||||||
chr2:112064390
|
T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.318+137T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064390 | ||||||
chr2:112064398
|
A | C | 6 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+145A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064398 | ||||||
chr2:112064410
|
T | C | 1 | a0002c0002t0004g0296 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.318+157T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064410 | ||||||
chr2:112064507
|
A | G | 126 | a0001c0001t0001g0123a0001c0001t0001g0274a0001c0001t0001g0275others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.318+254A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064507 | ||||||
chr2:112064596
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318+343A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064596 | ||||||
chr2:112064626
|
G | A | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+373G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064626 | ||||||
chr2:112064727
|
C | T | 72 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.318+474C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064727 | ||||||
chr2:112064921
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.318+668T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064921 | ||||||
chr2:112064936
|
A | G | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+683A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064936 | ||||||
chr2:112065022
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0185others(12): Show | 17 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.318+769G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065022 | ||||||
chr2:112065066
|
C | T | 54 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(51): Show | 54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.318+813C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065066 | ||||||
chr2:112065254
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.318+1001A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065254 | ||||||
chr2:112065304
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.318+1051T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065304 | ||||||
chr2:112065357
|
A | G | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1104A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065357 | ||||||
chr2:112065399
|
G | T | 25 | a0001c0001t0001g0123a0001c0001t0002g0119a0001c0001t0004g0082others(22): Show | 26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+1146G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065399 | ||||||
chr2:112065463
|
A | C | 25 | a0001c0001t0001g0123a0001c0001t0002g0119a0001c0001t0004g0082others(22): Show | 26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+1210A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065463 | ||||||
chr2:112065537
|
C | T | 37 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(34): Show | 37 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.318+1284C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065537 | ||||||
chr2:112065551
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.318+1298C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065551 | ||||||
chr2:112065576
|
T | G | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1323T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065576 | ||||||
chr2:112065643
|
C | CA | 9 | a0001c0001t0001g0191a0001c0001t0002g0037a0001c0001t0002g0038others(6): Show | 9 | HG00438.hp1 HG01258.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-1270dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | |||||
chr2:112065643
|
C | CAA | 9 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(6): Show | 9 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-1271_319-1270d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | |||||
chr2:112065643
|
CA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(91): Show | 96 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.319-1270delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | |||||
chr2:112065664
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0232others(26): Show | 30 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.319-1272A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065664 | ||||||
chr2:112065715
|
C | T | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.319-1221C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065715 | ||||||
chr2:112065727
|
A | G | 1 | a0002c0002t0004g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319-1209A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065727 | ||||||
chr2:112065743
|
C | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.319-1193C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065743 | ||||||
chr2:112066048
|
T | C | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-888T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066048 | ||||||
chr2:112066249
|
A | G | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.319-687A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066249 | ||||||
chr2:112066413
|
T | A | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319-523T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066413 | ||||||
chr2:112066499
|
G | T | 2 | a0001c0001t0013g0284a0001c0001t0013g0285 | 2 | HG00323.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.319-437G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066499 | ||||||
chr2:112066834
|
A | G | 1 | a0002c0002t0004g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319-102A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066834 | ||||||
chr2:112067324
|
G | A | 53 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(50): Show | 53 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.450+257G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067324 | ||||||
chr2:112067363
|
C | T | 78 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(75): Show | 79 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.450+296C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067363 | ||||||
chr2:112067742
|
C | T | 1 | a0002c0002t0003g0132 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.450+675C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067742 | ||||||
chr2:112067939
|
C | T | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+872C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067939 | ||||||
chr2:112067969
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.450+902T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067969 | ||||||
chr2:112068138
|
C | T | 38 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(35): Show | 38 | HG01257.hp2 HG01516.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.450+1071C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068138 | ||||||
chr2:112068170
|
C | T | 74 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(71): Show | 75 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+1103C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068170 | ||||||
chr2:112068210
|
G | A | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.450+1143G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068210 | ||||||
chr2:112068501
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.450+1434G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068501 | ||||||
chr2:112068564
|
C | T | 1 | a0002c0002t0003g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.450+1497C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068564 | ||||||
chr2:112068661
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011 | 4 | HG02572.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1594G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068661 | ||||||
chr2:112068663
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+1596C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068663 | ||||||
chr2:112068664
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.450+1597G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068664 | ||||||
chr2:112068678
|
T | C | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.450+1611T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068678 | ||||||
chr2:112068698
|
C | T | 1 | a0001c0001t0005g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.450+1631C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068698 | ||||||
chr2:112068898
|
G | A | 21 | a0001c0001t0001g0123a0001c0001t0002g0119a0001c0001t0005g0008others(18): Show | 22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.450+1831G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068898 | ||||||
chr2:112068914
|
C | T | 6 | a0003c0003t0009g0300a0003c0003t0009g0303a0003c0003t0009g0304others(3): Show | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1847C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068914 | ||||||
chr2:112068915
|
G | A | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1848G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068915 | ||||||
chr2:112068921
|
G | A | 74 | a0001c0001t0001g0123a0001c0001t0002g0080a0001c0001t0002g0088others(71): Show | 75 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+1854G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068921 | ||||||
chr2:112068963
|
C | T | 1 | a0001c0001t0026g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450+1896C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068963 | ||||||
chr2:112069016
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.450+1949C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069016 | ||||||
chr2:112069019
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.450+1952C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069019 | ||||||
chr2:112069177
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0017g0224a0001c0001t0017g0231 | 3 | HG02451.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.450+2110C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069177 | ||||||
chr2:112069182
|
G | C | 5 | a0002c0002t0003g0137a0002c0002t0003g0138a0002c0002t0003g0139others(2): Show | 5 | HG02056.hp2 HG04115.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+2115G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069182 | ||||||
chr2:112069198
|
C | CA | 59 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0185others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.450+2154dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | |||||
chr2:112069198
|
C | CAA | 46 | a0001c0001t0001g0123a0001c0001t0002g0088a0001c0001t0002g0095others(43): Show | 47 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.450+2153_450+2154d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | |||||
chr2:112069198
|
C | CAAA | 24 | a0001c0001t0002g0080a0001c0001t0002g0089a0001c0001t0002g0090others(21): Show | 24 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.450+2152_450+2154d others(5): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | |||||
chr2:112069221
|
A | C | 3 | a0001c0004t0010g0289a0001c0004t0010g0290a0001c0004t0010g0291 | 3 | HG02895.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.450+2154A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069221 | ||||||
chr2:112069392
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450+2325C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069392 | ||||||
chr2:112069711
|
C | T | 3 | a0001c0001t0040g0295a0002c0002t0018g0293a0002c0002t0018g0294 | 3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.450+2644C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069711 | ||||||
chr2:112069834
|
G | C | 54 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(51): Show | 54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.450+2767G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069834 | ||||||
chr2:112069862
|
A | G | 54 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0002g0089others(51): Show | 54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.450+2795A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069862 | ||||||
chr2:112070218
|
T | G | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.450+3151T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070218 | ||||||
chr2:112070242
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.450+3175C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070242 | ||||||
chr2:112070401
|
AGT | A | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG01433.hp1 NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.450+3335_450+3336d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070401 | ||||||
chr2:112070722
|
G | A | 2 | a0002c0002t0008g0142a0002c0002t0008g0146 | 2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.450+3655G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070722 | ||||||
chr2:112070868
|
C | G | 1 | a0002c0002t0004g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+3801C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070868 | ||||||
chr2:112070882
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0232others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.450+3815C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070882 | ||||||
chr2:112070915
|
G | A | 1 | a0001c0001t0039g0201 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.450+3848G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070915 | ||||||
chr2:112071046
|
T | C | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3866T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071046 | ||||||
chr2:112071047
|
G | A | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3865G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071047 | ||||||
chr2:112071058
|
T | C | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3854T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071058 | ||||||
chr2:112071201
|
T | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.451-3711T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071201 | ||||||
chr2:112071297
|
T | TC | 18 | a0001c0001t0001g0202a0001c0001t0001g0226a0001c0001t0001g0238others(15): Show | 18 | HG01109.hp2 HG01192.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-3607dupC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071297 | |||||
chr2:112071306
|
G | C | 4 | a0001c0001t0001g0246a0001c0001t0001g0270a0001c0001t0002g0063others(1): Show | 4 | HG00642.hp1 HG03669.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3606G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071306 | ||||||
chr2:112071306
|
G | GC | 16 | a0001c0001t0001g0183a0001c0001t0001g0191a0001c0001t0001g0203others(13): Show | 16 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-3599dupC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071306 | |||||
chr2:112071308
|
C | G | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.451-3604C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071308 | ||||||
chr2:112071314
|
G | C | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.451-3598G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071314 | ||||||
chr2:112071328
|
T | G | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.451-3584T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071328 | ||||||
chr2:112071462
|
C | T | 1 | a0003c0003t0009g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.451-3450C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071462 | ||||||
chr2:112071524
|
C | A | 1 | a0001c0001t0026g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-3388C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071524 | ||||||
chr2:112071598
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.451-3314C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071598 | ||||||
chr2:112071806
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0191a0001c0001t0001g0193others(30): Show | 35 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.451-3106C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071806 | ||||||
chr2:112071810
|
C | T | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-3102C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071810 | ||||||
chr2:112071936
|
T | TA | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2975dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071936 | |||||
chr2:112071941
|
T | G | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-2971T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071941 | ||||||
chr2:112072105
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.451-2807G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072105 | ||||||
chr2:112072332
|
G | A | 5 | a0001c0001t0033g0087a0001c0004t0010g0288a0001c0004t0010g0289others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-2580G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072332 | ||||||
chr2:112072396
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(11): Show | 16 | HG00621.hp1 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-2516T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072396 | ||||||
chr2:112072409
|
C | G | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-2503C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072409 | ||||||
chr2:112072410
|
G | A | 1 | a0002c0002t0043g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.451-2502G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072410 | ||||||
chr2:112072588
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(193): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.451-2324C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072588 | ||||||
chr2:112072703
|
C | A | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-2209C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072703 | ||||||
chr2:112072788
|
A | G | 20 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.451-2124A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072788 | ||||||
chr2:112072895
|
C | CT | 85 | a0001c0001t0001g0123a0001c0001t0001g0214a0001c0001t0001g0215others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.451-1995dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112072895 | |||||
chr2:112072895
|
CT | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0187a0001c0001t0001g0248others(11): Show | 14 | HG01070.hp1 HG01167.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-1995delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112072895 | |||||
chr2:112073097
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.451-1815G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073097 | ||||||
chr2:112073244
|
C | T | 1 | a0002c0002t0003g0176 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.451-1668C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073244 | ||||||
chr2:112073259
|
T | C | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.451-1653T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073259 | ||||||
chr2:112073344
|
C | T | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-1568C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073344 | ||||||
chr2:112073414
|
C | T | 1 | a0001c0004t0010g0288 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.451-1498C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073414 | ||||||
chr2:112073491
|
T | C | 4 | a0001c0001t0011g0184a0001c0001t0011g0206a0001c0001t0011g0216others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1421T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073491 | ||||||
chr2:112073558
|
A | T | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.451-1354A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073558 | ||||||
chr2:112073573
|
A | G | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-1339A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073573 | ||||||
chr2:112073769
|
G | A | 1 | a0001c0001t0007g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.451-1143G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073769 | ||||||
chr2:112073848
|
G | T | 1 | a0001c0001t0002g0100 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.451-1064G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073848 | ||||||
chr2:112074041
|
T | C | 1 | a0002c0002t0008g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.451-871T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074041 | ||||||
chr2:112074085
|
G | A | 23 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(20): Show | 24 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.451-827G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074085 | ||||||
chr2:112074106
|
G | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.451-806G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074106 | ||||||
chr2:112075005
|
A | T | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.501+43A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075005 | ||||||
chr2:112075092
|
A | G | 3 | a0001c0001t0011g0184a0001c0001t0011g0206a0001c0001t0011g0216 | 3 | HG02922.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.501+130A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075092 | ||||||
chr2:112075107
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.501+145G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075107 | ||||||
chr2:112075245
|
C | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.501+283C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075245 | ||||||
chr2:112075531
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.501+569C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075531 | ||||||
chr2:112075534
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.501+572C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075534 | ||||||
chr2:112075850
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.501+888G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075850 | ||||||
chr2:112075940
|
G | A | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+978G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075940 | ||||||
chr2:112076123
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011 | 4 | HG02572.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-1069G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076123 | ||||||
chr2:112076426
|
G | C | 1 | a0001c0001t0005g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502-766G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076426 | ||||||
chr2:112076567
|
T | C | 1 | a0001c0001t0031g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.502-625T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076567 | ||||||
chr2:112076587
|
A | C | 31 | a0001c0001t0001g0050a0001c0001t0002g0037a0001c0001t0002g0038others(28): Show | 31 | HG00408.hp2 HG00558.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.502-605A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076587 | ||||||
chr2:112076822
|
C | T | 2 | a0002c0002t0003g0166a0002c0002t0003g0178 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.502-370C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076822 | ||||||
chr2:112076841
|
TTTGTGTG others(12): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.502-349_502-331del others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076841 | |||||
chr2:112076842
|
T | TTG | 10 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036others(7): Show | 10 | HG01361.hp1 HG01928.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-304_502-303dup others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
T | TTGTG | 27 | a0001c0001t0002g0026a0001c0001t0002g0030a0001c0001t0002g0031others(24): Show | 27 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.502-306_502-303dup others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
T | TTGTGTG | 9 | a0001c0001t0001g0050a0001c0001t0002g0037a0001c0001t0002g0042others(6): Show | 9 | HG01255.hp2 HG01516.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-308_502-303dup others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0002g0047a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 5 | HG01257.hp2 HG01433.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-310_502-303dup others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.502-316_502-303dup others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTG | T | 23 | a0001c0001t0002g0025a0001c0001t0002g0241a0001c0001t0004g0082others(20): Show | 24 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-308_502-303del others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(1): Show |
T | 23 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 24 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-310_502-303del others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(3): Show |
T | 16 | a0001c0001t0001g0013a0001c0001t0002g0088a0001c0001t0002g0089others(13): Show | 16 | HG00140.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.502-312_502-303del others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502-314_502-303del others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0002g0242a0002c0002t0004g0296 | 2 | HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.502-316_502-303del others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0221a0001c0001t0001g0245 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.502-318_502-303del others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0001g0270 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-320_502-303del others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076842
|
TTGTGTGT others(13): Show |
T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.502-322_502-303del others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | |||||
chr2:112076852
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.502-340G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076852 | ||||||
chr2:112076929
|
T | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.502-263T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076929 | ||||||
chr2:112077028
|
A | G | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.502-164A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112077028 | ||||||
chr2:112077038
|
C | CA | 83 | a0001c0001t0001g0195a0001c0001t0001g0217a0001c0001t0002g0068others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.502-136dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112077038 | |||||
chr2:112077038
|
CA | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 39 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.502-136delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112077038 | |||||
chr2:112077299
|
T | C | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+17T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077299 | ||||||
chr2:112077562
|
A | T | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.592+280A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077562 | ||||||
chr2:112077563
|
T | A | 23 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(20): Show | 24 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.592+281T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077563 | ||||||
chr2:112077564
|
T | A | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.592+282T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077564 | ||||||
chr2:112077737
|
G | T | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.592+455G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077737 | ||||||
chr2:112077748
|
T | G | 2 | a0002c0002t0004g0126a0002c0002t0004g0128 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.592+466T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077748 | ||||||
chr2:112078061
|
C | T | 6 | a0001c0001t0002g0047a0001c0001t0002g0049a0001c0001t0002g0058others(3): Show | 6 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+779C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078061 | ||||||
chr2:112078096
|
G | A | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+814G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078096 | ||||||
chr2:112078126
|
G | A | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+844G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078126 | ||||||
chr2:112078274
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592+992G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078274 | ||||||
chr2:112078285
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+1003G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078285 | ||||||
chr2:112078360
|
C | T | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+1078C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078360 | ||||||
chr2:112078435
|
G | A | 20 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1153G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078435 | ||||||
chr2:112078533
|
C | G | 6 | a0002c0002t0001g0018a0002c0002t0012g0280a0002c0002t0012g0281others(3): Show | 6 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+1251C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078533 | ||||||
chr2:112078538
|
C | T | 1 | a0002c0002t0003g0164 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.592+1256C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078538 | ||||||
chr2:112078736
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.592+1454C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078736 | ||||||
chr2:112078749
|
A | G | 3 | a0001c0001t0002g0065a0001c0001t0002g0071a0001c0001t0002g0079 | 3 | HG00558.hp1 NA18948.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.592+1467A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078749 | ||||||
chr2:112079005
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.592+1723T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079005 | ||||||
chr2:112079083
|
A | G | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+1801A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079083 | ||||||
chr2:112079311
|
C | T | 6 | a0001c0001t0005g0077a0001c0001t0007g0021a0001c0001t0007g0084others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-1746C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079311 | ||||||
chr2:112079384
|
C | A | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1673C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079384 | ||||||
chr2:112079763
|
C | T | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-1294C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079763 | ||||||
chr2:112079926
|
C | CT | 76 | a0001c0001t0001g0195a0001c0001t0002g0056a0001c0001t0002g0068others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.593-1110dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | |||||
chr2:112079926
|
C | CTT | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 108 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.593-1111_593-1110d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | |||||
chr2:112079926
|
CT | C | 25 | a0001c0001t0001g0123a0001c0001t0002g0039a0001c0001t0002g0089others(22): Show | 26 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-1110delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | |||||
chr2:112079962
|
C | T | 20 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.593-1095C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079962 | ||||||
chr2:112079981
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.593-1076G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079981 | ||||||
chr2:112080079
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.593-978G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080079 | ||||||
chr2:112080149
|
G | A | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-908G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080149 | ||||||
chr2:112080252
|
A | T | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.593-805A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080252 | ||||||
chr2:112080452
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.593-605T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080452 | ||||||
chr2:112080461
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.593-596G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080461 | ||||||
chr2:112080481
|
G | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0062a0001c0001t0002g0182others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-576G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080481 | ||||||
chr2:112080626
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.593-431T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080626 | ||||||
chr2:112080728
|
A | T | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-329A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080728 | ||||||
chr2:112080771
|
G | A | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.593-286G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080771 | ||||||
chr2:112080796
|
A | C | 5 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-261A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080796 | ||||||
chr2:112081268
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.655-67A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 7/18 | chr2 | 112081268 | ||||||
chr2:112081710
|
A | G | 5 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0194others(2): Show | 5 | HG01175.hp2 HG01346.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+192A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081710 | ||||||
chr2:112081888
|
T | C | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838+370T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081888 | ||||||
chr2:112081891
|
C | T | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838+373C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081891 | ||||||
chr2:112081892
|
C | T | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+374C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081892 | ||||||
chr2:112081918
|
G | A | 6 | a0001c0001t0005g0077a0001c0001t0007g0021a0001c0001t0007g0084others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+400G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081918 | ||||||
chr2:112082056
|
C | T | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+538C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082056 | ||||||
chr2:112082086
|
A | G | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.838+568A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082086 | ||||||
chr2:112082088
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.838+570G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082088 | ||||||
chr2:112082111
|
T | C | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+593T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082111 | ||||||
chr2:112082112
|
G | A | 6 | a0001c0001t0005g0077a0001c0001t0007g0021a0001c0001t0007g0084others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+594G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082112 | ||||||
chr2:112082216
|
A | G | 21 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(18): Show | 22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+698A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082216 | ||||||
chr2:112082284
|
G | A | 3 | a0001c0001t0005g0127a0001c0001t0017g0224a0001c0001t0017g0231 | 3 | HG02055.hp2 HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.838+766G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082284 | ||||||
chr2:112082301
|
G | A | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838+783G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082301 | ||||||
chr2:112082657
|
G | GGT | 6 | a0001c0001t0002g0212a0001c0004t0010g0288a0001c0004t0010g0289others(3): Show | 6 | HG02165.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+1157_838+1158d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | |||||
chr2:112082657
|
GGTGT | G | 6 | a0001c0001t0005g0077a0001c0001t0007g0021a0001c0001t0007g0084others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1155_838+1158d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | |||||
chr2:112082657
|
GGTGTGT | G | 3 | a0001c0001t0002g0092a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG01928.hp2 HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.838+1153_838+1158d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | |||||
chr2:112082841
|
T | C | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+1323T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082841 | ||||||
chr2:112082926
|
C | T | 21 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(18): Show | 22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+1408C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082926 | ||||||
chr2:112083102
|
A | G | 1 | a0001c0001t0007g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.838+1584A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083102 | ||||||
chr2:112083344
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.838+1826C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083344 | ||||||
chr2:112083568
|
G | A | 5 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+2050G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083568 | ||||||
chr2:112084029
|
A | G | 1 | a0001c0001t0005g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.839-1976A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084029 | ||||||
chr2:112084183
|
G | A | 21 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(18): Show | 22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-1822G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084183 | ||||||
chr2:112084225
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.839-1780G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084225 | ||||||
chr2:112084261
|
G | T | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1744G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084261 | ||||||
chr2:112084269
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.839-1736A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084269 | ||||||
chr2:112084279
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.839-1726T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084279 | ||||||
chr2:112084470
|
T | C | 24 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(21): Show | 25 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.839-1535T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084470 | ||||||
chr2:112084473
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.839-1532C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084473 | ||||||
chr2:112084513
|
C | T | 1 | a0002c0002t0008g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.839-1492C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084513 | ||||||
chr2:112084589
|
A | AGATCTAT others(7): Show |
6 | a0001c0001t0001g0197a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG00438.hp2 NA18939.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-1414_839-1401d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112084589 | |||||
chr2:112084642
|
A | G | 1 | a0002c0002t0004g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.839-1363A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084642 | ||||||
chr2:112085231
|
A | C | 21 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.839-774A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085231 | ||||||
chr2:112085346
|
T | A | 73 | a0002c0002t0001g0018a0002c0002t0001g0199a0002c0002t0001g0207others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.839-659T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085346 | ||||||
chr2:112085667
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.839-338A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085667 | ||||||
chr2:112085672
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.839-333A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085672 | ||||||
chr2:112085768
|
G | A | 1 | a0002c0002t0003g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.839-237G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085768 | ||||||
chr2:112085820
|
G | T | 24 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0081others(21): Show | 25 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.839-185G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085820 | ||||||
chr2:112085825
|
G | A | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.839-180G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085825 | ||||||
chr2:112085988
|
AT | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(46): Show | 52 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.839-10delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112085988 | |||||
chr2:112086398
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+294G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112086398 | ||||||
chr2:112086514
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.938+410T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112086514 | ||||||
chr2:112087066
|
G | A | 3 | a0001c0001t0026g0015a0001c0001t0027g0298a0001c0001t0042g0299 | 3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938+962G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087066 | ||||||
chr2:112087291
|
A | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.938+1187A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087291 | ||||||
chr2:112087390
|
A | G | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+1286A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087390 | ||||||
chr2:112087407
|
T | TC | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.938+1303_938+1304i others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087407 | ||||||
chr2:112087416
|
ACT | A | 3 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0024g0012 | 3 | HG00323.hp2 HG02723.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.938+1315_938+1316d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 112087416 | |||||
chr2:112087422
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.938+1318C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087422 | ||||||
chr2:112087526
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+1422G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087526 | ||||||
chr2:112087756
|
C | G | 1 | a0002c0002t0003g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.938+1652C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087756 | ||||||
chr2:112087818
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.938+1714A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087818 | ||||||
chr2:112088017
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.939-1608C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088017 | ||||||
chr2:112088027
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.939-1598C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088027 | ||||||
chr2:112088487
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0202a0001c0001t0001g0223others(1): Show | 4 | NA18948.hp1 NA18960.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.939-1138A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088487 | ||||||
chr2:112088674
|
A | G | 1 | a0001c0001t0019g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.939-951A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088674 | ||||||
chr2:112088783
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.939-842A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088783 | ||||||
chr2:112088798
|
G | A | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-827G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088798 | ||||||
chr2:112088846
|
C | G | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-779C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088846 | ||||||
chr2:112088861
|
C | T | 1 | a0001c0001t0013g0284 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.939-764C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088861 | ||||||
chr2:112088962
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.939-663C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088962 | ||||||
chr2:112089416
|
A | C | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.939-209A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089416 | ||||||
chr2:112089454
|
C | T | 1 | a0001c0001t0023g0048 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.939-171C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089454 | ||||||
chr2:112089511
|
A | C | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.939-114A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089511 | ||||||
chr2:112089577
|
C | G | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.939-48C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089577 | ||||||
chr2:112089587
|
C | T | 75 | a0002c0002t0001g0018a0002c0002t0001g0199a0002c0002t0001g0207others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.939-38C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089587 | ||||||
chr2:112090020
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1032+302G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090020 | ||||||
chr2:112090041
|
T | A | 2 | a0001c0001t0001g0197a0001c0001t0039g0201 | 2 | NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1032+323T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090041 | ||||||
chr2:112090169
|
A | G | 3 | a0002c0002t0004g0022a0002c0002t0004g0126a0002c0002t0004g0128 | 3 | HG03195.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1032+451A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090169 | ||||||
chr2:112090324
|
T | G | 1 | a0001c0001t0002g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1032+606T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090324 | ||||||
chr2:112090379
|
A | ATTGG | 24 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1032+704_1032+707d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | |||||
chr2:112090379
|
ATTGG | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 107 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1032+704_1032+707d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | |||||
chr2:112090379
|
ATTGGTTG others(1): Show |
A | 5 | a0001c0001t0001g0221a0001c0001t0001g0272a0001c0001t0002g0212others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+700_1032+707d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | |||||
chr2:112090379
|
ATTGGTTG others(5): Show |
A | 72 | a0001c0001t0037g0243a0002c0002t0001g0018a0002c0002t0001g0199others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1032+696_1032+707d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | |||||
chr2:112090522
|
A | G | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1032+804A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090522 | ||||||
chr2:112090627
|
A | C | 5 | a0002c0002t0001g0018a0002c0002t0012g0280a0002c0002t0012g0282others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+909A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090627 | ||||||
chr2:112090821
|
A | G | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1033-891A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090821 | ||||||
chr2:112090903
|
G | A | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1033-809G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090903 | ||||||
chr2:112091196
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1033-516C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091196 | ||||||
chr2:112091240
|
CA | C | 7 | a0001c0001t0001g0020a0001c0001t0002g0067a0001c0001t0005g0261others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-456delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112091240 | |||||
chr2:112091256
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0211 | 2 | NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1033-456A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091256 | ||||||
chr2:112091328
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | NA18747.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1033-384C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091328 | ||||||
chr2:112091516
|
AT | A | 19 | a0001c0001t0005g0008a0001c0001t0005g0081a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1033-195delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091516 | ||||||
chr2:112091656
|
C | T | 3 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170 | 3 | HG02615.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1033-56C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091656 | ||||||
chr2:112092310
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1104+527A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092310 | ||||||
chr2:112092429
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1104+646C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092429 | ||||||
chr2:112092734
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1104+951T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092734 | ||||||
chr2:112093004
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1104+1221T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093004 | ||||||
chr2:112093056
|
C | T | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104+1273C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093056 | ||||||
chr2:112093066
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1104+1283T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093066 | ||||||
chr2:112093202
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1104+1419G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093202 | ||||||
chr2:112093319
|
G | A | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1104+1536G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093319 | ||||||
chr2:112093354
|
T | G | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104+1571T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093354 | ||||||
chr2:112093430
|
A | T | 1 | a0002c0002t0004g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1104+1647A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093430 | ||||||
chr2:112093488
|
T | C | 1 | a0001c0001t0015g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1104+1705T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093488 | ||||||
chr2:112093847
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1104+2064A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093847 | ||||||
chr2:112093947
|
G | A | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1104+2164G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093947 | ||||||
chr2:112093987
|
T | C | 1 | a0002c0002t0012g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1104+2204T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093987 | ||||||
chr2:112094112
|
A | G | 1 | a0002c0002t0004g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1104+2329A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094112 | ||||||
chr2:112094161
|
C | CT | 8 | a0001c0001t0001g0225a0001c0001t0001g0263a0001c0001t0002g0041others(5): Show | 8 | HG00621.hp1 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104+2397dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112094161 | |||||
chr2:112094194
|
G | A | 2 | a0002c0002t0004g0126a0002c0002t0004g0128 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1104+2411G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094194 | ||||||
chr2:112094246
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1104+2463C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094246 | ||||||
chr2:112094380
|
C | G | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1104+2597C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094380 | ||||||
chr2:112094409
|
C | T | 3 | a0002c0002t0004g0023a0002c0002t0004g0024a0002c0002t0004g0117 | 3 | HG01175.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1104+2626C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094409 | ||||||
chr2:112094953
|
G | A | 2 | a0001c0001t0002g0119a0001c0001t0002g0229 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1105-2091G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094953 | ||||||
chr2:112095051
|
A | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1105-1993A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095051 | ||||||
chr2:112095140
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1105-1904C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095140 | ||||||
chr2:112095141
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1105-1903G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095141 | ||||||
chr2:112095161
|
CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1105-1879_1105-186 others(21): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095161 | |||||
chr2:112095165
|
C | CT | 7 | a0001c0001t0002g0066a0001c0001t0002g0068a0001c0001t0002g0070others(4): Show | 7 | HG00140.hp1 HG01081.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1832dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(2): Show |
7 | a0002c0002t0003g0130a0002c0002t0003g0131a0002c0002t0003g0134others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1840_1105-183 others(13): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(3): Show |
2 | a0002c0002t0003g0148a0002c0002t0003g0164 | 2 | HG03491.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1105-1841_1105-183 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(5): Show |
3 | a0001c0005t0020g0292a0002c0002t0001g0199a0002c0002t0003g0161 | 3 | HG01109.hp2 HG03654.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1105-1843_1105-183 others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(6): Show |
2 | a0002c0002t0001g0222a0002c0002t0008g0162 | 2 | HG02698.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1105-1844_1105-183 others(17): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(7): Show |
1 | a0002c0002t0008g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1105-1845_1105-183 others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(8): Show |
1 | a0002c0002t0003g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1105-1846_1105-183 others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(9): Show |
1 | a0002c0002t0003g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1105-1847_1105-183 others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(12): Show |
3 | a0002c0002t0003g0157a0002c0002t0014g0149a0002c0002t0014g0150 | 3 | HG00099.hp2 HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1105-1850_1105-183 others(23): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
C | CTTTTTTT others(13): Show |
1 | a0002c0002t0014g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1105-1851_1105-183 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTT | C | 6 | a0001c0001t0002g0078a0001c0001t0007g0021a0001c0001t0007g0085others(3): Show | 6 | HG01109.hp1 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1834_1105-183 others(7): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTT | C | 16 | a0001c0001t0001g0050a0001c0001t0002g0040a0001c0001t0002g0042others(13): Show | 16 | HG01175.hp2 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1105-1835_1105-183 others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTT | C | 14 | a0001c0001t0002g0025a0001c0001t0002g0037a0001c0001t0002g0041others(11): Show | 14 | HG00099.hp1 HG00408.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1105-1836_1105-183 others(9): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT | C | 7 | a0001c0001t0002g0036a0001c0001t0002g0103a0001c0001t0002g0253others(4): Show | 7 | HG00140.hp2 HG01257.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1838_1105-183 others(11): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0093others(7): Show | 10 | HG02129.hp2 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1105-1839_1105-183 others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0173others(1): Show | 4 | HG02647.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1841_1105-183 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0003g0139a0002c0002t0003g0141 | 2 | HG04115.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1105-1842_1105-183 others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(5): Show |
C | 4 | a0002c0002t0003g0137a0002c0002t0003g0138a0002c0002t0003g0140others(1): Show | 4 | HG02056.hp2 HG03195.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1843_1105-183 others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0002g0095a0002c0002t0004g0114a0002c0002t0004g0126others(1): Show | 4 | HG01258.hp1 HG02135.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1844_1105-183 others(17): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0096a0002c0002t0001g0018a0002c0002t0004g0113 | 3 | HG01256.hp2 HG02965.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1105-1845_1105-183 others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(8): Show |
C | 5 | a0002c0002t0004g0111a0002c0002t0004g0112a0002c0002t0004g0116others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105-1846_1105-183 others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0005g0081a0001c0001t0005g0125a0001c0001t0005g0258others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105-1847_1105-183 others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(10): Show |
C | 19 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0120others(16): Show | 20 | HG00639.hp1 HG01346.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1105-1848_1105-183 others(21): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1105-1849_1105-183 others(22): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1105-1850_1105-183 others(23): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(13): Show |
C | 1 | a0002c0002t0003g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1105-1851_1105-183 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(14): Show |
C | 6 | a0001c0001t0026g0015a0001c0001t0042g0299a0002c0002t0001g0207others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1852_1105-183 others(25): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0040g0295a0002c0002t0004g0017 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1105-1853_1105-183 others(26): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(16): Show |
C | 10 | a0001c0001t0001g0190a0001c0001t0001g0225a0001c0001t0001g0238others(7): Show | 10 | HG00438.hp1 HG00438.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1105-1854_1105-183 others(27): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(17): Show |
C | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 94 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1105-1855_1105-183 others(28): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(18): Show |
C | 7 | a0001c0001t0001g0185a0001c0001t0001g0220a0001c0001t0001g0228others(4): Show | 7 | HG00323.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1856_1105-183 others(29): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(19): Show |
C | 6 | a0001c0001t0002g0027a0001c0001t0002g0055a0001c0001t0002g0056others(3): Show | 6 | HG02145.hp2 NA18942.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105-1857_1105-183 others(30): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0002g0026 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1105-1858_1105-183 others(31): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(21): Show |
C | 1 | a0002c0002t0003g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1105-1859_1105-183 others(32): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(25): Show |
C | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1105-1863_1105-183 others(36): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095165
|
CTTTTTTT others(28): Show |
C | 1 | a0002c0002t0008g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1105-1866_1105-183 others(39): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | |||||
chr2:112095195
|
T | C | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1105-1849T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095195 | ||||||
chr2:112095208
|
TTTTTG | T | 7 | a0001c0001t0002g0030a0001c0001t0002g0035a0001c0001t0002g0047others(4): Show | 7 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1835_1105-183 others(9): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095208 | ||||||
chr2:112095213
|
G | T | 1 | a0001c0001t0002g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1105-1831G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095213 | ||||||
chr2:112095281
|
C | T | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-1763C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095281 | ||||||
chr2:112095464
|
C | A | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1105-1580C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095464 | ||||||
chr2:112095508
|
A | AT | 6 | a0001c0001t0001g0050a0001c0001t0002g0037a0001c0001t0002g0039others(3): Show | 6 | HG02132.hp2 HG02165.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1527dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095508 | |||||
chr2:112095642
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1105-1402T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095642 | ||||||
chr2:112095725
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1105-1319T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095725 | ||||||
chr2:112095762
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1105-1282A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095762 | ||||||
chr2:112095840
|
G | A | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1105-1204G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095840 | ||||||
chr2:112096037
|
G | C | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1105-1007G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096037 | ||||||
chr2:112096068
|
C | T | 2 | a0002c0002t0001g0199a0002c0002t0001g0222 | 2 | NA18940.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1105-976C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096068 | ||||||
chr2:112096118
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0236others(9): Show | 13 | HG00558.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1105-926A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096118 | ||||||
chr2:112096146
|
G | A | 73 | a0002c0002t0001g0018a0002c0002t0001g0199a0002c0002t0001g0207others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1105-898G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096146 | ||||||
chr2:112096166
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-878G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096166 | ||||||
chr2:112096336
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1105-708G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096336 | ||||||
chr2:112096401
|
A | G | 4 | a0001c0001t0011g0184a0001c0001t0011g0206a0001c0001t0011g0216others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-643A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096401 | ||||||
chr2:112096477
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1105-567G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096477 | ||||||
chr2:112096490
|
G | A | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1105-554G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096490 | ||||||
chr2:112096507
|
A | G | 1 | a0002c0002t0004g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1105-537A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096507 | ||||||
chr2:112096758
|
G | A | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1105-286G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096758 | ||||||
chr2:112096819
|
G | A | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-225G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096819 | ||||||
chr2:112097007
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 102 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1105-37A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112097007 | ||||||
chr2:112097354
|
C | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1272+63C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097354 | ||||||
chr2:112097356
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1272+65A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097356 | ||||||
chr2:112097390
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1272+99A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097390 | ||||||
chr2:112097554
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1272+263G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097554 | ||||||
chr2:112097582
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0185 | 3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1272+291G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097582 | ||||||
chr2:112097712
|
C | CA | 24 | a0001c0001t0001g0238a0001c0001t0002g0027a0001c0001t0002g0040others(21): Show | 24 | HG01069.hp2 HG01109.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1272+446dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr2 | 112097712 | |||||
chr2:112097712
|
CA | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1272+446delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr2 | 112097712 | |||||
chr2:112097731
|
A | C | 2 | a0001c0001t0001g0269a0001c0001t0038g0192 | 2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1272+440A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097731 | ||||||
chr2:112097737
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1272+446A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097737 | ||||||
chr2:112097818
|
T | A | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1272+527T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097818 | ||||||
chr2:112097908
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1272+617A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097908 | ||||||
chr2:112097956
|
C | G | 4 | a0001c0001t0007g0084a0001c0001t0007g0085a0001c0001t0007g0086others(1): Show | 4 | HG01243.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-639C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097956 | ||||||
chr2:112097981
|
TC | T | 5 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-613delC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097981 | ||||||
chr2:112098376
|
C | T | 21 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1273-219C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098376 | ||||||
chr2:112098520
|
G | A | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1273-75G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098520 | ||||||
chr2:112098588
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
splice_region_variant&intron_variant | LOW | c.1273-7C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098588 | ||||||
chr2:112098731
|
G | A | 6 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0235others(3): Show | 6 | HG02027.hp2 NA18978.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376+33G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098731 | ||||||
chr2:112098745
|
C | T | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1376+47C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098745 | ||||||
chr2:112098749
|
T | C | 1 | a0002c0002t0003g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1376+51T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098749 | ||||||
chr2:112098757
|
C | A | 5 | a0002c0002t0004g0112a0002c0002t0004g0113a0002c0002t0004g0114others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376+59C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098757 | ||||||
chr2:112098790
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1376+92C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098790 | ||||||
chr2:112098908
|
C | T | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+210C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098908 | ||||||
chr2:112098915
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1376+217C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098915 | ||||||
chr2:112098917
|
A | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+219A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098917 | ||||||
chr2:112099020
|
T | C | 1 | a0001c0001t0007g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1376+322T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099020 | ||||||
chr2:112099178
|
C | T | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+480C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099178 | ||||||
chr2:112099351
|
T | C | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1376+653T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099351 | ||||||
chr2:112099499
|
G | A | 8 | a0001c0001t0001g0123a0001c0001t0001g0196a0001c0001t0001g0225others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376+801G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099499 | ||||||
chr2:112099525
|
C | CAT | 22 | a0001c0001t0001g0013a0001c0001t0001g0218a0001c0001t0001g0228others(19): Show | 22 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1376+857_1376+858d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATAT | 6 | a0001c0001t0001g0014a0001c0001t0002g0031a0001c0001t0002g0034others(3): Show | 6 | HG01361.hp1 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+855_1376+858d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATAT | 6 | a0001c0001t0002g0090a0001c0001t0002g0093a0001c0001t0002g0094others(3): Show | 6 | HG02698.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+853_1376+858d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATATA others(1): Show |
5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0103others(2): Show | 5 | HG02056.hp1 HG03017.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+851_1376+858d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATATA others(3): Show |
6 | a0001c0001t0002g0091a0001c0001t0002g0101a0001c0001t0002g0229others(3): Show | 6 | HG00280.hp1 HG01934.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+849_1376+858d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATATA others(5): Show |
1 | a0001c0001t0002g0100 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1376+847_1376+858d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATATA others(7): Show |
2 | a0001c0001t0002g0102a0001c0001t0002g0253 | 2 | HG00140.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1376+845_1376+858d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
C | CATATATA others(9): Show |
1 | a0001c0001t0002g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1376+843_1376+858d others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
CAT | C | 3 | a0001c0001t0001g0183a0001c0001t0002g0068a0001c0001t0011g0230 | 3 | HG02027.hp1 HG02148.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1376+857_1376+858d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
CATATAT | C | 10 | a0001c0001t0026g0015a0002c0002t0004g0109a0002c0002t0004g0111others(7): Show | 10 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1376+853_1376+858d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099525
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1376+849_1376+858d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | |||||
chr2:112099527
|
T | C | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+829T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099527 | ||||||
chr2:112099529
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0039g0201 | 2 | NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1376+831T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099529 | ||||||
chr2:112099545
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0027g0298a0003c0003t0009g0305 | 2 | HG02145.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1376+849_1376+860d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099545 | |||||
chr2:112099547
|
TATATATA others(3): Show |
T | 19 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1376+851_1376+860d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099547 | |||||
chr2:112099549
|
TATATATA others(1): Show |
T | 8 | a0002c0002t0003g0133a0002c0002t0003g0134a0002c0002t0003g0136others(5): Show | 8 | NA18941.hp1 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+853_1376+860d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099549 | |||||
chr2:112099551
|
TATATAC | T | 54 | a0001c0001t0001g0205a0001c0001t0013g0284a0001c0001t0013g0286others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.1376+855_1376+860d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099551 | |||||
chr2:112099553
|
TATAC | T | 8 | a0001c0001t0001g0225a0001c0001t0001g0274a0001c0001t0013g0285others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+857_1376+860d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099553 | |||||
chr2:112099555
|
T | C | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376+857T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099555 | ||||||
chr2:112099555
|
TAC | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1376+868_1376+869d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099555 | |||||
chr2:112099557
|
C | T | 18 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0211others(15): Show | 18 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1376+859C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099557 | ||||||
chr2:112099854
|
G | T | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1377-768G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099854 | ||||||
chr2:112099882
|
C | CA | 50 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0001g0246others(47): Show | 51 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1377-722dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099882 | |||||
chr2:112099882
|
CA | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0208others(10): Show | 13 | HG02056.hp1 HG02109.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377-722delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099882 | |||||
chr2:112099956
|
T | A | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1377-666T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099956 | ||||||
chr2:112100021
|
A | G | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1377-601A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100021 | ||||||
chr2:112100065
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1377-557A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100065 | ||||||
chr2:112100233
|
C | T | 1 | a0001c0001t0040g0295 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1377-389C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100233 | ||||||
chr2:112100288
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1377-334A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100288 | ||||||
chr2:112100545
|
C | T | 73 | a0002c0002t0001g0018a0002c0002t0001g0199a0002c0002t0001g0207others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1377-77C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100545 | ||||||
chr2:112100908
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(97): Show | 106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1450+213C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112100908 | ||||||
chr2:112101442
|
T | C | 2 | a0002c0002t0003g0172a0002c0002t0003g0180 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1450+747T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101442 | ||||||
chr2:112101442
|
T | G | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+747T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101442 | ||||||
chr2:112101457
|
T | G | 3 | a0001c0001t0001g0123a0001c0001t0002g0287a0001c0001t0002g0297 | 3 | HG01167.hp2 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1450+762T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101457 | ||||||
chr2:112101617
|
T | C | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+922T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101617 | ||||||
chr2:112101890
|
GACAAGTT others(11): Show |
G | 1 | a0001c0001t0006g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1450+1217_1450+123 others(22): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr2 | 112101890 | |||||
chr2:112102007
|
T | A | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1450+1312T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102007 | ||||||
chr2:112102118
|
T | C | 5 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085others(2): Show | 5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450+1423T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102118 | ||||||
chr2:112102186
|
A | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1450+1491A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102186 | ||||||
chr2:112102346
|
G | GCAAGGCT others(2956): Show |
1 | a0001c0001t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1450+1663_1450+166 others(2967): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr2 | 112102346 | |||||
chr2:112102387
|
C | T | 2 | a0002c0002t0004g0111a0002c0002t0004g0115 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1450+1692C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102387 | ||||||
chr2:112102421
|
C | T | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1450+1726C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102421 | ||||||
chr2:112102491
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1450+1796C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102491 | ||||||
chr2:112102644
|
A | C | 2 | a0002c0002t0018g0293a0002c0002t0018g0294 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+1949A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102644 | ||||||
chr2:112102658
|
A | T | 2 | a0001c0001t0004g0082a0001c0001t0004g0083 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1450+1963A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102658 | ||||||
chr2:112102733
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450+2038T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102733 | ||||||
chr2:112102923
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1450+2228C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102923 | ||||||
chr2:112103124
|
T | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1450+2429T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103124 | ||||||
chr2:112103357
|
C | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1451-2645C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103357 | ||||||
chr2:112103382
|
A | G | 1 | a0002c0002t0012g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1451-2620A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103382 | ||||||
chr2:112103543
|
A | C | 1 | a0001c0001t0002g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1451-2459A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103543 | ||||||
chr2:112103575
|
T | G | 2 | a0001c0001t0007g0084a0001c0001t0007g0086 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2427T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103575 | ||||||
chr2:112103576
|
T | G | 2 | a0001c0001t0007g0084a0001c0001t0007g0086 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2426T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103576 | ||||||
chr2:112103578
|
T | C | 2 | a0001c0001t0007g0084a0001c0001t0007g0086 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2424T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103578 | ||||||
chr2:112103579
|
G | T | 2 | a0001c0001t0007g0084a0001c0001t0007g0086 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2423G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103579 | ||||||
chr2:112103610
|
C | T | 5 | a0002c0002t0001g0207a0002c0002t0003g0171a0002c0002t0003g0172others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-2392C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103610 | ||||||
chr2:112104385
|
T | C | 1 | a0001c0001t0030g0045 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1451-1617T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104385 | ||||||
chr2:112104510
|
A | G | 1 | a0001c0001t0011g0230 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1451-1492A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104510 | ||||||
chr2:112104575
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1451-1427A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104575 | ||||||
chr2:112104642
|
G | A | 4 | a0001c0001t0002g0067a0001c0001t0002g0069a0001c0001t0002g0072others(1): Show | 4 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451-1360G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104642 | ||||||
chr2:112105094
|
T | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1451-908T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105094 | ||||||
chr2:112105218
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0003g0151 | 2 | HG00558.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1451-784C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105218 | ||||||
chr2:112105317
|
G | A | 3 | a0001c0001t0002g0030a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG01361.hp1 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1451-685G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105317 | ||||||
chr2:112105390
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1451-612A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105390 | ||||||
chr2:112105567
|
T | G | 2 | a0001c0001t0001g0014a0002c0002t0012g0281 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1451-435T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105567 | ||||||
chr2:112105698
|
T | C | 1 | a0002c0002t0004g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1451-304T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105698 | ||||||
chr2:112105913
|
T | C | 2 | a0001c0001t0006g0233a0001c0001t0006g0239 | 2 | HG02027.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1451-89T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105913 | ||||||
chr2:112106161
|
C | G | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1524+86C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106161 | ||||||
chr2:112106225
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(6): Show | 10 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+150T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106225 | ||||||
chr2:112106250
|
A | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1524+175A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106250 | ||||||
chr2:112106274
|
A | G | 1 | a0002c0002t0004g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1524+199A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106274 | ||||||
chr2:112106353
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1524+278C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106353 | ||||||
chr2:112106515
|
A | G | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1524+440A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106515 | ||||||
chr2:112106568
|
A | AT | 11 | a0001c0001t0001g0195a0001c0001t0001g0226a0001c0001t0002g0031others(8): Show | 11 | HG00323.hp2 HG01978.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+507dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112106568 | |||||
chr2:112106684
|
A | G | 5 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+609A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106684 | ||||||
chr2:112106792
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1524+717C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106792 | ||||||
chr2:112107085
|
C | T | 2 | a0002c0002t0008g0142a0002c0002t0008g0146 | 2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1525-703C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107085 | ||||||
chr2:112107156
|
G | A | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-632G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107156 | ||||||
chr2:112107290
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1525-498A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107290 | ||||||
chr2:112107317
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | NA18747.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1525-471C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107317 | ||||||
chr2:112107357
|
C | CA | 36 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0193others(33): Show | 37 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1525-412dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107357 | |||||
chr2:112107357
|
C | CAA | 72 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0001t0001g0215others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.1525-413_1525-412d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107357 | |||||
chr2:112107396
|
A | AT | 8 | a0001c0001t0001g0215a0002c0002t0003g0134a0002c0002t0003g0136others(5): Show | 8 | NA18957.hp1 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-384dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107396 | |||||
chr2:112107496
|
A | G | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1525-292A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107496 | ||||||
chr2:112107514
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1525-274G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107514 | ||||||
chr2:112107677
|
A | G | 5 | a0002c0002t0001g0207a0002c0002t0003g0171a0002c0002t0003g0172others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-111A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107677 | ||||||
chr2:112107886
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1577+46G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112107886 | ||||||
chr2:112107940
|
G | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1577+100G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112107940 | ||||||
chr2:112107953
|
T | G | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1577+113T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112107953 | ||||||
chr2:112108055
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1577+215G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108055 | ||||||
chr2:112108089
|
A | G | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+249A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108089 | ||||||
chr2:112108262
|
A | G | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+422A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108262 | ||||||
chr2:112108393
|
T | C | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1577+553T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108393 | ||||||
chr2:112108527
|
A | C | 1 | a0001c0001t0002g0063 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1577+687A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108527 | ||||||
chr2:112108646
|
T | C | 3 | a0002c0002t0004g0022a0002c0002t0004g0126a0002c0002t0004g0128 | 3 | HG03195.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1577+806T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108646 | ||||||
chr2:112108743
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0003g0151 | 2 | HG00558.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1577+903C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108743 | ||||||
chr2:112108926
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0185 | 3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1577+1086C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108926 | ||||||
chr2:112108981
|
T | C | 21 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(18): Show | 23 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1577+1141T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108981 | ||||||
chr2:112109020
|
A | T | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1180A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109020 | ||||||
chr2:112109068
|
G | A | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1228G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109068 | ||||||
chr2:112109129
|
AT | A | 4 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0249others(1): Show | 4 | NA18992.hp1 NA19003.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1292delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109129 | |||||
chr2:112109272
|
C | A | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1432C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109272 | ||||||
chr2:112109409
|
T | C | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1577+1569T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109409 | ||||||
chr2:112109425
|
C | T | 5 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085others(2): Show | 5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1577+1585C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109425 | ||||||
chr2:112109664
|
C | CT | 24 | a0001c0001t0001g0032a0001c0001t0001g0217a0001c0001t0001g0232others(21): Show | 24 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1577+1846dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | |||||
chr2:112109664
|
CT | C | 10 | a0001c0001t0001g0248a0001c0001t0002g0053a0001c0001t0005g0260others(7): Show | 10 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+1846delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | |||||
chr2:112109664
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0007g0084a0001c0001t0007g0086 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1577+1836_1577+184 others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | |||||
chr2:112109699
|
T | C | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1577+1859T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109699 | ||||||
chr2:112109759
|
C | CT | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 126 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1577+1939dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109759 | |||||
chr2:112109759
|
C | CTT | 9 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0238others(6): Show | 9 | HG01192.hp2 HG01517.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1577+1938_1577+193 others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109759 | |||||
chr2:112109828
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1577+1988G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109828 | ||||||
chr2:112109915
|
C | T | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+2075C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109915 | ||||||
chr2:112109982
|
C | T | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1577+2142C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109982 | ||||||
chr2:112110270
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1577+2430C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110270 | ||||||
chr2:112110358
|
T | C | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1577+2518T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110358 | ||||||
chr2:112110584
|
C | A | 9 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085others(6): Show | 9 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1578-2315C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110584 | ||||||
chr2:112110732
|
G | A | 5 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0015g0170others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578-2167G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110732 | ||||||
chr2:112110738
|
C | G | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0286others(1): Show | 4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-2161C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110738 | ||||||
chr2:112110780
|
A | G | 2 | a0002c0002t0008g0142a0002c0002t0008g0146 | 2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1578-2119A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110780 | ||||||
chr2:112110791
|
A | G | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-2108A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110791 | ||||||
chr2:112110836
|
G | A | 5 | a0001c0001t0007g0084a0001c0001t0007g0086a0001c0001t0011g0184others(2): Show | 5 | HG01243.hp2 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578-2063G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110836 | ||||||
chr2:112110849
|
G | A | 29 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(26): Show | 30 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1578-2050G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110849 | ||||||
chr2:112110892
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1578-2007G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110892 | ||||||
chr2:112111271
|
C | G | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-1628C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111271 | ||||||
chr2:112111464
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 220 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1578-1435C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111464 | ||||||
chr2:112111695
|
GTGGAAAT others(31): Show |
G | 1 | a0002c0002t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1578-1202_1578-116 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112111695 | |||||
chr2:112111869
|
G | A | 2 | a0001c0001t0002g0119a0001c0001t0002g0229 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1578-1030G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111869 | ||||||
chr2:112111889
|
A | G | 4 | a0001c0004t0010g0288a0001c0004t0010g0289a0001c0004t0010g0290others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-1010A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111889 | ||||||
chr2:112111995
|
C | T | 1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1578-904C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111995 | ||||||
chr2:112112038
|
A | T | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1578-861A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112038 | ||||||
chr2:112112185
|
C | G | 23 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578-714C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112185 | ||||||
chr2:112112278
|
G | C | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1578-621G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112278 | ||||||
chr2:112112284
|
C | T | 5 | a0002c0002t0001g0018a0002c0002t0012g0280a0002c0002t0012g0282others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578-615C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112284 | ||||||
chr2:112112431
|
C | T | 6 | a0002c0002t0004g0017a0002c0002t0004g0023a0002c0002t0004g0024others(3): Show | 6 | HG01175.hp1 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578-468C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112431 | ||||||
chr2:112112448
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0185 | 3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1578-451A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112448 | ||||||
chr2:112112467
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1578-432C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112467 | ||||||
chr2:112112539
|
A | G | 2 | a0001c0001t0026g0015a0001c0001t0042g0299 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1578-360A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112539 | ||||||
chr2:112112596
|
G | C | 5 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085others(2): Show | 5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578-303G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112596 | ||||||
chr2:112112724
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1578-175A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112724 | ||||||
chr2:112112832
|
C | T | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1578-67C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112832 | ||||||
chr2:112112973
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1608+44C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112112973 | ||||||
chr2:112113042
|
CAG | C | 4 | a0001c0001t0011g0184a0001c0001t0011g0206a0001c0001t0011g0216others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+115_1608+116d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113042 | |||||
chr2:112113125
|
ATACT | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1608+201_1608+204d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113125 | |||||
chr2:112113153
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1608+224G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113153 | ||||||
chr2:112113424
|
C | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0297 | 2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1608+495C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113424 | ||||||
chr2:112113564
|
GGGATGGG others(7): Show |
G | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1608+637_1608+650d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113564 | |||||
chr2:112113573
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+644A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113573 | ||||||
chr2:112113575
|
G | T | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+646G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113575 | ||||||
chr2:112113578
|
T | A | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+649T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113578 | ||||||
chr2:112113610
|
CAAGATTC others(31): Show |
C | 2 | a0001c0001t0026g0015a0001c0005t0020g0292 | 2 | HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1608+782_1608+819d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113610 | |||||
chr2:112113617
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1608+688C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113617 | ||||||
chr2:112113700
|
CTACAGAA others(11): Show |
C | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+783_1608+800d others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113700 | |||||
chr2:112113711
|
T | G | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+782T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113711 | ||||||
chr2:112113735
|
A | C | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+806A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113735 | ||||||
chr2:112113736
|
C | T | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+807C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113736 | ||||||
chr2:112113749
|
G | T | 3 | a0001c0001t0005g0127a0001c0001t0015g0174a0001c0001t0042g0299 | 3 | HG02055.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1608+820G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113749 | ||||||
chr2:112113749
|
GGTAGCAT others(31): Show |
G | 3 | a0001c0001t0007g0084a0001c0001t0007g0085a0001c0001t0013g0285 | 3 | HG00323.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1608+896_1608+933d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113749 | |||||
chr2:112113761
|
G | GAAAGATT others(69): Show |
1 | a0001c0001t0013g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1608+895_1608+896i others(78): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113761 | |||||
chr2:112113785
|
GATGTAGC others(33): Show |
G | 1 | a0001c0001t0005g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+857_1608+896d others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113785 | ||||||
chr2:112113787
|
T | G | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+858T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113787 | ||||||
chr2:112113787
|
TGTAGCAT others(107): Show |
T | 5 | a0001c0001t0005g0008a0001c0001t0005g0258a0001c0001t0005g0259others(2): Show | 6 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+972_1608+1085 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113787 | |||||
chr2:112113787
|
TGTAGCAT others(183): Show |
T | 1 | a0001c0001t0028g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1608+934_1608+1123 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113787 | |||||
chr2:112113825
|
T | G | 6 | a0001c0001t0007g0021a0001c0001t0007g0086a0001c0001t0007g0110others(3): Show | 6 | HG01243.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+896T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113825 | ||||||
chr2:112113825
|
TGTAGCAT others(31): Show |
T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1608+972_1608+1009 others(41): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113825 | |||||
chr2:112113825
|
TGTAGCAT others(1361): Show |
T | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1608+972_1609-816d others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113825 | |||||
chr2:112113837
|
G | A | 5 | a0001c0001t0007g0021a0001c0001t0007g0086a0001c0001t0007g0110others(2): Show | 5 | HG01243.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+908G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113837 | ||||||
chr2:112113863
|
G | GGTAGCAT others(31): Show |
2 | a0001c0001t0001g0123a0001c0001t0027g0298 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1608+971_1608+972i others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113863 | |||||
chr2:112113863
|
G | T | 8 | a0001c0001t0002g0051a0001c0001t0007g0021a0001c0001t0007g0086others(5): Show | 8 | HG01243.hp2 HG02132.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1608+934G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113863 | ||||||
chr2:112113875
|
G | A | 3 | a0001c0001t0007g0084a0001c0001t0007g0085a0001c0001t0013g0285 | 3 | HG00323.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1608+946G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113875 | ||||||
chr2:112113901
|
G | GGTAGCAT others(69): Show |
1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1608+1047_1608+104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | |||||
chr2:112113901
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(46): Show | 49 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1608+972G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113901 | ||||||
chr2:112113901
|
GGTAGCAT others(31): Show |
G | 4 | a0002c0002t0003g0169a0002c0002t0008g0152a0002c0002t0008g0159others(1): Show | 4 | HG01109.hp1 HG01515.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+1010_1608+104 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | |||||
chr2:112113901
|
GGTAGCAT others(107): Show |
G | 1 | a0001c0001t0005g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1608+1048_1608+116 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | |||||
chr2:112113903
|
T | TAGCATTA others(6): Show |
1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+981_1608+982i others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113903 | |||||
chr2:112113925
|
ACTCTACA others(33): Show |
A | 2 | a0002c0002t0004g0113a0002c0002t0004g0114 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1608+999_1608+1038 others(43): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113925 | |||||
chr2:112113939
|
T | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1608+1010T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113939 | ||||||
chr2:112113949
|
C | T | 13 | a0001c0001t0005g0081a0001c0001t0005g0120a0001c0001t0005g0121others(10): Show | 13 | HG01070.hp2 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1608+1020C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113949 | ||||||
chr2:112113971
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1042G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113971 | ||||||
chr2:112113973
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1044A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113973 | ||||||
chr2:112113977
|
G | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1608+1048G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113977 | ||||||
chr2:112113977
|
GGTAGCAT others(31): Show |
G | 13 | a0001c0001t0001g0029a0001c0001t0002g0026a0001c0001t0002g0027others(10): Show | 13 | HG00323.hp1 HG01175.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1608+1314_1608+135 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113977 | |||||
chr2:112113977
|
GGTAGCAT others(69): Show |
G | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+1276_1608+135 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113977 | |||||
chr2:112113983
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1054A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113983 | ||||||
chr2:112113984
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1055T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113984 | ||||||
chr2:112113984
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1055T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113984 | ||||||
chr2:112113986
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1057A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113986 | ||||||
chr2:112113986
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1057A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113986 | ||||||
chr2:112114010
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1608+1081A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114010 | ||||||
chr2:112114015
|
T | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0065a0001c0001t0007g0084others(2): Show | 5 | HG00558.hp1 HG03239.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1086T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114015 | ||||||
chr2:112114021
|
A | T | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+1092A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114021 | ||||||
chr2:112114022
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(4): Show | 7 | HG02165.hp1 HG02886.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+1093T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114022 | ||||||
chr2:112114022
|
T | TACGAAGC others(13): Show |
1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+1093_1608+109 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114022 | ||||||
chr2:112114025
|
C | T | 6 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0258others(3): Show | 7 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+1096C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114025 | ||||||
chr2:112114032
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1608+1103A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114032 | ||||||
chr2:112114046
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1117A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114046 | ||||||
chr2:112114047
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1118G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114047 | ||||||
chr2:112114048
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1119A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114048 | ||||||
chr2:112114053
|
T | G | 7 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0258others(4): Show | 8 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+1124T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114053 | ||||||
chr2:112114060
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1608+1131T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114060 | ||||||
chr2:112114075
|
T | C | 1 | a0001c0001t0026g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+1146T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114075 | ||||||
chr2:112114085
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1156G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114085 | ||||||
chr2:112114091
|
T | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0002g0051others(3): Show | 6 | HG02055.hp2 HG02132.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+1162T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114091 | ||||||
chr2:112114093
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1164T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114093 | ||||||
chr2:112114098
|
T | C | 10 | a0001c0001t0001g0029a0002c0002t0004g0017a0002c0002t0004g0023others(7): Show | 10 | HG00323.hp1 HG01175.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1608+1169T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114098 | ||||||
chr2:112114104
|
AAAGATTC others(867): Show |
A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0002c0002t0012g0281 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1608+1200_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114104 | |||||
chr2:112114110
|
T | G | 2 | a0002c0002t0003g0172a0002c0002t0003g0180 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+1181T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114110 | ||||||
chr2:112114113
|
T | C | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+1184T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114113 | ||||||
chr2:112114115
|
ACTCTACA others(375): Show |
A | 1 | a0001c0001t0005g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+1189_1608+157 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114115 | |||||
chr2:112114129
|
T | G | 7 | a0001c0001t0025g0106a0002c0002t0003g0135a0002c0002t0003g0143others(4): Show | 7 | HG03239.hp2 NA18984.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+1200T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114129 | ||||||
chr2:112114167
|
T | TGTAGCAT others(107): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1275_1608+127 others(118): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114167 | |||||
chr2:112114174
|
T | C | 1 | a0002c0002t0003g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1608+1245T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114174 | ||||||
chr2:112114205
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1276T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114205 | ||||||
chr2:112114205
|
T | G | 2 | a0001c0001t0013g0285a0001c0001t0013g0286 | 2 | HG00323.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1608+1276T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114205 | ||||||
chr2:112114205
|
T | TGTAGCAT others(69): Show |
2 | a0001c0001t0002g0089a0001c0001t0002g0108 | 2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1608+1313_1608+131 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | |||||
chr2:112114205
|
TGTAGCAT others(107): Show |
T | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608+1352_1608+146 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | |||||
chr2:112114205
|
TGTAGCAT others(221): Show |
T | 1 | a0001c0001t0007g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1608+1352_1609-157 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | |||||
chr2:112114212
|
T | C | 5 | a0002c0002t0003g0135a0002c0002t0003g0143a0002c0002t0003g0167others(2): Show | 5 | NA18987.hp1 NA18995.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1283T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114212 | ||||||
chr2:112114238
|
AAAGATGT others(34): Show |
A | 1 | a0002c0002t0003g0155 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1608+1311_1608+135 others(45): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114238 | |||||
chr2:112114243
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1314T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114243 | ||||||
chr2:112114243
|
T | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(42): Show | 45 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1608+1314T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114243 | ||||||
chr2:112114243
|
TGTAGCAT others(31): Show |
T | 3 | a0001c0001t0001g0020a0001c0001t0007g0085a0002c0002t0003g0181 | 3 | HG02280.hp2 HG03579.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1608+1390_1608+142 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | |||||
chr2:112114243
|
TGTAGCAT others(69): Show |
T | 1 | a0002c0002t0003g0176 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1608+1352_1608+142 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | |||||
chr2:112114243
|
TGTAGCAT others(145): Show |
T | 3 | a0002c0002t0003g0135a0002c0002t0003g0165a0002c0002t0003g0167 | 3 | NA18947.hp2 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1608+1352_1608+150 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | |||||
chr2:112114281
|
G | C | 2 | a0001c0001t0002g0089a0001c0001t0002g0108 | 2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1608+1352G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114281 | ||||||
chr2:112114281
|
G | T | 26 | a0001c0001t0002g0065a0001c0001t0005g0008a0001c0001t0005g0077others(23): Show | 27 | HG00558.hp1 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1608+1352G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114281 | ||||||
chr2:112114319
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(7): Show | 10 | HG02886.hp1 HG02970.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+1390G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114319 | ||||||
chr2:112114319
|
G | T | 31 | a0001c0001t0002g0051a0001c0001t0002g0088a0001c0001t0002g0091others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1608+1390G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114319 | ||||||
chr2:112114319
|
GGTAGCAT others(31): Show |
G | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 67 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1608+1428_1608+146 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | |||||
chr2:112114319
|
GGTAGCAT others(69): Show |
G | 1 | a0002c0002t0004g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1608+1428_1608+150 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | |||||
chr2:112114319
|
GGTAGCAT others(145): Show |
G | 1 | a0001c0005t0020g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1608+1466_1609-153 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | |||||
chr2:112114319
|
GGTAGCAT others(1055): Show |
G | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1608+1466_1609-628 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | |||||
chr2:112114326
|
T | C | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608+1397T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114326 | ||||||
chr2:112114357
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1608+1428T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | ||||||
chr2:112114357
|
T | G | 34 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0005g0008others(31): Show | 35 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1608+1428T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | ||||||
chr2:112114357
|
T | TGTAGCAT others(31): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1465_1608+146 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114357 | |||||
chr2:112114357
|
TGTAGCAT others(31): Show |
T | 1 | a0001c0001t0026g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+1504_1608+154 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114357 | |||||
chr2:112114357
|
TGTAGCAT others(69): Show |
T | 4 | a0001c0001t0005g0257a0001c0001t0007g0021a0001c0001t0007g0110others(1): Show | 4 | HG00323.hp2 HG01891.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+1466_1608+154 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114357 | |||||
chr2:112114381
|
ACTCTACA others(33): Show |
A | 1 | a0002c0002t0004g0022 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1608+1455_1608+149 others(44): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114381 | |||||
chr2:112114395
|
C | G | 25 | a0001c0001t0001g0123a0001c0001t0005g0008a0001c0001t0005g0077others(22): Show | 26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+1466C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114395 | ||||||
chr2:112114395
|
C | T | 4 | a0001c0001t0013g0286a0002c0002t0003g0163a0002c0002t0003g0176others(1): Show | 4 | HG03669.hp2 NA18984.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+1466C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114395 | ||||||
chr2:112114395
|
CGTAGCAT others(107): Show |
C | 1 | a0002c0002t0003g0143 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1608+1504_1609-153 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114395 | |||||
chr2:112114403
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+1474T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114403 | ||||||
chr2:112114408
|
AAAGATTC others(563): Show |
A | 2 | a0001c0004t0010g0288a0001c0004t0010g0289 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1608+1504_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114408 | |||||
chr2:112114433
|
C | CGTAGCAT others(145): Show |
2 | a0001c0004t0010g0290a0001c0004t0010g0291 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1608+1541_1608+154 others(156): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | |||||
chr2:112114433
|
C | CGTAGCAT others(601): Show |
1 | a0002c0002t0003g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1608+1541_1608+154 others(612): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | |||||
chr2:112114433
|
C | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(7): Show | 10 | HG02109.hp1 HG02165.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1608+1504C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114433 | ||||||
chr2:112114433
|
C | T | 47 | a0001c0001t0002g0025a0001c0001t0002g0088a0001c0001t0002g0091others(44): Show | 48 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1608+1504C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114433 | ||||||
chr2:112114433
|
CGTAGCAT others(31): Show |
C | 2 | a0001c0001t0001g0019a0002c0002t0003g0163 | 2 | HG03041.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1609-1537_1609-150 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | |||||
chr2:112114433
|
CGTAGCAT others(69): Show |
C | 4 | a0001c0001t0001g0187a0001c0001t0001g0306a0002c0002t0004g0111others(1): Show | 4 | HG02145.hp1 HG02572.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1575_1609-150 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | |||||
chr2:112114433
|
CGTAGCAT others(221): Show |
C | 5 | a0001c0001t0001g0209a0002c0002t0003g0141a0002c0002t0003g0156others(2): Show | 5 | HG01109.hp1 HG02735.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1542_1609-138 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | |||||
chr2:112114471
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1608+1542T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114471 | ||||||
chr2:112114471
|
T | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 51 | HG00408.hp1 HG00738.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1608+1542T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114471 | ||||||
chr2:112114497
|
T | TCTACAGA others(865): Show |
2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1609-1538_1609-153 others(876): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114497 | |||||
chr2:112114509
|
T | C | 38 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0123others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1609-1575T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114509 | ||||||
chr2:112114509
|
T | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1609-1575T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114509 | ||||||
chr2:112114510
|
GTAGCATT others(30): Show |
G | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1609-1573_1609-153 others(41): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114510 | ||||||
chr2:112114547
|
T | C | 9 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0306others(6): Show | 9 | HG01256.hp2 HG01258.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1609-1537T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114547 | ||||||
chr2:112114547
|
T | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1609-1537T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114547 | ||||||
chr2:112114585
|
G | C | 6 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0003g0176others(3): Show | 6 | HG01257.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1499G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114585 | ||||||
chr2:112114585
|
G | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1609-1499G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114585 | ||||||
chr2:112114609
|
ACT | A | 19 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1609-1472_1609-147 others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114609 | |||||
chr2:112114623
|
G | C | 5 | a0002c0002t0001g0207a0002c0002t0003g0143a0002c0002t0003g0165others(2): Show | 5 | HG02257.hp1 NA18947.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-1461G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114623 | ||||||
chr2:112114623
|
G | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0220others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1609-1461G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114623 | ||||||
chr2:112114636
|
AAAGATTC others(335): Show |
A | 33 | a0002c0002t0001g0018a0002c0002t0003g0004a0002c0002t0003g0130others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1609-1423_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114636 | |||||
chr2:112114661
|
T | C | 8 | a0002c0002t0003g0135a0002c0002t0003g0143a0002c0002t0003g0155others(5): Show | 8 | NA18947.hp2 NA18984.hp2 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-1423T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114661 | ||||||
chr2:112114661
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1609-1423T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114661 | ||||||
chr2:112114674
|
AAAGATTC others(297): Show |
A | 28 | a0001c0001t0001g0220a0001c0001t0001g0221a0002c0002t0001g0199others(25): Show | 28 | HG00323.hp1 HG01081.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1609-1271_1609-968 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114674 | |||||
chr2:112114674
|
AAAGATTC others(335): Show |
A | 1 | a0002c0002t0003g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-1271_1609-930 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114674 | |||||
chr2:112114699
|
G | C | 11 | a0001c0001t0001g0209a0002c0002t0003g0135a0002c0002t0003g0141others(8): Show | 11 | HG01109.hp1 HG02735.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.1609-1385G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114699 | ||||||
chr2:112114699
|
G | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(45): Show | 50 | HG00408.hp1 HG00738.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1609-1385G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114699 | ||||||
chr2:112114712
|
AAAGATTC others(259): Show |
A | 1 | a0002c0002t0004g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1609-1271_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114712 | |||||
chr2:112114728
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1609-1356A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114728 | ||||||
chr2:112114737
|
G | C | 5 | a0002c0002t0003g0135a0002c0002t0003g0143a0002c0002t0003g0163others(2): Show | 5 | NA18947.hp2 NA18984.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-1347G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114737 | ||||||
chr2:112114737
|
G | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1609-1347G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114737 | ||||||
chr2:112114775
|
G | C | 3 | a0002c0002t0003g0135a0002c0002t0003g0163a0002c0002t0003g0167 | 3 | NA18984.hp2 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1609-1309G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114775 | ||||||
chr2:112114775
|
G | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1609-1309G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114775 | ||||||
chr2:112114788
|
AAAGATTC others(183): Show |
A | 2 | a0002c0002t0004g0111a0002c0002t0004g0115 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1609-1271_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114788 | |||||
chr2:112114813
|
T | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(56): Show | 60 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1609-1271T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114813 | ||||||
chr2:112114826
|
AAAGATTC others(145): Show |
A | 1 | a0002c0002t0003g0181 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1609-1233_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114826 | |||||
chr2:112114851
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(52): Show | 55 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1609-1233T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114851 | ||||||
chr2:112114851
|
T | TGTAGCAT others(31): Show |
1 | a0001c0001t0002g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1609-1157_1609-112 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114851 | |||||
chr2:112114851
|
TGTAGCAT others(31): Show |
T | 4 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0024g0012others(1): Show | 4 | HG00323.hp2 HG02723.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1157_1609-112 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114851 | |||||
chr2:112114858
|
T | TCGACCTA others(3): Show |
1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1609-1226_1609-122 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114858 | ||||||
chr2:112114864
|
AAAGATTC others(107): Show |
A | 6 | a0001c0001t0001g0009a0001c0001t0036g0001a0002c0002t0003g0156others(3): Show | 6 | HG01109.hp1 HG02735.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-1119_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114864 | |||||
chr2:112114889
|
G | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(45): Show | 49 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1609-1195G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114889 | ||||||
chr2:112114902
|
AAAGATTC others(69): Show |
A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(36): Show | 41 | HG00408.hp1 HG00738.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1609-1119_1609-104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114902 | |||||
chr2:112114902
|
AAAGATTC others(107): Show |
A | 1 | a0002c0002t0003g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1609-1119_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114902 | |||||
chr2:112114927
|
G | GGTAGCAT others(31): Show |
1 | a0001c0001t0027g0298 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1609-1144_1609-110 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114927 | |||||
chr2:112114927
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1609-1157G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114927 | ||||||
chr2:112114935
|
T | C | 2 | a0001c0004t0010g0290a0001c0004t0010g0291 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1609-1149T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114935 | ||||||
chr2:112114940
|
AAAGATTC others(31): Show |
A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(54): Show | 58 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1609-1119_1609-108 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114940 | |||||
chr2:112114940
|
AAAGATTC others(69): Show |
A | 3 | a0001c0001t0001g0245a0001c0001t0001g0270a0002c0002t0003g0143 | 3 | HG04115.hp2 NA18974.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1609-1119_1609-104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114940 | |||||
chr2:112114949
|
T | C | 1 | a0001c0001t0042g0299 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1609-1135T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114949 | ||||||
chr2:112114965
|
T | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1609-1119T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114965 | ||||||
chr2:112114965
|
T | TGTAGCAT others(31): Show |
4 | a0001c0001t0001g0123a0001c0001t0002g0049a0001c0001t0002g0093others(1): Show | 4 | HG02109.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1107_1609-110 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114965 | |||||
chr2:112114965
|
TGTAGCAT others(31): Show |
T | 2 | a0001c0001t0001g0306a0001c0001t0026g0015 | 2 | HG03453.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1609-1106_1609-106 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114965 | |||||
chr2:112114978
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0019others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1609-1106G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114978 | ||||||
chr2:112115071
|
C | A | 4 | a0002c0002t0001g0199a0002c0002t0001g0222a0002c0002t0003g0137others(1): Show | 4 | HG02056.hp2 HG04115.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1013C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115071 | ||||||
chr2:112115079
|
G | T | 1 | a0001c0001t0007g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-1005G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115079 | ||||||
chr2:112115117
|
G | T | 1 | a0001c0001t0013g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1609-967G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115117 | ||||||
chr2:112115141
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ACTCTACA others(33): Show |
A | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1609-940_1609-901d others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115141 | |||||
chr2:112115155
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G | T | 4 | a0001c0001t0005g0127a0001c0001t0007g0021a0001c0001t0007g0085others(1): Show | 4 | HG02055.hp2 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-929G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115155 | ||||||
chr2:112115155
|
GGTAGCAT others(107): Show |
G | 1 | a0001c0001t0007g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-891_1609-778d others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115155 | |||||
chr2:112115193
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G | T | 4 | a0001c0001t0001g0225a0001c0001t0002g0212a0001c0001t0013g0286others(1): Show | 4 | HG02145.hp2 HG02165.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-891G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115193 | ||||||
chr2:112115231
|
G | T | 26 | a0001c0001t0001g0225a0001c0001t0002g0212a0001c0001t0005g0008others(23): Show | 27 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1609-853G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115231 | ||||||
chr2:112115231
|
GGTAGCAT others(31): Show |
G | 3 | a0001c0001t0001g0250a0001c0001t0007g0021a0001c0001t0007g0085 | 3 | HG01074.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1609-750_1609-713d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115231 | |||||
chr2:112115269
|
T | G | 33 | a0001c0001t0001g0187a0001c0001t0001g0246a0001c0001t0002g0076others(30): Show | 34 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1609-815T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115269 | ||||||
chr2:112115269
|
T | GGTAGCAT others(31): Show |
1 | a0002c0002t0003g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1609-853_1609-816d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115269 | ||||||
chr2:112115269
|
T | TGTAGCAT others(219): Show |
1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-789_1609-788i others(228): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115269 | |||||
chr2:112115269
|
T | TGTAGCAT others(219): Show |
1 | a0001c0001t0013g0286 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1609-789_1609-788i others(228): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115269 | |||||
chr2:112115295
|
TCTACAGA others(67): Show |
T | 2 | a0001c0001t0005g0127a0001c0001t0042g0299 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1609-712_1609-639d others(76): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115295 | |||||
chr2:112115307
|
T | G | 22 | a0001c0001t0002g0212a0001c0001t0005g0008a0001c0001t0005g0077others(19): Show | 23 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1609-777T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115307 | ||||||
chr2:112115309
|
T | G | 4 | a0001c0001t0001g0225a0002c0002t0014g0149a0002c0002t0014g0150others(1): Show | 4 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-775T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115309 | ||||||
chr2:112115331
|
ACTCTACA others(69): Show |
A | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1609-750_1609-675d others(78): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115331 | |||||
chr2:112115333
|
TCTACAGA others(29): Show |
T | 1 | a0001c0001t0026g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-712_1609-677d others(38): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115333 | |||||
chr2:112115369
|
A | ACT | 27 | a0001c0001t0001g0225a0001c0001t0002g0076a0001c0001t0002g0212others(24): Show | 28 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1609-714_1609-713d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115369 | |||||
chr2:112115380
|
A | T | 3 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085 | 3 | HG03098.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1609-704A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115380 | ||||||
chr2:112115381
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-703T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115381 | ||||||
chr2:112115383
|
T | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1609-701T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115383 | ||||||
chr2:112115405
|
ACT | A | 6 | a0001c0001t0002g0076a0001c0001t0007g0086a0001c0001t0013g0284others(3): Show | 6 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-676_1609-675d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115405 | |||||
chr2:112115418
|
A | T | 2 | a0001c0001t0007g0086a0001c0001t0007g0110 | 2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1609-666A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115418 | ||||||
chr2:112115419
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1609-665T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115419 | ||||||
chr2:112115419
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-665T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115419 | ||||||
chr2:112115419
|
TGTAGCAT others(31): Show |
T | 3 | a0001c0001t0007g0021a0001c0001t0007g0084a0001c0001t0007g0085 | 3 | HG03098.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1609-627_1609-590d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115419 | |||||
chr2:112115457
|
G | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1609-627G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115457 | ||||||
chr2:112115470
|
A | G | 20 | a0001c0001t0005g0008a0001c0001t0005g0077a0001c0001t0005g0081others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1609-614A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115470 | ||||||
chr2:112115604
|
A | T | 1 | a0001c0001t0002g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1609-480A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115604 | ||||||
chr2:112115834
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1609-250C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115834 | ||||||
chr2:112115834
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1609-250C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115834 | ||||||
chr2:112115955
|
T | A | 1 | a0001c0001t0002g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1609-129T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115955 | ||||||
chr2:112116020
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1609-64T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112116020 |