| geneid | 57583 |
|---|---|
| ensemblid | ENSG00000146433.10 |
| hgncid | 20958 |
| symbol | TMEM181 |
| name | transmembrane protein 181 |
| refseq_nuc | NM_001376852.1 |
| refseq_prot | NP_001363781.1 |
| ensembl_nuc | ENST00000684151.1 |
| ensembl_prot | ENSP00000507085.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 158560091 |
| end | 158635429 |
| strand | + |
| ver | v1.2 |
| region | chr6:158560091-158635429 |
| region5000 | chr6:158555091-158640429 |
| regionname0 | TMEM181_chr6_158560091_158635429 |
| regionname5000 | TMEM181_chr6_158555091_158640429 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 475 | 328 | 86 | 73 | 117 | 12 | 38 | 95 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0002 | 0/0 | 475 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0003 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0004 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0005 | 0/0 | 475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0006 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1428 | 322 | 82 | 72 | 117 | 12 | 37 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0002 | 0/0 | 1428 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0003 | 0/0 | 1428 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0004 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0005 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0006 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0007 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| c0008 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3676 | 175 | 30 | 38 | 76 | 7 | 22 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0002 | 0/0 | 3676 | 47 | 15 | 3 | 25 | 0 | 4 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0003 | 0/0 | 3676 | 33 | 14 | 13 | 0 | 1 | 5 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0004 | 0/0 | 3674 | 27 | 9 | 15 | 1 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0005 | 0/0 | 3674 | 14 | 14 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0006 | 0/0 | 3676 | 7 | 1 | 3 | 0 | 3 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0007 | 0/0 | 3676 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0008 | 0/0 | 3675 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0009 | 0/0 | 3676 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0010 | 0/0 | 3676 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0011 | 0/0 | 3657 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0012 | 0/0 | 3676 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0013 | 0/0 | 3676 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0014 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0015 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0016 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0017 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0018 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0019 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0020 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0021 | 0/0 | 3676 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0022 | 0/0 | 3689 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0023 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0024 | 0/0 | 3674 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0025 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0026 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0027 | 0/0 | 3674 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0028 | 0/0 | 3674 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0029 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0030 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| t0031 | 0/0 | 3676 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0008 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 322 | 82 | 72 | 117 | 12 | 37 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0002 | 0/0 | 1428 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0008 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0002c0003 | 0/0 | 1428 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0003c0004 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0004c0005 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0005c0006 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0006c0007 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5103 | 168 | 26 | 37 | 75 | 7 | 21 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0002 | 0/0 | 5103 | 47 | 15 | 3 | 25 | 0 | 4 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0003 | 0/0 | 5103 | 32 | 13 | 13 | 0 | 1 | 5 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0004 | 0/0 | 5101 | 25 | 9 | 13 | 1 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0005 | 0/0 | 5101 | 14 | 14 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0006 | 0/0 | 5103 | 7 | 1 | 3 | 0 | 3 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0007 | 0/0 | 5103 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0008 | 0/0 | 5102 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0009 | 0/0 | 5103 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0010 | 0/0 | 5103 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0011 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0012 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0013 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0014 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0015 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0017 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0018 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0019 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0020 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0021 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0022 | 0/0 | 5116 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0023 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0024 | 0/0 | 5101 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0025 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0026 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0027 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0028 | 0/0 | 5101 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0029 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0001t0030 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0002t0001 | 0/0 | 5103 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0002t0031 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0001c0008t0001 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0002c0003t0004 | 0/0 | 5101 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0003c0004t0001 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0004c0005t0003 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0005c0006t0001 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| a0006c0007t0016 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | copy fasta | chr6 | 158555091 | 158640429 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0008 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0004 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0010g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0013g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0014g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0017g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0018g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0019g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0021g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0022g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0023g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0024g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0026g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0027g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0028g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0030g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0031g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0002c0003t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0003c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0004c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0005c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0006c0007t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0004 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00423 | hp1 | a0001 | c0001 | t0015 | g0028 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0285 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00733 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00741 | hp2 | a0001 | c0001 | t0028 | g0121 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01175 | hp2 | a0005 | c0006 | t0001 | g0043 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0061 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0113 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0065 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01934 | hp1 | a0001 | c0002 | t0031 | g0097 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01981 | hp2 | a0001 | c0001 | t0022 | g0243 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0284 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0280 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02300 | hp2 | a0001 | c0001 | t0024 | g0119 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02572 | hp2 | a0004 | c0005 | t0003 | g0020 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0041 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02683 | hp2 | a0001 | c0008 | t0001 | g0073 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0216 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0128 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0114 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0034 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03516 | hp2 | a0006 | c0007 | t0016 | g0130 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0306 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04204 | hp1 | a0001 | c0001 | t0027 | g0079 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | YRI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | YRI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18747 | hp1 | a0001 | c0001 | t0018 | g0277 | EAS | CHB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0281 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18980 | hp2 | a0001 | c0001 | t0014 | g0264 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18981 | hp1 | a0001 | c0001 | t0011 | g0051 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18987 | hp2 | a0001 | c0001 | t0029 | g0162 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18994 | hp1 | a0001 | c0001 | t0017 | g0295 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19012 | hp2 | a0001 | c0001 | t0019 | g0017 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19088 | hp1 | a0001 | c0001 | t0030 | g0031 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0256 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ASW | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ASW | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20752 | hp2 | a0001 | c0001 | t0013 | g0137 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0229 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | GIH | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01123 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0129 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG06807 | hp1 | a0001 | c0001 | t0020 | g0203 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:158585312
|
A | G | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.268A>G | p.Ile90Val | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/17 | 402/5103 | 268/1428 | 90/475 | chr6 | 158585312 | ||
| chr6:158608455
|
C | T | 1 | a0002 | 2 | HG00733.hp1 HG01123.hp2 |
missense_variant | MODERATE | c.796C>T | p.Arg266Cys | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 9/17 | 930/5103 | 796/1428 | 266/475 | chr6 | 158608455 | ||
| chr6:158623564
|
A | G | 1 | a0005 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.911A>G | p.His304Arg | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/17 | 1045/5103 | 911/1428 | 304/475 | chr6 | 158623564 | ||
| chr6:158631860
|
A | C | 1 | a0004 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1400A>C | p.Lys467Thr | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1534/5103 | 1400/1428 | 467/475 | chr6 | 158631860 | ||
| chr6:158631871
|
G | A | 1 | a0003 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1545/5103 | 1411/1428 | 471/475 | chr6 | 158631871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:158573465
|
C | G | 1 | a0001c0008 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.54C>G | p.Val18Val | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/17 | 188/5103 | 54/1428 | 18/475 | chr6 | 158573465 | ||
| chr6:158605347
|
T | C | 1 | a0001c0002 | 5 | HG01934.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.573T>C | p.Thr191Thr | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/17 | 707/5103 | 573/1428 | 191/475 | chr6 | 158605347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:158631935
|
C | T | 1 | a0001c0002t0031 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 47 | chr6 | 158631935 | |||||
| chr6:158632001
|
C | G | 1 | a0001c0001t0030 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 113 | chr6 | 158632001 | |||||
| chr6:158632216
|
ATCATTCA others(12): Show |
A | 1 | a0001c0001t0011 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332_*350delTTCACT others(13): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 332 | INFO_REALIGN_3_PRIME | chr6 | 158632216 | ||||
| chr6:158632311
|
G | C | 3 | a0001c0001t0003a0001c0001t0012a0004c0005t0003 | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 423 | chr6 | 158632311 | |||||
| chr6:158632311
|
G | T | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | 95 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 423 | chr6 | 158632311 | |||||
| chr6:158632414
|
T | TGGTCAGT others(6): Show |
1 | a0001c0001t0022 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*528_*540dupGTCAGT others(7): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 541 | INFO_REALIGN_3_PRIME | chr6 | 158632414 | ||||
| chr6:158632434
|
G | A | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(6): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*546G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 546 | chr6 | 158632434 | |||||
| chr6:158632465
|
G | A | 1 | a0001c0001t0023 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 577 | chr6 | 158632465 | |||||
| chr6:158632536
|
AG | A | 1 | a0001c0001t0008 | 3 | HG02071.hp2 HG02080.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*651delG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 651 | INFO_REALIGN_3_PRIME | chr6 | 158632536 | ||||
| chr6:158632676
|
G | A | 1 | a0001c0001t0024 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*788G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 788 | chr6 | 158632676 | |||||
| chr6:158632794
|
G | A | 1 | a0001c0001t0013 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*906G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 906 | chr6 | 158632794 | |||||
| chr6:158633016
|
C | T | 1 | a0001c0001t0028 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1128C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1128 | chr6 | 158633016 | |||||
| chr6:158633095
|
T | C | 1 | a0001c0001t0006 | 7 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1207T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1207 | chr6 | 158633095 | |||||
| chr6:158633229
|
G | A | 1 | a0001c0001t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1341 | chr6 | 158633229 | |||||
| chr6:158633335
|
G | A | 1 | a0001c0001t0014 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1447G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1447 | chr6 | 158633335 | |||||
| chr6:158633395
|
G | A | 3 | a0001c0001t0003a0001c0001t0012a0004c0005t0003 | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1507 | chr6 | 158633395 | |||||
| chr6:158633454
|
C | A | 1 | a0001c0001t0007 | 3 | NA18999.hp2 NA19062.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1566 | chr6 | 158633454 | |||||
| chr6:158633585
|
G | A | 1 | a0001c0001t0015 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1697 | chr6 | 158633585 | |||||
| chr6:158633599
|
G | GGT | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(6): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1712_*1713dupGT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1714 | INFO_REALIGN_3_PRIME | chr6 | 158633599 | ||||
| chr6:158633711
|
A | C | 1 | a0001c0001t0027 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1823 | chr6 | 158633711 | |||||
| chr6:158633711
|
A | G | 2 | a0001c0001t0002a0001c0001t0029 | 48 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1823A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1823 | chr6 | 158633711 | |||||
| chr6:158633758
|
G | A | 1 | a0006c0007t0016 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1870G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1870 | chr6 | 158633758 | |||||
| chr6:158633842
|
C | G | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1954C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1954 | chr6 | 158633842 | |||||
| chr6:158633860
|
A | G | 2 | a0001c0001t0020a0006c0007t0016 | 2 | HG03516.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1972A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 1972 | chr6 | 158633860 | |||||
| chr6:158634161
|
AAGTT | A | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(6): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2276_*2279delTTAG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2276 | INFO_REALIGN_3_PRIME | chr6 | 158634161 | ||||
| chr6:158634188
|
C | T | 1 | a0001c0001t0012 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2300C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2300 | chr6 | 158634188 | |||||
| chr6:158634228
|
G | T | 6 | a0001c0001t0004a0001c0001t0023a0001c0001t0024others(3): Show | 31 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2340G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2340 | chr6 | 158634228 | |||||
| chr6:158634250
|
T | C | 6 | a0001c0001t0004a0001c0001t0023a0001c0001t0024others(3): Show | 31 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2362T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2362 | chr6 | 158634250 | |||||
| chr6:158634307
|
G | A | 1 | a0001c0001t0017 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2419G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2419 | chr6 | 158634307 | |||||
| chr6:158634337
|
G | A | 1 | a0001c0001t0018 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2449G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2449 | chr6 | 158634337 | |||||
| chr6:158634391
|
A | C | 1 | a0001c0001t0010 | 2 | HG00673.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2503A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2503 | chr6 | 158634391 | |||||
| chr6:158634609
|
T | C | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | 95 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2721T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2721 | chr6 | 158634609 | |||||
| chr6:158634853
|
G | A | 1 | a0001c0001t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2965G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 2965 | chr6 | 158634853 | |||||
| chr6:158634898
|
C | T | 2 | a0001c0001t0002a0001c0001t0029 | 48 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3010C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3010 | chr6 | 158634898 | |||||
| chr6:158635005
|
G | A | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(6): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3117G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3117 | chr6 | 158635005 | |||||
| chr6:158635016
|
T | G | 1 | a0001c0001t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3128T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3128 | chr6 | 158635016 | |||||
| chr6:158635030
|
A | G | 1 | a0001c0001t0029 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3142A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3142 | chr6 | 158635030 | |||||
| chr6:158635109
|
T | G | 1 | a0001c0001t0019 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3221T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3221 | chr6 | 158635109 | |||||
| chr6:158635372
|
G | A | 1 | a0001c0001t0009 | 2 | HG02683.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3484G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 17/17 | 3484 | chr6 | 158635372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:158560243
|
G | C | 1 | a0001c0001t0002g0018 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.8+11G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560243 | ||||||
| chr6:158560250
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8+18C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560250 | ||||||
| chr6:158560311
|
C | T | 1 | a0001c0001t0003g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.8+79C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560311 | ||||||
| chr6:158560414
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 232 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.8+182C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560414 | ||||||
| chr6:158560466
|
T | G | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8+234T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560466 | ||||||
| chr6:158560473
|
C | G | 6 | a0001c0001t0002g0100a0001c0001t0005g0096a0001c0002t0001g0009others(3): Show | 7 | HG01934.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.8+241C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560473 | ||||||
| chr6:158560584
|
G | T | 1 | a0001c0001t0001g0311 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.8+352G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560584 | ||||||
| chr6:158560590
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0309a0001c0001t0001g0310others(1): Show | 4 | NA18960.hp2 NA19011.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.8+358C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560590 | ||||||
| chr6:158560665
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8+433G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560665 | ||||||
| chr6:158560751
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8+519C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560751 | ||||||
| chr6:158560777
|
T | A | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0003g0116others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+545T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560777 | ||||||
| chr6:158560790
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0003g0308a0001c0001t0003g0312 | 3 | HG02717.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.8+558C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560790 | ||||||
| chr6:158560815
|
CT | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(308): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.8+595delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158560815 | |||||
| chr6:158560858
|
T | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(219): Show | 230 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.8+626T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560858 | ||||||
| chr6:158560943
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8+711G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158560943 | ||||||
| chr6:158561034
|
A | C | 79 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0131others(76): Show | 81 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.8+802A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561034 | ||||||
| chr6:158561169
|
C | T | 39 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(36): Show | 41 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.8+937C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561169 | ||||||
| chr6:158561173
|
G | GGCT | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | NA18962.hp1 NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.8+943_8+945dupCTG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158561173 | |||||
| chr6:158561191
|
A | T | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194 | 3 | NA19063.hp2 NA19064.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.8+959A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561191 | ||||||
| chr6:158561423
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8+1191T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561423 | ||||||
| chr6:158561716
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 236 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.8+1484G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561716 | ||||||
| chr6:158561720
|
C | T | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8+1488C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561720 | ||||||
| chr6:158561881
|
A | C | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.8+1649A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561881 | ||||||
| chr6:158561889
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.8+1657G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561889 | ||||||
| chr6:158561952
|
C | G | 23 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0211others(20): Show | 24 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.8+1720C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561952 | ||||||
| chr6:158562138
|
T | G | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0003g0116others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+1906T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562138 | ||||||
| chr6:158562214
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.8+1982A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562214 | ||||||
| chr6:158562316
|
G | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 157 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.8+2084G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562316 | ||||||
| chr6:158562446
|
T | G | 2 | a0001c0001t0003g0132a0001c0001t0005g0133 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.8+2214T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562446 | ||||||
| chr6:158562446
|
T | TTG | 19 | a0001c0001t0001g0095a0001c0001t0001g0299a0001c0001t0001g0300others(16): Show | 20 | HG00673.hp2 HG01168.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.8+2242_8+2243dupGT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTG | 37 | a0001c0001t0001g0017a0001c0001t0001g0159a0001c0001t0001g0172others(34): Show | 39 | HG00558.hp1 HG00735.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.8+2240_8+2243dupGT others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTGTG | 20 | a0001c0001t0001g0103a0001c0001t0001g0195a0001c0001t0001g0196others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.8+2238_8+2243dupGT others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTGTGT others(1): Show |
37 | a0001c0001t0001g0117a0001c0001t0001g0183a0001c0001t0001g0187others(34): Show | 39 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.8+2236_8+2243dupGT others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTGTGT others(3): Show |
14 | a0001c0001t0003g0019a0001c0001t0003g0225a0001c0001t0003g0226others(11): Show | 14 | HG00741.hp1 HG01074.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.8+2234_8+2243dupGT others(8): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTGTGT others(5): Show |
6 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.8+2232_8+2243dupGT others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
T | TTGTGTGT others(7): Show |
1 | a0006c0007t0016g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8+2230_8+2243dupGT others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562446
|
TTGTG | T | 3 | a0001c0001t0004g0104a0001c0001t0005g0101a0004c0005t0003g0020 | 3 | HG02572.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.8+2240_8+2243delGT others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562446 | |||||
| chr6:158562462
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8+2230G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562462 | ||||||
| chr6:158562466
|
GTGTGTGT others(3): Show |
G | 5 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0004g0135others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.8+2236_8+2245delGT others(8): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158562466 | |||||
| chr6:158562476
|
C | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(126): Show | 134 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.8+2244C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562476 | ||||||
| chr6:158562476
|
CTT | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 16 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.8+2245_8+2246delTT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562476 | ||||||
| chr6:158562478
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(133): Show | 141 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.8+2246T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562478 | ||||||
| chr6:158562488
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8+2256G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562488 | ||||||
| chr6:158562591
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 235 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.8+2359A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562591 | ||||||
| chr6:158562744
|
G | A | 8 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0124others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.8+2512G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562744 | ||||||
| chr6:158562798
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.8+2566T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562798 | ||||||
| chr6:158562847
|
C | G | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8+2615C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158562847 | ||||||
| chr6:158563241
|
T | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 227 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.8+3009T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563241 | ||||||
| chr6:158563331
|
T | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 233 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.8+3099T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563331 | ||||||
| chr6:158563334
|
G | C | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00609.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.8+3102G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563334 | ||||||
| chr6:158563435
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.8+3203C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563435 | ||||||
| chr6:158563544
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.8+3312C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563544 | ||||||
| chr6:158563553
|
C | G | 1 | a0001c0001t0003g0224 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8+3321C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563553 | ||||||
| chr6:158563582
|
T | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(216): Show | 227 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.8+3350T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563582 | ||||||
| chr6:158563649
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.8+3417A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563649 | ||||||
| chr6:158563679
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0143others(10): Show | 15 | HG00438.hp1 HG01243.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.8+3447C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563679 | ||||||
| chr6:158563680
|
G | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 12 | HG00423.hp1 HG00438.hp2 HG03492.hp1 others(9): Show |
intron_variant | MODIFIER | c.8+3448G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563680 | ||||||
| chr6:158563701
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(310): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.8+3469A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563701 | ||||||
| chr6:158563729
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 236 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.8+3497A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563729 | ||||||
| chr6:158563740
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.8+3508A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563740 | ||||||
| chr6:158563749
|
C | T | 3 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022 | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.8+3517C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563749 | ||||||
| chr6:158563787
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8+3555T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563787 | ||||||
| chr6:158563969
|
G | A | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8+3737G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563969 | ||||||
| chr6:158564234
|
C | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.8+4002C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564234 | ||||||
| chr6:158564269
|
C | T | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8+4037C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564269 | ||||||
| chr6:158564311
|
C | T | 2 | a0001c0001t0003g0222a0001c0001t0003g0223 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.8+4079C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564311 | ||||||
| chr6:158564704
|
AGATGAGG others(36): Show |
A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4474_8+4516delAT others(41): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158564704 | |||||
| chr6:158564761
|
G | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4529G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564761 | ||||||
| chr6:158564763
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4531A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564763 | ||||||
| chr6:158564781
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4549C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564781 | ||||||
| chr6:158564782
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4550A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564782 | ||||||
| chr6:158564783
|
G | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4551G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564783 | ||||||
| chr6:158564789
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4557A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564789 | ||||||
| chr6:158564793
|
C | T | 6 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0001t0002g0184others(3): Show | 6 | NA18947.hp1 NA18961.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.8+4561C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564793 | ||||||
| chr6:158564797
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4565A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564797 | ||||||
| chr6:158564802
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4570G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564802 | ||||||
| chr6:158564803
|
G | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4571G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564803 | ||||||
| chr6:158564804
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4572G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564804 | ||||||
| chr6:158564806
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(220): Show | 231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.8+4574C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564806 | ||||||
| chr6:158564809
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4577A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564809 | ||||||
| chr6:158564811
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4579G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564811 | ||||||
| chr6:158564825
|
T | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4593T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564825 | ||||||
| chr6:158564837
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4605G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564837 | ||||||
| chr6:158564838
|
G | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4606G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564838 | ||||||
| chr6:158564849
|
A | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4617A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564849 | ||||||
| chr6:158564857
|
G | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4625G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564857 | ||||||
| chr6:158564862
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4630A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564862 | ||||||
| chr6:158564868
|
C | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4636C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564868 | ||||||
| chr6:158564878
|
T | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4646T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564878 | ||||||
| chr6:158564901
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4669A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564901 | ||||||
| chr6:158564908
|
T | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4676T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564908 | ||||||
| chr6:158564909
|
T | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4677T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564909 | ||||||
| chr6:158564912
|
T | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4680T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564912 | ||||||
| chr6:158564914
|
A | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4682A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564914 | ||||||
| chr6:158564918
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4686C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564918 | ||||||
| chr6:158564919
|
T | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4687T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564919 | ||||||
| chr6:158564921
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4689A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564921 | ||||||
| chr6:158564928
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4696A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564928 | ||||||
| chr6:158564935
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8+4703G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564935 | ||||||
| chr6:158564947
|
A | C | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4715A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564947 | ||||||
| chr6:158564948
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4716C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564948 | ||||||
| chr6:158564950
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8+4718A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158564950 | ||||||
| chr6:158565133
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.8+4901G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565133 | ||||||
| chr6:158565173
|
T | G | 1 | a0001c0001t0005g0189 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.8+4941T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565173 | ||||||
| chr6:158565251
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.8+5019C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565251 | ||||||
| chr6:158565359
|
A | G | 3 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022 | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.8+5127A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565359 | ||||||
| chr6:158565387
|
A | T | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.8+5155A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565387 | ||||||
| chr6:158565394
|
C | T | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.8+5162C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565394 | ||||||
| chr6:158565439
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 100 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.8+5207G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565439 | ||||||
| chr6:158565479
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0002g0011a0001c0001t0002g0100others(2): Show | 6 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8+5247C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565479 | ||||||
| chr6:158565534
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.8+5302G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565534 | ||||||
| chr6:158565620
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 209 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.8+5388C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565620 | ||||||
| chr6:158565645
|
T | G | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.8+5413T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565645 | ||||||
| chr6:158565666
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8+5434A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565666 | ||||||
| chr6:158565723
|
G | A | 30 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(27): Show | 31 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.8+5491G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565723 | ||||||
| chr6:158565774
|
G | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(185): Show | 194 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.8+5542G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565774 | ||||||
| chr6:158565928
|
G | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(237): Show | 250 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.8+5696G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565928 | ||||||
| chr6:158566289
|
C | G | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8+6057C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566289 | ||||||
| chr6:158566325
|
C | T | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107 | 3 | HG01070.hp2 HG01071.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.8+6093C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566325 | ||||||
| chr6:158566476
|
T | TGGGGTGA others(143): Show |
28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6246_8+6247insGG others(148): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158566476 | |||||
| chr6:158566482
|
G | T | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6250G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566482 | ||||||
| chr6:158566483
|
C | G | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6251C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566483 | ||||||
| chr6:158566484
|
T | G | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6252T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566484 | ||||||
| chr6:158566485
|
C | G | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6253C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566485 | ||||||
| chr6:158566486
|
C | G | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6254C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566486 | ||||||
| chr6:158566522
|
G | A | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6290G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566522 | ||||||
| chr6:158566544
|
TG | T | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6314delG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158566544 | |||||
| chr6:158566552
|
G | A | 28 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0001g0195others(25): Show | 28 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.8+6320G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566552 | ||||||
| chr6:158566552
|
G | GGTGATAC others(279): Show |
1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.8+6348_8+6349insCT others(284): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158566552 | |||||
| chr6:158566552
|
G | GGTGATAC others(165): Show |
192 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(189): Show | 200 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.8+6367_8+6538dupGG others(170): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158566552 | |||||
| chr6:158566707
|
G | GGTGATGG others(165): Show |
1 | a0001c0001t0003g0224 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8+6538_8+6539insGG others(170): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158566707 | |||||
| chr6:158566771
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 245 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.8+6539A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566771 | ||||||
| chr6:158566839
|
C | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.9-6581C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566839 | ||||||
| chr6:158566883
|
T | A | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9-6537T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158566883 | ||||||
| chr6:158567098
|
C | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(221): Show | 232 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.9-6322C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567098 | ||||||
| chr6:158567151
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.9-6269A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567151 | ||||||
| chr6:158567160
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02148.hp2 HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.9-6260T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567160 | ||||||
| chr6:158567295
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.9-6125G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567295 | ||||||
| chr6:158567383
|
G | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.9-6037G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567383 | ||||||
| chr6:158567440
|
C | A | 2 | a0001c0001t0001g0050a0001c0001t0011g0051 | 2 | NA18981.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.9-5980C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567440 | ||||||
| chr6:158567453
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.9-5967G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567453 | ||||||
| chr6:158567648
|
G | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 234 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.9-5772G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567648 | ||||||
| chr6:158567665
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0086a0001c0001t0001g0091 | 4 | NA18944.hp2 NA18963.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-5755A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567665 | ||||||
| chr6:158567684
|
T | C | 8 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0124others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-5736T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567684 | ||||||
| chr6:158567708
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.9-5712G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567708 | ||||||
| chr6:158567837
|
C | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 233 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.9-5583C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567837 | ||||||
| chr6:158567857
|
T | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.9-5563T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567857 | ||||||
| chr6:158567921
|
C | T | 1 | a0001c0001t0004g0046 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.9-5499C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567921 | ||||||
| chr6:158567975
|
C | T | 1 | a0001c0001t0028g0121 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.9-5445C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158567975 | ||||||
| chr6:158568058
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9-5362G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568058 | ||||||
| chr6:158568111
|
A | G | 1 | a0001c0001t0004g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.9-5309A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568111 | ||||||
| chr6:158568119
|
C | G | 19 | a0001c0001t0001g0103a0001c0001t0001g0117a0001c0001t0003g0116others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.9-5301C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568119 | ||||||
| chr6:158568215
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.9-5205T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568215 | ||||||
| chr6:158568412
|
G | C | 1 | a0001c0001t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.9-5008G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568412 | ||||||
| chr6:158568558
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9-4862C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568558 | ||||||
| chr6:158568601
|
T | G | 12 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(9): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.9-4819T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568601 | ||||||
| chr6:158568696
|
C | G | 10 | a0001c0001t0001g0036a0001c0001t0001g0195a0001c0001t0001g0196others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.9-4724C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568696 | ||||||
| chr6:158568722
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.9-4698A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568722 | ||||||
| chr6:158568768
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.9-4652G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568768 | ||||||
| chr6:158568778
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.9-4642C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568778 | ||||||
| chr6:158568894
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.9-4526A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568894 | ||||||
| chr6:158568910
|
T | C | 2 | a0001c0001t0004g0115a0001c0001t0025g0114 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.9-4510T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568910 | ||||||
| chr6:158568942
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 16 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.9-4478G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568942 | ||||||
| chr6:158568955
|
G | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(223): Show | 236 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.9-4465G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568955 | ||||||
| chr6:158568955
|
G | T | 9 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0124others(6): Show | 9 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.9-4465G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158568955 | ||||||
| chr6:158569003
|
G | T | 1 | a0001c0001t0001g0293 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9-4417G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569003 | ||||||
| chr6:158569007
|
C | T | 1 | a0001c0001t0007g0084 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.9-4413C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569007 | ||||||
| chr6:158569031
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.9-4389A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569031 | ||||||
| chr6:158569089
|
C | G | 3 | a0001c0001t0001g0307a0001c0001t0003g0308a0001c0001t0003g0312 | 3 | HG02717.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.9-4331C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569089 | ||||||
| chr6:158569379
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | NA18946.hp2 NA18962.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.9-4041C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569379 | ||||||
| chr6:158569573
|
G | A | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-3847G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569573 | ||||||
| chr6:158569597
|
CT | C | 10 | a0001c0001t0001g0037a0001c0001t0001g0195a0001c0001t0001g0234others(7): Show | 10 | HG01070.hp2 HG01169.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.9-3807delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158569597 | |||||
| chr6:158569599
|
T | C | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.9-3821T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569599 | ||||||
| chr6:158569623
|
C | T | 8 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0124others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-3797C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569623 | ||||||
| chr6:158569640
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.9-3780G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569640 | ||||||
| chr6:158569671
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.9-3749G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569671 | ||||||
| chr6:158569863
|
G | T | 2 | a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01884.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.9-3557G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158569863 | ||||||
| chr6:158570006
|
A | C | 11 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.9-3414A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570006 | ||||||
| chr6:158570075
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.9-3345A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570075 | ||||||
| chr6:158570130
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0083a0001c0001t0001g0086others(1): Show | 5 | HG00609.hp1 NA18944.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-3290C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570130 | ||||||
| chr6:158570283
|
G | A | 46 | a0001c0001t0001g0017a0001c0001t0001g0159a0001c0001t0001g0172others(43): Show | 48 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.9-3137G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570283 | ||||||
| chr6:158570333
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.9-3087C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570333 | ||||||
| chr6:158570358
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(100): Show | 108 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.9-3062G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570358 | ||||||
| chr6:158570381
|
C | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-3039C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570381 | ||||||
| chr6:158570432
|
A | G | 1 | a0001c0001t0013g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.9-2988A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570432 | ||||||
| chr6:158570442
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0139others(15): Show | 20 | HG00438.hp1 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.9-2978C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570442 | ||||||
| chr6:158570463
|
G | C | 1 | a0001c0001t0001g0251 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.9-2957G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570463 | ||||||
| chr6:158570483
|
C | T | 3 | a0001c0001t0001g0290a0001c0001t0017g0295a0001c0001t0021g0306 | 3 | HG03688.hp1 NA18980.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.9-2937C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570483 | ||||||
| chr6:158570487
|
C | T | 1 | a0001c0001t0009g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.9-2933C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570487 | ||||||
| chr6:158570513
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9-2907T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570513 | ||||||
| chr6:158570532
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.9-2888C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570532 | ||||||
| chr6:158570536
|
C | T | 101 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(98): Show | 104 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.9-2884C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570536 | ||||||
| chr6:158570564
|
A | C | 21 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(18): Show | 21 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.9-2856A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570564 | ||||||
| chr6:158570726
|
C | G | 1 | a0001c0001t0005g0016 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.9-2694C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570726 | ||||||
| chr6:158570734
|
C | CT | 135 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 140 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.9-2685dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158570734 | |||||
| chr6:158570738
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01255.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.9-2682C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570738 | ||||||
| chr6:158570739
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.9-2681G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570739 | ||||||
| chr6:158570802
|
T | C | 14 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(11): Show | 14 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.9-2618T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570802 | ||||||
| chr6:158570823
|
T | A | 8 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(5): Show | 9 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.9-2597T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570823 | ||||||
| chr6:158570914
|
A | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 237 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.9-2506A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570914 | ||||||
| chr6:158570920
|
G | GT | 15 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 15 | HG01243.hp1 HG02071.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.9-2489dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158570920 | |||||
| chr6:158570920
|
GT | G | 11 | a0001c0001t0001g0054a0001c0001t0001g0235a0001c0001t0002g0012others(8): Show | 12 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.9-2489delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158570920 | |||||
| chr6:158570961
|
G | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-2459G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570961 | ||||||
| chr6:158570972
|
G | T | 31 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(28): Show | 32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.9-2448G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570972 | ||||||
| chr6:158571041
|
C | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(5): Show | 9 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.9-2379C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571041 | ||||||
| chr6:158571076
|
C | CTAATTTT others(21): Show |
1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.9-2334_9-2307dupAA others(26): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571076 | |||||
| chr6:158571089
|
A | AAATT | 7 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(4): Show | 8 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.9-2314_9-2311dupAA others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571089 | |||||
| chr6:158571119
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9-2301T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571119 | ||||||
| chr6:158571127
|
C | T | 44 | a0001c0001t0001g0140a0001c0001t0001g0183a0001c0001t0001g0187others(41): Show | 47 | HG00558.hp1 HG01074.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.9-2293C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571127 | ||||||
| chr6:158571129
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9-2291T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571129 | ||||||
| chr6:158571131
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9-2289C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571131 | ||||||
| chr6:158571135
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.9-2285T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571135 | ||||||
| chr6:158571146
|
A | G | 3 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022 | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-2274A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571146 | ||||||
| chr6:158571150
|
G | A | 3 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022 | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-2270G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571150 | ||||||
| chr6:158571189
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 8 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.9-2231C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571189 | ||||||
| chr6:158571196
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.9-2224G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571196 | ||||||
| chr6:158571299
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.9-2121G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571299 | ||||||
| chr6:158571305
|
G | GC | 39 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0183others(36): Show | 40 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.9-2114dupC | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571305 | |||||
| chr6:158571318
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.9-2102G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571318 | ||||||
| chr6:158571318
|
GATCTCCT others(195): Show |
G | 3 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022 | 4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-2089_9-1888del | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571318 | |||||
| chr6:158571331
|
T | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0259a0001c0001t0003g0089others(2): Show | 5 | HG00642.hp2 HG01081.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.9-2089T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571331 | ||||||
| chr6:158571331
|
T | TGTGATCC others(397): Show |
1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9-2045_9-2044insAT others(402): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571331 | |||||
| chr6:158571331
|
TGTGATCC others(37): Show |
T | 2 | a0001c0001t0001g0276a0001c0001t0018g0277 | 2 | NA18747.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.9-2082_9-2039delCG others(42): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571331 | |||||
| chr6:158571331
|
TGTGATCC others(195): Show |
T | 1 | a0001c0001t0004g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.9-2077_9-1876del | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571331 | |||||
| chr6:158571343
|
A | ACCTTGGC others(59): Show |
1 | a0001c0001t0005g0189 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.9-2045_9-2044insAT others(64): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571343 | |||||
| chr6:158571343
|
A | G | 2 | a0001c0001t0001g0140a0004c0005t0003g0020 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.9-2077A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571343 | ||||||
| chr6:158571343
|
ACCTTGGC others(59): Show |
A | 10 | a0001c0001t0002g0010a0001c0001t0002g0155a0001c0001t0002g0157others(7): Show | 11 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.9-2055_9-1990delGG others(64): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571343 | |||||
| chr6:158571343
|
ACCTTGGC others(195): Show |
A | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9-2044_9-1843del | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571343 | |||||
| chr6:158571356
|
AAAGTGCT others(52): Show |
A | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.9-2063_9-2005delAA others(57): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571356 | ||||||
| chr6:158571365
|
GGATTATA others(59): Show |
G | 35 | a0001c0001t0001g0183a0001c0001t0001g0294a0001c0001t0001g0300others(32): Show | 36 | HG02027.hp2 HG02071.hp1 HG02083.hp1 others(33): Show |
intron_variant | MODIFIER | c.9-2049_9-1984delTA others(64): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571365 | |||||
| chr6:158571371
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0002g0179 | 2 | HG02622.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.9-2049T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571371 | ||||||
| chr6:158571375
|
C | CATGATCT others(15): Show |
1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.9-2045_9-2044insAT others(20): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571375 | ||||||
| chr6:158571375
|
C | CGTGATCT others(15): Show |
2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.9-2023_9-2002dupTG others(20): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571375 | |||||
| chr6:158571376
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 145 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.9-2044G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571376 | ||||||
| chr6:158571376
|
GTGATCTG others(195): Show |
G | 33 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.9-2040_9-1839del | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158571376 | |||||
| chr6:158571418
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.9-2002T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571418 | ||||||
| chr6:158571431
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0002g0179 | 2 | NA18998.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.9-1989A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571431 | ||||||
| chr6:158571442
|
C | G | 1 | a0001c0001t0002g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.9-1978C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571442 | ||||||
| chr6:158571442
|
C | T | 16 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(13): Show | 17 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.9-1978C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571442 | ||||||
| chr6:158571445
|
A | C | 16 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(13): Show | 17 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.9-1975A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571445 | ||||||
| chr6:158571498
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0001g0138others(4): Show | 7 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.9-1922T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571498 | ||||||
| chr6:158571505
|
G | A | 5 | a0001c0001t0001g0236a0001c0001t0002g0155a0001c0001t0002g0164others(2): Show | 5 | HG00558.hp1 HG01175.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-1915G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571505 | ||||||
| chr6:158571520
|
A | G | 3 | a0001c0001t0004g0044a0001c0001t0004g0046a0002c0003t0004g0003 | 4 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-1900A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571520 | ||||||
| chr6:158571533
|
C | T | 3 | a0001c0001t0004g0044a0001c0001t0004g0046a0002c0003t0004g0003 | 4 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-1887C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571533 | ||||||
| chr6:158571545
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(196): Show | 209 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.9-1875G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571545 | ||||||
| chr6:158571578
|
A | G | 4 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0076others(1): Show | 5 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-1842A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571578 | ||||||
| chr6:158571587
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0089a0001c0001t0003g0090others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.9-1833C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571587 | ||||||
| chr6:158571590
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.9-1830G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571590 | ||||||
| chr6:158571593
|
C | T | 51 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(48): Show | 55 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.9-1827C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571593 | ||||||
| chr6:158571599
|
T | C | 2 | a0001c0001t0005g0209a0001c0001t0005g0210 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.9-1821T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571599 | ||||||
| chr6:158571706
|
C | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(114): Show | 121 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.9-1714C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571706 | ||||||
| chr6:158571764
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-1656C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571764 | ||||||
| chr6:158571807
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9-1613G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571807 | ||||||
| chr6:158571938
|
G | A | 1 | a0001c0001t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.9-1482G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158571938 | ||||||
| chr6:158572061
|
C | T | 37 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(34): Show | 38 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.9-1359C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572061 | ||||||
| chr6:158572093
|
T | C | 7 | a0001c0001t0005g0096a0001c0001t0005g0191a0001c0001t0005g0207others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.9-1327T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572093 | ||||||
| chr6:158572114
|
C | T | 1 | a0001c0001t0030g0031 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.9-1306C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572114 | ||||||
| chr6:158572135
|
T | C | 122 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.9-1285T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572135 | ||||||
| chr6:158572137
|
C | T | 3 | a0001c0001t0005g0096a0001c0001t0005g0191a0001c0001t0026g0129 | 3 | HG02109.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.9-1283C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572137 | ||||||
| chr6:158572181
|
G | A | 1 | a0001c0001t0027g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.9-1239G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572181 | ||||||
| chr6:158572238
|
G | A | 1 | a0001c0001t0029g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.9-1182G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572238 | ||||||
| chr6:158572309
|
CATA | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 247 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.9-1110_9-1108delAT others(1): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572309 | ||||||
| chr6:158572539
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.9-881G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572539 | ||||||
| chr6:158572557
|
C | T | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.9-863C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572557 | ||||||
| chr6:158572605
|
G | GA | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-815_9-814insA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572605 | ||||||
| chr6:158572763
|
CTG | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-653_9-652delGT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158572763 | |||||
| chr6:158572848
|
ATGTGGGC others(61): Show |
A | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107 | 3 | HG01070.hp2 HG01071.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.9-538_9-471delGGCT others(64): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158572848 | |||||
| chr6:158572878
|
AGTGGGCT others(1): Show |
A | 110 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(107): Show | 114 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.9-528_9-521delCTTG others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158572878 | |||||
| chr6:158572968
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.9-452G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158572968 | ||||||
| chr6:158573038
|
G | C | 36 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(33): Show | 37 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.9-382G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573038 | ||||||
| chr6:158573063
|
A | G | 2 | a0001c0001t0004g0135a0001c0001t0004g0136 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.9-357A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573063 | ||||||
| chr6:158573092
|
CTG | C | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194 | 3 | NA19063.hp2 NA19064.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.9-325_9-324delTG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 158573092 | |||||
| chr6:158573108
|
T | C | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.9-312T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573108 | ||||||
| chr6:158573160
|
T | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9-260T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573160 | ||||||
| chr6:158573166
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9-254G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573166 | ||||||
| chr6:158573175
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-245G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573175 | ||||||
| chr6:158573176
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.9-244C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573176 | ||||||
| chr6:158573178
|
G | A | 1 | a0001c0001t0001g0311 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.9-242G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573178 | ||||||
| chr6:158573213
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9-207C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573213 | ||||||
| chr6:158573363
|
T | C | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.9-57T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573363 | ||||||
| chr6:158573386
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.9-34C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573386 | ||||||
| chr6:158573396
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.9-24C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573396 | ||||||
| chr6:158573399
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.9-21A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158573399 | ||||||
| chr6:158573545
|
T | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(310): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.112+22T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158573545 | ||||||
| chr6:158573811
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.112+288C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158573811 | ||||||
| chr6:158573822
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112+299G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158573822 | ||||||
| chr6:158573836
|
C | T | 1 | a0001c0001t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112+313C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158573836 | ||||||
| chr6:158574019
|
C | A | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.112+496C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574019 | ||||||
| chr6:158574027
|
T | C | 113 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.112+504T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574027 | ||||||
| chr6:158574036
|
G | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+513G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574036 | ||||||
| chr6:158574085
|
C | T | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+562C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574085 | ||||||
| chr6:158574089
|
A | AGCC | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+567_112+569dup others(3): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158574089 | |||||
| chr6:158574183
|
T | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+660T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574183 | ||||||
| chr6:158574227
|
G | A | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112+704G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574227 | ||||||
| chr6:158574264
|
G | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+741G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574264 | ||||||
| chr6:158574412
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+889T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574412 | ||||||
| chr6:158574558
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1035A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574558 | ||||||
| chr6:158574640
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.112+1117A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574640 | ||||||
| chr6:158574835
|
C | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.112+1312C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574835 | ||||||
| chr6:158574900
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.112+1377A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574900 | ||||||
| chr6:158574908
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.112+1385A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574908 | ||||||
| chr6:158574922
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.112+1399T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574922 | ||||||
| chr6:158574936
|
T | A | 2 | a0001c0001t0005g0133a0006c0007t0016g0130 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.112+1413T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158574936 | ||||||
| chr6:158575072
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1549C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575072 | ||||||
| chr6:158575357
|
C | CT | 93 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(90): Show | 96 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.112+1844dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158575357 | |||||
| chr6:158575401
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.112+1878T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575401 | ||||||
| chr6:158575516
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1993C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575516 | ||||||
| chr6:158575560
|
C | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(113): Show | 120 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.112+2037C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575560 | ||||||
| chr6:158575561
|
G | T | 3 | a0001c0001t0002g0174a0001c0001t0005g0189a0001c0001t0005g0190 | 3 | HG02145.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.112+2038G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575561 | ||||||
| chr6:158575741
|
G | A | 118 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.112+2218G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575741 | ||||||
| chr6:158575796
|
G | A | 113 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.112+2273G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575796 | ||||||
| chr6:158575826
|
T | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+2303T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575826 | ||||||
| chr6:158575881
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.112+2358A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575881 | ||||||
| chr6:158575961
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0206 | 3 | HG02622.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.112+2438G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158575961 | ||||||
| chr6:158576009
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2486T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576009 | ||||||
| chr6:158576021
|
G | A | 1 | a0001c0001t0003g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.112+2498G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576021 | ||||||
| chr6:158576184
|
G | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2661G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576184 | ||||||
| chr6:158576314
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2791C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576314 | ||||||
| chr6:158576469
|
G | C | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+2946G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576469 | ||||||
| chr6:158576536
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.112+3013A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576536 | ||||||
| chr6:158576613
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112+3090T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576613 | ||||||
| chr6:158576770
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.112+3247G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576770 | ||||||
| chr6:158576828
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.112+3305C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158576828 | ||||||
| chr6:158577009
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.112+3486C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577009 | ||||||
| chr6:158577019
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+3496G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577019 | ||||||
| chr6:158577057
|
A | G | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112+3534A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577057 | ||||||
| chr6:158577061
|
C | CA | 13 | a0001c0001t0001g0027a0001c0001t0001g0050a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp2 HG01361.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+3559dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158577061 | |||||
| chr6:158577061
|
CA | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 142 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.112+3559delA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158577061 | |||||
| chr6:158577061
|
CAA | C | 39 | a0001c0001t0001g0045a0001c0001t0001g0311a0001c0001t0002g0010others(36): Show | 41 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+3558_112+3559d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158577061 | |||||
| chr6:158577205
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.112+3682A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577205 | ||||||
| chr6:158577221
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.112+3698A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577221 | ||||||
| chr6:158577374
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-3566T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577374 | ||||||
| chr6:158577446
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-3494G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577446 | ||||||
| chr6:158577539
|
G | A | 118 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.113-3401G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577539 | ||||||
| chr6:158577549
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.113-3391G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577549 | ||||||
| chr6:158577908
|
T | C | 1 | a0001c0001t0004g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.113-3032T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577908 | ||||||
| chr6:158577986
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2954A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577986 | ||||||
| chr6:158577993
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-2947G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577993 | ||||||
| chr6:158577993
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2947G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158577993 | ||||||
| chr6:158578013
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2927C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578013 | ||||||
| chr6:158578020
|
G | C | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113-2920G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578020 | ||||||
| chr6:158578208
|
A | G | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.113-2732A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578208 | ||||||
| chr6:158578410
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.113-2530A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578410 | ||||||
| chr6:158578666
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.113-2274G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578666 | ||||||
| chr6:158578728
|
A | G | 2 | a0001c0001t0004g0115a0001c0001t0025g0114 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.113-2212A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578728 | ||||||
| chr6:158578913
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.113-2027G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578913 | ||||||
| chr6:158578971
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1969G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158578971 | ||||||
| chr6:158579075
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0100a0001c0001t0002g0173 | 4 | HG02717.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1865A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579075 | ||||||
| chr6:158579208
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1732G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579208 | ||||||
| chr6:158579265
|
T | TA | 113 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.113-1662dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 158579265 | |||||
| chr6:158579304
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.113-1636A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579304 | ||||||
| chr6:158579436
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1504G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579436 | ||||||
| chr6:158579486
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1454G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579486 | ||||||
| chr6:158579537
|
TG | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.113-1402delG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579537 | ||||||
| chr6:158579576
|
G | A | 1 | a0001c0001t0003g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-1364G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579576 | ||||||
| chr6:158579697
|
C | T | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.113-1243C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579697 | ||||||
| chr6:158579700
|
CAA | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1239_113-1238d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579700 | ||||||
| chr6:158579751
|
G | A | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-1189G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579751 | ||||||
| chr6:158579909
|
G | C | 3 | a0001c0001t0004g0044a0001c0001t0004g0046a0002c0003t0004g0003 | 4 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1031G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579909 | ||||||
| chr6:158579912
|
C | T | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-1028C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579912 | ||||||
| chr6:158580018
|
C | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0029g0162 | 3 | NA18987.hp2 NA19062.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.113-922C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580018 | ||||||
| chr6:158580040
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.113-900G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580040 | ||||||
| chr6:158580105
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-835C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580105 | ||||||
| chr6:158580120
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-820C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580120 | ||||||
| chr6:158580147
|
A | G | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-793A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580147 | ||||||
| chr6:158580187
|
G | A | 48 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(45): Show | 50 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-753G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580187 | ||||||
| chr6:158580198
|
C | T | 1 | a0001c0001t0005g0016 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.113-742C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580198 | ||||||
| chr6:158580286
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-654C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580286 | ||||||
| chr6:158580290
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.113-650A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580290 | ||||||
| chr6:158580346
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-594A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580346 | ||||||
| chr6:158580363
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-577G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580363 | ||||||
| chr6:158580391
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-549T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580391 | ||||||
| chr6:158580873
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113-67T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158580873 | ||||||
| chr6:158581067
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+72C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581067 | ||||||
| chr6:158581073
|
G | C | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107 | 3 | HG01070.hp2 HG01071.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.168+78G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581073 | ||||||
| chr6:158581238
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0093 | 3 | HG00099.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.168+243A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581238 | ||||||
| chr6:158581363
|
T | C | 114 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(111): Show | 118 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.168+368T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581363 | ||||||
| chr6:158581453
|
A | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+458A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581453 | ||||||
| chr6:158581480
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+485G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581480 | ||||||
| chr6:158581631
|
T | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+636T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581631 | ||||||
| chr6:158581679
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+684C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581679 | ||||||
| chr6:158581696
|
C | T | 122 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.168+701C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581696 | ||||||
| chr6:158581753
|
C | CA | 14 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0058others(11): Show | 15 | HG00423.hp1 HG01167.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+779dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 158581753 | |||||
| chr6:158581753
|
C | CAA | 109 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 114 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.168+778_168+779dup others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 158581753 | |||||
| chr6:158581753
|
C | CAAA | 48 | a0001c0001t0001g0042a0001c0001t0001g0140a0001c0001t0001g0143others(45): Show | 49 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.168+777_168+779dup others(3): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 158581753 | |||||
| chr6:158581753
|
C | CAAAA | 69 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(66): Show | 72 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.168+776_168+779dup others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 158581753 | |||||
| chr6:158581753
|
C | CAAAAA | 10 | a0001c0001t0001g0038a0001c0001t0002g0032a0001c0001t0003g0019others(7): Show | 10 | HG01175.hp1 HG01358.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+775_168+779dup others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 158581753 | |||||
| chr6:158581796
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.168+801T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581796 | ||||||
| chr6:158581999
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.168+1004C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158581999 | ||||||
| chr6:158582023
|
G | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.168+1028G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582023 | ||||||
| chr6:158582066
|
A | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+1071A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582066 | ||||||
| chr6:158582080
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1085C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582080 | ||||||
| chr6:158582350
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0093 | 3 | HG00099.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.168+1355A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582350 | ||||||
| chr6:158582503
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-1451A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582503 | ||||||
| chr6:158582658
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-1296C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582658 | ||||||
| chr6:158582960
|
C | T | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-994C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582960 | ||||||
| chr6:158582963
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-991A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582963 | ||||||
| chr6:158582989
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169-965C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158582989 | ||||||
| chr6:158583072
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(309): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.169-882G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583072 | ||||||
| chr6:158583175
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.169-779G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583175 | ||||||
| chr6:158583177
|
G | T | 1 | a0001c0001t0001g0287 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.169-777G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583177 | ||||||
| chr6:158583226
|
C | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.169-728C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583226 | ||||||
| chr6:158583310
|
T | C | 1 | a0001c0001t0027g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169-644T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583310 | ||||||
| chr6:158583367
|
T | C | 7 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0004g0124others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-587T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583367 | ||||||
| chr6:158583440
|
C | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0236a0001c0001t0001g0237others(7): Show | 11 | HG01192.hp2 HG01255.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-514C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583440 | ||||||
| chr6:158583521
|
G | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.169-433G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583521 | ||||||
| chr6:158583575
|
C | T | 78 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(75): Show | 81 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.169-379C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583575 | ||||||
| chr6:158583596
|
C | T | 41 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(38): Show | 42 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.169-358C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583596 | ||||||
| chr6:158583616
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0302 | 2 | HG02083.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.169-338C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583616 | ||||||
| chr6:158583668
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.169-286C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583668 | ||||||
| chr6:158583713
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169-241T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583713 | ||||||
| chr6:158583778
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-176C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 3/16 | chr6 | 158583778 | ||||||
| chr6:158584198
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+154C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584198 | ||||||
| chr6:158584250
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+206G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584250 | ||||||
| chr6:158584281
|
A | G | 118 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(115): Show | 122 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.259+237A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584281 | ||||||
| chr6:158584331
|
G | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.259+287G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584331 | ||||||
| chr6:158584435
|
A | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.259+391A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584435 | ||||||
| chr6:158584477
|
C | A | 1 | a0001c0001t0003g0013 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.259+433C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584477 | ||||||
| chr6:158584489
|
A | G | 1 | a0001c0001t0004g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.259+445A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584489 | ||||||
| chr6:158584602
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.259+558G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584602 | ||||||
| chr6:158584628
|
A | G | 1 | a0001c0001t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259+584A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584628 | ||||||
| chr6:158584644
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.259+600C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584644 | ||||||
| chr6:158584649
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.259+605C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584649 | ||||||
| chr6:158584653
|
G | A | 36 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(33): Show | 37 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.259+609G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584653 | ||||||
| chr6:158584739
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0004g0076 | 2 | HG00140.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.260-565C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584739 | ||||||
| chr6:158584838
|
T | C | 7 | a0001c0001t0002g0174a0001c0001t0005g0189a0001c0001t0005g0190others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-466T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158584838 | ||||||
| chr6:158585084
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.260-220C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158585084 | ||||||
| chr6:158585301
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG02080.hp1 | splice_region_variant&intron_variant | LOW | c.260-3T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 4/16 | chr6 | 158585301 | ||||||
| chr6:158585606
|
A | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+181A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585606 | ||||||
| chr6:158585619
|
C | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+194C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585619 | ||||||
| chr6:158585698
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+273C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585698 | ||||||
| chr6:158585733
|
G | A | 1 | a0001c0001t0006g0004 | 2 | HG00140.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.381+308G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585733 | ||||||
| chr6:158585790
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381+365C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585790 | ||||||
| chr6:158585795
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.381+370G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585795 | ||||||
| chr6:158585804
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+379A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585804 | ||||||
| chr6:158585895
|
G | T | 1 | a0001c0001t0002g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.381+470G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585895 | ||||||
| chr6:158585896
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.381+471C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585896 | ||||||
| chr6:158585949
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+524C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585949 | ||||||
| chr6:158585972
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(242): Show | 255 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(252): Show |
intron_variant | MODIFIER | c.381+547A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158585972 | ||||||
| chr6:158586095
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.381+670C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586095 | ||||||
| chr6:158586156
|
T | TG | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+734dupG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr6 | 158586156 | |||||
| chr6:158586184
|
C | T | 9 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG00609.hp2 HG02148.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+759C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586184 | ||||||
| chr6:158586413
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+988T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586413 | ||||||
| chr6:158586525
|
C | T | 116 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(113): Show | 120 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.381+1100C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586525 | ||||||
| chr6:158586612
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+1187G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586612 | ||||||
| chr6:158586651
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+1226A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586651 | ||||||
| chr6:158586727
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+1302C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158586727 | ||||||
| chr6:158587011
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.381+1586C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587011 | ||||||
| chr6:158587016
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.381+1591G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587016 | ||||||
| chr6:158587319
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(219): Show | 230 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.381+1894C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587319 | ||||||
| chr6:158587455
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0015g0028 | 3 | HG00423.hp1 NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.381+2030T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587455 | ||||||
| chr6:158587499
|
C | CT | 6 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0245others(3): Show | 6 | HG01070.hp1 HG02145.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+2087dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr6 | 158587499 | |||||
| chr6:158587639
|
T | A | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.382-2033T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587639 | ||||||
| chr6:158587679
|
G | A | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382-1993G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587679 | ||||||
| chr6:158587710
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1962G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587710 | ||||||
| chr6:158587850
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.382-1822T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587850 | ||||||
| chr6:158587962
|
C | T | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-1710C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158587962 | ||||||
| chr6:158588216
|
C | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1456C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588216 | ||||||
| chr6:158588437
|
CTTTTTGT others(3): Show |
C | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-1221_382-1212d others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr6 | 158588437 | |||||
| chr6:158588611
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0160a0001c0001t0002g0161 | 4 | NA18960.hp1 NA18978.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-1061G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588611 | ||||||
| chr6:158588677
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-995G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588677 | ||||||
| chr6:158588738
|
A | G | 4 | a0001c0001t0008g0254a0001c0001t0008g0280a0001c0001t0008g0284others(1): Show | 4 | HG00673.hp1 HG02071.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-934A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588738 | ||||||
| chr6:158588845
|
C | T | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.382-827C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588845 | ||||||
| chr6:158588925
|
C | G | 42 | a0001c0001t0001g0244a0001c0001t0001g0268a0001c0001t0001g0269others(39): Show | 44 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.382-747C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158588925 | ||||||
| chr6:158589025
|
G | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | NA18971.hp1 NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.382-647G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158589025 | ||||||
| chr6:158589347
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 216 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.382-325T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158589347 | ||||||
| chr6:158589464
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.382-208A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158589464 | ||||||
| chr6:158589619
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-53C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 5/16 | chr6 | 158589619 | ||||||
| chr6:158589899
|
T | A | 1 | a0001c0001t0001g0287 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.492+117T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158589899 | ||||||
| chr6:158590264
|
C | T | 1 | a0001c0008t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.492+482C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590264 | ||||||
| chr6:158590328
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.492+546T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590328 | ||||||
| chr6:158590342
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+560G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590342 | ||||||
| chr6:158590376
|
C | CA | 198 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 206 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.492+604dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158590376 | |||||
| chr6:158590376
|
C | CAA | 11 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 12 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.492+603_492+604dup others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158590376 | |||||
| chr6:158590402
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+620A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590402 | ||||||
| chr6:158590431
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG01928.hp1 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+649C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590431 | ||||||
| chr6:158590453
|
TG | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+672delG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590453 | ||||||
| chr6:158590552
|
C | T | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+770C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590552 | ||||||
| chr6:158590669
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.492+887G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590669 | ||||||
| chr6:158590676
|
A | C | 2 | a0001c0001t0001g0033a0001c0001t0012g0216 | 2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.492+894A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590676 | ||||||
| chr6:158590681
|
C | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(209): Show | 221 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.492+899C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590681 | ||||||
| chr6:158590692
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0070others(1): Show | 8 | HG00639.hp1 HG00738.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+910G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590692 | ||||||
| chr6:158590723
|
A | G | 33 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.492+941A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590723 | ||||||
| chr6:158590751
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+969C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158590751 | ||||||
| chr6:158591509
|
A | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+1727A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591509 | ||||||
| chr6:158591535
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.492+1753C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591535 | ||||||
| chr6:158591625
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.492+1843C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591625 | ||||||
| chr6:158591778
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(238): Show | 251 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.492+1996A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591778 | ||||||
| chr6:158591792
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+2010C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591792 | ||||||
| chr6:158591800
|
G | A | 75 | a0001c0001t0001g0103a0001c0001t0001g0307a0001c0001t0003g0013others(72): Show | 77 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.492+2018G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591800 | ||||||
| chr6:158591818
|
G | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+2036G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591818 | ||||||
| chr6:158591873
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.492+2091T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591873 | ||||||
| chr6:158591913
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.492+2131A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158591913 | ||||||
| chr6:158592067
|
C | T | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.492+2285C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592067 | ||||||
| chr6:158592135
|
G | A | 1 | a0001c0001t0003g0227 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.492+2353G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592135 | ||||||
| chr6:158592266
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.492+2484A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592266 | ||||||
| chr6:158592334
|
T | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+2552T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592334 | ||||||
| chr6:158592395
|
A | G | 48 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(45): Show | 50 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.492+2613A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592395 | ||||||
| chr6:158592476
|
CT | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 191 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.492+2706delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158592476 | |||||
| chr6:158592535
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+2753C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592535 | ||||||
| chr6:158592548
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.492+2766C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592548 | ||||||
| chr6:158592728
|
G | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+2946G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592728 | ||||||
| chr6:158592842
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 183 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.492+3060T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592842 | ||||||
| chr6:158592903
|
G | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(166): Show | 177 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.492+3121G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592903 | ||||||
| chr6:158592988
|
G | C | 1 | a0001c0001t0014g0264 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.492+3206G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592988 | ||||||
| chr6:158592994
|
T | G | 34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.492+3212T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592994 | ||||||
| chr6:158593008
|
G | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+3226G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593008 | ||||||
| chr6:158593018
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(170): Show | 181 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.492+3236G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593018 | ||||||
| chr6:158593128
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+3346C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593128 | ||||||
| chr6:158593270
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+3488A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593270 | ||||||
| chr6:158593296
|
G | A | 4 | a0001c0002t0001g0009a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 5 | HG01934.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+3514G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593296 | ||||||
| chr6:158593522
|
C | T | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.492+3740C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593522 | ||||||
| chr6:158593668
|
G | A | 1 | a0001c0001t0005g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.492+3886G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593668 | ||||||
| chr6:158593785
|
A | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+4003A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593785 | ||||||
| chr6:158593863
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.492+4081G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593863 | ||||||
| chr6:158593900
|
A | G | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.492+4118A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593900 | ||||||
| chr6:158593911
|
C | G | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+4129C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593911 | ||||||
| chr6:158593988
|
G | A | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.492+4206G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158593988 | ||||||
| chr6:158594016
|
C | G | 51 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(48): Show | 53 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.492+4234C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594016 | ||||||
| chr6:158594026
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.492+4244T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594026 | ||||||
| chr6:158594026
|
T | C | 54 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(51): Show | 56 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.492+4244T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594026 | ||||||
| chr6:158594083
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 183 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.492+4301A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594083 | ||||||
| chr6:158594099
|
CT | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.492+4338delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158594099 | |||||
| chr6:158594099
|
CTT | C | 50 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0301others(47): Show | 52 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.492+4337_492+4338d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158594099 | |||||
| chr6:158594120
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.492+4338T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594120 | ||||||
| chr6:158594211
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 183 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.492+4429A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594211 | ||||||
| chr6:158594215
|
T | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+4433T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594215 | ||||||
| chr6:158594250
|
C | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.492+4468C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594250 | ||||||
| chr6:158594254
|
A | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+4472A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594254 | ||||||
| chr6:158594263
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+4481T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594263 | ||||||
| chr6:158594350
|
C | T | 2 | a0001c0001t0008g0280a0001c0001t0008g0284 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.492+4568C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594350 | ||||||
| chr6:158594441
|
T | C | 3 | a0001c0001t0005g0096a0001c0001t0005g0133a0001c0001t0005g0191 | 3 | HG03041.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.492+4659T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594441 | ||||||
| chr6:158594481
|
A | T | 47 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.492+4699A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594481 | ||||||
| chr6:158594570
|
T | A | 34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.492+4788T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594570 | ||||||
| chr6:158594593
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.492+4811C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594593 | ||||||
| chr6:158594602
|
T | G | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.492+4820T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594602 | ||||||
| chr6:158594807
|
C | A | 48 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(45): Show | 50 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.492+5025C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594807 | ||||||
| chr6:158594877
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.492+5095G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594877 | ||||||
| chr6:158595044
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+5262A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595044 | ||||||
| chr6:158595161
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.492+5379C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595161 | ||||||
| chr6:158595314
|
C | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 175 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.492+5532C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595314 | ||||||
| chr6:158595323
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+5541T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595323 | ||||||
| chr6:158595361
|
G | A | 55 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(52): Show | 59 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.492+5579G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595361 | ||||||
| chr6:158595457
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+5675C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595457 | ||||||
| chr6:158595483
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+5701T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595483 | ||||||
| chr6:158595592
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 183 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.492+5810T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595592 | ||||||
| chr6:158595595
|
C | T | 2 | a0001c0001t0004g0135a0001c0001t0004g0136 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.492+5813C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595595 | ||||||
| chr6:158595617
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.492+5835C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595617 | ||||||
| chr6:158595688
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+5906G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595688 | ||||||
| chr6:158595775
|
G | C | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.492+5993G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595775 | ||||||
| chr6:158595822
|
G | A | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.492+6040G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595822 | ||||||
| chr6:158595863
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492+6081G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595863 | ||||||
| chr6:158595944
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.492+6162C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595944 | ||||||
| chr6:158595982
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.492+6200C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595982 | ||||||
| chr6:158596026
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.492+6244A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596026 | ||||||
| chr6:158596166
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.492+6384C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596166 | ||||||
| chr6:158596211
|
G | T | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.492+6429G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596211 | ||||||
| chr6:158596245
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.492+6463G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596245 | ||||||
| chr6:158596267
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.492+6485C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596267 | ||||||
| chr6:158596275
|
A | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+6493A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596275 | ||||||
| chr6:158596280
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+6498G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596280 | ||||||
| chr6:158596300
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+6518C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596300 | ||||||
| chr6:158596313
|
G | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.492+6531G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596313 | ||||||
| chr6:158596316
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(4): Show | 8 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+6534C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596316 | ||||||
| chr6:158596655
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+6873C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596655 | ||||||
| chr6:158596823
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(172): Show | 183 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.492+7041G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596823 | ||||||
| chr6:158596824
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.492+7042T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596824 | ||||||
| chr6:158596879
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.492+7097G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596879 | ||||||
| chr6:158596887
|
C | G | 34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.492+7105C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596887 | ||||||
| chr6:158596975
|
T | C | 3 | a0001c0001t0004g0044a0001c0001t0004g0046a0002c0003t0004g0003 | 4 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+7193T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596975 | ||||||
| chr6:158597147
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.492+7365G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597147 | ||||||
| chr6:158597181
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.492+7399C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597181 | ||||||
| chr6:158597369
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+7587A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597369 | ||||||
| chr6:158597545
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.493-7722A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597545 | ||||||
| chr6:158597588
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-7679C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597588 | ||||||
| chr6:158597709
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-7558C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597709 | ||||||
| chr6:158597914
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.493-7353G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158597914 | ||||||
| chr6:158598084
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(168): Show | 179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.493-7183C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598084 | ||||||
| chr6:158598273
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-6994G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598273 | ||||||
| chr6:158598507
|
C | T | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493-6760C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598507 | ||||||
| chr6:158598508
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(238): Show | 251 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.493-6759A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598508 | ||||||
| chr6:158598625
|
GT | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(164): Show | 174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.493-6631delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158598625 | |||||
| chr6:158598631
|
T | A | 1 | a0001c0001t0004g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.493-6636T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598631 | ||||||
| chr6:158598738
|
A | G | 2 | a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01884.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.493-6529A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598738 | ||||||
| chr6:158598763
|
T | C | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493-6504T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598763 | ||||||
| chr6:158598814
|
C | T | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-6453C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598814 | ||||||
| chr6:158598822
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.493-6445C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598822 | ||||||
| chr6:158598831
|
G | A | 1 | a0001c0001t0014g0264 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.493-6436G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598831 | ||||||
| chr6:158598856
|
G | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-6411G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598856 | ||||||
| chr6:158598863
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-6404T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598863 | ||||||
| chr6:158598931
|
G | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493-6336G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598931 | ||||||
| chr6:158599241
|
A | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.493-6026A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599241 | ||||||
| chr6:158599334
|
T | C | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.493-5933T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599334 | ||||||
| chr6:158599441
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.493-5826A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599441 | ||||||
| chr6:158599529
|
T | A | 1 | a0001c0001t0003g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.493-5738T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599529 | ||||||
| chr6:158599639
|
C | T | 1 | a0001c0001t0006g0004 | 2 | HG00140.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.493-5628C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599639 | ||||||
| chr6:158599809
|
C | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-5458C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599809 | ||||||
| chr6:158599865
|
G | T | 47 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.493-5402G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599865 | ||||||
| chr6:158599935
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-5332C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599935 | ||||||
| chr6:158599998
|
C | T | 2 | a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01884.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.493-5269C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158599998 | ||||||
| chr6:158600040
|
A | G | 5 | a0001c0001t0001g0095a0001c0002t0001g0009a0001c0002t0001g0098others(2): Show | 6 | HG01934.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-5227A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600040 | ||||||
| chr6:158600199
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-5068G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600199 | ||||||
| chr6:158600317
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-4950C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600317 | ||||||
| chr6:158600365
|
G | C | 1 | a0001c0001t0030g0031 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.493-4902G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600365 | ||||||
| chr6:158600458
|
A | ATTTTTTT others(1): Show |
15 | a0001c0001t0003g0089a0001c0001t0003g0116a0001c0001t0003g0132others(12): Show | 15 | HG01074.hp1 HG01081.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.493-4788_493-4781d others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
A | ATTTTTTT others(2): Show |
10 | a0001c0001t0001g0307a0001c0001t0003g0019a0001c0001t0003g0090others(7): Show | 10 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.493-4789_493-4781d others(11): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0003g0013a0001c0001t0003g0214a0001c0001t0003g0308 | 4 | HG01243.hp2 HG02717.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-4790_493-4781d others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0003g0217a0001c0001t0003g0228a0001c0001t0012g0216 | 3 | HG01346.hp1 HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.493-4791_493-4781d others(13): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
AT | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.493-4781delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
ATT | A | 10 | a0001c0001t0001g0054a0001c0001t0004g0044a0001c0001t0004g0046others(7): Show | 10 | HG01106.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.493-4782_493-4781d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
ATTT | A | 26 | a0001c0001t0001g0103a0001c0001t0004g0092a0001c0001t0004g0105others(23): Show | 28 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.493-4783_493-4781d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0236a0001c0001t0001g0240a0001c0001t0001g0248others(4): Show | 7 | HG01978.hp1 HG02148.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-4790_493-4781d others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
ATTTTTTT others(4): Show |
A | 157 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 164 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.493-4791_493-4781d others(13): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600458
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0183a0001c0001t0001g0187 | 2 | NA19063.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.493-4792_493-4781d others(14): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158600458 | |||||
| chr6:158600631
|
C | T | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.493-4636C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600631 | ||||||
| chr6:158600715
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.493-4552C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600715 | ||||||
| chr6:158600755
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-4512G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600755 | ||||||
| chr6:158600891
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.493-4376C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600891 | ||||||
| chr6:158600940
|
C | T | 16 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(13): Show | 17 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.493-4327C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600940 | ||||||
| chr6:158600944
|
T | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.493-4323T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600944 | ||||||
| chr6:158601087
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(202): Show | 214 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.493-4180T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601087 | ||||||
| chr6:158601111
|
TATA | T | 5 | a0001c0001t0001g0095a0001c0002t0001g0009a0001c0002t0001g0098others(2): Show | 6 | HG01934.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-4153_493-4151d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158601111 | |||||
| chr6:158601270
|
C | T | 1 | a0001c0001t0022g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.493-3997C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601270 | ||||||
| chr6:158601347
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.493-3920G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601347 | ||||||
| chr6:158601545
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-3722G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601545 | ||||||
| chr6:158601595
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.493-3672C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601595 | ||||||
| chr6:158601628
|
G | A | 1 | a0001c0001t0007g0084 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.493-3639G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601628 | ||||||
| chr6:158601673
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493-3594C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601673 | ||||||
| chr6:158601684
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-3583G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601684 | ||||||
| chr6:158601758
|
G | GA | 21 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0066others(18): Show | 22 | HG00423.hp1 HG01109.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.493-3492dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158601758 | |||||
| chr6:158601771
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.493-3496A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601771 | ||||||
| chr6:158601776
|
C | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-3491C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601776 | ||||||
| chr6:158601796
|
A | G | 2 | a0001c0001t0002g0158a0001c0001t0002g0166 | 2 | NA18964.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.493-3471A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601796 | ||||||
| chr6:158601843
|
C | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-3424C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601843 | ||||||
| chr6:158601986
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-3281G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158601986 | ||||||
| chr6:158602012
|
C | T | 3 | a0001c0001t0006g0005a0001c0001t0006g0061a0001c0001t0006g0065 | 4 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-3255C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602012 | ||||||
| chr6:158602097
|
C | G | 1 | a0001c0001t0004g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.493-3170C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602097 | ||||||
| chr6:158602212
|
T | C | 1 | a0001c0001t0007g0056 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.493-3055T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602212 | ||||||
| chr6:158602401
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-2866T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602401 | ||||||
| chr6:158602409
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.493-2858A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602409 | ||||||
| chr6:158602483
|
C | T | 2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.493-2784C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602483 | ||||||
| chr6:158602491
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.493-2776G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602491 | ||||||
| chr6:158602563
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.493-2704A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602563 | ||||||
| chr6:158602566
|
C | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.493-2701C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602566 | ||||||
| chr6:158602567
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.493-2700G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602567 | ||||||
| chr6:158602616
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0083a0001c0001t0001g0086others(1): Show | 5 | HG00609.hp1 NA18944.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-2651C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602616 | ||||||
| chr6:158602616
|
CT | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.493-2639delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158602616 | |||||
| chr6:158602684
|
C | T | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493-2583C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602684 | ||||||
| chr6:158602725
|
C | T | 49 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(46): Show | 51 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.493-2542C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602725 | ||||||
| chr6:158602807
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.493-2460C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602807 | ||||||
| chr6:158602866
|
G | C | 2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.493-2401G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602866 | ||||||
| chr6:158602972
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-2295T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602972 | ||||||
| chr6:158602981
|
A | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(206): Show | 218 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(215): Show |
intron_variant | MODIFIER | c.493-2286A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602981 | ||||||
| chr6:158602982
|
A | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(206): Show | 218 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(215): Show |
intron_variant | MODIFIER | c.493-2285A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602982 | ||||||
| chr6:158602990
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-2277A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602990 | ||||||
| chr6:158603055
|
C | T | 1 | a0001c0008t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493-2212C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603055 | ||||||
| chr6:158603063
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-2204G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603063 | ||||||
| chr6:158603151
|
T | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493-2116T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603151 | ||||||
| chr6:158603219
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-2048C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603219 | ||||||
| chr6:158603237
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.493-2030G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603237 | ||||||
| chr6:158603300
|
A | G | 2 | a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01884.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.493-1967A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603300 | ||||||
| chr6:158603336
|
GT | G | 46 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0010others(43): Show | 48 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.493-1930delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603336 | ||||||
| chr6:158603345
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.493-1922G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603345 | ||||||
| chr6:158603399
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.493-1868G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603399 | ||||||
| chr6:158603520
|
G | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-1747G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603520 | ||||||
| chr6:158603566
|
T | A | 1 | a0001c0001t0001g0287 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.493-1701T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603566 | ||||||
| chr6:158603588
|
G | GT | 31 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(28): Show | 32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.493-1660dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158603588 | |||||
| chr6:158603588
|
GT | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.493-1660delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158603588 | |||||
| chr6:158603588
|
GTT | G | 6 | a0001c0001t0001g0238a0001c0001t0001g0273a0001c0001t0002g0156others(3): Show | 6 | HG01175.hp2 HG02602.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-1661_493-1660d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158603588 | |||||
| chr6:158603588
|
GTTT | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 164 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.493-1662_493-1660d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158603588 | |||||
| chr6:158603595
|
T | G | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.493-1672T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603595 | ||||||
| chr6:158603655
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.493-1612T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603655 | ||||||
| chr6:158603689
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-1578A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603689 | ||||||
| chr6:158603769
|
C | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.493-1498C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603769 | ||||||
| chr6:158603775
|
T | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493-1492T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158603775 | ||||||
| chr6:158604224
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.493-1043A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604224 | ||||||
| chr6:158604311
|
A | G | 7 | a0001c0001t0001g0307a0001c0001t0003g0211a0001c0001t0003g0212others(4): Show | 7 | HG01243.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-956A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604311 | ||||||
| chr6:158604320
|
G | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0093 | 3 | HG00099.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.493-947G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604320 | ||||||
| chr6:158604327
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.493-940C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604327 | ||||||
| chr6:158604331
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.493-936C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604331 | ||||||
| chr6:158604332
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.493-935A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604332 | ||||||
| chr6:158604335
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.493-932C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604335 | ||||||
| chr6:158604335
|
CGT | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-916_493-915del others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158604335 | |||||
| chr6:158604335
|
CGTGT | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 149 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.493-918_493-915del others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158604335 | |||||
| chr6:158604462
|
T | A | 34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.493-805T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604462 | ||||||
| chr6:158604468
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.493-799C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604468 | ||||||
| chr6:158604510
|
T | C | 1 | a0001c0001t0010g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.493-757T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604510 | ||||||
| chr6:158604578
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.493-689C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604578 | ||||||
| chr6:158604580
|
T | G | 40 | a0001c0001t0001g0103a0001c0001t0002g0012a0001c0001t0002g0204others(37): Show | 42 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.493-687T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604580 | ||||||
| chr6:158604615
|
G | A | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493-652G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604615 | ||||||
| chr6:158604633
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.493-634C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604633 | ||||||
| chr6:158604661
|
T | C | 5 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0092others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-606T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604661 | ||||||
| chr6:158604700
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-567C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604700 | ||||||
| chr6:158604976
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 183 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.493-291T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604976 | ||||||
| chr6:158605129
|
AAAGT | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(101): Show | 108 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.493-137_493-134del others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605129 | ||||||
| chr6:158605130
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0005g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493-137_493-136ins others(18): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605130 | ||||||
| chr6:158605130
|
AAGTGTGT others(2): Show |
A | 33 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(30): Show | 34 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.493-136_493-128del others(9): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605130 | ||||||
| chr6:158605131
|
A | AAGTGTGT others(4): Show |
1 | a0001c0001t0002g0193 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.493-136_493-135ins others(11): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605131 | ||||||
| chr6:158605131
|
A | AGTGT | 10 | a0001c0001t0001g0081a0001c0001t0002g0032a0001c0001t0002g0175others(7): Show | 10 | HG02071.hp1 HG02647.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.493-111_493-108dup others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | AGTGTGT | 10 | a0001c0001t0002g0011a0001c0001t0002g0100a0001c0001t0002g0171others(7): Show | 12 | HG00733.hp1 HG01123.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-113_493-108dup others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | AGTGTGTG others(1): Show |
44 | a0001c0001t0001g0103a0001c0001t0001g0274a0001c0001t0001g0276others(41): Show | 45 | HG00140.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.493-115_493-108dup others(8): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | AGTGTGTG others(3): Show |
12 | a0001c0001t0002g0077a0001c0001t0002g0167a0001c0001t0002g0184others(9): Show | 12 | HG01109.hp2 HG02300.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.493-117_493-108dup others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0002g0012a0001c0001t0002g0102a0001c0001t0002g0206others(1): Show | 5 | HG02622.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-119_493-108dup others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | AGTGTGTG others(11): Show |
3 | a0001c0001t0005g0207a0001c0001t0005g0209a0001c0001t0005g0210 | 3 | HG02486.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.493-125_493-108dup others(18): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605131
|
A | T | 1 | a0001c0001t0005g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493-136A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605131 | ||||||
| chr6:158605131
|
AGTGTGTG others(3): Show |
A | 5 | a0001c0001t0001g0095a0001c0002t0001g0009a0001c0002t0001g0098others(2): Show | 6 | HG01934.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-117_493-108del others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605131 | |||||
| chr6:158605152
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(99): Show | 106 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.493-115G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605152 | ||||||
| chr6:158605154
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 115 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.493-113G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605154 | ||||||
| chr6:158605154
|
G | GTGTGTGT others(3): Show |
4 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0189others(1): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-108_493-107ins others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr6 | 158605154 | |||||
| chr6:158605156
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.493-111G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605156 | ||||||
| chr6:158605158
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.493-109G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605158 | ||||||
| chr6:158605159
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.493-108T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605159 | ||||||
| chr6:158605162
|
G | A | 21 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(18): Show | 22 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.493-105G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605162 | ||||||
| chr6:158605232
|
T | A | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.493-35T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605232 | ||||||
| chr6:158605468
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.573+121G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158605468 | ||||||
| chr6:158605869
|
GC | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(228): Show | 240 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.573+529delC | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158605869 | |||||
| chr6:158605869
|
GCC | G | 10 | a0001c0001t0001g0014a0001c0001t0001g0236a0001c0001t0001g0237others(7): Show | 11 | HG01192.hp2 HG01255.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+528_573+529del others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158605869 | |||||
| chr6:158606066
|
CTG | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG01255.hp1 HG01981.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.573+722_573+723del others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158606066 | |||||
| chr6:158606090
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.573+743G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606090 | ||||||
| chr6:158606127
|
C | T | 34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.573+780C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606127 | ||||||
| chr6:158606170
|
C | T | 6 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0001t0001g0276others(3): Show | 6 | HG00673.hp1 NA18747.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+823C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606170 | ||||||
| chr6:158606197
|
GGGGCGTG others(30): Show |
G | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.573+918_574-943del others(37): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158606197 | |||||
| chr6:158606239
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01496.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.573+892G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606239 | ||||||
| chr6:158606281
|
C | CGCTAGAG others(65): Show |
34 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(31): Show | 35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.573+945_573+946ins others(72): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158606281 | |||||
| chr6:158606281
|
C | CGCTAGAG others(65): Show |
1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.573+945_573+946ins others(72): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158606281 | |||||
| chr6:158606281
|
C | CGCTAGAG others(65): Show |
110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.573+945_573+946ins others(72): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 158606281 | |||||
| chr6:158606345
|
A | G | 35 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.574-899A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606345 | ||||||
| chr6:158606354
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-890G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606354 | ||||||
| chr6:158606629
|
A | T | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.574-615A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606629 | ||||||
| chr6:158606647
|
G | T | 35 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.574-597G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606647 | ||||||
| chr6:158606759
|
T | C | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-485T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606759 | ||||||
| chr6:158606816
|
G | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-428G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606816 | ||||||
| chr6:158606840
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.574-404C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606840 | ||||||
| chr6:158606866
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-378G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606866 | ||||||
| chr6:158606907
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.574-337A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606907 | ||||||
| chr6:158606927
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0160a0001c0001t0002g0161 | 4 | NA18960.hp1 NA18978.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-317G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606927 | ||||||
| chr6:158607117
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.574-127C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158607117 | ||||||
| chr6:158607171
|
G | A | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.574-73G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158607171 | ||||||
| chr6:158607444
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.673+101G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607444 | ||||||
| chr6:158607456
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.673+113C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607456 | ||||||
| chr6:158607501
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.673+158G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607501 | ||||||
| chr6:158607682
|
A | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.673+339A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607682 | ||||||
| chr6:158607746
|
G | C | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.673+403G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607746 | ||||||
| chr6:158607802
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18946.hp2 NA18962.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.673+459T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607802 | ||||||
| chr6:158607860
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.674-473C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607860 | ||||||
| chr6:158608011
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.674-322G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608011 | ||||||
| chr6:158608029
|
T | C | 32 | a0001c0001t0001g0103a0001c0001t0004g0044a0001c0001t0004g0046others(29): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.674-304T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608029 | ||||||
| chr6:158608150
|
GATGGGGT others(69): Show |
G | 1 | a0001c0001t0001g0059 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.674-149_674-74delC others(75): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr6 | 158608150 | |||||
| chr6:158608180
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.674-153C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608180 | ||||||
| chr6:158608205
|
CAGGTGCT others(31): Show |
C | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 115 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.674-96_674-59delCT others(36): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr6 | 158608205 | |||||
| chr6:158608218
|
C | T | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-115C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608218 | ||||||
| chr6:158608234
|
G | A | 1 | a0001c0001t0004g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.674-99G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608234 | ||||||
| chr6:158608237
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.674-96C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608237 | ||||||
| chr6:158608257
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.674-76G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608257 | ||||||
| chr6:158608310
|
G | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 150 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.674-23G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158608310 | ||||||
| chr6:158608770
|
G | A | 5 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(2): Show | 6 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+20G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158608770 | ||||||
| chr6:158608836
|
G | A | 35 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.896+86G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158608836 | ||||||
| chr6:158608841
|
T | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0236others(11): Show | 15 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+91T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158608841 | ||||||
| chr6:158608842
|
A | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0236others(11): Show | 15 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+92A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158608842 | ||||||
| chr6:158608921
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.896+171C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158608921 | ||||||
| chr6:158609027
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+277G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609027 | ||||||
| chr6:158609097
|
C | CA | 7 | a0001c0001t0001g0038a0001c0001t0001g0072a0001c0001t0001g0286others(4): Show | 7 | HG00733.hp2 HG00735.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+362dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158609097 | |||||
| chr6:158609097
|
C | CAA | 30 | a0001c0001t0001g0307a0001c0001t0003g0013a0001c0001t0003g0019others(27): Show | 31 | HG00642.hp2 HG01074.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.896+361_896+362dup others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158609097 | |||||
| chr6:158609112
|
A | AG | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+364dupG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158609112 | |||||
| chr6:158609142
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.896+392C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609142 | ||||||
| chr6:158609162
|
G | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.896+412G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609162 | ||||||
| chr6:158609203
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(196): Show | 206 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.896+453A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609203 | ||||||
| chr6:158609480
|
A | G | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.896+730A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609480 | ||||||
| chr6:158609499
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.896+749C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609499 | ||||||
| chr6:158609515
|
A | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0206 | 3 | HG02622.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.896+765A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609515 | ||||||
| chr6:158609601
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.896+851C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609601 | ||||||
| chr6:158609613
|
C | T | 1 | a0001c0001t0005g0016 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.896+863C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609613 | ||||||
| chr6:158609912
|
C | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0248 | 2 | HG02602.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.896+1162C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609912 | ||||||
| chr6:158609923
|
T | C | 6 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(3): Show | 7 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+1173T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609923 | ||||||
| chr6:158609940
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.896+1190C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609940 | ||||||
| chr6:158609966
|
A | G | 2 | a0001c0001t0004g0106a0001c0001t0004g0107 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.896+1216A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609966 | ||||||
| chr6:158609999
|
G | A | 1 | a0006c0007t0016g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.896+1249G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158609999 | ||||||
| chr6:158610146
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.896+1396A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610146 | ||||||
| chr6:158610219
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.896+1469A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610219 | ||||||
| chr6:158610269
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.896+1519A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610269 | ||||||
| chr6:158610333
|
A | G | 1 | a0001c0001t0003g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.896+1583A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610333 | ||||||
| chr6:158610338
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0054others(12): Show | 18 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.896+1588C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610338 | ||||||
| chr6:158610417
|
G | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02809.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.896+1667G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610417 | ||||||
| chr6:158610531
|
C | A | 48 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(45): Show | 51 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.896+1781C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610531 | ||||||
| chr6:158610611
|
CTT | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(103): Show | 110 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.896+1864_896+1865d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158610611 | |||||
| chr6:158610695
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 248 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.896+1945C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610695 | ||||||
| chr6:158610844
|
A | G | 52 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0100others(49): Show | 56 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.896+2094A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610844 | ||||||
| chr6:158610905
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.896+2155G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158610905 | ||||||
| chr6:158611202
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0070others(1): Show | 8 | HG00639.hp1 HG00738.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+2452A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611202 | ||||||
| chr6:158611447
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.896+2697T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611447 | ||||||
| chr6:158611522
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.896+2772G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611522 | ||||||
| chr6:158611638
|
C | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 204 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.896+2888C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611638 | ||||||
| chr6:158611752
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3002G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611752 | ||||||
| chr6:158611763
|
CAA | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+3015_896+3016d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158611763 | |||||
| chr6:158611835
|
T | C | 1 | a0001c0001t0017g0295 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.896+3085T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611835 | ||||||
| chr6:158611976
|
A | AC | 35 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.896+3234dupC | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158611976 | |||||
| chr6:158611976
|
A | ACCC | 19 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0117others(16): Show | 21 | HG00438.hp1 HG01069.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3232_896+3234d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158611976 | |||||
| chr6:158611978
|
C | CCT | 44 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(41): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.896+3229_896+3230i others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158611978 | |||||
| chr6:158611984
|
C | A | 1 | a0001c0001t0022g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.896+3234C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611984 | ||||||
| chr6:158611984
|
C | CCCA | 74 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(71): Show | 75 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.896+3234_896+3235i others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611984 | ||||||
| chr6:158611998
|
C | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+3248C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611998 | ||||||
| chr6:158612020
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 11 | HG00099.hp1 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.896+3270G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612020 | ||||||
| chr6:158612080
|
G | T | 2 | a0001c0001t0004g0111a0001c0001t0004g0112 | 2 | HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.896+3330G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612080 | ||||||
| chr6:158612086
|
C | T | 1 | a0001c0001t0021g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.896+3336C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612086 | ||||||
| chr6:158612141
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.896+3391G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612141 | ||||||
| chr6:158612160
|
C | T | 41 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0018others(38): Show | 43 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.896+3410C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612160 | ||||||
| chr6:158612283
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.896+3533C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612283 | ||||||
| chr6:158612285
|
G | C | 85 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(82): Show | 87 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.896+3535G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612285 | ||||||
| chr6:158612335
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3585C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612335 | ||||||
| chr6:158612379
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.896+3629A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612379 | ||||||
| chr6:158612418
|
G | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.896+3668G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612418 | ||||||
| chr6:158612710
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.896+3960A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612710 | ||||||
| chr6:158612745
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.896+3995T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158612745 | ||||||
| chr6:158613053
|
ATTTC | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+4307_896+4310d others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158613053 | |||||
| chr6:158613183
|
A | C | 1 | a0001c0001t0005g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.896+4433A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613183 | ||||||
| chr6:158613416
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0054others(12): Show | 18 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.896+4666G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613416 | ||||||
| chr6:158613416
|
G | T | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896+4666G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613416 | ||||||
| chr6:158613432
|
T | G | 3 | a0001c0001t0001g0259a0001c0001t0001g0265a0001c0001t0001g0311 | 3 | HG04184.hp2 NA18952.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.896+4682T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613432 | ||||||
| chr6:158613477
|
G | A | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.896+4727G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613477 | ||||||
| chr6:158613536
|
C | CAG | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 248 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.896+4787_896+4788i others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158613536 | |||||
| chr6:158613665
|
A | G | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+4915A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613665 | ||||||
| chr6:158613731
|
T | C | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.896+4981T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613731 | ||||||
| chr6:158613762
|
T | A | 1 | a0001c0001t0003g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.896+5012T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613762 | ||||||
| chr6:158613787
|
T | C | 4 | a0001c0001t0002g0011a0001c0001t0002g0100a0001c0001t0002g0173others(1): Show | 5 | HG02145.hp1 HG02717.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.896+5037T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613787 | ||||||
| chr6:158613868
|
G | C | 1 | a0001c0001t0005g0016 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.896+5118G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613868 | ||||||
| chr6:158613919
|
T | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+5169T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158613919 | ||||||
| chr6:158614048
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.896+5298A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614048 | ||||||
| chr6:158614065
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.896+5315A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614065 | ||||||
| chr6:158614095
|
A | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0206 | 3 | HG02622.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.896+5345A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614095 | ||||||
| chr6:158614221
|
G | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | NA18971.hp1 NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.896+5471G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614221 | ||||||
| chr6:158614245
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+5495C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614245 | ||||||
| chr6:158614479
|
T | TTTAA | 194 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(191): Show | 202 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.896+5730_896+5733d others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158614479 | |||||
| chr6:158614489
|
A | T | 41 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(38): Show | 42 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.896+5739A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614489 | ||||||
| chr6:158614490
|
T | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.896+5740T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614490 | ||||||
| chr6:158614541
|
G | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+5791G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614541 | ||||||
| chr6:158614756
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0205a0001c0001t0002g0206 | 4 | HG02622.hp2 HG02922.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+6006C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614756 | ||||||
| chr6:158614887
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.896+6137T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614887 | ||||||
| chr6:158614913
|
G | C | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+6163G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614913 | ||||||
| chr6:158614922
|
G | C | 1 | a0001c0001t0005g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.896+6172G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614922 | ||||||
| chr6:158614984
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(159): Show | 169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.896+6234A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158614984 | ||||||
| chr6:158615000
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+6250T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615000 | ||||||
| chr6:158615095
|
C | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.896+6345C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615095 | ||||||
| chr6:158615265
|
T | C | 2 | a0001c0001t0003g0211a0001c0001t0003g0219 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.896+6515T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615265 | ||||||
| chr6:158615559
|
C | A | 1 | a0001c0001t0003g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.896+6809C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615559 | ||||||
| chr6:158615576
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.896+6826T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615576 | ||||||
| chr6:158615909
|
C | T | 41 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0018others(38): Show | 43 | HG00558.hp1 HG01074.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.896+7159C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158615909 | ||||||
| chr6:158615985
|
ATAAACTT | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0299 | 3 | HG00642.hp1 HG01496.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.896+7240_896+7246d others(9): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158615985 | |||||
| chr6:158616027
|
C | A | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+7277C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616027 | ||||||
| chr6:158616038
|
A | G | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+7288A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616038 | ||||||
| chr6:158616042
|
T | G | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+7292T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616042 | ||||||
| chr6:158616092
|
G | A | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.896+7342G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616092 | ||||||
| chr6:158616249
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 203 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.897-7301G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616249 | ||||||
| chr6:158616276
|
CTCTT | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 203 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.897-7272_897-7269d others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158616276 | |||||
| chr6:158616304
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-7246G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616304 | ||||||
| chr6:158616316
|
A | AT | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-7229dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158616316 | |||||
| chr6:158616562
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.897-6988C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616562 | ||||||
| chr6:158616696
|
C | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-6854C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616696 | ||||||
| chr6:158616745
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-6805C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616745 | ||||||
| chr6:158616845
|
G | A | 1 | a0001c0001t0020g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.897-6705G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616845 | ||||||
| chr6:158616907
|
T | C | 7 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(4): Show | 8 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.897-6643T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616907 | ||||||
| chr6:158616995
|
C | G | 1 | a0001c0001t0004g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.897-6555C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616995 | ||||||
| chr6:158617061
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-6489G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617061 | ||||||
| chr6:158617104
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG00639.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.897-6446G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617104 | ||||||
| chr6:158617220
|
A | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.897-6330A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617220 | ||||||
| chr6:158617287
|
C | G | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.897-6263C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617287 | ||||||
| chr6:158617368
|
CTCTCTTC others(8): Show |
C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-6178_897-6164d others(17): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158617368 | |||||
| chr6:158617394
|
G | A | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.897-6156G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617394 | ||||||
| chr6:158617410
|
C | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.897-6140C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617410 | ||||||
| chr6:158617438
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0260 | 2 | HG03239.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.897-6112T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617438 | ||||||
| chr6:158617454
|
GT | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-6088delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158617454 | |||||
| chr6:158617469
|
C | CT | 105 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(102): Show | 109 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-6080dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158617469 | |||||
| chr6:158617560
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.897-5990T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617560 | ||||||
| chr6:158617742
|
AGTC | A | 3 | a0001c0001t0001g0249a0001c0001t0001g0255a0001c0001t0001g0291 | 3 | HG02735.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.897-5807_897-5805d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617742 | ||||||
| chr6:158617867
|
T | C | 8 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(5): Show | 9 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-5683T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158617867 | ||||||
| chr6:158618023
|
C | G | 1 | a0005c0006t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.897-5527C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618023 | ||||||
| chr6:158618023
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.897-5527C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618023 | ||||||
| chr6:158618041
|
T | C | 1 | a0001c0001t0025g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.897-5509T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618041 | ||||||
| chr6:158618121
|
TTGTAGGT others(5): Show |
T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5428_897-5417d others(14): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618121 | ||||||
| chr6:158618180
|
T | C | 44 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(41): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.897-5370T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618180 | ||||||
| chr6:158618181
|
A | G | 44 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(41): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.897-5369A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618181 | ||||||
| chr6:158618188
|
A | T | 44 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(41): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.897-5362A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618188 | ||||||
| chr6:158618222
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.897-5328C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618222 | ||||||
| chr6:158618235
|
G | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5315G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618235 | ||||||
| chr6:158618239
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5311T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618239 | ||||||
| chr6:158618299
|
A | G | 40 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(37): Show | 42 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.897-5251A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618299 | ||||||
| chr6:158618302
|
C | CGTTTTTG | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5248_897-5247i others(9): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618302 | ||||||
| chr6:158618303
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5247C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618303 | ||||||
| chr6:158618306
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5244C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618306 | ||||||
| chr6:158618308
|
T | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5242T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618308 | ||||||
| chr6:158618308
|
T | TTTGTTGT others(2): Show |
42 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0172others(39): Show | 44 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.897-5227_897-5219d others(11): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158618308 | |||||
| chr6:158618355
|
A | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-5195A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618355 | ||||||
| chr6:158618378
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-5172A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618378 | ||||||
| chr6:158618422
|
C | G | 1 | a0001c0001t0003g0013 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.897-5128C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618422 | ||||||
| chr6:158618569
|
T | C | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.897-4981T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618569 | ||||||
| chr6:158618576
|
T | G | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.897-4974T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618576 | ||||||
| chr6:158618581
|
C | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.897-4969C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618581 | ||||||
| chr6:158618656
|
T | G | 1 | a0001c0001t0005g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.897-4894T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618656 | ||||||
| chr6:158618819
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.897-4731C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618819 | ||||||
| chr6:158618862
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 248 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.897-4688A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618862 | ||||||
| chr6:158618967
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0007g0056a0001c0001t0007g0057others(1): Show | 4 | HG02056.hp2 NA18999.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-4583C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158618967 | ||||||
| chr6:158619262
|
C | G | 1 | a0001c0001t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.897-4288C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619262 | ||||||
| chr6:158619274
|
C | G | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.897-4276C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619274 | ||||||
| chr6:158619281
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.897-4269G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619281 | ||||||
| chr6:158619339
|
T | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.897-4211T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619339 | ||||||
| chr6:158619426
|
C | T | 1 | a0001c0001t0025g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.897-4124C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619426 | ||||||
| chr6:158619507
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-4043A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619507 | ||||||
| chr6:158619597
|
G | A | 1 | a0005c0006t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.897-3953G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619597 | ||||||
| chr6:158619710
|
A | T | 1 | a0001c0001t0004g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897-3840A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619710 | ||||||
| chr6:158619833
|
C | T | 4 | a0001c0001t0006g0005a0001c0001t0006g0061a0001c0001t0006g0065others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-3717C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619833 | ||||||
| chr6:158619862
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.897-3688C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619862 | ||||||
| chr6:158619867
|
C | CA | 37 | a0001c0001t0001g0036a0001c0001t0001g0072a0001c0001t0001g0081others(34): Show | 38 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.897-3661dupA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619867 | |||||
| chr6:158619867
|
C | CAA | 11 | a0001c0001t0001g0048a0001c0001t0002g0010a0001c0001t0002g0032others(8): Show | 12 | HG02027.hp2 HG02145.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.897-3662_897-3661d others(4): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619867 | |||||
| chr6:158619867
|
CA | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(131): Show | 138 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.897-3661delA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619867 | |||||
| chr6:158619881
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0136a0001c0001t0006g0005a0001c0001t0006g0061 | 4 | HG01069.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-3667_897-3658d others(12): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619881 | |||||
| chr6:158619882
|
AAAAAAAA others(2): Show |
A | 40 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(37): Show | 43 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.897-3666_897-3658d others(11): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619882 | |||||
| chr6:158619888
|
AAGG | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0054others(10): Show | 15 | HG00140.hp2 HG01496.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.897-3657_897-3655d others(5): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158619888 | |||||
| chr6:158619977
|
G | A | 1 | a0001c0001t0014g0264 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.897-3573G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158619977 | ||||||
| chr6:158620122
|
G | A | 1 | a0001c0001t0004g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.897-3428G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620122 | ||||||
| chr6:158620305
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0004g0107 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.897-3245C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620305 | ||||||
| chr6:158620497
|
A | G | 44 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(41): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.897-3053A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620497 | ||||||
| chr6:158620523
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.897-3027G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620523 | ||||||
| chr6:158620630
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.897-2920G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620630 | ||||||
| chr6:158620684
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 203 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.897-2866G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620684 | ||||||
| chr6:158620751
|
C | G | 1 | a0001c0001t0025g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.897-2799C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620751 | ||||||
| chr6:158620807
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-2743C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620807 | ||||||
| chr6:158620809
|
G | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-2741G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620809 | ||||||
| chr6:158620821
|
A | G | 3 | a0001c0001t0006g0005a0001c0001t0006g0061a0001c0001t0006g0065 | 4 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-2729A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620821 | ||||||
| chr6:158620840
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.897-2710A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620840 | ||||||
| chr6:158620876
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.897-2674A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158620876 | ||||||
| chr6:158621079
|
T | A | 1 | a0001c0001t0002g0163 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.897-2471T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621079 | ||||||
| chr6:158621210
|
A | G | 1 | a0001c0001t0004g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.897-2340A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621210 | ||||||
| chr6:158621311
|
T | C | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.897-2239T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621311 | ||||||
| chr6:158621315
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.897-2235A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621315 | ||||||
| chr6:158621321
|
G | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.897-2229G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621321 | ||||||
| chr6:158621456
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.897-2094A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621456 | ||||||
| chr6:158621505
|
C | T | 1 | a0001c0001t0003g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.897-2045C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621505 | ||||||
| chr6:158621521
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00609.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.897-2029G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621521 | ||||||
| chr6:158621570
|
C | G | 30 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(27): Show | 31 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.897-1980C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621570 | ||||||
| chr6:158621819
|
T | G | 1 | a0001c0001t0003g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.897-1731T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621819 | ||||||
| chr6:158621844
|
C | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.897-1706C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621844 | ||||||
| chr6:158621885
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.897-1665G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621885 | ||||||
| chr6:158621945
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0172 | 3 | HG02559.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.897-1605C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621945 | ||||||
| chr6:158621946
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.897-1604G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621946 | ||||||
| chr6:158621963
|
C | T | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.897-1587C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158621963 | ||||||
| chr6:158622409
|
G | A | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.897-1141G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622409 | ||||||
| chr6:158622537
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0205a0001c0001t0002g0206 | 4 | HG02622.hp2 HG02922.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-1013G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622537 | ||||||
| chr6:158622556
|
C | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.897-994C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622556 | ||||||
| chr6:158622622
|
C | T | 1 | a0001c0001t0001g0151 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.897-928C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622622 | ||||||
| chr6:158622643
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 204 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.897-907T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622643 | ||||||
| chr6:158622772
|
A | T | 1 | a0001c0001t0005g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.897-778A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622772 | ||||||
| chr6:158622822
|
CTTG | C | 41 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0018others(38): Show | 43 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.897-723_897-721del others(3): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr6 | 158622822 | |||||
| chr6:158622895
|
T | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.897-655T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622895 | ||||||
| chr6:158622895
|
T | G | 27 | a0001c0001t0003g0013a0001c0001t0003g0116a0001c0001t0003g0118others(24): Show | 28 | HG00733.hp2 HG00735.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.897-655T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622895 | ||||||
| chr6:158622911
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0236others(11): Show | 15 | HG01106.hp1 HG01192.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.897-639C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158622911 | ||||||
| chr6:158623243
|
G | A | 3 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0110 | 3 | HG00738.hp1 HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.897-307G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623243 | ||||||
| chr6:158623263
|
T | G | 3 | a0001c0001t0005g0021a0001c0001t0005g0189a0001c0001t0005g0190 | 3 | HG02886.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.897-287T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623263 | ||||||
| chr6:158623284
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 119 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.897-266A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623284 | ||||||
| chr6:158623408
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.897-142T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623408 | ||||||
| chr6:158623762
|
AT | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(227): Show | 239 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.954+171delT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr6 | 158623762 | |||||
| chr6:158623762
|
ATT | A | 7 | a0001c0001t0001g0289a0001c0001t0002g0012a0001c0001t0002g0204others(4): Show | 8 | HG00558.hp2 HG01109.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+170_954+171del others(2): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr6 | 158623762 | |||||
| chr6:158623836
|
C | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.954+229C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158623836 | ||||||
| chr6:158623909
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+302C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158623909 | ||||||
| chr6:158623979
|
C | T | 91 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(88): Show | 93 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.954+372C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158623979 | ||||||
| chr6:158623993
|
C | T | 1 | a0001c0001t0027g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.954+386C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158623993 | ||||||
| chr6:158624052
|
G | A | 9 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0005g0016others(6): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+445G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624052 | ||||||
| chr6:158624132
|
C | T | 30 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(27): Show | 31 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.954+525C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624132 | ||||||
| chr6:158624148
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0227 | 2 | HG01074.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.954+541G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624148 | ||||||
| chr6:158624162
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.954+555C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624162 | ||||||
| chr6:158624206
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.954+599A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624206 | ||||||
| chr6:158624262
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.954+655G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624262 | ||||||
| chr6:158624327
|
A | G | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+720A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624327 | ||||||
| chr6:158624330
|
T | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+723T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624330 | ||||||
| chr6:158624331
|
G | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+724G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624331 | ||||||
| chr6:158624333
|
T | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+726T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624333 | ||||||
| chr6:158624337
|
G | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+730G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624337 | ||||||
| chr6:158624338
|
A | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+731A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624338 | ||||||
| chr6:158624339
|
G | C | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+732G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624339 | ||||||
| chr6:158624340
|
A | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+733A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624340 | ||||||
| chr6:158624341
|
A | C | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+734A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624341 | ||||||
| chr6:158624345
|
T | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+738T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624345 | ||||||
| chr6:158624347
|
A | C | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+740A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624347 | ||||||
| chr6:158624348
|
T | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+741T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624348 | ||||||
| chr6:158624351
|
C | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.954+744C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624351 | ||||||
| chr6:158624386
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.955-718G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624386 | ||||||
| chr6:158624410
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.955-694C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624410 | ||||||
| chr6:158624468
|
G | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.955-636G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624468 | ||||||
| chr6:158624678
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-426T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624678 | ||||||
| chr6:158624690
|
C | T | 41 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0018others(38): Show | 43 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.955-414C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624690 | ||||||
| chr6:158624778
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-326C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624778 | ||||||
| chr6:158624787
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.955-317G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624787 | ||||||
| chr6:158624835
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.955-269C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624835 | ||||||
| chr6:158624928
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.955-176C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624928 | ||||||
| chr6:158624960
|
G | A | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.955-144G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624960 | ||||||
| chr6:158625044
|
T | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 248 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.955-60T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158625044 | ||||||
| chr6:158625084
|
G | A | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-20G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158625084 | ||||||
| chr6:158625259
|
G | T | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1057+53G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 12/16 | chr6 | 158625259 | ||||||
| chr6:158625342
|
C | A | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1057+136C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 12/16 | chr6 | 158625342 | ||||||
| chr6:158625379
|
C | T | 1 | a0001c0001t0006g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1057+173C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 12/16 | chr6 | 158625379 | ||||||
| chr6:158625409
|
G | A | 43 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(40): Show | 46 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1057+203G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 12/16 | chr6 | 158625409 | ||||||
| chr6:158625470
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1058-233G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 12/16 | chr6 | 158625470 | ||||||
| chr6:158625765
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1109+11C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158625765 | ||||||
| chr6:158625937
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1109+183T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158625937 | ||||||
| chr6:158625988
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109+234C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158625988 | ||||||
| chr6:158625997
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1109+243C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158625997 | ||||||
| chr6:158626037
|
G | T | 1 | a0001c0001t0002g0018 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1109+283G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626037 | ||||||
| chr6:158626055
|
A | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 248 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.1109+301A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626055 | ||||||
| chr6:158626112
|
C | T | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1109+358C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626112 | ||||||
| chr6:158626125
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0252a0001c0001t0001g0257others(4): Show | 8 | HG02080.hp1 HG03688.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1109+371C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626125 | ||||||
| chr6:158626185
|
G | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0042others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109+431G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626185 | ||||||
| chr6:158626211
|
G | C | 1 | a0001c0001t0002g0170 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1109+457G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626211 | ||||||
| chr6:158626309
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1109+555G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626309 | ||||||
| chr6:158626350
|
T | C | 43 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(40): Show | 46 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1109+596T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626350 | ||||||
| chr6:158626408
|
C | T | 2 | a0001c0001t0003g0132a0001c0001t0003g0141 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1109+654C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626408 | ||||||
| chr6:158626453
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0035 | 2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1109+699G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626453 | ||||||
| chr6:158626504
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1109+750C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626504 | ||||||
| chr6:158626607
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1109+853C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626607 | ||||||
| chr6:158626636
|
TTTCA | T | 30 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(27): Show | 31 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1109+887_1109+890d others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626636 | |||||
| chr6:158626773
|
C | CTCACTCA others(16): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0054others(12): Show | 18 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1109+1029_1109+105 others(27): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626773 | |||||
| chr6:158626870
|
ACT | A | 31 | a0001c0001t0003g0213a0001c0001t0004g0044a0001c0001t0004g0046others(28): Show | 32 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1109+1120_1109+112 others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626870 | |||||
| chr6:158626880
|
T | A | 32 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(29): Show | 33 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1109+1126T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626880 | ||||||
| chr6:158626910
|
CCTCACCC others(5): Show |
C | 2 | a0001c0001t0001g0036a0001c0001t0026g0129 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1109+1179_1109+119 others(16): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626910 | |||||
| chr6:158626913
|
C | T | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1109+1159C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626913 | ||||||
| chr6:158626926
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1109+1172A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626926 | ||||||
| chr6:158626928
|
CCTCATT | C | 35 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(32): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1109+1179_1109+118 others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626928 | |||||
| chr6:158626932
|
ATTCT | A | 75 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(72): Show | 79 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.1109+1179_1109+118 others(8): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626932 | ||||||
| chr6:158626933
|
T | C | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1109+1179T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626933 | ||||||
| chr6:158626934
|
T | TCTCACC | 120 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1109+1198_1109+120 others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626934 | |||||
| chr6:158626936
|
T | A | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1109+1182T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626936 | ||||||
| chr6:158626954
|
TCACTCA | T | 20 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(17): Show | 21 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1109+1204_1109+120 others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158626954 | |||||
| chr6:158626958
|
T | C | 11 | a0001c0001t0004g0104a0001c0001t0004g0115a0001c0001t0004g0120others(8): Show | 11 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1109+1204T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626958 | ||||||
| chr6:158626960
|
A | T | 10 | a0001c0001t0004g0104a0001c0001t0004g0115a0001c0001t0004g0120others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1109+1206A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158626960 | ||||||
| chr6:158627017
|
TCTCA | T | 2 | a0001c0001t0005g0016a0001c0001t0005g0022 | 3 | HG01884.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1109+1267_1109+127 others(8): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158627017 | |||||
| chr6:158627045
|
C | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0217a0001c0001t0012g0216 | 4 | HG02602.hp2 HG02738.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109+1291C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627045 | ||||||
| chr6:158627052
|
C | G | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1109+1298C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627052 | ||||||
| chr6:158627072
|
C | G | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1109+1318C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627072 | ||||||
| chr6:158627077
|
ACACCCT | A | 34 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(31): Show | 35 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110-1317_1110-131 others(10): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158627077 | |||||
| chr6:158627107
|
T | TCA | 237 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(234): Show | 247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1110-1300_1110-129 others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158627107 | |||||
| chr6:158627135
|
A | T | 1 | a0001c0001t0003g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1110-1273A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627135 | ||||||
| chr6:158627136
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-1272C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627136 | ||||||
| chr6:158627144
|
A | C | 1 | a0001c0001t0005g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1110-1264A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627144 | ||||||
| chr6:158627157
|
C | T | 37 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0018others(34): Show | 39 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1110-1251C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627157 | ||||||
| chr6:158627183
|
C | G | 4 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0189others(1): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110-1225C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627183 | ||||||
| chr6:158627293
|
A | G | 8 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(5): Show | 9 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110-1115A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627293 | ||||||
| chr6:158627507
|
T | G | 1 | a0001c0001t0002g0165 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110-901T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627507 | ||||||
| chr6:158627520
|
G | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1110-888G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627520 | ||||||
| chr6:158627610
|
G | GT | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-798_1110-797i others(3): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627610 | ||||||
| chr6:158627611
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-797C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627611 | ||||||
| chr6:158627611
|
C | T | 1 | a0001c0001t0025g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1110-797C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627611 | ||||||
| chr6:158627612
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-796A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627612 | ||||||
| chr6:158627613
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-795C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627613 | ||||||
| chr6:158627615
|
G | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-793G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627615 | ||||||
| chr6:158627660
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0011g0051 | 2 | NA18981.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1110-748C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627660 | ||||||
| chr6:158627790
|
G | A | 1 | a0005c0006t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1110-618G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627790 | ||||||
| chr6:158627805
|
T | TAATG | 237 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(234): Show | 247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1110-601_1110-600i others(6): Show |
TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 158627805 | |||||
| chr6:158627828
|
A | G | 1 | a0001c0001t0010g0256 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1110-580A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627828 | ||||||
| chr6:158627908
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1110-500G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627908 | ||||||
| chr6:158627963
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1110-445C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627963 | ||||||
| chr6:158627997
|
A | G | 1 | a0001c0001t0018g0277 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1110-411A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627997 | ||||||
| chr6:158628027
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198 | 3 | HG02109.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1110-381C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628027 | ||||||
| chr6:158628079
|
G | C | 1 | a0006c0007t0016g0130 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1110-329G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628079 | ||||||
| chr6:158628121
|
C | T | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1110-287C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628121 | ||||||
| chr6:158628124
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1110-284G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628124 | ||||||
| chr6:158628146
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(241): Show | 254 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.1110-262T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628146 | ||||||
| chr6:158628176
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1110-232G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628176 | ||||||
| chr6:158628179
|
C | T | 1 | a0004c0005t0003g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1110-229C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628179 | ||||||
| chr6:158628287
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0029 | 2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1110-121C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628287 | ||||||
| chr6:158628313
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110-95C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628313 | ||||||
| chr6:158628335
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1110-73T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628335 | ||||||
| chr6:158628344
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1110-64C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628344 | ||||||
| chr6:158628401
|
T | C | 2 | a0001c0001t0005g0096a0001c0001t0005g0191 | 2 | HG03041.hp1 HG03540.hp2 |
splice_region_variant&intron_variant | LOW | c.1110-7T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158628401 | ||||||
| chr6:158628504
|
T | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0217 | 3 | HG02602.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1192+14T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628504 | ||||||
| chr6:158628612
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1192+122G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628612 | ||||||
| chr6:158628648
|
C | T | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192+158C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628648 | ||||||
| chr6:158628795
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1192+305C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628795 | ||||||
| chr6:158628857
|
G | A | 7 | a0001c0001t0001g0259a0001c0001t0001g0265a0001c0001t0001g0311others(4): Show | 8 | HG02145.hp1 HG02717.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192+367G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628857 | ||||||
| chr6:158628957
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1192+467C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628957 | ||||||
| chr6:158628984
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(111): Show | 118 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1192+494T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158628984 | ||||||
| chr6:158629394
|
G | A | 1 | a0001c0001t0022g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1193-336G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629394 | ||||||
| chr6:158629502
|
T | A | 7 | a0001c0001t0005g0016a0001c0001t0005g0021a0001c0001t0005g0022others(4): Show | 8 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193-228T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629502 | ||||||
| chr6:158629507
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1193-223G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629507 | ||||||
| chr6:158629508
|
G | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1193-222G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629508 | ||||||
| chr6:158629539
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0204a0001c0001t0002g0205others(1): Show | 5 | HG01109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1193-191C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629539 | ||||||
| chr6:158629562
|
C | CT | 45 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(42): Show | 48 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1193-167dupT | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr6 | 158629562 | |||||
| chr6:158629600
|
T | C | 45 | a0001c0001t0004g0044a0001c0001t0004g0046a0001c0001t0004g0052others(42): Show | 47 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1193-130T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629600 | ||||||
| chr6:158629665
|
G | C | 1 | a0001c0001t0026g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1193-65G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 14/16 | chr6 | 158629665 | ||||||
| chr6:158629857
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1282+38C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158629857 | ||||||
| chr6:158629883
|
C | T | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+64C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158629883 | ||||||
| chr6:158630002
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1282+183A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630002 | ||||||
| chr6:158630097
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1282+278T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630097 | ||||||
| chr6:158630154
|
A | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 127 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1282+335A>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630154 | ||||||
| chr6:158630346
|
A | G | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+527A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630346 | ||||||
| chr6:158630578
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1283-745G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630578 | ||||||
| chr6:158630698
|
G | A | 1 | a0001c0001t0014g0264 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1283-625G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630698 | ||||||
| chr6:158630714
|
TA | T | 117 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(114): Show | 123 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.1283-596delA | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr6 | 158630714 | |||||
| chr6:158630828
|
G | A | 1 | a0001c0001t0003g0215 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1283-495G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630828 | ||||||
| chr6:158630842
|
C | T | 1 | a0001c0001t0003g0229 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1283-481C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630842 | ||||||
| chr6:158630876
|
C | T | 115 | a0001c0001t0001g0307a0001c0001t0002g0010a0001c0001t0002g0011others(112): Show | 121 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1283-447C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630876 | ||||||
| chr6:158630880
|
C | T | 115 | a0001c0001t0001g0307a0001c0001t0002g0010a0001c0001t0002g0011others(112): Show | 121 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.1283-443C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630880 | ||||||
| chr6:158630954
|
C | T | 1 | a0001c0001t0005g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1283-369C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630954 | ||||||
| chr6:158630976
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1283-347C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 15/16 | chr6 | 158630976 | ||||||
| chr6:158631439
|
G | A | 33 | a0001c0001t0003g0013a0001c0001t0003g0019a0001c0001t0003g0089others(30): Show | 34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1349+50G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631439 | ||||||
| chr6:158631510
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1349+121T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631510 | ||||||
| chr6:158631573
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349+184T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631573 | ||||||
| chr6:158631650
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1350-160G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631650 | ||||||
| chr6:158631664
|
G | C | 1 | a0001c0001t0014g0264 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1350-146G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631664 | ||||||
| chr6:158631689
|
G | A | 45 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(42): Show | 48 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1350-121G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 16/16 | chr6 | 158631689 |