Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| a0002 | 0/0 | 475 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| a0003 | 0/0 | 475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| a0004 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| a0005 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| a0006 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | MEPLA others(470): Show |
chr6 | 158555091 | 158640429 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1425 | 322 | 82 | 72 | 117 | 12 | 37 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0001c0002 | 0/0 | 1425 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0001c0008 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0002c0003 | 0/0 | 1425 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0003c0006 | 0/0 | 1425 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0004c0005 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0005c0007 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
chr6 | 158555091 | 158640429 | ||
| a0006c0004 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | ATGGA others(1420): Show |
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 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0002 | 0/0 | 5103 | 47 | 15 | 3 | 25 | 0 | 4 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0003 | 0/0 | 5103 | 32 | 13 | 13 | 0 | 1 | 5 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0004 | 0/0 | 5101 | 25 | 9 | 13 | 1 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0005 | 0/0 | 5101 | 14 | 14 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0006 | 0/0 | 5103 | 7 | 1 | 3 | 0 | 3 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0007 | 0/0 | 5103 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0008 | 0/0 | 5102 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5097): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0009 | 0/0 | 5103 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0010 | 0/0 | 5103 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0011 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5079): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0012 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0013 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0014 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0015 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0017 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0018 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0019 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0020 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0021 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0022 | 0/0 | 5116 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5111): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0023 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0024 | 0/0 | 5101 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0025 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0026 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0027 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0028 | 0/0 | 5101 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0029 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0001t0030 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0002t0001 | 0/0 | 5103 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0002t0031 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0001c0008t0001 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0002c0003t0004 | 0/0 | 5101 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5096): Show |
chr6 | 158555091 | 158640429 |
| a0003c0006t0001 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0004c0005t0003 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0005c0007t0016 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| a0006c0004t0001 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | GAGTT others(5098): Show |
chr6 | 158555091 | 158640429 |
| actghapid | grch38/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 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0019 | 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 |
| a0001c0001t0001g0028 | 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 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0141 | 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 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0264 | 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 |
| 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 |
| 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 | 0 | 1 | 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 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0280 | 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 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0311 | 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 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0187 | 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 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0092 | 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 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0134 | 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 |
| a0001c0001t0003g0143 | 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 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0117 | 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 |
| 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 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0005g0135 | 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 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0012g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0014g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0015g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0017g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0018g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0019g0019 | 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 |
| a0001c0001t0021g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0022g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0023g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0024g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0025g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0026g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0027g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0001t0028g0123 | 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 |
| a0001c0001t0030g0033 | 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 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0002t0031g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0001c0008t0001g0075 | 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 |
| a0003c0006t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0004c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0005c0007t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| a0006c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0044 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | 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 | g0030 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0073 | 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 | g0261 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0271 | EAS | CHS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0302 | 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 | g0221 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG00741 | hp2 | a0001 | c0001 | t0028 | g0123 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0137 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0095 | 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 | g0047 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0094 | 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 | g0118 | 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 | g0055 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01175 | hp2 | a0003 | c0006 | t0001 | g0045 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0151 | 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 | g0048 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0110 | 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 | g0021 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0297 | 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 | g0115 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0064 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0018 | 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 | g0144 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01934 | hp1 | a0001 | c0002 | t0031 | g0099 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01981 | hp2 | a0001 | c0001 | t0022 | g0291 | 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 | g0295 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0173 | 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 | g0018 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0270 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0266 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02300 | hp2 | a0001 | c0001 | t0024 | g0121 | AMR | PEL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02572 | hp2 | a0004 | c0005 | t0003 | g0022 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0043 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02683 | hp2 | a0001 | c0008 | t0001 | g0075 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0215 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0101 | 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 | g0219 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0013 | 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 | g0106 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0130 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0202 | 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 | g0299 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0116 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0145 | 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 | g0305 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0208 | 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 | g0198 | 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 | g0127 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0036 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03516 | hp2 | a0005 | c0007 | t0016 | g0132 | AFR | ESN | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0179 | 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 | g0076 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03688 | hp1 | a0001 | c0001 | t0021 | g0304 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0104 | 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 | g0229 | SAS | PJL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04204 | hp1 | a0001 | c0001 | t0027 | g0081 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | STU | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0212 | 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 | g0263 | EAS | CHB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0079 | 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 | g0148 | AFR | YRI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18944 | hp1 | a0006 | c0004 | t0001 | g0267 | 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 | g0243 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0308 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0025 | 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 | g0230 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0058 | 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 | g0276 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18980 | hp2 | a0001 | c0001 | t0014 | g0249 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18981 | hp1 | a0001 | c0001 | t0011 | g0053 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0170 | 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 | g0250 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0056 | 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 | g0242 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18994 | hp1 | a0001 | c0001 | t0017 | g0281 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0239 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19012 | hp2 | a0001 | c0001 | t0019 | g0019 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0146 | 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 | g0117 | AFR | LWK | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0282 | 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 | g0031 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | 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 | g0172 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19088 | hp1 | a0001 | c0001 | t0030 | g0033 | 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 | g0256 | EAS | JPT | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0241 | 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 | g0260 | AFR | ASW | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20752 | hp2 | a0001 | c0001 | t0013 | g0139 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0225 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | GIH | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | GIH | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0217 | 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 | g0131 | 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 | g0040 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | MSL | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | 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 | g0122 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | USA | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | TMEM181_chr6_158555091_158640429 | TMEM181 | chr6 | 158555091 | 158640429 |
| view | 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 | a0005 | 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 | a0003 | 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 | a0006 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0003 a0001c0001t0012 a0004c0005t0003 |
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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0023 others(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 | a0001c0001t0003 a0001c0001t0012 a0004c0005t0003 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0023 others(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 | a0001c0001t0002 a0001c0001t0029 |
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 | a0005c0007t0016 | 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 | a0001c0001t0020 a0005c0007t0016 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0023 others(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 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(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 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(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 | a0001c0001t0002 a0001c0001t0029 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0023 others(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 |
| view | 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 | a0001c0001t0002g0020 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0003g0310 | 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 | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0002g0102 a0001c0001t0005g0098 a0001c0002t0001g0009 others(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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0307 a0001c0001t0001g0308 others(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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0003g0118 others(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 | a0001c0001t0001g0305 a0001c0001t0003g0306 a0001c0001t0003g0310 |
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 | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(305): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | 219 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(216): Show |
229 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(226): 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0133 others(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 | 38 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(35): 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
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 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
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 | a0001c0001t0001g0105 | 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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(221): Show |
235 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(232): 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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
230 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.8+1657G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158561889 | |||||||
| chr6:158561952 | C | G | 22 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(19): 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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0003g0118 others(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 | a0001c0001t0001g0095 | 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 | 149 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(146): Show |
156 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(153): 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 | a0001c0001t0003g0134 a0001c0001t0005g0135 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0297 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 |
35 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0002g0013 others(32): 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 | a0001c0001t0003g0021 a0001c0001t0003g0223 a0001c0001t0003g0224 others(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 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0128 others(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 | a0005c0007t0016g0132 | 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 | a0001c0001t0004g0106 a0001c0001t0005g0103 a0004c0005t0003g0022 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0004g0137 others(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 | 127 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(124): Show |
133 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(130): 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 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(131): Show |
140 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(137): 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 | a0001c0001t0001g0140 | 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 | 223 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(220): Show |
234 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(231): 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 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(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 | a0001c0001t0001g0025 | 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 | 216 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(213): Show |
226 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.8+3009T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563241 | |||||||
| chr6:158563331 | T | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(218): Show |
232 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(229): 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 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | a0001c0001t0005g0024 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0003g0222 | 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 | 216 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(213): Show |
226 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.8+3350T>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563582 | |||||||
| chr6:158563649 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
230 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.8+3417A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563649 | |||||||
| chr6:158563679 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0144 a0001c0001t0001g0145 others(9): Show |
14 | HG00438.hp1 HG01243.hp1 HG01258.hp1 others(11): 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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(307): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.8+3469A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158563701 | |||||||
| chr6:158563729 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(221): Show |
235 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(232): 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 |
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 | a0001c0001t0002g0156 | 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 | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
230 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(227): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0003g0220 a0001c0001t0003g0221 |
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 | 5 | a0001c0001t0001g0012 a0001c0001t0002g0185 a0001c0001t0002g0186 others(2): 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 | 220 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
230 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(227): 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 | a0001c0001t0002g0157 | 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 | a0001c0001t0004g0107 | 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 |
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 | a0001c0001t0017g0281 | 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 | a0001c0001t0017g0281 | 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(92): Show |
99 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(96): 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 | a0001c0001t0001g0174 a0001c0001t0002g0011 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0038 | 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 | 198 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(195): Show |
208 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(205): 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 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
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 | a0001c0001t0001g0311 | 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 | 29 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(26): 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 | 186 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(183): Show |
193 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.8+5542G>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158565774 | |||||||
| chr6:158565928 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(234): Show |
249 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(246): 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 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0235 | 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 |
189 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(186): Show |
199 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(196): 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 | a0001c0001t0003g0222 | 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 | 232 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(229): Show |
244 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(241): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 221 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(218): Show |
231 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(228): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0236 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0052 a0001c0001t0011g0053 |
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 | a0001c0001t0001g0237 | 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 | 223 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(220): Show |
233 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(230): 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 | a0001c0001t0001g0007 a0001c0001t0001g0088 a0001c0001t0001g0093 |
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 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(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 | a0001c0001t0001g0238 | 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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(219): Show |
232 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(229): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0004g0048 | 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 | a0001c0001t0028g0123 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0004g0114 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0003g0118 others(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 | a0001c0001t0002g0177 | 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 | a0001c0001t0005g0023 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0195 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0004g0054 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0004g0117 a0001c0001t0025g0116 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | 223 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(220): Show |
235 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(232): 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 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0007g0086 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0305 a0001c0001t0003g0306 a0001c0001t0003g0310 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0089 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0195 a0001c0001t0001g0232 others(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 | a0001c0001t0005g0135 | 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 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(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 | a0001c0001t0005g0135 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0024 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0088 others(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 | 45 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0159 others(42): 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 | a0001c0001t0001g0302 | 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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(99): Show |
107 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(104): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0013g0139 | 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 | 17 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0144 others(14): Show |
19 | HG00438.hp1 HG01167.hp1 HG01243.hp1 others(16): 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0276 a0001c0001t0017g0281 a0001c0001t0021g0304 |
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 | a0001c0001t0009g0036 | 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 | a0001c0001t0005g0024 | 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 | a0001c0001t0001g0084 | 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 | 100 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(97): Show |
103 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(100): 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | a0001c0001t0005g0018 | 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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(131): Show |
139 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(136): 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 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
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 | a0001c0001t0002g0020 | 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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(221): Show |
236 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.9-2506A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 1/16 | chr6 | 158570914 | |||||||
| chr6:158570920 | G | GT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0152 a0001c0001t0001g0195 others(11): Show |
14 | HG01243.hp1 HG02071.hp1 HG02109.hp2 others(11): 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 | a0001c0001t0001g0056 a0001c0001t0001g0283 a0001c0001t0002g0013 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 30 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(27): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0135 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0240 | 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 | 43 | a0001c0001t0001g0012 a0001c0001t0001g0141 a0001c0001t0002g0010 others(40): 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 |
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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0205 a0001c0001t0002g0206 others(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 | a0001c0001t0001g0297 | 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 | a0001c0001t0002g0175 | 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 | 38 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0174 others(35): 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 | a0001c0001t0004g0054 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0253 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0262 a0001c0001t0018g0263 |
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 | a0001c0001t0004g0078 | 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 | a0001c0001t0001g0141 a0004c0005t0003g0022 |
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 | a0001c0001t0002g0010 a0001c0001t0002g0157 a0001c0001t0002g0160 others(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 | a0001c0001t0026g0131 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0280 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0038 a0001c0001t0002g0181 |
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 | a0001c0001t0001g0141 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 |
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 | 138 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(135): Show |
144 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(141): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0012 a0001c0001t0002g0181 |
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 | a0001c0001t0002g0157 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0021 a0001c0001t0003g0091 others(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 | a0001c0001t0003g0015 a0001c0001t0003g0021 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0136 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0288 a0001c0001t0002g0157 a0001c0001t0002g0169 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0002c0003t0004g0003 |
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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0002c0003t0004g0003 |
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 | 196 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(193): Show |
208 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(205): 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0078 others(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 | a0001c0001t0003g0021 a0001c0001t0003g0091 a0001c0001t0003g0092 others(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 | a0001c0001t0001g0307 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 |
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 | 115 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(112): Show |
120 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(117): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0005g0023 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0005g0098 a0001c0001t0005g0191 a0001c0001t0005g0207 others(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 | a0001c0001t0030g0033 | 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 | 121 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0039 others(118): 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 a0001c0001t0026g0131 |
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 | a0001c0001t0027g0081 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
246 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(243): 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0017g0281 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 |
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 | 109 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0004g0137 a0001c0001t0004g0138 |
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 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0004g0107 | 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0005g0098 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0002g0173 | 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 | a0001c0001t0001g0032 | 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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(307): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0005g0023 | 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 | a0001c0001t0004g0106 | 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 | 112 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(109): 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 | a0001c0001t0026g0131 | 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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0261 | 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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): 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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0005g0135 a0005c0007t0016g0132 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 92 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(89): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(111): Show |
119 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(116): 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 | a0001c0001t0002g0176 a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(114): 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 | 112 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(109): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0206 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0003g0306 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0004c0005t0003g0022 | 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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0103 | 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 | 12 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0057 others(9): 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 | 135 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(132): Show |
141 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(138): 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 | a0001c0001t0001g0047 a0001c0001t0001g0309 a0001c0001t0002g0010 others(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 | a0001c0001t0001g0274 | 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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(114): 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0004g0054 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0005g0098 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0004g0117 a0001c0001t0025g0116 |
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 | a0001c0001t0001g0244 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0102 a0001c0001t0002g0175 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 112 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(109): 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.113-1402delG | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 2/16 | chr6 | 158579537 | |||||||
| chr6:158579576 | G | A | 1 | a0001c0001t0003g0306 | 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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0002c0003t0004g0003 |
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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0002g0020 a0001c0001t0002g0172 a0001c0001t0029g0162 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0005g0018 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0165 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0095 |
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 | 113 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(110): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 121 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(118): 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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0057 others(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 | 107 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(104): Show |
113 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(110): 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 | a0001c0001t0001g0044 a0001c0001t0001g0141 a0001c0001t0001g0145 others(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 | 68 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): 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 | a0001c0001t0001g0040 a0001c0001t0002g0034 a0001c0001t0003g0021 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0095 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0103 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0004g0122 | 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 | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(306): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
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 | a0001c0001t0027g0081 | 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 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0284 a0001c0001t0001g0288 others(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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | 40 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(37): 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 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
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 | a0001c0002t0001g0101 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(114): 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 | a0001c0001t0026g0131 | 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 | 127 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(124): Show |
134 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(131): 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 | a0001c0001t0003g0015 | 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 | a0001c0001t0004g0114 | 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 | 127 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(124): Show |
134 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(131): 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 | a0001c0001t0005g0023 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0078 |
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 | a0001c0001t0002g0176 a0001c0001t0005g0189 a0001c0001t0005g0190 others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 242 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(239): Show |
254 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(251): 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 | a0001c0001t0003g0229 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 115 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(112): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0002g0186 | 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 | 219 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(216): Show |
229 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(226): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0015g0030 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0076 a0001c0001t0001g0293 others(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 | a0001c0001t0017g0281 | 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 | a0004c0005t0003g0022 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0163 a0001c0001t0002g0164 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0008g0239 a0001c0001t0008g0266 a0001c0001t0008g0270 others(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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0247 |
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 | 204 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(201): Show |
215 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(212): 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0273 | 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 | a0001c0008t0001g0075 | 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 | a0001c0001t0005g0024 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 195 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(192): Show |
205 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(202): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0035 a0001c0001t0012g0215 |
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 | 209 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(206): Show |
220 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(217): 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0072 others(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 | 32 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(29): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0003g0217 | 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 | a0001c0001t0001g0153 | 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(235): Show |
250 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(247): 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 | a0001c0001t0026g0131 | 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 | 74 | a0001c0001t0001g0105 a0001c0001t0001g0305 a0001c0001t0003g0014 others(71): 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0017g0281 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(179): Show |
190 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(187): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0248 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
182 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.492+3060T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158592842 | |||||||
| chr6:158592903 | G | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(164): Show |
176 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(173): 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 | a0001c0001t0014g0249 | 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 | 33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(168): Show |
180 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(177): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0002t0001g0009 a0001c0002t0001g0100 a0001c0002t0001g0101 others(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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | a0001c0001t0005g0023 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0001g0299 | 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 | a0004c0005t0003g0022 | 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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 117 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(114): Show |
124 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(121): 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
182 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.492+4301A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594083 | |||||||
| chr6:158594099 | CT | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(114): Show |
124 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(121): 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0001g0299 others(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 | 117 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(114): Show |
124 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.492+4338T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158594120 | |||||||
| chr6:158594211 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
182 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(179): 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 | a0001c0001t0026g0131 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): 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 | a0001c0001t0026g0131 | 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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0001t0008g0266 a0001c0001t0008g0270 |
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 | a0001c0001t0005g0098 a0001c0001t0005g0135 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0004g0106 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | a0001c0001t0004g0106 | 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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0001t0002g0169 | 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 | 165 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(162): Show |
174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.492+5532C>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595314 | |||||||
| chr6:158595323 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.492+5675C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595457 | |||||||
| chr6:158595483 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.492+5701T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158595483 | |||||||
| chr6:158595592 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
182 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(179): 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 | a0001c0001t0004g0137 a0001c0001t0004g0138 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0103 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0005g0135 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0003g0142 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.492+6518C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596300 | |||||||
| chr6:158596313 | G | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.492+6873C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596655 | |||||||
| chr6:158596823 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
182 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(179): 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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.492+7097G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158596879 | |||||||
| chr6:158596887 | C | G | 33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0002c0003t0004g0003 |
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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0084 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0034 | 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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(166): Show |
178 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.493-7183C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598084 | |||||||
| chr6:158598273 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0005g0135 | 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(235): Show |
250 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.493-6759A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598508 | |||||||
| chr6:158598625 | GT | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(162): Show |
173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): 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 | a0001c0001t0004g0128 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0024 |
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 | a0001c0001t0005g0103 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0014g0249 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.493-6411G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158598856 | |||||||
| chr6:158598863 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0026g0131 | 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 | 162 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(159): Show |
170 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(167): 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0003g0224 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0005g0018 a0001c0001t0005g0024 |
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 | a0001c0001t0001g0097 a0001c0002t0001g0009 a0001c0002t0001g0100 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0030g0033 | 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 |
14 | a0001c0001t0003g0014 a0001c0001t0003g0091 a0001c0001t0003g0118 others(11): 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 | a0001c0001t0001g0305 a0001c0001t0003g0021 a0001c0001t0003g0092 others(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 | a0001c0001t0003g0015 a0001c0001t0003g0213 a0001c0001t0003g0306 |
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 | a0001c0001t0003g0216 a0001c0001t0003g0224 a0001c0001t0012g0215 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0056 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0094 a0001c0001t0004g0107 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0269 a0001c0001t0001g0287 others(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 | 156 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(153): Show |
163 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(160): 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 | 1 | a0001c0001t0001g0012 | 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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0021 a0001c0001t0003g0091 others(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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.493-4323T>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158600944 | |||||||
| chr6:158601087 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(199): Show |
213 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(210): 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 | a0001c0001t0001g0097 a0001c0002t0001g0009 a0001c0002t0001g0100 others(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 | a0001c0001t0022g0291 | 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 | a0001c0001t0001g0105 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0005g0024 | 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 | a0001c0001t0007g0086 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(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 | 107 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(104): Show |
112 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(109): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0161 a0001c0001t0002g0168 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0006g0005 a0001c0001t0006g0060 a0001c0001t0006g0064 |
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 | a0001c0001t0004g0078 | 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 | a0001c0001t0007g0066 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0003g0218 a0001c0001t0003g0219 |
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 | a0001c0001t0002g0163 | 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 | a0001c0001t0001g0069 | 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 | 163 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(160): Show |
171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0088 others(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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(116): Show |
125 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(122): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): 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 | a0001c0001t0003g0218 a0001c0001t0003g0219 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(203): Show |
217 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.493-2286A>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158602981 | |||||||
| chr6:158602982 | A | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(203): Show |
217 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(214): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0008t0001g0075 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0026g0131 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0024 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0262 a0001c0001t0002g0010 others(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 | a0001c0001t0001g0251 | 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 | 164 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0273 | 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 | 30 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(27): 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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0255 a0001c0001t0001g0285 a0001c0001t0002g0158 others(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 | 155 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(152): Show |
163 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(160): 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0002g0156 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 162 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(159): Show |
170 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(167): 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 | a0001c0001t0026g0131 | 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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.493-1043A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604224 | |||||||
| chr6:158604311 | A | G | 6 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0211 others(3): 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 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
148 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(145): 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 | 33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0010g0271 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0105 a0001c0001t0002g0013 a0001c0001t0002g0204 others(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 | a0001c0001t0005g0103 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0094 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 174 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(171): Show |
182 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.493-291T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158604976 | |||||||
| chr6:158605129 | AAAGT | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(99): Show |
107 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(104): 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 | a0001c0001t0005g0210 | 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 | 32 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(29): 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 | a0001c0001t0001g0083 a0001c0001t0002g0034 a0001c0001t0002g0177 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0102 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0257 a0001c0001t0001g0262 others(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 | a0001c0001t0002g0079 a0001c0001t0002g0170 a0001c0001t0002g0185 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0104 a0001c0001t0002g0206 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 |
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 | a0001c0001t0005g0210 | 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 | a0001c0001t0001g0097 a0001c0002t0001g0009 a0001c0002t0001g0100 others(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 | 100 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(97): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.493-115G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605152 | |||||||
| chr6:158605154 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(106): Show |
114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): 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 | a0001c0001t0005g0018 a0001c0001t0005g0024 a0001c0001t0005g0189 others(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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.493-111G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 6/16 | chr6 | 158605156 | |||||||
| chr6:158605158 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0002g0183 | 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 | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(225): Show |
239 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(236): 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 | a0001c0001t0001g0017 a0001c0001t0001g0284 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0082 a0001c0001t0001g0083 |
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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.573+743G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 7/16 | chr6 | 158606090 | |||||||
| chr6:158606127 | C | T | 33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | 5 | a0001c0001t0001g0012 a0001c0001t0001g0262 a0001c0001t0010g0241 others(2): 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 | a0001c0001t0004g0106 | 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 |
33 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(30): 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 | a0001c0001t0026g0131 | 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 |
108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): 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 | 34 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(31): 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0004g0106 | 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 | 34 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(31): 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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0308 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0163 a0001c0001t0002g0164 |
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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.673+101G>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 8/16 | chr6 | 158607444 | |||||||
| chr6:158607456 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0002g0165 | 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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0003g0222 | 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 | 109 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(106): Show |
114 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(111): 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0004g0129 | 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 | a0001c0001t0002g0177 | 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 | a0001c0001t0001g0197 | 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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(139): Show |
149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | 34 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(31): 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 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | 148 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(145): Show |
155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0272 others(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 | 29 | a0001c0001t0001g0305 a0001c0001t0003g0014 a0001c0001t0003g0015 others(26): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(110): 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | 196 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(193): Show |
205 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(202): 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0206 |
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 | a0001c0001t0001g0275 | 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 | a0001c0001t0005g0018 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0296 |
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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0004g0108 a0001c0001t0004g0109 |
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 | a0005c0007t0016g0132 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0003g0310 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 104 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(101): Show |
109 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(106): 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): 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 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0057 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0152 | 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.896+2772G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158611522 | |||||||
| chr6:158611638 | C | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(190): Show |
203 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(200): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0017g0281 | 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 | 34 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(31): 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 | 18 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0119 others(15): Show |
20 | HG00438.hp1 HG01069.hp2 HG01167.hp1 others(17): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0022g0291 | 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 | 73 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(70): 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
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 | a0001c0001t0021g0304 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0057 | 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 | 84 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0240 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0004c0005t0003g0022 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0309 |
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 | a0001c0001t0005g0103 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): 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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0004c0005t0003g0022 | 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 | a0001c0001t0003g0091 | 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 | a0001c0001t0002g0011 a0001c0001t0002g0102 a0001c0001t0002g0175 others(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 | a0001c0001t0005g0018 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0003g0223 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0206 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0247 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 191 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(188): Show |
201 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(198): 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 | 40 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(37): 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0205 a0001c0001t0002g0206 |
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 | a0001c0001t0001g0297 | 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 | a0001c0001t0004g0122 | 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 | a0001c0001t0005g0209 | 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 | 160 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(157): Show |
168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0026g0131 | 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 | 1 | a0001c0001t0003g0014 | 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 | a0001c0001t0003g0228 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0297 |
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 | a0001c0001t0004g0122 | 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 | a0001c0001t0004g0122 | 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 | a0001c0001t0004g0122 | 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 | a0001c0001t0026g0131 | 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 | 192 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(189): Show |
202 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.897-7301G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158616249 | |||||||
| chr6:158616276 | CTCTT | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(189): Show |
202 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(199): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0004g0112 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0004g0106 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0098 | 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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0001g0062 a0001c0001t0001g0244 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(100): Show |
108 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(105): 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0251 a0001c0001t0001g0277 |
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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0003c0006t0001g0045 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0025g0116 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0174 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0003g0015 | 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 | a0001c0001t0005g0135 | 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | a0001c0001t0005g0207 | 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 | a0001c0001t0002g0173 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): 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 | a0001c0001t0001g0069 a0001c0001t0007g0066 a0001c0001t0007g0067 others(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 | a0001c0001t0003g0229 | 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0025g0116 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0003c0006t0001g0045 | 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 | a0001c0001t0004g0126 | 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 | a0001c0001t0006g0005 a0001c0001t0006g0060 a0001c0001t0006g0064 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0050 a0001c0001t0002g0010 a0001c0001t0002g0034 others(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 | 131 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(128): Show |
137 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(134): 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 | a0001c0001t0004g0138 a0001c0001t0006g0005 a0001c0001t0006g0060 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0014g0249 | 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 | a0001c0001t0004g0117 | 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 | a0001c0001t0004g0108 a0001c0001t0004g0109 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0301 | 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 | 192 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(189): Show |
202 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(199): 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 | a0001c0001t0025g0116 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0006g0005 a0001c0001t0006g0060 a0001c0001t0006g0064 |
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 | a0001c0001t0003g0021 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0002g0165 | 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 | a0001c0001t0004g0117 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0003g0212 | 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 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0003g0143 | 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 | 159 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(156): Show |
167 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(164): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0174 |
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 | a0001c0001t0001g0051 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0026g0131 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0205 a0001c0001t0002g0206 |
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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | |||||||
| chr6:158622643 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(190): Show |
203 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(200): 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(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 | a0001c0001t0003g0021 a0001c0001t0003g0091 a0001c0001t0003g0092 others(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 | 26 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0118 others(23): 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 | a0001c0001t0001g0017 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | a0001c0001t0004g0110 a0001c0001t0004g0111 a0001c0001t0004g0112 |
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 | a0001c0001t0005g0023 a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(110): Show |
118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.897-266A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623284 | |||||||
| chr6:158623408 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.897-142T>C | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 10/16 | chr6 | 158623408 | |||||||
| chr6:158623762 | AT | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(224): Show |
238 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(235): 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 | a0001c0001t0001g0275 a0001c0001t0002g0013 a0001c0001t0002g0204 others(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 | 159 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(156): Show |
167 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(164): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 90 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(87): 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 | a0001c0001t0027g0081 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0005g0018 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0003g0217 a0001c0001t0003g0223 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0003g0224 | 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 | 159 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(156): Show |
167 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.954+655G>A | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624262 | |||||||
| chr6:158624327 | A | G | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | a0001c0001t0001g0140 | 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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.955-694C>T | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 11/16 | chr6 | 158624410 | |||||||
| chr6:158624468 | G | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(108): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0005g0024 | 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 | a0001c0001t0026g0131 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0006g0064 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0004g0110 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0301 | 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 | a0001c0001t0002g0020 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
247 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(244): 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0044 others(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 | a0001c0001t0002g0172 | 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 | a0001c0001t0004g0054 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0003g0134 a0001c0001t0003g0142 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0003g0212 a0001c0001t0004g0046 a0001c0001t0004g0048 others(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 | 31 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(28): 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 | a0001c0001t0001g0038 a0001c0001t0026g0131 |
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 | a0001c0001t0005g0189 a0001c0001t0005g0190 |
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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | 34 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(31): 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(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 | a0001c0001t0005g0103 | 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 | 118 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(115): Show |
124 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(121): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0004g0106 a0001c0001t0004g0117 a0001c0001t0004g0122 others(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 | a0001c0001t0004g0106 a0001c0001t0004g0117 a0001c0001t0004g0122 others(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 | a0001c0001t0005g0018 a0001c0001t0005g0024 |
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 | a0001c0001t0003g0015 a0001c0001t0003g0216 a0001c0001t0012g0215 |
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 | a0001c0001t0001g0283 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | 234 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(231): Show |
246 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(243): 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 | a0001c0001t0003g0221 | 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | a0001c0001t0005g0103 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(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 | a0001c0001t0005g0018 a0001c0001t0005g0024 a0001c0001t0005g0189 others(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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0002g0167 | 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | a0001c0001t0025g0116 | 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1110-796A>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627612 | |||||||
| chr6:158627613 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1110-795C>G | TMEM181 | ENSG00000146433.10 | transcript | ENST00000684151.1 | protein_coding | 13/16 | chr6 | 158627613 | |||||||
| chr6:158627615 | G | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | a0001c0001t0001g0052 a0001c0001t0011g0053 |
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 | a0003c0006t0001g0045 | 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 | 234 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(231): Show |
246 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(243): 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 | a0001c0001t0010g0241 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0018g0263 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0202 |
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 | a0005c0007t0016g0132 | 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 | a0001c0001t0026g0131 | 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 | a0001c0001t0003g0143 | 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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(238): Show |
253 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(250): 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 | a0001c0001t0001g0282 | 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 | a0004c0005t0003g0022 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 |
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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0005g0098 a0001c0001t0005g0191 |
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 | a0001c0001t0003g0015 a0001c0001t0003g0216 |
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 | a0001c0001t0004g0122 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0309 others(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 | a0001c0001t0005g0098 | 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 | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
117 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(114): 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 | a0001c0001t0022g0291 | 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 | a0001c0001t0005g0018 a0001c0001t0005g0023 a0001c0001t0005g0024 others(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 | a0001c0001t0001g0302 | 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | a0001c0001t0002g0013 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0048 a0001c0001t0004g0054 others(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 | a0001c0001t0026g0131 | 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 | 110 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(107): Show |
115 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(112): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0200 | 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 | 120 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(117): Show |
126 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(123): 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0005g0135 | 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 | a0001c0001t0014g0249 | 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 | 116 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(113): 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0003g0225 | 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 | 114 | a0001c0001t0001g0305 a0001c0001t0002g0010 a0001c0001t0002g0011 others(111): 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 | 114 | a0001c0001t0001g0305 a0001c0001t0002g0010 a0001c0001t0002g0011 others(111): 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 | a0001c0001t0005g0135 | 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 | a0001c0001t0001g0253 | 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 | 32 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0021 others(29): 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(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 | a0001c0001t0001g0289 | 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 | a0001c0001t0014g0249 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(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 |